हनटिंग्टन रोग (Hindi Wikipedia)

Analysis of information sources in references of the Wikipedia article "हनटिंग्टन रोग" in Hindi language version.

refsWebsite

Global rank Hindi rank

94nih.gov

4^th place

7^th place

68doi.org

2^nd place

5^th place

34web.archive.org

1^st place

11archive.org

6^th place

4wikipedia.org

low place

2,315^th place

3elsevier.com

610^th place

1,030^th place

3hdfoundation.org

low place

3oxfordjournals.org

1,389^th place

574^th place

3sagepub.com

731^st place

398^th place

2archive.today

14^th place

26^th place

2stanford.edu

179^th place

115^th place

2wkhealth.com

low place

3,532^nd place

2hdsa.org

low place

1cma.ca

low place

1hdac.org

low place

1bentham-direct.org

low place

1bmjjournals.com

low place

2,126^th place

1nature.com

234^th place

288^th place

1wiley.com

222^nd place

151^st place

1jbc.org

4,455^th place

7,293^rd place

1huntington-study-group.org

low place

1adisonline.com

low place

1fda.gov

447^th place

1,057^th place

1webcitation.org

24^th place

38^th place

1medscape.com

719^th place

1,511^th place

1yale.edu

565^th place

1,400^th place

1ama-assn.org

3,257^th place

1,014^th place

1lww.com

2,769^th place

7,313^th place

1psychiatryonline.org

4,032^nd place

4,438^th place

1google.co.uk

504^th place

117^th place

1royalsociety.org

2,415^th place

1,234^th place

1hda.org.uk

low place

1bbc.co.uk

8^th place

13^th place

1huntington-assoc.com

low place

1jneurosci.org

low place

1sciencedaily.com

993^rd place

647^th place

1plosone.org

4,730^th place

5,779^th place

adisonline.com

Frank S, Jankovic J. (2010). "Advances in the Pharmacological Management of Huntington's Disease". Drugs. 70 (5): 561–71. डीओआई:10.2165/11534430-000000000-00000. पीएमआईडी 20329804. मूल से से 8 अक्तूबर 2011 को पुरालेखित।. अभिगमन तिथि: 15 जनवरी 2011. {{cite journal}}: Check date values in: |archive-date= (help)

ama-assn.org

archneur.ama-assn.org

Irwin A Brody, Robert H Wilkins (1967). "Huntington's Chorea". Arch Neurol. 17 (3): 331. डीओआई:10.1001/archneur.1967.00470270109013. पीएमआईडी 4228262. 8 मार्च 2012 को मूल से पुरालेखित. अभिगमन तिथि: 15 जनवरी 2011.

archive.org

Kremer B (2002). "Clinical neurology of Huntington's disease". In Bates G, Harper P, and Jones L (ed.). Huntington's Disease – Third Edition. Oxford: Oxford University Press. pp. 28–53. ISBN 0-19-851060-8.{{cite book}}: CS1 maint: multiple names: editors list (link)
van Duijn E, Kingma EM, van der Mast RC (2007). "Psychopathology in verified Huntington's disease gene carriers". J Neuropsychiatry Clin Neurosci. 19 (4): 441–8. डीओआई:10.1176/appi.neuropsych.19.4.441. पीएमआईडी 18070848.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Passarge, E (2001). Color Atlas of Genetics (2nd ed.). Thieme. p. 142. ISBN 0-86577-958-9.
Wexler NS, Young AB, Tanzi RE; et al. (1987). "Homozygotes for Huntington's disease". Nature. 326 (6109): 194–197. डीओआई:10.1038/326194a0. पीएमआईडी 2881213. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
"Guidelines for the molecular genetics predictive test in Huntington's disease. International Huntington Association (IHA) and the World Federation of Neurology (WFN) Research Group on Huntington's Chorea". Neurology. 44 (8): 1533–6. 1994. पीएमआईडी 8058167.
Harper P (2002). "Genetic counselling and presymptomatic testing". In Bates G, Harper P, and Jones L (ed.). Huntington's Disease – Third Edition. Oxford: Oxford University Press. pp. 198–242. ISBN 0-19-851060-8.{{cite book}}: CS1 maint: multiple names: editors list (link)
Crauford D and Snowden J (2002). "Neuropyschological and neuropsychiatric aspects of Huntington's disease". In Bates G, Harper P, and Jones L (ed.). Huntington's Disease – Third Edition. Oxford: Oxford University Press. pp. 62–87. ISBN 0-19-851060-8.{{cite book}}: CS1 maint: multiple names: editors list (link)
Harper P (2002). "The epidemiology of Huntington's disease". In Bates G, Harper P, and Jones L (ed.). Huntington's Disease – Third Edition. Oxford: Oxford University Press. pp. 159–189. ISBN 0-19-851060-8.{{cite book}}: CS1 maint: multiple names: editors list (link)
Driver-Dunckley E, Caviness JN. (2007). "Huntington's disease". In Schapira AHV (ed.). Neurology and Clinical Neuroscience. Mosby Elsevier. pp. 879–885. ISBN 978-0323033541.
Wexler AR (2002). "Chorea and community in a 19th-century town". Bull Hist Med. 76 (3): 495–527. डीओआई:10.1353/bhm.2002.0150. पीएमआईडी 12486915.
Braude PR, De Wert GM, Evers-Kiebooms G, Pettigrew RA, Geraedts JP (1998). "Non-disclosure preimplantation genetic diagnosis for Huntington's disease: practical and ethical dilemmas". Prenat. Diagn. 18 (13): 1422–6. डीओआई:10.1002/(SICI)1097-0223(199812)18:13<1422::AID-PD499>3.0.CO;2-R. पीएमआईडी 9949442. अभिगमन तिथि: 2009-04-01.{{cite journal}}: CS1 maint: multiple names: authors list (link)

archive.today

Ridley RM, Frith CD, Crow TJ, Conneally PM (1988). "Anticipation in Huntington's disease is inherited through the male line but may originate in the female". Journal of Medical Genetics. 25 (9): 589–595. डीओआई:10.1136/jmg.25.9.589. पीएमसी 1051535. पीएमआईडी 2972838. 14 जुलाई 2012 को मूल से पुरालेखित. अभिगमन तिथि: 15 जनवरी 2011.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Squitieri F, Gellera C, Cannella M; et al. (2003). "Homozygosity for CAG mutation in Huntington disease is associated with a more severe clinical course". Brain. 126 (Pt 4): 946–55. डीओआई:10.1093/brain/awg077. पीएमआईडी 12615650. 20 दिसंबर 2012 को मूल से पुरालेखित. अभिगमन तिथि: 15 जनवरी 2011. {{cite journal}}: Check date values in: |archive-date= (help); Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)

bbc.co.uk

news.bbc.co.uk

"BBC article: Genetic data banned for insurers". BBC. 2008-06-13. अभिगमन तिथि: 2008-08-10.

bentham-direct.org

Katsuno M, Banno H, Suzuki K; et al. (2008). "Molecular genetics and biomarkers of polyglutamine diseases". Curr. Mol. Med. 8 (3): 221–34. डीओआई:10.2174/156652408784221298. पीएमआईडी 18473821. मूल से से 13 फ़रवरी 2009 को पुरालेखित।. अभिगमन तिथि: 2009-04-01. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)

bmjjournals.com

jmg.bmjjournals.com

Ridley RM, Frith CD, Crow TJ, Conneally PM (1988). "Anticipation in Huntington's disease is inherited through the male line but may originate in the female". Journal of Medical Genetics. 25 (9): 589–595. डीओआई:10.1136/jmg.25.9.589. पीएमसी 1051535. पीएमआईडी 2972838. 14 जुलाई 2012 को मूल से पुरालेखित. अभिगमन तिथि: 15 जनवरी 2011.{{cite journal}}: CS1 maint: multiple names: authors list (link)

cma.ca

Montoya A, Price BH, Menear M, Lepage M (2006). "Brain imaging and cognitive dysfunctions in Huntington's disease" (PDF). J Psychiatry Neurosci. 31 (1): 21–9. पीएमसी 1325063. पीएमआईडी 16496032. मूल से (PDF) से 23 मार्च 2016 को पुरालेखित।. अभिगमन तिथि: 2009-04-01.{{cite journal}}: CS1 maint: multiple names: authors list (link)

doi.org

Walker FO (2007). "Huntington's disease". Lancet. 369 (9557): 218. डीओआई:10.1016/S0140-6736(07)60111-1. पीएमआईडी 17240289.
Walker FO (2007). "Huntington's disease". Lancet. 369 (9557): 219. डीओआई:10.1016/S0140-6736(07)60111-1. पीएमआईडी 17240289.
Aziz NA, van der Marck MA, Pijl H, Olde Rikkert MG, Bloem BR, Roos RA (2008). "Weight loss in neurodegenerative disorders". J. Neurol. 255 (12): 1872–80. डीओआई:10.1007/s00415-009-0062-8. पीएमआईडी 19165531.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Gagnon JF, Petit D, Latreille V, Montplaisir J (2008). "Neurobiology of sleep disturbances in neurodegenerative disorders". Curr. Pharm. Des. 14 (32): 3430–45. डीओआई:10.2174/138161208786549353. पीएमआईडी 19075719.{{cite journal}}: CS1 maint: multiple names: authors list (link)
van Duijn E, Kingma EM, van der Mast RC (2007). "Psychopathology in verified Huntington's disease gene carriers". J Neuropsychiatry Clin Neurosci. 19 (4): 441–8. डीओआई:10.1176/appi.neuropsych.19.4.441. पीएमआईडी 18070848.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Walker FO (2007). "Huntington's disease". Lancet. 369 (9557): 221. डीओआई:10.1016/S0140-6736(07)60111-1. पीएमआईडी 17240289.
Walker FO (2007). "Huntington's disease". Lancet. 369 (9557): 220. डीओआई:10.1016/S0140-6736(07)60111-1. पीएमआईडी 17240289.
Katsuno M, Banno H, Suzuki K; et al. (2008). "Molecular genetics and biomarkers of polyglutamine diseases". Curr. Mol. Med. 8 (3): 221–34. डीओआई:10.2174/156652408784221298. पीएमआईडी 18473821. मूल से से 13 फ़रवरी 2009 को पुरालेखित।. अभिगमन तिथि: 2009-04-01. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
Walker FO (2007). "Huntington's disease". Lancet. 369 (9557): 222. डीओआई:10.1016/S0140-6736(07)60111-1. पीएमआईडी 17240289.
Nance MA, Myers RH (2001). "Juvenile onset Huntington's disease—clinical and research perspectives". Ment Retard Dev Disabil Res Rev. 7 (3): 153–7. डीओआई:10.1002/mrdd.1022. पीएमआईडी 11553930.
Ridley RM, Frith CD, Crow TJ, Conneally PM (1988). "Anticipation in Huntington's disease is inherited through the male line but may originate in the female". Journal of Medical Genetics. 25 (9): 589–595. डीओआई:10.1136/jmg.25.9.589. पीएमसी 1051535. पीएमआईडी 2972838. 14 जुलाई 2012 को मूल से पुरालेखित. अभिगमन तिथि: 15 जनवरी 2011.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Semaka A, Creighton S, Warby S, Hayden MR (2006). "Predictive testing for Huntington disease: interpretation and significance of intermediate alleles". Clin. Genet. 70 (4): 283–94. डीओआई:10.1111/j.1399-0004.2006.00668.x. पीएमआईडी 16965319.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Squitieri F, Gellera C, Cannella M; et al. (2003). "Homozygosity for CAG mutation in Huntington disease is associated with a more severe clinical course". Brain. 126 (Pt 4): 946–55. डीओआई:10.1093/brain/awg077. पीएमआईडी 12615650. 20 दिसंबर 2012 को मूल से पुरालेखित. अभिगमन तिथि: 15 जनवरी 2011. {{cite journal}}: Check date values in: |archive-date= (help); Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
Wexler NS, Young AB, Tanzi RE; et al. (1987). "Homozygotes for Huntington's disease". Nature. 326 (6109): 194–197. डीओआई:10.1038/326194a0. पीएमआईडी 2881213. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
Goehler H, Lalowski M, Stelzl U; et al. (2004). "A protein interaction network links GIT1, an enhancer of Huntingtin aggregation, to Huntington's disease". Mol. Cell. 15 (6): 853–65. डीओआई:10.1016/j.molcel.2004.09.016. पीएमआईडी 15383276. 5 अक्तूबर 2017 को मूल से पुरालेखित. अभिगमन तिथि: 2009-04-27. {{cite journal}}: Check date values in: |archive-date= (help); Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
Harjes P, Wanker EE (2003). "The hunt for huntingtin function: interaction partners tell many different stories". Trends Biochem. Sci. 28 (8): 425–33. डीओआई:10.1016/S0968-0004(03)00168-3. पीएमआईडी 12932731. 5 अक्तूबर 2017 को मूल से पुरालेखित. अभिगमन तिथि: 2009-04-27. {{cite journal}}: Check date values in: |archive-date= (help)
Cattaneo E, Zuccato C, Tartari M (2005). "Normal huntingtin function: an alternative approach to Huntington's disease". Nat. Rev. Neurosci. 6 (12): 919–30. डीओआई:10.1038/nrn1806. पीएमआईडी 16288298.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Rubinsztein DC, Carmichael J (2003). "Huntington's disease: Molecular basis of neurodegeneration". Expert Rev Mol Med. 5 (20): 1–21. डीओआई:10.1017/S1462399403006549. पीएमआईडी 14585171.
Subramaniam S, Sixt KM, Barrow R, Snyder SH (2009). "Rhes, a striatal specific protein, mediates mutant-huntingtin cytotoxicity". Science. 324 (5932): 1327–30. डीओआई:10.1126/science.1172871. पीएमसी 2745286. पीएमआईडी 19498170.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Lobsiger CS, Cleveland DW (2007). "Glial cells as intrinsic components of non-cell-autonomous neurodegenerative disease". Nat. Neurosci. 10 (11): 1355–60. डीओआई:10.1038/nn1988. पीएमआईडी 17965655.
Crossman AR (2000). "Functional anatomy of movement disorders" (PDF). J. Anat. 196 (Pt 4): 519–25. डीओआई:10.1046/j.1469-7580.2000.19640519.x. पीएमसी 1468094. पीएमआईडी 10923984.^{[मृत कड़ियाँ]}
Myers RH (2004). "Huntington's disease genetics". NeuroRx. 1 (2): 255–62. डीओआई:10.1602/neurorx.1.2.255. पीएमसी 534940. पीएमआईडी 15717026.
Burson CM, Markey KR (2001). "Genetic counseling issues in predictive genetic testing for familial adult-onset neurologic diseases". Semin Pediatr Neurol. 8 (3): 177–86. डीओआई:10.1053/spen.2001.26451. पीएमआईडी 11575847.
Hayden MR (2003). "Predictive testing for Huntington's disease: a universal model?". Lancet Neurol. 2 (3): 141–2. डीओआई:10.1016/S1474-4422(03)00317-X. पीएमआईडी 12849232. {{cite journal}}: Unknown parameter |month= ignored (help)
Kuliev A, Verlinsky Y (2005). "Preimplantation diagnosis: A realistic option for assisted reproduction and genetic practice". Curr. Opin. Obstet. Gynecol. 17 (2): 179–83. डीओआई:10.1097/01.gco.0000162189.76349.c5. पीएमआईडी 15758612. 13 अगस्त 2011 को मूल से पुरालेखित. अभिगमन तिथि: 2009-04-01.
Schneider SA, Walker RH, Bhatia KP (2007). "The Huntington's disease-like syndromes: what to consider in patients with a negative Huntington's disease gene test". Nat Clin Pract Neurol. 3 (9): 517–25. डीओआई:10.1038/ncpneuro0606. पीएमआईडी 17805246. {{cite journal}}: |access-date= requires |url= (help)CS1 maint: multiple names: authors list (link)
Frank S, Jankovic J. (2010). "Advances in the Pharmacological Management of Huntington's Disease". Drugs. 70 (5): 561–71. डीओआई:10.2165/11534430-000000000-00000. पीएमआईडी 20329804. मूल से से 8 अक्तूबर 2011 को पुरालेखित।. अभिगमन तिथि: 15 जनवरी 2011. {{cite journal}}: Check date values in: |archive-date= (help)
Walker FO (2007). "Huntington's disease". Lancet. 369 (9557): 224. डीओआई:10.1016/S0140-6736(07)60111-1. पीएमआईडी 17240289.
Bonelli RM, Wenning GK, Kapfhammer HP (2004). "Huntington's disease: present treatments and future therapeutic modalities". Int Clin Psychopharmacol. 19 (2): 51–62. डीओआई:10.1097/00004850-200403000-00001. पीएमआईडी 15076012. 1 जून 2012 को मूल से पुरालेखित. अभिगमन तिथि: 2009-04-01.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Walker FO (2007). "Huntington's disease". Lancet. 369 (9557): 225. डीओआई:10.1016/S0140-6736(07)60111-1. पीएमआईडी 17240289.
Panagiotakis PH, DiSario JA, Hilden K, Ogara M, Fang JC (2008). "DPEJ tube placement prevents aspiration pneumonia in high-risk patients". Nutr Clin Pract. 23 (2): 172–5. डीओआई:10.1177/0884533608314537. पीएमआईडी 18390785.{{cite journal}}: CS1 maint: multiple names: authors list (link)^{[मृत कड़ियाँ]}
Bilney B, Morris ME, Perry A (2003). "Effectiveness of physiotherapy, occupational therapy, and speech pathology for people with Huntington's disease: a systematic review". Neurorehabil Neural Repair. 17 (1): 12–24. डीओआई:10.1177/0888439002250448. पीएमआईडी 12645441.{{cite journal}}: CS1 maint: multiple names: authors list (link)^{[मृत कड़ियाँ]}
Zinzi P, Salmaso D, De Grandis R; et al. (2007). "Effects of an intensive rehabilitation programme on patients with Huntington's disease: a pilot study". Clin Rehabil. 21 (7): 603–13. डीओआई:10.1177/0269215507075495. पीएमआईडी 17702702. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)^{[मृत कड़ियाँ]}
Harper PS (1999). "Huntington's disease: A clinical, genetic and molecular model for polyglutamine repeat disorders". Philos. Trans. R. Soc. Lond., B, Biol. Sci. 354 (1386): 957–61. डीओआई:10.1098/rstb.1999.0446. पीएमसी 1692597. पीएमआईडी 10434293.
Andrew SE, Goldberg YP, Kremer B; et al. (1993). "The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease". Nat. Genet. 4 (4): 398–403. डीओआई:10.1038/ng0893-398. पीएमआईडी 8401589. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
Di Maio L, Squitieri F, Napolitano G; et al. (1993). "Suicide risk in Huntington's disease". J. Med. Genet. 30 (4): 293–5. डीओआई:10.1136/jmg.30.4.293. पीएमसी 1016335. पीएमआईडी 8487273. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
Gusella JF, Wexler NS, Conneally PM; et al. (1983). "A polymorphic DNA marker genetically linked to Huntington's disease". Nature. 306 (5940): 234–8. डीओआई:10.1038/306234a0. पीएमआईडी 6316146. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
Squitieri F, Andrew SE, Goldberg YP; et al. (1994). "DNA haplotype analysis of Huntington disease reveals clues to the origins and mechanisms of CAG expansion and reasons for geographic variations of prevalence". Hum. Mol. Genet. 3 (12): 2103–14. डीओआई:10.1093/hmg/3.12.2103. पीएमआईडी 7881406. 15 मार्च 2020 को मूल से पुरालेखित. अभिगमन तिथि: 15 जनवरी 2011. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
Almqvist EW, Elterman DS, MacLeod PM, Hayden MR (2001). "High incidence rate and absent family histories in one quarter of patients newly diagnosed with Huntington disease in British Columbia". Clin. Genet. 60 (3): 198–205. डीओआई:10.1034/j.1399-0004.2001.600305.x. पीएमआईडी 11595021.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Lanska DJ (2000). "George Huntington (1850–1916) and hereditary chorea". J Hist Neurosci. 9 (1): 76–89. डीओआई:10.1076/0964-704X(200004)9:1;1-2;FT076. पीएमआईडी 11232352.
Irwin A Brody, Robert H Wilkins (1967). "Huntington's Chorea". Arch Neurol. 17 (3): 331. डीओआई:10.1001/archneur.1967.00470270109013. पीएमआईडी 4228262. 8 मार्च 2012 को मूल से पुरालेखित. अभिगमन तिथि: 15 जनवरी 2011.
Davenport CB, Muncey EB (1916). "Huntington's chorea in relation to heredity and eugenics". American Journal of Insanity. 73: 195–222. डीओआई:10.1176/appi.ajp.73.2.195. 11 जून 2011 को मूल से पुरालेखित. अभिगमन तिथि: 15 जनवरी 2011.
Vessie, PR (1932). "On the transmission of Huntington's chorea for 300 years – the Bures family group". Nervous and Mental Disease. 76 (6). Baltimore: 553–573. डीओआई:10.1097/00005053-193212000-00001. अभिगमन तिथि: 2009-04-01.
Wexler AR (2002). "Chorea and community in a 19th-century town". Bull Hist Med. 76 (3): 495–527. डीओआई:10.1353/bhm.2002.0150. पीएमआईडी 12486915.
Macdonald M (1993). "A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. The Huntington's Disease Collaborative Research Group". Cell. 72 (6): 971–83. डीओआई:10.1016/0092-8674(93)90585-E. पीएमआईडी 8458085. 5 अक्तूबर 2017 को मूल से पुरालेखित. अभिगमन तिथि: 15 जनवरी 2011. {{cite journal}}: Check date values in: |archive-date= (help)
Bertram L, Tanzi RE (2005). "The genetic epidemiology of neurodegenerative disease". J. Clin. Invest. 115 (6): 1449–57. डीओआई:10.1172/JCI24761. पीएमसी 1137006. पीएमआईडी 15931380. {{cite journal}}: |access-date= requires |url= (help)
La Spada AR, Roling DB, Harding AE; et al. (1992). "Meiotic stability and genotype-phenotype correlation of the trinucleotide repeat in X-linked spinal and bulbar muscular atrophy". Nat. Genet. 2 (4): 301–4. डीओआई:10.1038/ng1292-301. पीएमआईडी 1303283. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
Sathasivam K, Hobbs C, Mangiarini L; et al. (1999). "Transgenic models of Huntington's disease". Philos. Trans. R. Soc. Lond., B, Biol. Sci. 354 (1386): 963–9. डीओआई:10.1098/rstb.1999.0447. पीएमसी 1692600. पीएमआईडी 10434294. मूल से से 23 फ़रवरी 2020 को पुरालेखित।. अभिगमन तिथि: 15 जनवरी 2011. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
Li JY, Popovic N, Brundin P (2005). "The use of the R6 transgenic mouse models of Huntington's disease in attempts to develop novel therapeutic strategies". NeuroRx. 2 (3): 447–64. डीओआई:10.1602/neurorx.2.3.447. पीएमसी 1144488. पीएमआईडी 16389308.{{cite journal}}: CS1 maint: multiple names: authors list (link)
DiFiglia M, Sapp E, Chase KO; et al. (1997). "Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brain". Science. 277 (5334): 1990–3. डीओआई:10.1126/science.277.5334.1990. पीएमआईडी 9302293. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
Davenport CB (1915). "Huntington's chorea in relation to heredity and eugenics". Proc. Natl. Acad. Sci. U.S.A. 1 (5): 283–5. डीओआई:10.1073/pnas.1.5.283. पीएमसी 1090803. पीएमआईडी 16575999.
Rollin, Bernard E. (2006). "The Regulation of Animal Research and the Emergence of Animal Ethics: A Conceptual History". Theoretical Medicine and Bioethics. 27 (4): 285–304. डीओआई:10.1007/s11017-006-9007-8. पीएमआईडी 16937023.
Doerflinger RM (2008). "The problem of deception in embryonic stem cell research". Cell Prolif. 41 Suppl 1: 65–70. डीओआई:10.1111/j.1365-2184.2008.00492.x. पीएमआईडी 18181947.
Binedell J, Soldan JR, Scourfield J, Harper PS (1996). "Huntington's disease predictive testing: the case for an assessment approach to requests from adolescents". J. Med. Genet. 33 (11): 912–8. डीओआई:10.1136/jmg.33.11.912. पीएमसी 1050784. पीएमआईडी 8950670.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Borry P, Goffin T, Nys H, Dierickx K (2008). "Predictive genetic testing in minors for adult-onset genetic diseases". Mt. Sinai J. Med. 75 (3): 287–96. डीओआई:10.1002/msj.20038. पीएमआईडी 18704981.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Braude PR, De Wert GM, Evers-Kiebooms G, Pettigrew RA, Geraedts JP (1998). "Non-disclosure preimplantation genetic diagnosis for Huntington's disease: practical and ethical dilemmas". Prenat. Diagn. 18 (13): 1422–6. डीओआई:10.1002/(SICI)1097-0223(199812)18:13<1422::AID-PD499>3.0.CO;2-R. पीएमआईडी 9949442. अभिगमन तिथि: 2009-04-01.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Walker FO (2007). "Huntington's disease". Lancet. 369 (9557): 223. डीओआई:10.1016/S0140-6736(07)60111-1. पीएमआईडी 17240289.
Coyle JT, Schwarcz R (1976). "Lesion of striatal neurones with kainic acid provides a model for Huntington's chorea". Nature. 263 (5574): 244–6. डीओआई:10.1038/263244a0. पीएमआईडी 8731.
Brouillet E, Hantraye P, Ferrante RJ, Dolan R, Leroy-Willig A, Kowall NW, Beal MF (1995). "Chronic mitochondrial energy impairment produces selective striatal degeneration and abnormal choreiform movements in primates". Proc Natl Acad Sci USA. 92 (15): 7105–7109. डीओआई:10.1073/pnas.92.15.7105. पीएमसी 41480. पीएमआईडी 7624378.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Mangiarini L, Sathasivam K, Seller M, Cozens B, Harper A, Hetherington C, Lawton M, Trottier Y, Lehrach H, Davies SW, Bates GP (1996). "Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological genotype in transgenic mice". Cell. 87 (3): 493–506. डीओआई:10.1016/S0092-8674(00)81369-0. पीएमआईडी 8898202.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Marsh JL, Pallos J and Thompson LM (2003). "Fly models of Huntington's disease". Human Molecular Genetics. 12 (2): 187–193. डीओआई:10.1093/hmg/ddg271. पीएमआईडी 12925571. 24 दिसंबर 2009 को मूल से पुरालेखित. अभिगमन तिथि: 2009-04-01. {{cite journal}}: Check date values in: |archive-date= (help)
Voisine C, Varma H, Walker N, Bates EA, Stockwell BR, Hart AC (2007). "Identification of potential therapeutic drugs for huntington's disease using Caenorhabditis elegans". PLoS ONE. 2 (6): e504. डीओआई:10.1371/journal.pone.0000504. पीएमसी 1876812. पीएमआईडी 17551584. 13 सितंबर 2011 को मूल से पुरालेखित. अभिगमन तिथि: 15 जनवरी 2011.{{cite journal}}: CS1 maint: multiple names: authors list (link) CS1 maint: unflagged free DOI (link)
Lecerf JM, Shirley TL, Zhu Q; et al. (2001). "Human single-chain Fv intrabodies counteract in situ huntingtin aggregation in cellular models of Huntington's disease". Proc. Natl. Acad. Sci. U.S.A. 98 (8): 4764–9. डीओआई:10.1073/pnas.071058398. पीएमसी 31908. पीएमआईडी 11296304. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
Miller TW, Zhou C, Gines S; et al. (2005). "A human single-chain Fv intrabody preferentially targets amino-terminal huntingtin's fragments in striatal models of Huntington's disease". Neurobiol. Dis. 19 (1–2): 47–56. डीओआई:10.1016/j.nbd.2004.11.003. पीएमआईडी 15837560. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
Harper SQ, Staber PD, He X; et al. (2005). "RNA interference improves motor and neuropathological abnormalities in a Huntington's disease mouse model". Proc. Natl. Acad. Sci. U.S.A. 102 (16): 5820–5. डीओआई:10.1073/pnas.0501507102. पीएमसी 556303. पीएमआईडी 15811941. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
Díaz-Hernández M, Torres-Peraza J, Salvatori-Abarca A; et al. (2005). "Full Motor Recovery Despite Striatal Neuron Loss and Formation of Irreversible Amyloid-Like Inclusions in a Conditional Mouse Model of Huntington's Disease". The Journal of Neuroscience. 25 (42): 9773–9781. डीओआई:10.1523/JNEUROSCI.3183-05.2005. पीएमआईडी 16237181. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
Clelland CD, Barker RA, Watts C (2008). "Cell therapy in Huntington disease". Neurosurg Focus. 24 (3–4): E9. डीओआई:10.3171/FOC/2008/24/3-4/E8. पीएमआईडी 18341412.{{cite journal}}: CS1 maint: multiple names: authors list (link)

dx.doi.org

वैन डर बर्ग जेएम, जोर्क्विस्ट एम, ब्रंडीन पी. (2009). बियॉन्ड द ब्रेन: वाइडस्प्रेड पेथॉलोजी इन हनटिंग्टन्स डिज़ीस. लैनसेट न्यूरोल. 8(8):765-74. doi:10.1016/S1474-4422(09)70178-4पमिड 19608102

elsevier.com

linkinghub.elsevier.com

Goehler H, Lalowski M, Stelzl U; et al. (2004). "A protein interaction network links GIT1, an enhancer of Huntingtin aggregation, to Huntington's disease". Mol. Cell. 15 (6): 853–65. डीओआई:10.1016/j.molcel.2004.09.016. पीएमआईडी 15383276. 5 अक्तूबर 2017 को मूल से पुरालेखित. अभिगमन तिथि: 2009-04-27. {{cite journal}}: Check date values in: |archive-date= (help); Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
Harjes P, Wanker EE (2003). "The hunt for huntingtin function: interaction partners tell many different stories". Trends Biochem. Sci. 28 (8): 425–33. डीओआई:10.1016/S0968-0004(03)00168-3. पीएमआईडी 12932731. 5 अक्तूबर 2017 को मूल से पुरालेखित. अभिगमन तिथि: 2009-04-27. {{cite journal}}: Check date values in: |archive-date= (help)
Macdonald M (1993). "A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. The Huntington's Disease Collaborative Research Group". Cell. 72 (6): 971–83. डीओआई:10.1016/0092-8674(93)90585-E. पीएमआईडी 8458085. 5 अक्तूबर 2017 को मूल से पुरालेखित. अभिगमन तिथि: 15 जनवरी 2011. {{cite journal}}: Check date values in: |archive-date= (help)

fda.gov

"FDA Approves First Drug for Treatment of Chorea in Huntington's Disease". FDA Approves First Drug for Treatment of Chorea in Huntington's Disease. U.S. Food and Drug Administration. अगस्त 15, 2008. 1 जून 2012 को मूल से पुरालेखित. अभिगमन तिथि: 2008-08-10.

google.co.uk

scholar.google.co.uk

Vessie, PR (1932). "On the transmission of Huntington's chorea for 300 years – the Bures family group". Nervous and Mental Disease. 76 (6). Baltimore: 553–573. डीओआई:10.1097/00005053-193212000-00001. अभिगमन तिथि: 2009-04-01.

hda.org.uk

"HDA research news—medical research into treatment & prevention on hda.org.uk". Huntington's Disease Association-United Kingdom. 2009. 31 मई 2009 को मूल से पुरालेखित. अभिगमन तिथि: 2008-08-10.

hdac.org

"Booklet by the Huntington Society of Canada" (PDF). Caregiver's Handbook for Advanced-Stage Huntington Disease. HD Society of Canada. 2007-04-11. मूल से (PDF) से 25 जून 2008 को पुरालेखित।. अभिगमन तिथि: 2008-08-10.

hdfoundation.org

"The Venezuela Huntington's disease project". Hereditary Disease Foundation website. Hereditary Disease Foundation. 2008. मूल से से 26 अक्तूबर 2008 को पुरालेखित।. अभिगमन तिथि: 2008-09-08. {{cite web}}: Check date values in: |archive-date= (help)
"Achievements of Hereditary Disease Foundation". Achievements of Hereditary Disease Foundation. Hereditary Disease Foundation. मूल से से 16 जुलाई 2011 को पुरालेखित।. अभिगमन तिथि: 2008-08-10.
"Hereditary Disease Foundation – About Us". Hereditary disease foundation. 2008. मूल से से 12 मार्च 2009 को पुरालेखित।. अभिगमन तिथि: 2009-03-27.

hdsa.org

"Huntington's Disease Society of America – History". Huntington's Disease Society of America. 2008. 24 नवंबर 2010 को मूल से पुरालेखित. अभिगमन तिथि: 2009-03-17. {{cite web}}: Check date values in: |archive-date= (help)
"US Senate s. resolution 531" (PDF). S. Res. 531. US Senate. 2008-04-06. 21 जुलाई 2011 को मूल से पुरालेखित (PDF). अभिगमन तिथि: 2008-08-10.

huntington-assoc.com

"IHA Profile". International Huntington Association. 2004. 12 जून 2011 को मूल से पुरालेखित. अभिगमन तिथि: 2009-04-03.

huntington-study-group.org

"Unified Huntington's Disease Rating Scale (UHDRS)". UHDRS and Database. HSG. 2009-02-01. मूल से से 2 मई 2009 को पुरालेखित।. अभिगमन तिथि: 2009-04-14.

jbc.org

"Analysis of Strand Slippage in DNA Polymerase Expansions of CAG/CTG Triplet Repeats Associated with Neurodegenerative Disease — JBC". 8 सितंबर 2017 को मूल से पुरालेखित.

jneurosci.org

Carter RJ, Lione LA, Humby T, Mangiarini L, Mahal A, Bates GP, Dunnett SB, and Morton AJ (15 अप्रैल 1999). "Characterization of Progressive Motor Deficits in Mice Transgenic for the Human Huntington's Disease Mutation". The Journal of Neuroscience. 19 (8): 3248–3257. पीएमआईडी 10191337. 7 जनवरी 2009 को मूल से पुरालेखित. अभिगमन तिथि: 2009-04-01.{{cite journal}}: CS1 maint: multiple names: authors list (link)

lww.com

journals.lww.com

Jelliffe SE, Muncey EB, Davenport CB (1913). "Huntington's Chorea: A Study in Heredity". The Journal of Nervous and Mental Disease. 40 (12): 796. 12 मई 2012 को मूल से पुरालेखित. अभिगमन तिथि: 15 जनवरी 2011.{{cite journal}}: CS1 maint: multiple names: authors list (link)

medscape.com

emedicine.medscape.com

Sharon I (2010). "Huntington Disease Dementia". emedicine, WebMD. Medscape. 5 मार्च 2010 को मूल से पुरालेखित. अभिगमन तिथि: 2010-05-16. {{cite web}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)

nature.com

"Nature Clinical Practice Neurology | Mechanisms of Disease: histone modifications in Huntington's disease | Article". 26 नवंबर 2011 को मूल से पुरालेखित. {{cite web}}: Check date values in: |archive-date= (help)

nih.gov

pubmed.ncbi.nlm.nih.gov

Walker FO (2007). "Huntington's disease". Lancet. 369 (9557): 218. डीओआई:10.1016/S0140-6736(07)60111-1. पीएमआईडी 17240289.
Walker FO (2007). "Huntington's disease". Lancet. 369 (9557): 219. डीओआई:10.1016/S0140-6736(07)60111-1. पीएमआईडी 17240289.
Montoya A, Price BH, Menear M, Lepage M (2006). "Brain imaging and cognitive dysfunctions in Huntington's disease" (PDF). J Psychiatry Neurosci. 31 (1): 21–9. पीएमसी 1325063. पीएमआईडी 16496032. मूल से (PDF) से 23 मार्च 2016 को पुरालेखित।. अभिगमन तिथि: 2009-04-01.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Aziz NA, van der Marck MA, Pijl H, Olde Rikkert MG, Bloem BR, Roos RA (2008). "Weight loss in neurodegenerative disorders". J. Neurol. 255 (12): 1872–80. डीओआई:10.1007/s00415-009-0062-8. पीएमआईडी 19165531.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Gagnon JF, Petit D, Latreille V, Montplaisir J (2008). "Neurobiology of sleep disturbances in neurodegenerative disorders". Curr. Pharm. Des. 14 (32): 3430–45. डीओआई:10.2174/138161208786549353. पीएमआईडी 19075719.{{cite journal}}: CS1 maint: multiple names: authors list (link)
van Duijn E, Kingma EM, van der Mast RC (2007). "Psychopathology in verified Huntington's disease gene carriers". J Neuropsychiatry Clin Neurosci. 19 (4): 441–8. डीओआई:10.1176/appi.neuropsych.19.4.441. पीएमआईडी 18070848.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Walker FO (2007). "Huntington's disease". Lancet. 369 (9557): 221. डीओआई:10.1016/S0140-6736(07)60111-1. पीएमआईडी 17240289.
Walker FO (2007). "Huntington's disease". Lancet. 369 (9557): 220. डीओआई:10.1016/S0140-6736(07)60111-1. पीएमआईडी 17240289.
Katsuno M, Banno H, Suzuki K; et al. (2008). "Molecular genetics and biomarkers of polyglutamine diseases". Curr. Mol. Med. 8 (3): 221–34. डीओआई:10.2174/156652408784221298. पीएमआईडी 18473821. मूल से से 13 फ़रवरी 2009 को पुरालेखित।. अभिगमन तिथि: 2009-04-01. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
Walker FO (2007). "Huntington's disease". Lancet. 369 (9557): 222. डीओआई:10.1016/S0140-6736(07)60111-1. पीएमआईडी 17240289.
Nance MA, Myers RH (2001). "Juvenile onset Huntington's disease—clinical and research perspectives". Ment Retard Dev Disabil Res Rev. 7 (3): 153–7. डीओआई:10.1002/mrdd.1022. पीएमआईडी 11553930.
Ridley RM, Frith CD, Crow TJ, Conneally PM (1988). "Anticipation in Huntington's disease is inherited through the male line but may originate in the female". Journal of Medical Genetics. 25 (9): 589–595. डीओआई:10.1136/jmg.25.9.589. पीएमसी 1051535. पीएमआईडी 2972838. 14 जुलाई 2012 को मूल से पुरालेखित. अभिगमन तिथि: 15 जनवरी 2011.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Semaka A, Creighton S, Warby S, Hayden MR (2006). "Predictive testing for Huntington disease: interpretation and significance of intermediate alleles". Clin. Genet. 70 (4): 283–94. डीओआई:10.1111/j.1399-0004.2006.00668.x. पीएमआईडी 16965319.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Squitieri F, Gellera C, Cannella M; et al. (2003). "Homozygosity for CAG mutation in Huntington disease is associated with a more severe clinical course". Brain. 126 (Pt 4): 946–55. डीओआई:10.1093/brain/awg077. पीएमआईडी 12615650. 20 दिसंबर 2012 को मूल से पुरालेखित. अभिगमन तिथि: 15 जनवरी 2011. {{cite journal}}: Check date values in: |archive-date= (help); Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
Wexler NS, Young AB, Tanzi RE; et al. (1987). "Homozygotes for Huntington's disease". Nature. 326 (6109): 194–197. डीओआई:10.1038/326194a0. पीएमआईडी 2881213. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
Goehler H, Lalowski M, Stelzl U; et al. (2004). "A protein interaction network links GIT1, an enhancer of Huntingtin aggregation, to Huntington's disease". Mol. Cell. 15 (6): 853–65. डीओआई:10.1016/j.molcel.2004.09.016. पीएमआईडी 15383276. 5 अक्तूबर 2017 को मूल से पुरालेखित. अभिगमन तिथि: 2009-04-27. {{cite journal}}: Check date values in: |archive-date= (help); Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
Harjes P, Wanker EE (2003). "The hunt for huntingtin function: interaction partners tell many different stories". Trends Biochem. Sci. 28 (8): 425–33. डीओआई:10.1016/S0968-0004(03)00168-3. पीएमआईडी 12932731. 5 अक्तूबर 2017 को मूल से पुरालेखित. अभिगमन तिथि: 2009-04-27. {{cite journal}}: Check date values in: |archive-date= (help)
Cattaneo E, Zuccato C, Tartari M (2005). "Normal huntingtin function: an alternative approach to Huntington's disease". Nat. Rev. Neurosci. 6 (12): 919–30. डीओआई:10.1038/nrn1806. पीएमआईडी 16288298.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Rubinsztein DC, Carmichael J (2003). "Huntington's disease: Molecular basis of neurodegeneration". Expert Rev Mol Med. 5 (20): 1–21. डीओआई:10.1017/S1462399403006549. पीएमआईडी 14585171.
Bloch M, Hayden MR (1990). "Opinion: predictive testing for Huntington disease in childhood: challenges and implications". Am. J. Hum. Genet. 46 (1): 1–4. पीएमसी 1683548. पीएमआईडी 2136787.
Subramaniam S, Sixt KM, Barrow R, Snyder SH (2009). "Rhes, a striatal specific protein, mediates mutant-huntingtin cytotoxicity". Science. 324 (5932): 1327–30. डीओआई:10.1126/science.1172871. पीएमसी 2745286. पीएमआईडी 19498170.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Lobsiger CS, Cleveland DW (2007). "Glial cells as intrinsic components of non-cell-autonomous neurodegenerative disease". Nat. Neurosci. 10 (11): 1355–60. डीओआई:10.1038/nn1988. पीएमआईडी 17965655.
Crossman AR (2000). "Functional anatomy of movement disorders" (PDF). J. Anat. 196 (Pt 4): 519–25. डीओआई:10.1046/j.1469-7580.2000.19640519.x. पीएमसी 1468094. पीएमआईडी 10923984.^{[मृत कड़ियाँ]}
Myers RH (2004). "Huntington's disease genetics". NeuroRx. 1 (2): 255–62. डीओआई:10.1602/neurorx.1.2.255. पीएमसी 534940. पीएमआईडी 15717026.
Burson CM, Markey KR (2001). "Genetic counseling issues in predictive genetic testing for familial adult-onset neurologic diseases". Semin Pediatr Neurol. 8 (3): 177–86. डीओआई:10.1053/spen.2001.26451. पीएमआईडी 11575847.
Hayden MR (2003). "Predictive testing for Huntington's disease: a universal model?". Lancet Neurol. 2 (3): 141–2. डीओआई:10.1016/S1474-4422(03)00317-X. पीएमआईडी 12849232. {{cite journal}}: Unknown parameter |month= ignored (help)
"Guidelines for the molecular genetics predictive test in Huntington's disease. International Huntington Association (IHA) and the World Federation of Neurology (WFN) Research Group on Huntington's Chorea". Neurology. 44 (8): 1533–6. 1994. पीएमआईडी 8058167.
Kuliev A, Verlinsky Y (2005). "Preimplantation diagnosis: A realistic option for assisted reproduction and genetic practice". Curr. Opin. Obstet. Gynecol. 17 (2): 179–83. डीओआई:10.1097/01.gco.0000162189.76349.c5. पीएमआईडी 15758612. 13 अगस्त 2011 को मूल से पुरालेखित. अभिगमन तिथि: 2009-04-01.
Schneider SA, Walker RH, Bhatia KP (2007). "The Huntington's disease-like syndromes: what to consider in patients with a negative Huntington's disease gene test". Nat Clin Pract Neurol. 3 (9): 517–25. डीओआई:10.1038/ncpneuro0606. पीएमआईडी 17805246. {{cite journal}}: |access-date= requires |url= (help)CS1 maint: multiple names: authors list (link)
Frank S, Jankovic J. (2010). "Advances in the Pharmacological Management of Huntington's Disease". Drugs. 70 (5): 561–71. डीओआई:10.2165/11534430-000000000-00000. पीएमआईडी 20329804. मूल से से 8 अक्तूबर 2011 को पुरालेखित।. अभिगमन तिथि: 15 जनवरी 2011. {{cite journal}}: Check date values in: |archive-date= (help)
Walker FO (2007). "Huntington's disease". Lancet. 369 (9557): 224. डीओआई:10.1016/S0140-6736(07)60111-1. पीएमआईडी 17240289.
Bonelli RM, Wenning GK, Kapfhammer HP (2004). "Huntington's disease: present treatments and future therapeutic modalities". Int Clin Psychopharmacol. 19 (2): 51–62. डीओआई:10.1097/00004850-200403000-00001. पीएमआईडी 15076012. 1 जून 2012 को मूल से पुरालेखित. अभिगमन तिथि: 2009-04-01.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Walker FO (2007). "Huntington's disease". Lancet. 369 (9557): 225. डीओआई:10.1016/S0140-6736(07)60111-1. पीएमआईडी 17240289.
Panagiotakis PH, DiSario JA, Hilden K, Ogara M, Fang JC (2008). "DPEJ tube placement prevents aspiration pneumonia in high-risk patients". Nutr Clin Pract. 23 (2): 172–5. डीओआई:10.1177/0884533608314537. पीएमआईडी 18390785.{{cite journal}}: CS1 maint: multiple names: authors list (link)^{[मृत कड़ियाँ]}
Bilney B, Morris ME, Perry A (2003). "Effectiveness of physiotherapy, occupational therapy, and speech pathology for people with Huntington's disease: a systematic review". Neurorehabil Neural Repair. 17 (1): 12–24. डीओआई:10.1177/0888439002250448. पीएमआईडी 12645441.{{cite journal}}: CS1 maint: multiple names: authors list (link)^{[मृत कड़ियाँ]}
Zinzi P, Salmaso D, De Grandis R; et al. (2007). "Effects of an intensive rehabilitation programme on patients with Huntington's disease: a pilot study". Clin Rehabil. 21 (7): 603–13. डीओआई:10.1177/0269215507075495. पीएमआईडी 17702702. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)^{[मृत कड़ियाँ]}
Harper PS (1999). "Huntington's disease: A clinical, genetic and molecular model for polyglutamine repeat disorders". Philos. Trans. R. Soc. Lond., B, Biol. Sci. 354 (1386): 957–61. डीओआई:10.1098/rstb.1999.0446. पीएमसी 1692597. पीएमआईडी 10434293.
Andrew SE, Goldberg YP, Kremer B; et al. (1993). "The relationship between trinucleotide (CAG) repeat length and clinical features of Huntington's disease". Nat. Genet. 4 (4): 398–403. डीओआई:10.1038/ng0893-398. पीएमआईडी 8401589. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
Di Maio L, Squitieri F, Napolitano G; et al. (1993). "Suicide risk in Huntington's disease". J. Med. Genet. 30 (4): 293–5. डीओआई:10.1136/jmg.30.4.293. पीएमसी 1016335. पीएमआईडी 8487273. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
Gusella JF, Wexler NS, Conneally PM; et al. (1983). "A polymorphic DNA marker genetically linked to Huntington's disease". Nature. 306 (5940): 234–8. डीओआई:10.1038/306234a0. पीएमआईडी 6316146. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
Squitieri F, Andrew SE, Goldberg YP; et al. (1994). "DNA haplotype analysis of Huntington disease reveals clues to the origins and mechanisms of CAG expansion and reasons for geographic variations of prevalence". Hum. Mol. Genet. 3 (12): 2103–14. डीओआई:10.1093/hmg/3.12.2103. पीएमआईडी 7881406. 15 मार्च 2020 को मूल से पुरालेखित. अभिगमन तिथि: 15 जनवरी 2011. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
Almqvist EW, Elterman DS, MacLeod PM, Hayden MR (2001). "High incidence rate and absent family histories in one quarter of patients newly diagnosed with Huntington disease in British Columbia". Clin. Genet. 60 (3): 198–205. डीओआई:10.1034/j.1399-0004.2001.600305.x. पीएमआईडी 11595021.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Lanska DJ (2000). "George Huntington (1850–1916) and hereditary chorea". J Hist Neurosci. 9 (1): 76–89. डीओआई:10.1076/0964-704X(200004)9:1;1-2;FT076. पीएमआईडी 11232352.
Irwin A Brody, Robert H Wilkins (1967). "Huntington's Chorea". Arch Neurol. 17 (3): 331. डीओआई:10.1001/archneur.1967.00470270109013. पीएमआईडी 4228262. 8 मार्च 2012 को मूल से पुरालेखित. अभिगमन तिथि: 15 जनवरी 2011.
Wexler AR (2002). "Chorea and community in a 19th-century town". Bull Hist Med. 76 (3): 495–527. डीओआई:10.1353/bhm.2002.0150. पीएमआईडी 12486915.
Conneally PM (1984). "Huntington disease: genetics and epidemiology". Am. J. Hum. Genet. 36 (3): 506–26. पीएमसी 1684448. पीएमआईडी 6233902.
Macdonald M (1993). "A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. The Huntington's Disease Collaborative Research Group". Cell. 72 (6): 971–83. डीओआई:10.1016/0092-8674(93)90585-E. पीएमआईडी 8458085. 5 अक्तूबर 2017 को मूल से पुरालेखित. अभिगमन तिथि: 15 जनवरी 2011. {{cite journal}}: Check date values in: |archive-date= (help)
Bertram L, Tanzi RE (2005). "The genetic epidemiology of neurodegenerative disease". J. Clin. Invest. 115 (6): 1449–57. डीओआई:10.1172/JCI24761. पीएमसी 1137006. पीएमआईडी 15931380. {{cite journal}}: |access-date= requires |url= (help)
La Spada AR, Roling DB, Harding AE; et al. (1992). "Meiotic stability and genotype-phenotype correlation of the trinucleotide repeat in X-linked spinal and bulbar muscular atrophy". Nat. Genet. 2 (4): 301–4. डीओआई:10.1038/ng1292-301. पीएमआईडी 1303283. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
Sathasivam K, Hobbs C, Mangiarini L; et al. (1999). "Transgenic models of Huntington's disease". Philos. Trans. R. Soc. Lond., B, Biol. Sci. 354 (1386): 963–9. डीओआई:10.1098/rstb.1999.0447. पीएमसी 1692600. पीएमआईडी 10434294. मूल से से 23 फ़रवरी 2020 को पुरालेखित।. अभिगमन तिथि: 15 जनवरी 2011. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
Li JY, Popovic N, Brundin P (2005). "The use of the R6 transgenic mouse models of Huntington's disease in attempts to develop novel therapeutic strategies". NeuroRx. 2 (3): 447–64. डीओआई:10.1602/neurorx.2.3.447. पीएमसी 1144488. पीएमआईडी 16389308.{{cite journal}}: CS1 maint: multiple names: authors list (link)
DiFiglia M, Sapp E, Chase KO; et al. (1997). "Aggregation of huntingtin in neuronal intranuclear inclusions and dystrophic neurites in brain". Science. 277 (5334): 1990–3. डीओआई:10.1126/science.277.5334.1990. पीएमआईडी 9302293. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
Davenport CB (1915). "Huntington's chorea in relation to heredity and eugenics". Proc. Natl. Acad. Sci. U.S.A. 1 (5): 283–5. डीओआई:10.1073/pnas.1.5.283. पीएमसी 1090803. पीएमआईडी 16575999.
Rollin, Bernard E. (2006). "The Regulation of Animal Research and the Emergence of Animal Ethics: A Conceptual History". Theoretical Medicine and Bioethics. 27 (4): 285–304. डीओआई:10.1007/s11017-006-9007-8. पीएमआईडी 16937023.
Doerflinger RM (2008). "The problem of deception in embryonic stem cell research". Cell Prolif. 41 Suppl 1: 65–70. डीओआई:10.1111/j.1365-2184.2008.00492.x. पीएमआईडी 18181947.
Chapman MA (1990). "Predictive testing for adult-onset genetic disease: ethical and legal implications of the use of linkage analysis for Huntington disease". Am. J. Hum. Genet. 47 (1): 1–3. पीएमसी 1683745. पीएमआईडी 2140926.
Huggins M, Bloch M, Kanani S; et al. (1990). "Ethical and legal dilemmas arising during predictive testing for adult-onset disease: the experience of Huntington disease". Am. J. Hum. Genet. 47 (1): 4–12. पीएमसी 1683755. पीएमआईडी 1971997. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
Binedell J, Soldan JR, Scourfield J, Harper PS (1996). "Huntington's disease predictive testing: the case for an assessment approach to requests from adolescents". J. Med. Genet. 33 (11): 912–8. डीओआई:10.1136/jmg.33.11.912. पीएमसी 1050784. पीएमआईडी 8950670.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Borry P, Goffin T, Nys H, Dierickx K (2008). "Predictive genetic testing in minors for adult-onset genetic diseases". Mt. Sinai J. Med. 75 (3): 287–96. डीओआई:10.1002/msj.20038. पीएमआईडी 18704981.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Braude PR, De Wert GM, Evers-Kiebooms G, Pettigrew RA, Geraedts JP (1998). "Non-disclosure preimplantation genetic diagnosis for Huntington's disease: practical and ethical dilemmas". Prenat. Diagn. 18 (13): 1422–6. डीओआई:10.1002/(SICI)1097-0223(199812)18:13<1422::AID-PD499>3.0.CO;2-R. पीएमआईडी 9949442. अभिगमन तिथि: 2009-04-01.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Walker FO (2007). "Huntington's disease". Lancet. 369 (9557): 223. डीओआई:10.1016/S0140-6736(07)60111-1. पीएमआईडी 17240289.
Coyle JT, Schwarcz R (1976). "Lesion of striatal neurones with kainic acid provides a model for Huntington's chorea". Nature. 263 (5574): 244–6. डीओआई:10.1038/263244a0. पीएमआईडी 8731.
Brouillet E, Hantraye P, Ferrante RJ, Dolan R, Leroy-Willig A, Kowall NW, Beal MF (1995). "Chronic mitochondrial energy impairment produces selective striatal degeneration and abnormal choreiform movements in primates". Proc Natl Acad Sci USA. 92 (15): 7105–7109. डीओआई:10.1073/pnas.92.15.7105. पीएमसी 41480. पीएमआईडी 7624378.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Mangiarini L, Sathasivam K, Seller M, Cozens B, Harper A, Hetherington C, Lawton M, Trottier Y, Lehrach H, Davies SW, Bates GP (1996). "Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological genotype in transgenic mice". Cell. 87 (3): 493–506. डीओआई:10.1016/S0092-8674(00)81369-0. पीएमआईडी 8898202.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Carter RJ, Lione LA, Humby T, Mangiarini L, Mahal A, Bates GP, Dunnett SB, and Morton AJ (15 अप्रैल 1999). "Characterization of Progressive Motor Deficits in Mice Transgenic for the Human Huntington's Disease Mutation". The Journal of Neuroscience. 19 (8): 3248–3257. पीएमआईडी 10191337. 7 जनवरी 2009 को मूल से पुरालेखित. अभिगमन तिथि: 2009-04-01.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Marsh JL, Pallos J and Thompson LM (2003). "Fly models of Huntington's disease". Human Molecular Genetics. 12 (2): 187–193. डीओआई:10.1093/hmg/ddg271. पीएमआईडी 12925571. 24 दिसंबर 2009 को मूल से पुरालेखित. अभिगमन तिथि: 2009-04-01. {{cite journal}}: Check date values in: |archive-date= (help)
Voisine C, Varma H, Walker N, Bates EA, Stockwell BR, Hart AC (2007). "Identification of potential therapeutic drugs for huntington's disease using Caenorhabditis elegans". PLoS ONE. 2 (6): e504. डीओआई:10.1371/journal.pone.0000504. पीएमसी 1876812. पीएमआईडी 17551584. 13 सितंबर 2011 को मूल से पुरालेखित. अभिगमन तिथि: 15 जनवरी 2011.{{cite journal}}: CS1 maint: multiple names: authors list (link) CS1 maint: unflagged free DOI (link)
Lecerf JM, Shirley TL, Zhu Q; et al. (2001). "Human single-chain Fv intrabodies counteract in situ huntingtin aggregation in cellular models of Huntington's disease". Proc. Natl. Acad. Sci. U.S.A. 98 (8): 4764–9. डीओआई:10.1073/pnas.071058398. पीएमसी 31908. पीएमआईडी 11296304. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
Miller TW, Zhou C, Gines S; et al. (2005). "A human single-chain Fv intrabody preferentially targets amino-terminal huntingtin's fragments in striatal models of Huntington's disease". Neurobiol. Dis. 19 (1–2): 47–56. डीओआई:10.1016/j.nbd.2004.11.003. पीएमआईडी 15837560. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
Harper SQ, Staber PD, He X; et al. (2005). "RNA interference improves motor and neuropathological abnormalities in a Huntington's disease mouse model". Proc. Natl. Acad. Sci. U.S.A. 102 (16): 5820–5. डीओआई:10.1073/pnas.0501507102. पीएमसी 556303. पीएमआईडी 15811941. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
Díaz-Hernández M, Torres-Peraza J, Salvatori-Abarca A; et al. (2005). "Full Motor Recovery Despite Striatal Neuron Loss and Formation of Irreversible Amyloid-Like Inclusions in a Conditional Mouse Model of Huntington's Disease". The Journal of Neuroscience. 25 (42): 9773–9781. डीओआई:10.1523/JNEUROSCI.3183-05.2005. पीएमआईडी 16237181. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
Clelland CD, Barker RA, Watts C (2008). "Cell therapy in Huntington disease". Neurosurg Focus. 24 (3–4): E9. डीओआई:10.3171/FOC/2008/24/3-4/E8. पीएमआईडी 18341412.{{cite journal}}: CS1 maint: multiple names: authors list (link)

ncbi.nlm.nih.gov

"Huntington Disease". genereviews bookshelf. University of Washington. 2007-07-19. 2 जून 2010 को मूल से पुरालेखित. अभिगमन तिथि: 2009-03-12.
Montoya A, Price BH, Menear M, Lepage M (2006). "Brain imaging and cognitive dysfunctions in Huntington's disease" (PDF). J Psychiatry Neurosci. 31 (1): 21–9. पीएमसी 1325063. पीएमआईडी 16496032. मूल से (PDF) से 23 मार्च 2016 को पुरालेखित।. अभिगमन तिथि: 2009-04-01.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Ridley RM, Frith CD, Crow TJ, Conneally PM (1988). "Anticipation in Huntington's disease is inherited through the male line but may originate in the female". Journal of Medical Genetics. 25 (9): 589–595. डीओआई:10.1136/jmg.25.9.589. पीएमसी 1051535. पीएमआईडी 2972838. 14 जुलाई 2012 को मूल से पुरालेखित. अभिगमन तिथि: 15 जनवरी 2011.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Bloch M, Hayden MR (1990). "Opinion: predictive testing for Huntington disease in childhood: challenges and implications". Am. J. Hum. Genet. 46 (1): 1–4. पीएमसी 1683548. पीएमआईडी 2136787.
Subramaniam S, Sixt KM, Barrow R, Snyder SH (2009). "Rhes, a striatal specific protein, mediates mutant-huntingtin cytotoxicity". Science. 324 (5932): 1327–30. डीओआई:10.1126/science.1172871. पीएमसी 2745286. पीएमआईडी 19498170.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Purves D, Augustine GA, Fitzpatrick D, Hall W, LaMantia A-S, McNamara JO, Williams SM (2001). "Modulation of Movement by the Basal Ganglia – Circuits within the Basal Ganglia System". In Purves D (ed.). Neuroscience (2nd ed.). Sunderland, MA: Sinauer Associates. ISBN 0-87893-742-0. 17 अगस्त 2009 को मूल से पुरालेखित. अभिगमन तिथि: 2009-04-01. {{cite book}}: External link in |chapterurl= (help); Unknown parameter |chapterurl= ignored (help)CS1 maint: multiple names: authors list (link)
Crossman AR (2000). "Functional anatomy of movement disorders" (PDF). J. Anat. 196 (Pt 4): 519–25. डीओआई:10.1046/j.1469-7580.2000.19640519.x. पीएमसी 1468094. पीएमआईडी 10923984.^{[मृत कड़ियाँ]}
Myers RH (2004). "Huntington's disease genetics". NeuroRx. 1 (2): 255–62. डीओआई:10.1602/neurorx.1.2.255. पीएमसी 534940. पीएमआईडी 15717026.
Harper PS (1999). "Huntington's disease: A clinical, genetic and molecular model for polyglutamine repeat disorders". Philos. Trans. R. Soc. Lond., B, Biol. Sci. 354 (1386): 957–61. डीओआई:10.1098/rstb.1999.0446. पीएमसी 1692597. पीएमआईडी 10434293.
Di Maio L, Squitieri F, Napolitano G; et al. (1993). "Suicide risk in Huntington's disease". J. Med. Genet. 30 (4): 293–5. डीओआई:10.1136/jmg.30.4.293. पीएमसी 1016335. पीएमआईडी 8487273. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
Conneally PM (1984). "Huntington disease: genetics and epidemiology". Am. J. Hum. Genet. 36 (3): 506–26. पीएमसी 1684448. पीएमआईडी 6233902.
Bertram L, Tanzi RE (2005). "The genetic epidemiology of neurodegenerative disease". J. Clin. Invest. 115 (6): 1449–57. डीओआई:10.1172/JCI24761. पीएमसी 1137006. पीएमआईडी 15931380. {{cite journal}}: |access-date= requires |url= (help)
Sathasivam K, Hobbs C, Mangiarini L; et al. (1999). "Transgenic models of Huntington's disease". Philos. Trans. R. Soc. Lond., B, Biol. Sci. 354 (1386): 963–9. डीओआई:10.1098/rstb.1999.0447. पीएमसी 1692600. पीएमआईडी 10434294. मूल से से 23 फ़रवरी 2020 को पुरालेखित।. अभिगमन तिथि: 15 जनवरी 2011. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
Li JY, Popovic N, Brundin P (2005). "The use of the R6 transgenic mouse models of Huntington's disease in attempts to develop novel therapeutic strategies". NeuroRx. 2 (3): 447–64. डीओआई:10.1602/neurorx.2.3.447. पीएमसी 1144488. पीएमआईडी 16389308.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Davenport CB (1915). "Huntington's chorea in relation to heredity and eugenics". Proc. Natl. Acad. Sci. U.S.A. 1 (5): 283–5. डीओआई:10.1073/pnas.1.5.283. पीएमसी 1090803. पीएमआईडी 16575999.
Chapman MA (1990). "Predictive testing for adult-onset genetic disease: ethical and legal implications of the use of linkage analysis for Huntington disease". Am. J. Hum. Genet. 47 (1): 1–3. पीएमसी 1683745. पीएमआईडी 2140926.
Huggins M, Bloch M, Kanani S; et al. (1990). "Ethical and legal dilemmas arising during predictive testing for adult-onset disease: the experience of Huntington disease". Am. J. Hum. Genet. 47 (1): 4–12. पीएमसी 1683755. पीएमआईडी 1971997. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
Binedell J, Soldan JR, Scourfield J, Harper PS (1996). "Huntington's disease predictive testing: the case for an assessment approach to requests from adolescents". J. Med. Genet. 33 (11): 912–8. डीओआई:10.1136/jmg.33.11.912. पीएमसी 1050784. पीएमआईडी 8950670.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Brouillet E, Hantraye P, Ferrante RJ, Dolan R, Leroy-Willig A, Kowall NW, Beal MF (1995). "Chronic mitochondrial energy impairment produces selective striatal degeneration and abnormal choreiform movements in primates". Proc Natl Acad Sci USA. 92 (15): 7105–7109. डीओआई:10.1073/pnas.92.15.7105. पीएमसी 41480. पीएमआईडी 7624378.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Voisine C, Varma H, Walker N, Bates EA, Stockwell BR, Hart AC (2007). "Identification of potential therapeutic drugs for huntington's disease using Caenorhabditis elegans". PLoS ONE. 2 (6): e504. डीओआई:10.1371/journal.pone.0000504. पीएमसी 1876812. पीएमआईडी 17551584. 13 सितंबर 2011 को मूल से पुरालेखित. अभिगमन तिथि: 15 जनवरी 2011.{{cite journal}}: CS1 maint: multiple names: authors list (link) CS1 maint: unflagged free DOI (link)
Lecerf JM, Shirley TL, Zhu Q; et al. (2001). "Human single-chain Fv intrabodies counteract in situ huntingtin aggregation in cellular models of Huntington's disease". Proc. Natl. Acad. Sci. U.S.A. 98 (8): 4764–9. डीओआई:10.1073/pnas.071058398. पीएमसी 31908. पीएमआईडी 11296304. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
Harper SQ, Staber PD, He X; et al. (2005). "RNA interference improves motor and neuropathological abnormalities in a Huntington's disease mouse model". Proc. Natl. Acad. Sci. U.S.A. 102 (16): 5820–5. डीओआई:10.1073/pnas.0501507102. पीएमसी 556303. पीएमआईडी 15811941. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)

oxfordjournals.org

hmg.oxfordjournals.org

Squitieri F, Andrew SE, Goldberg YP; et al. (1994). "DNA haplotype analysis of Huntington disease reveals clues to the origins and mechanisms of CAG expansion and reasons for geographic variations of prevalence". Hum. Mol. Genet. 3 (12): 2103–14. डीओआई:10.1093/hmg/3.12.2103. पीएमआईडी 7881406. 15 मार्च 2020 को मूल से पुरालेखित. अभिगमन तिथि: 15 जनवरी 2011. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
Marsh JL, Pallos J and Thompson LM (2003). "Fly models of Huntington's disease". Human Molecular Genetics. 12 (2): 187–193. डीओआई:10.1093/hmg/ddg271. पीएमआईडी 12925571. 24 दिसंबर 2009 को मूल से पुरालेखित. अभिगमन तिथि: 2009-04-01. {{cite journal}}: Check date values in: |archive-date= (help)

brain.oxfordjournals.org

Squitieri F, Gellera C, Cannella M; et al. (2003). "Homozygosity for CAG mutation in Huntington disease is associated with a more severe clinical course". Brain. 126 (Pt 4): 946–55. डीओआई:10.1093/brain/awg077. पीएमआईडी 12615650. 20 दिसंबर 2012 को मूल से पुरालेखित. अभिगमन तिथि: 15 जनवरी 2011. {{cite journal}}: Check date values in: |archive-date= (help); Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)

plosone.org

Voisine C, Varma H, Walker N, Bates EA, Stockwell BR, Hart AC (2007). "Identification of potential therapeutic drugs for huntington's disease using Caenorhabditis elegans". PLoS ONE. 2 (6): e504. डीओआई:10.1371/journal.pone.0000504. पीएमसी 1876812. पीएमआईडी 17551584. 13 सितंबर 2011 को मूल से पुरालेखित. अभिगमन तिथि: 15 जनवरी 2011.{{cite journal}}: CS1 maint: multiple names: authors list (link) CS1 maint: unflagged free DOI (link)

psychiatryonline.org

ajp.psychiatryonline.org

Davenport CB, Muncey EB (1916). "Huntington's chorea in relation to heredity and eugenics". American Journal of Insanity. 73: 195–222. डीओआई:10.1176/appi.ajp.73.2.195. 11 जून 2011 को मूल से पुरालेखित. अभिगमन तिथि: 15 जनवरी 2011.

royalsociety.org

journals.royalsociety.org

Sathasivam K, Hobbs C, Mangiarini L; et al. (1999). "Transgenic models of Huntington's disease". Philos. Trans. R. Soc. Lond., B, Biol. Sci. 354 (1386): 963–9. डीओआई:10.1098/rstb.1999.0447. पीएमसी 1692600. पीएमआईडी 10434294. मूल से से 23 फ़रवरी 2020 को पुरालेखित।. अभिगमन तिथि: 15 जनवरी 2011. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)

sagepub.com

sciencedaily.com

"First Transgenic Monkey Model Of Huntington's Disease Developed". ScienceDaily. 2008-05-19. 5 जून 2011 को मूल से पुरालेखित. अभिगमन तिथि: 2008-08-10.

stanford.edu

hopes.stanford.edu

"Huntingtin Protein and Protein Aggregation | HOPES - A guide to the science of Huntington's disease". मूल से से 31 अगस्त 2010 को पुरालेखित।.
"The Basic Neurobiology of Huntington's Disease (Text and Audio) | HOPES - A guide to the science of Huntington's disease". मूल से से 20 नवंबर 2010 को पुरालेखित।. {{cite web}}: Check date values in: |archive-date= (help)

web.archive.org

"Huntington Disease". genereviews bookshelf. University of Washington. 2007-07-19. 2 जून 2010 को मूल से पुरालेखित. अभिगमन तिथि: 2009-03-12.
Montoya A, Price BH, Menear M, Lepage M (2006). "Brain imaging and cognitive dysfunctions in Huntington's disease" (PDF). J Psychiatry Neurosci. 31 (1): 21–9. पीएमसी 1325063. पीएमआईडी 16496032. मूल से (PDF) से 23 मार्च 2016 को पुरालेखित।. अभिगमन तिथि: 2009-04-01.{{cite journal}}: CS1 maint: multiple names: authors list (link)
"Booklet by the Huntington Society of Canada" (PDF). Caregiver's Handbook for Advanced-Stage Huntington Disease. HD Society of Canada. 2007-04-11. मूल से (PDF) से 25 जून 2008 को पुरालेखित।. अभिगमन तिथि: 2008-08-10.
Katsuno M, Banno H, Suzuki K; et al. (2008). "Molecular genetics and biomarkers of polyglutamine diseases". Curr. Mol. Med. 8 (3): 221–34. डीओआई:10.2174/156652408784221298. पीएमआईडी 18473821. मूल से से 13 फ़रवरी 2009 को पुरालेखित।. अभिगमन तिथि: 2009-04-01. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
Goehler H, Lalowski M, Stelzl U; et al. (2004). "A protein interaction network links GIT1, an enhancer of Huntingtin aggregation, to Huntington's disease". Mol. Cell. 15 (6): 853–65. डीओआई:10.1016/j.molcel.2004.09.016. पीएमआईडी 15383276. 5 अक्तूबर 2017 को मूल से पुरालेखित. अभिगमन तिथि: 2009-04-27. {{cite journal}}: Check date values in: |archive-date= (help); Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
Harjes P, Wanker EE (2003). "The hunt for huntingtin function: interaction partners tell many different stories". Trends Biochem. Sci. 28 (8): 425–33. डीओआई:10.1016/S0968-0004(03)00168-3. पीएमआईडी 12932731. 5 अक्तूबर 2017 को मूल से पुरालेखित. अभिगमन तिथि: 2009-04-27. {{cite journal}}: Check date values in: |archive-date= (help)
"Huntingtin Protein and Protein Aggregation | HOPES - A guide to the science of Huntington's disease". मूल से से 31 अगस्त 2010 को पुरालेखित।.
"The Basic Neurobiology of Huntington's Disease (Text and Audio) | HOPES - A guide to the science of Huntington's disease". मूल से से 20 नवंबर 2010 को पुरालेखित।. {{cite web}}: Check date values in: |archive-date= (help)
"Nature Clinical Practice Neurology | Mechanisms of Disease: histone modifications in Huntington's disease | Article". 26 नवंबर 2011 को मूल से पुरालेखित. {{cite web}}: Check date values in: |archive-date= (help)
Purves D, Augustine GA, Fitzpatrick D, Hall W, LaMantia A-S, McNamara JO, Williams SM (2001). "Modulation of Movement by the Basal Ganglia – Circuits within the Basal Ganglia System". In Purves D (ed.). Neuroscience (2nd ed.). Sunderland, MA: Sinauer Associates. ISBN 0-87893-742-0. 17 अगस्त 2009 को मूल से पुरालेखित. अभिगमन तिथि: 2009-04-01. {{cite book}}: External link in |chapterurl= (help); Unknown parameter |chapterurl= ignored (help)CS1 maint: multiple names: authors list (link)
"Analysis of Strand Slippage in DNA Polymerase Expansions of CAG/CTG Triplet Repeats Associated with Neurodegenerative Disease — JBC". 8 सितंबर 2017 को मूल से पुरालेखित.
"Unified Huntington's Disease Rating Scale (UHDRS)". UHDRS and Database. HSG. 2009-02-01. मूल से से 2 मई 2009 को पुरालेखित।. अभिगमन तिथि: 2009-04-14.
Kuliev A, Verlinsky Y (2005). "Preimplantation diagnosis: A realistic option for assisted reproduction and genetic practice". Curr. Opin. Obstet. Gynecol. 17 (2): 179–83. डीओआई:10.1097/01.gco.0000162189.76349.c5. पीएमआईडी 15758612. 13 अगस्त 2011 को मूल से पुरालेखित. अभिगमन तिथि: 2009-04-01.
Frank S, Jankovic J. (2010). "Advances in the Pharmacological Management of Huntington's Disease". Drugs. 70 (5): 561–71. डीओआई:10.2165/11534430-000000000-00000. पीएमआईडी 20329804. मूल से से 8 अक्तूबर 2011 को पुरालेखित।. अभिगमन तिथि: 15 जनवरी 2011. {{cite journal}}: Check date values in: |archive-date= (help)
Bonelli RM, Wenning GK, Kapfhammer HP (2004). "Huntington's disease: present treatments and future therapeutic modalities". Int Clin Psychopharmacol. 19 (2): 51–62. डीओआई:10.1097/00004850-200403000-00001. पीएमआईडी 15076012. 1 जून 2012 को मूल से पुरालेखित. अभिगमन तिथि: 2009-04-01.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Sharon I (2010). "Huntington Disease Dementia". emedicine, WebMD. Medscape. 5 मार्च 2010 को मूल से पुरालेखित. अभिगमन तिथि: 2010-05-16. {{cite web}}: Unknown parameter |coauthors= ignored (|author= suggested) (help)
Squitieri F, Andrew SE, Goldberg YP; et al. (1994). "DNA haplotype analysis of Huntington disease reveals clues to the origins and mechanisms of CAG expansion and reasons for geographic variations of prevalence". Hum. Mol. Genet. 3 (12): 2103–14. डीओआई:10.1093/hmg/3.12.2103. पीएमआईडी 7881406. 15 मार्च 2020 को मूल से पुरालेखित. अभिगमन तिथि: 15 जनवरी 2011. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
Wexler A, Wexler N (2008). The Woman Who Walked Into the Sea. Huntington's and the Making of a Genetic Disease. Yale University Press. p. 288. ISBN 9780300105025. 6 जून 2011 को मूल से पुरालेखित. अभिगमन तिथि: 15 जनवरी 2011.
Irwin A Brody, Robert H Wilkins (1967). "Huntington's Chorea". Arch Neurol. 17 (3): 331. डीओआई:10.1001/archneur.1967.00470270109013. पीएमआईडी 4228262. 8 मार्च 2012 को मूल से पुरालेखित. अभिगमन तिथि: 15 जनवरी 2011.
Jelliffe SE, Muncey EB, Davenport CB (1913). "Huntington's Chorea: A Study in Heredity". The Journal of Nervous and Mental Disease. 40 (12): 796. 12 मई 2012 को मूल से पुरालेखित. अभिगमन तिथि: 15 जनवरी 2011.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Davenport CB, Muncey EB (1916). "Huntington's chorea in relation to heredity and eugenics". American Journal of Insanity. 73: 195–222. डीओआई:10.1176/appi.ajp.73.2.195. 11 जून 2011 को मूल से पुरालेखित. अभिगमन तिथि: 15 जनवरी 2011.
"The Venezuela Huntington's disease project". Hereditary Disease Foundation website. Hereditary Disease Foundation. 2008. मूल से से 26 अक्तूबर 2008 को पुरालेखित।. अभिगमन तिथि: 2008-09-08. {{cite web}}: Check date values in: |archive-date= (help)
Macdonald M (1993). "A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. The Huntington's Disease Collaborative Research Group". Cell. 72 (6): 971–83. डीओआई:10.1016/0092-8674(93)90585-E. पीएमआईडी 8458085. 5 अक्तूबर 2017 को मूल से पुरालेखित. अभिगमन तिथि: 15 जनवरी 2011. {{cite journal}}: Check date values in: |archive-date= (help)
Sathasivam K, Hobbs C, Mangiarini L; et al. (1999). "Transgenic models of Huntington's disease". Philos. Trans. R. Soc. Lond., B, Biol. Sci. 354 (1386): 963–9. डीओआई:10.1098/rstb.1999.0447. पीएमसी 1692600. पीएमआईडी 10434294. मूल से से 23 फ़रवरी 2020 को पुरालेखित।. अभिगमन तिथि: 15 जनवरी 2011. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)
"Achievements of Hereditary Disease Foundation". Achievements of Hereditary Disease Foundation. Hereditary Disease Foundation. मूल से से 16 जुलाई 2011 को पुरालेखित।. अभिगमन तिथि: 2008-08-10.
"HDA research news—medical research into treatment & prevention on hda.org.uk". Huntington's Disease Association-United Kingdom. 2009. 31 मई 2009 को मूल से पुरालेखित. अभिगमन तिथि: 2008-08-10.
"Hereditary Disease Foundation – About Us". Hereditary disease foundation. 2008. मूल से से 12 मार्च 2009 को पुरालेखित।. अभिगमन तिथि: 2009-03-27.
"Huntington's Disease Society of America – History". Huntington's Disease Society of America. 2008. 24 नवंबर 2010 को मूल से पुरालेखित. अभिगमन तिथि: 2009-03-17. {{cite web}}: Check date values in: |archive-date= (help)
"IHA Profile". International Huntington Association. 2004. 12 जून 2011 को मूल से पुरालेखित. अभिगमन तिथि: 2009-04-03.
"US Senate s. resolution 531" (PDF). S. Res. 531. US Senate. 2008-04-06. 21 जुलाई 2011 को मूल से पुरालेखित (PDF). अभिगमन तिथि: 2008-08-10.
Carter RJ, Lione LA, Humby T, Mangiarini L, Mahal A, Bates GP, Dunnett SB, and Morton AJ (15 अप्रैल 1999). "Characterization of Progressive Motor Deficits in Mice Transgenic for the Human Huntington's Disease Mutation". The Journal of Neuroscience. 19 (8): 3248–3257. पीएमआईडी 10191337. 7 जनवरी 2009 को मूल से पुरालेखित. अभिगमन तिथि: 2009-04-01.{{cite journal}}: CS1 maint: multiple names: authors list (link)
Marsh JL, Pallos J and Thompson LM (2003). "Fly models of Huntington's disease". Human Molecular Genetics. 12 (2): 187–193. डीओआई:10.1093/hmg/ddg271. पीएमआईडी 12925571. 24 दिसंबर 2009 को मूल से पुरालेखित. अभिगमन तिथि: 2009-04-01. {{cite journal}}: Check date values in: |archive-date= (help)
"First Transgenic Monkey Model Of Huntington's Disease Developed". ScienceDaily. 2008-05-19. 5 जून 2011 को मूल से पुरालेखित. अभिगमन तिथि: 2008-08-10.
Voisine C, Varma H, Walker N, Bates EA, Stockwell BR, Hart AC (2007). "Identification of potential therapeutic drugs for huntington's disease using Caenorhabditis elegans". PLoS ONE. 2 (6): e504. डीओआई:10.1371/journal.pone.0000504. पीएमसी 1876812. पीएमआईडी 17551584. 13 सितंबर 2011 को मूल से पुरालेखित. अभिगमन तिथि: 15 जनवरी 2011.{{cite journal}}: CS1 maint: multiple names: authors list (link) CS1 maint: unflagged free DOI (link)

webcitation.org

"FDA Approves First Drug for Treatment of Chorea in Huntington's Disease". FDA Approves First Drug for Treatment of Chorea in Huntington's Disease. U.S. Food and Drug Administration. अगस्त 15, 2008. 1 जून 2012 को मूल से पुरालेखित. अभिगमन तिथि: 2008-08-10.

wikipedia.org

en.wikipedia.org

Crossman AR (2000). "Functional anatomy of movement disorders" (PDF). J. Anat. 196 (Pt 4): 519–25. डीओआई:10.1046/j.1469-7580.2000.19640519.x. पीएमसी 1468094. पीएमआईडी 10923984.^{[मृत कड़ियाँ]}
Panagiotakis PH, DiSario JA, Hilden K, Ogara M, Fang JC (2008). "DPEJ tube placement prevents aspiration pneumonia in high-risk patients". Nutr Clin Pract. 23 (2): 172–5. डीओआई:10.1177/0884533608314537. पीएमआईडी 18390785.{{cite journal}}: CS1 maint: multiple names: authors list (link)^{[मृत कड़ियाँ]}
Bilney B, Morris ME, Perry A (2003). "Effectiveness of physiotherapy, occupational therapy, and speech pathology for people with Huntington's disease: a systematic review". Neurorehabil Neural Repair. 17 (1): 12–24. डीओआई:10.1177/0888439002250448. पीएमआईडी 12645441.{{cite journal}}: CS1 maint: multiple names: authors list (link)^{[मृत कड़ियाँ]}
Zinzi P, Salmaso D, De Grandis R; et al. (2007). "Effects of an intensive rehabilitation programme on patients with Huntington's disease: a pilot study". Clin Rehabil. 21 (7): 603–13. डीओआई:10.1177/0269215507075495. पीएमआईडी 17702702. {{cite journal}}: Explicit use of et al. in: |author= (help)CS1 maint: multiple names: authors list (link)^{[मृत कड़ियाँ]}

wiley.com

www3.interscience.wiley.com

Crossman AR (2000). "Functional anatomy of movement disorders" (PDF). J. Anat. 196 (Pt 4): 519–25. डीओआई:10.1046/j.1469-7580.2000.19640519.x. पीएमसी 1468094. पीएमआईडी 10923984.^{[मृत कड़ियाँ]}

wkhealth.com

meta.wkhealth.com

Kuliev A, Verlinsky Y (2005). "Preimplantation diagnosis: A realistic option for assisted reproduction and genetic practice". Curr. Opin. Obstet. Gynecol. 17 (2): 179–83. डीओआई:10.1097/01.gco.0000162189.76349.c5. पीएमआईडी 15758612. 13 अगस्त 2011 को मूल से पुरालेखित. अभिगमन तिथि: 2009-04-01.
Bonelli RM, Wenning GK, Kapfhammer HP (2004). "Huntington's disease: present treatments and future therapeutic modalities". Int Clin Psychopharmacol. 19 (2): 51–62. डीओआई:10.1097/00004850-200403000-00001. पीएमआईडी 15076012. 1 जून 2012 को मूल से पुरालेखित. अभिगमन तिथि: 2009-04-01.{{cite journal}}: CS1 maint: multiple names: authors list (link)

yale.edu

yalepress.yale.edu

Wexler A, Wexler N (2008). The Woman Who Walked Into the Sea. Huntington's and the Making of a Genetic Disease. Yale University Press. p. 288. ISBN 9780300105025. 6 जून 2011 को मूल से पुरालेखित. अभिगमन तिथि: 15 जनवरी 2011.

हनटिंग्टन रोग (Hindi Wikipedia)

adisonline.com

ama-assn.org

archneur.ama-assn.org

archive.org

archive.today

bbc.co.uk

news.bbc.co.uk

bentham-direct.org

bmjjournals.com

jmg.bmjjournals.com

cma.ca

doi.org

doi.org

dx.doi.org

elsevier.com

linkinghub.elsevier.com

fda.gov

google.co.uk

scholar.google.co.uk

hda.org.uk

hdac.org

hdfoundation.org

hdsa.org

huntington-assoc.com

huntington-study-group.org

jbc.org

jneurosci.org

lww.com

journals.lww.com

medscape.com

emedicine.medscape.com

nature.com

nih.gov

pubmed.ncbi.nlm.nih.gov

ncbi.nlm.nih.gov

oxfordjournals.org

hmg.oxfordjournals.org

brain.oxfordjournals.org

plosone.org

psychiatryonline.org

ajp.psychiatryonline.org

royalsociety.org

journals.royalsociety.org

sagepub.com

ncp.sagepub.com

nnr.sagepub.com

cre.sagepub.com

sciencedaily.com

stanford.edu

hopes.stanford.edu

web.archive.org

webcitation.org

wikipedia.org

en.wikipedia.org

wiley.com

www3.interscience.wiley.com

wkhealth.com

meta.wkhealth.com

yale.edu

yalepress.yale.edu