Huntingtons sjukdom (Swedish Wikipedia)

Analysis of information sources in references of the Wikipedia article "Huntingtons sjukdom" in Swedish language version.

refsWebsite

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10doi.org

2^nd place

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10worldcat.org

5^th place

9^th place

5nih.gov

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17^th place

2web.archive.org

1^st place

2wiley.com

222^nd place

202^nd place

2clinicaltrials.gov

5,225^th place

5,934^th place

1socialstyrelsen.se

low place

189^th place

1lakartidningen.se

low place

148^th place

1if-pan.krakow.pl

low place

1neuroguiden.se

low place

5,807^th place

1bmj.com

1,226^th place

1,106^th place

1nature.com

234^th place

206^th place

1smer.se

low place

5,085^th place

1medra.org

low place

1uu.se

3,805^th place

152^nd place

1roche.com

low place

1hdbuzz.net

low place

1plos.org

2,112^th place

1,407^th place

1jamanetwork.com

2,650^th place

1,558^th place

bmj.com

jmg.bmj.com

Semaka, Alicia; Kay, Chris; Doty, Crystal; Collins, Jennifer A.; Bijlsma, Emilia K.; Richards, Fiona. ”CAG size-specific risk estimates for intermediate allele repeat instability in Huntington disease” (på engelska). Journal of Medical Genetics 50 (10): sid. 696–703. doi:10.1136/jmedgenet-2013-101796. ISSN 0022-2593. http://jmg.bmj.com/content/50/10/696. Läst 5 juni 2017.

clinicaltrials.gov

UniQure Biopharma B.V. (2021-01-08). A Phase I/II, Randomized, Double-blind, Sham Control Study to Explore Safety, Tolerability, and Efficacy Signals of Multiple Ascending Doses of Striatally-Administered rAAV5-miHTT Total Huntingtin Gene (HTT) Lowering Therapy (AMT-130) in Early Manifest Huntington Disease. https://clinicaltrials.gov/ct2/show/NCT04120493. Läst 11 januari 2021.
”Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of IONIS-HTTRx in Patients With Early Manifest Huntington's Disease - Full Text View - ClinicalTrials.gov” (på engelska). clinicaltrials.gov. https://clinicaltrials.gov/ct2/show/NCT02519036?cond=Huntington+Disease&draw=5&rank=15. Läst 29 augusti 2017.

doi.org

dx.doi.org

Pringsheim, Tamara; Wiltshire, Katie; Day, Lundy; Dykeman, Jonathan; Steeves, Thomas; Jette, Nathalie. ”The incidence and prevalence of Huntington's disease: A systematic review and meta-analysis” (på engelska). Movement Disorders 27 (9): sid. 1083–1091. doi:10.1002/mds.25075. ISSN 1531-8257. http://onlinelibrary.wiley.com/doi/10.1002/mds.25075/abstract. Läst 6 juni 2017.
Roos, A-K.; Wiklund, L.; Laurell, K.. ”Discrepancy in prevalence of Huntington's disease in two Swedish regions” (på engelska). Acta Neurologica Scandinavica: sid. n/a–n/a. doi:10.1111/ane.12762. ISSN 1600-0404. http://onlinelibrary.wiley.com/doi/10.1111/ane.12762/abstract. Läst 6 juni 2017.
Semaka, Alicia; Kay, Chris; Doty, Crystal; Collins, Jennifer A.; Bijlsma, Emilia K.; Richards, Fiona. ”CAG size-specific risk estimates for intermediate allele repeat instability in Huntington disease” (på engelska). Journal of Medical Genetics 50 (10): sid. 696–703. doi:10.1136/jmedgenet-2013-101796. ISSN 0022-2593. http://jmg.bmj.com/content/50/10/696. Läst 5 juni 2017.
Sundblom, Jimmy; Niemelä, Valter; Ghazarian, Maria; Strand, Ann-Sofi; Bergdahl, Ingvar A.; Jansson, Jan-Håkan (2020-06-17). ”High frequency of intermediary alleles in the HTT gene in Northern Sweden - The Swedish Huntingtin Alleles and Phenotype (SHAPE) study” (på engelska). Scientific Reports 10 (1): sid. 9853. doi:10.1038/s41598-020-66643-0. ISSN 2045-2322. PMID 32555394. PMC: PMC7299994. https://www.nature.com/articles/s41598-020-66643-0. Läst 9 februari 2022.
Warby, Simon C.; Montpetit, Alexandre; Hayden, Anna R.; Carroll, Jeffrey B.; Butland, Stefanie L.; Visscher, Henk. ”CAG Expansion in the Huntington Disease Gene Is Associated with a Specific and Targetable Predisposing Haplogroup”. American Journal of Human Genetics 84 (3): sid. 351–366. doi:10.1016/j.ajhg.2009.02.003. ISSN 0002-9297. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2668007/. Läst 5 juni 2017.
Liu, Jeh-Ping; Zeitlin, Scott O.. ”Is Huntingtin Dispensable in the Adult Brain?” (på engelska). Journal of Huntington's Disease 6 (1): sid. 1–17. doi:10.3233/jhd-170235. ISSN 1879-6397. http://www.medra.org/servlet/aliasResolver?alias=iospress&doi=10.3233/JHD-170235. Läst 7 juni 2017.
Shin, Jun Wan; Kim, Kyung-Hee; Chao, Michael J.; Atwal, Ranjit S.; Gillis, Tammy; MacDonald, Marcy E.. ”Permanent inactivation of Huntington's disease mutation by personalized allele-specific CRISPR/Cas9”. Human Molecular Genetics. doi:10.1093/hmg/ddw286. https://doi-org.ezproxy.its.uu.se/10.1093/hmg/ddw286. Läst 8 juni 2017.
Wild, Edward J.; Boggio, Roberto; Langbehn, Douglas; Robertson, Nicola; Haider, Salman; Miller, James R. C.. ”Quantification of mutant huntingtin protein in cerebrospinal fluid from Huntington’s disease patients” (på engelska). The Journal of Clinical Investigation 125 (5): sid. 1979. doi:10.1172/JCI80743. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4463213/. Läst 29 maj 2017.
Niemelä, Valter; Landtblom, Anne-Marie; Blennow, Kaj; Sundblom, Jimmy. ”Tau or neurofilament light—Which is the more suitable biomarker for Huntington’s disease?”. PLOS ONE 12 (2): sid. e0172762. doi:10.1371/journal.pone.0172762. ISSN 1932-6203. http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0172762. Läst 29 maj 2017.
Huntington, George. ”ON CHOREA”. Archives of Neurology 17 (3): sid. 332–333. doi:10.1001/archneur.1967.00470270110014. ISSN 0003-9942. http://jamanetwork.com/journals/jamaneurology/fullarticle/567551. Läst 29 maj 2017.

hdbuzz.net

en.hdbuzz.net

”Disappointing Results from Wave’s PRECISION-HD1 and 2 Trials” (på engelska). HDBuzz. https://en.hdbuzz.net/301. Läst 16 april 2021.

if-pan.krakow.pl

Huntington’s disease: pathogenesis to animal models - if-pan.krakow.pl 2 februari 2010 PDF

jamanetwork.com

Huntington, George. ”ON CHOREA”. Archives of Neurology 17 (3): sid. 332–333. doi:10.1001/archneur.1967.00470270110014. ISSN 0003-9942. http://jamanetwork.com/journals/jamaneurology/fullarticle/567551. Läst 29 maj 2017.

lakartidningen.se

neurovetenskap, P. O. Lundberg professor emeritus; båda vid institutionen för; neurologi; sjukhuset, Akademiska (18 oktober 2005). ”Genetiska (van)föreställningar i olika tider”. Läkartidningen. https://lakartidningen.se/korrespondens/2005/10/genetiska-vanforestallningar-i-olika-tider/. Läst 1 maj 2020.

medra.org

Liu, Jeh-Ping; Zeitlin, Scott O.. ”Is Huntingtin Dispensable in the Adult Brain?” (på engelska). Journal of Huntington's Disease 6 (1): sid. 1–17. doi:10.3233/jhd-170235. ISSN 1879-6397. http://www.medra.org/servlet/aliasResolver?alias=iospress&doi=10.3233/JHD-170235. Läst 7 juni 2017.

nature.com

Sundblom, Jimmy; Niemelä, Valter; Ghazarian, Maria; Strand, Ann-Sofi; Bergdahl, Ingvar A.; Jansson, Jan-Håkan (2020-06-17). ”High frequency of intermediary alleles in the HTT gene in Northern Sweden - The Swedish Huntingtin Alleles and Phenotype (SHAPE) study” (på engelska). Scientific Reports 10 (1): sid. 9853. doi:10.1038/s41598-020-66643-0. ISSN 2045-2322. PMID 32555394. PMC: PMC7299994. https://www.nature.com/articles/s41598-020-66643-0. Läst 9 februari 2022.

neuroguiden.se

Hjärnan Arkiverad 11 februari 2011 hämtat från the Wayback Machine. neuroguiden.se

nih.gov

ncbi.nlm.nih.gov

”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): sid. 971–983. 1993-03-26. ISSN 0092-8674. PMID 8458085. https://www.ncbi.nlm.nih.gov/pubmed/8458085. Läst 13 oktober 2018.
Nopoulos, Peggy C.. ”Huntington disease: a single-gene degenerative disorder of the striatum”. Dialogues in Clinical Neuroscience 18 (1): sid. 91–98. ISSN 1294-8322. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4826775/. Läst 6 juni 2017.
Sundblom, Jimmy; Niemelä, Valter; Ghazarian, Maria; Strand, Ann-Sofi; Bergdahl, Ingvar A.; Jansson, Jan-Håkan (2020-06-17). ”High frequency of intermediary alleles in the HTT gene in Northern Sweden - The Swedish Huntingtin Alleles and Phenotype (SHAPE) study” (på engelska). Scientific Reports 10 (1): sid. 9853. doi:10.1038/s41598-020-66643-0. ISSN 2045-2322. PMID 32555394. PMC: PMC7299994. https://www.nature.com/articles/s41598-020-66643-0. Läst 9 februari 2022.
Warby, Simon C.; Montpetit, Alexandre; Hayden, Anna R.; Carroll, Jeffrey B.; Butland, Stefanie L.; Visscher, Henk. ”CAG Expansion in the Huntington Disease Gene Is Associated with a Specific and Targetable Predisposing Haplogroup”. American Journal of Human Genetics 84 (3): sid. 351–366. doi:10.1016/j.ajhg.2009.02.003. ISSN 0002-9297. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2668007/. Läst 5 juni 2017.
Wild, Edward J.; Boggio, Roberto; Langbehn, Douglas; Robertson, Nicola; Haider, Salman; Miller, James R. C.. ”Quantification of mutant huntingtin protein in cerebrospinal fluid from Huntington’s disease patients” (på engelska). The Journal of Clinical Investigation 125 (5): sid. 1979. doi:10.1172/JCI80743. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4463213/. Läst 29 maj 2017.

plos.org

journals.plos.org

Niemelä, Valter; Landtblom, Anne-Marie; Blennow, Kaj; Sundblom, Jimmy. ”Tau or neurofilament light—Which is the more suitable biomarker for Huntington’s disease?”. PLOS ONE 12 (2): sid. e0172762. doi:10.1371/journal.pone.0172762. ISSN 1932-6203. http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0172762. Läst 29 maj 2017.

roche.com

”Roche provides update on tominersen programme in manifest Huntington’s disease” (på engelska). www.roche.com. https://www.roche.com/media/releases/med-cor-2021-03-22b.htm. Läst 16 april 2021.

smer.se

”Preimplantatorisk genetisk diagnostik | Statens medicinsk-etiska råd (SMER)”. www.smer.se. http://www.smer.se/teman/preimplantatorisk-genetisk-diagnostik/. Läst 5 juni 2017.

socialstyrelsen.se

”Socialstyrelsen - Huntingtons sjukdom”. Arkiverad från originalet den 5 februari 2015. https://web.archive.org/web/20150205050938/http://www.socialstyrelsen.se/ovanligadiagnoser/huntingtonssjukdom. Läst 13 december 2014.

uu.se

doi-org.ezproxy.its.uu.se

Shin, Jun Wan; Kim, Kyung-Hee; Chao, Michael J.; Atwal, Ranjit S.; Gillis, Tammy; MacDonald, Marcy E.. ”Permanent inactivation of Huntington's disease mutation by personalized allele-specific CRISPR/Cas9”. Human Molecular Genetics. doi:10.1093/hmg/ddw286. https://doi-org.ezproxy.its.uu.se/10.1093/hmg/ddw286. Läst 8 juni 2017.

web.archive.org

”Socialstyrelsen - Huntingtons sjukdom”. Arkiverad från originalet den 5 februari 2015. https://web.archive.org/web/20150205050938/http://www.socialstyrelsen.se/ovanligadiagnoser/huntingtonssjukdom. Läst 13 december 2014.
Hjärnan Arkiverad 11 februari 2011 hämtat från the Wayback Machine. neuroguiden.se

wiley.com

onlinelibrary.wiley.com

Pringsheim, Tamara; Wiltshire, Katie; Day, Lundy; Dykeman, Jonathan; Steeves, Thomas; Jette, Nathalie. ”The incidence and prevalence of Huntington's disease: A systematic review and meta-analysis” (på engelska). Movement Disorders 27 (9): sid. 1083–1091. doi:10.1002/mds.25075. ISSN 1531-8257. http://onlinelibrary.wiley.com/doi/10.1002/mds.25075/abstract. Läst 6 juni 2017.
Roos, A-K.; Wiklund, L.; Laurell, K.. ”Discrepancy in prevalence of Huntington's disease in two Swedish regions” (på engelska). Acta Neurologica Scandinavica: sid. n/a–n/a. doi:10.1111/ane.12762. ISSN 1600-0404. http://onlinelibrary.wiley.com/doi/10.1111/ane.12762/abstract. Läst 6 juni 2017.

worldcat.org

Pringsheim, Tamara; Wiltshire, Katie; Day, Lundy; Dykeman, Jonathan; Steeves, Thomas; Jette, Nathalie. ”The incidence and prevalence of Huntington's disease: A systematic review and meta-analysis” (på engelska). Movement Disorders 27 (9): sid. 1083–1091. doi:10.1002/mds.25075. ISSN 1531-8257. http://onlinelibrary.wiley.com/doi/10.1002/mds.25075/abstract. Läst 6 juni 2017.
Roos, A-K.; Wiklund, L.; Laurell, K.. ”Discrepancy in prevalence of Huntington's disease in two Swedish regions” (på engelska). Acta Neurologica Scandinavica: sid. n/a–n/a. doi:10.1111/ane.12762. ISSN 1600-0404. http://onlinelibrary.wiley.com/doi/10.1111/ane.12762/abstract. Läst 6 juni 2017.
”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): sid. 971–983. 1993-03-26. ISSN 0092-8674. PMID 8458085. https://www.ncbi.nlm.nih.gov/pubmed/8458085. Läst 13 oktober 2018.
Nopoulos, Peggy C.. ”Huntington disease: a single-gene degenerative disorder of the striatum”. Dialogues in Clinical Neuroscience 18 (1): sid. 91–98. ISSN 1294-8322. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4826775/. Läst 6 juni 2017.
Semaka, Alicia; Kay, Chris; Doty, Crystal; Collins, Jennifer A.; Bijlsma, Emilia K.; Richards, Fiona. ”CAG size-specific risk estimates for intermediate allele repeat instability in Huntington disease” (på engelska). Journal of Medical Genetics 50 (10): sid. 696–703. doi:10.1136/jmedgenet-2013-101796. ISSN 0022-2593. http://jmg.bmj.com/content/50/10/696. Läst 5 juni 2017.
Sundblom, Jimmy; Niemelä, Valter; Ghazarian, Maria; Strand, Ann-Sofi; Bergdahl, Ingvar A.; Jansson, Jan-Håkan (2020-06-17). ”High frequency of intermediary alleles in the HTT gene in Northern Sweden - The Swedish Huntingtin Alleles and Phenotype (SHAPE) study” (på engelska). Scientific Reports 10 (1): sid. 9853. doi:10.1038/s41598-020-66643-0. ISSN 2045-2322. PMID 32555394. PMC: PMC7299994. https://www.nature.com/articles/s41598-020-66643-0. Läst 9 februari 2022.
Warby, Simon C.; Montpetit, Alexandre; Hayden, Anna R.; Carroll, Jeffrey B.; Butland, Stefanie L.; Visscher, Henk. ”CAG Expansion in the Huntington Disease Gene Is Associated with a Specific and Targetable Predisposing Haplogroup”. American Journal of Human Genetics 84 (3): sid. 351–366. doi:10.1016/j.ajhg.2009.02.003. ISSN 0002-9297. http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2668007/. Läst 5 juni 2017.
Liu, Jeh-Ping; Zeitlin, Scott O.. ”Is Huntingtin Dispensable in the Adult Brain?” (på engelska). Journal of Huntington's Disease 6 (1): sid. 1–17. doi:10.3233/jhd-170235. ISSN 1879-6397. http://www.medra.org/servlet/aliasResolver?alias=iospress&doi=10.3233/JHD-170235. Läst 7 juni 2017.
Niemelä, Valter; Landtblom, Anne-Marie; Blennow, Kaj; Sundblom, Jimmy. ”Tau or neurofilament light—Which is the more suitable biomarker for Huntington’s disease?”. PLOS ONE 12 (2): sid. e0172762. doi:10.1371/journal.pone.0172762. ISSN 1932-6203. http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0172762. Läst 29 maj 2017.
Huntington, George. ”ON CHOREA”. Archives of Neurology 17 (3): sid. 332–333. doi:10.1001/archneur.1967.00470270110014. ISSN 0003-9942. http://jamanetwork.com/journals/jamaneurology/fullarticle/567551. Läst 29 maj 2017.