Միոտոնիկ դիստրոֆիա (Armenian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Միոտոնիկ դիստրոֆիա" in Armenian language version.

refsWebsite

Global rank Armenian rank

31nih.gov

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22doi.org

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6web.archive.org

1^st place

5archive.org

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2wikidata.org

43^rd place

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2wikipedia.org

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2worldcat.org

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2handle.net

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2,318^th place

1harvard.edu

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1mda.org

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1uptodate.com

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1myotonic.org

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archive.org

Harley HG, Walsh KV, Rundle S, Brook JD, Sarfarazi M, Koch MC, Floyd JL, Harper PS, Shaw DJ (May 1991). «Localisation of the myotonic dystrophy locus to 19q13.2-19q13.3 and its relationship to twelve polymorphic loci on 19q». Hum. Genet. 87 (1): 73–80. doi:10.1007/BF01213096. PMID 2037285.
Le Ber I, Martinez M, Campion D, Laquerrière A, Bétard C, Bassez G, Girard C, Saugier-Veber P, Raux G, Sergeant N, Magnier P, Maisonobe T, Eymard B, Duyckaerts C, Delacourte A, Frebourg T, Hannequin D (September 2004). «A non-DM1, non-DM2 multisystem myotonic disorder with frontotemporal dementia: phenotype and suggestive mapping of the DM3 locus to chromosome 15q21-24». Brain. 127 (Pt 9): 1979–92. doi:10.1093/brain/awh216. PMID 15215218.
Wheeler TM, Lueck JD, Swanson MS, Dirksen RT, Thornton CA (December 2007). «Correction of ClC-1 splicing eliminates chloride channelopathy and myotonia in mouse models of myotonic dystrophy». J. Clin. Invest. 117 (12): 3952–7. doi:10.1172/JCI33355. PMC 2075481. PMID 18008009.
Cup EH, Pieterse AJ, Ten Broek-Pastoor JM, Munneke M, van Engelen BG, Hendricks HT, van der Wilt GJ, Oostendorp RA (November 2007). «Exercise therapy and other types of physical therapy for patients with neuromuscular diseases: a systematic review». Arch Phys Med Rehabil. 88 (11): 1452–64. doi:10.1016/j.apmr.2007.07.024. PMID 17964887.
Orngreen MC, Olsen DB, Vissing J (May 2005). «Aerobic training in patients with myotonic dystrophy type 1». Ann. Neurol. 57 (5): 754–7. doi:10.1002/ana.20460. PMID 15852373.

doi.org

Meola, G; Cardani, R (April 2015). «Myotonic dystrophies: An update on clinical aspects, genetic, pathology, and molecular pathomechanisms». Biochimica et Biophysica Acta. 1852 (4): 594–606. doi:10.1016/j.bbadis.2014.05.019. PMID 24882752.
Klein, AF; Dastidar, S; Furling, D; Chuah, MK (2015). «Therapeutic Approaches for Dominant Muscle Diseases: Highlight on Myotonic Dystrophy». Current Gene Therapy. 15 (4): 329–37. doi:10.2174/1566523215666150630120537. PMID 26122101.
Mahadevan M, Tsilfidis C, Sabourin L, Shutler G, Amemiya C, Jansen G, Neville C, Narang M, Barceló J, O'Hoy K (March 1992). «Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene». Science. 255 (5049): 1253–5. Bibcode:1992Sci...255.1253M. doi:10.1126/science.1546325. PMID 1546325.
van der Ven PF, Jansen G, van Kuppevelt TH, Perryman MB, Lupa M, Dunne PW, ter Laak HJ, Jap PH, Veerkamp JH, Epstein HF (November 1993). «Myotonic dystrophy kinase is a component of neuromuscular junctions». Hum. Mol. Genet. 2 (11): 1889–94. doi:10.1093/hmg/2.11.1889. PMID 8281152.
Harley HG, Walsh KV, Rundle S, Brook JD, Sarfarazi M, Koch MC, Floyd JL, Harper PS, Shaw DJ (May 1991). «Localisation of the myotonic dystrophy locus to 19q13.2-19q13.3 and its relationship to twelve polymorphic loci on 19q». Hum. Genet. 87 (1): 73–80. doi:10.1007/BF01213096. PMID 2037285.
Turner C, Hilton-Jones D (April 2010). «The myotonic dystrophies: diagnosis and management». J. Neurol. Neurosurg. Psychiatry. 81 (4): 358–67. doi:10.1136/jnnp.2008.158261. PMID 20176601.
Usdin K, House NC, Freudenreich CH (2015). «Repeat instability during DNA repair: Insights from model systems». Crit. Rev. Biochem. Mol. Biol. 50 (2): 142–67. doi:10.3109/10409238.2014.999192. PMC 4454471. PMID 25608779.
Ho TH, Savkur RS, Poulos MG, Mancini MA, Swanson MS, Cooper TA (July 2005). «Colocalization of muscleblind with RNA foci is separable from mis-regulation of alternative splicing in myotonic dystrophy». J. Cell Sci. 118 (Pt 13): 2923–33. doi:10.1242/jcs.02404. PMID 15961406.
Day JW, Ricker K, Jacobsen JF, Rasmussen LJ, Dick KA, Kress W, Schneider C, Koch MC, Beilman GJ, Harrison AR, Dalton JC, Ranum LP (February 2003). «Myotonic dystrophy type 2: molecular, diagnostic and clinical spectrum». Neurology. 60 (4): 657–64. doi:10.1001/archneur.60.5.657. PMID 12601109.
Liquori CL, Ricker K, Moseley ML, Jacobsen JF, Kress W, Naylor SL, Day JW, Ranum LP (August 2001). «Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9». Science. 293 (5531): 864–7. doi:10.1126/science.1062125. PMID 11486088.
Le Ber I, Martinez M, Campion D, Laquerrière A, Bétard C, Bassez G, Girard C, Saugier-Veber P, Raux G, Sergeant N, Magnier P, Maisonobe T, Eymard B, Duyckaerts C, Delacourte A, Frebourg T, Hannequin D (September 2004). «A non-DM1, non-DM2 multisystem myotonic disorder with frontotemporal dementia: phenotype and suggestive mapping of the DM3 locus to chromosome 15q21-24». Brain. 127 (Pt 9): 1979–92. doi:10.1093/brain/awh216. PMID 15215218.
Udd B, Meola G, Krahe R, Thornton C, Ranum LP, Bassez G, Kress W, Schoser B, Moxley R (June 2006). «140th ENMC International Workshop: Myotonic Dystrophy DM2/PROMM and other myotonic dystrophies with guidelines on management». Neuromuscul. Disord. 16 (6): 403–13. doi:10.1016/j.nmd.2006.03.010. PMID 16684600.
Nakamori M, Taylor K, Mochizuki H, Sobczak K, Takahashi MP (January 2016). «Oral administration of erythromycin decreases RNA toxicity in myotonic dystrophy». Ann Clin Transl Neurol. 3 (1): 42–54. doi:10.1002/acn3.271. PMC 4704483. PMID 26783549.
Rönnblom A, Andersson S, Hellström PM, Danielsson A (August 2002). «Gastric emptying in myotonic dystrophy». Eur. J. Clin. Invest. 32 (8): 570–4. doi:10.1046/j.1365-2362.2002.01028.x. PMID 12190956.
Wheeler TM, Lueck JD, Swanson MS, Dirksen RT, Thornton CA (December 2007). «Correction of ClC-1 splicing eliminates chloride channelopathy and myotonia in mouse models of myotonic dystrophy». J. Clin. Invest. 117 (12): 3952–7. doi:10.1172/JCI33355. PMC 2075481. PMID 18008009.
Voet NB, van der Kooi EL, Riphagen II, Lindeman E, van Engelen BG, Geurts AC (July 2013). «Strength training and aerobic exercise training for muscle disease». Cochrane Database Syst Rev (7): CD003907. doi:10.1002/14651858.CD003907.pub4. hdl:2066/123481. PMID 23835682.
Cup EH, Pieterse AJ, Ten Broek-Pastoor JM, Munneke M, van Engelen BG, Hendricks HT, van der Wilt GJ, Oostendorp RA (November 2007). «Exercise therapy and other types of physical therapy for patients with neuromuscular diseases: a systematic review». Arch Phys Med Rehabil. 88 (11): 1452–64. doi:10.1016/j.apmr.2007.07.024. PMID 17964887.
Orngreen MC, Olsen DB, Vissing J (May 2005). «Aerobic training in patients with myotonic dystrophy type 1». Ann. Neurol. 57 (5): 754–7. doi:10.1002/ana.20460. PMID 15852373.
Voet NB, van der Kooi EL, Riphagen II, Lindeman E, van Engelen BG, Geurts AC (January 2010). «Strength training and aerobic exercise training for muscle disease». Cochrane Database Syst Rev (1): CD003907. doi:10.1002/14651858.CD003907.pub3. hdl:2066/123481. PMID 20091552.
Mishra SK, Singh S, Lee B, Khosa S, Moheb N, Tandon VA (2018). «"Dystrophia Myotonica" and the Legacy of Hans Gustav Wilhelm Steinert». Ann Indian Acad Neurol. 21 (2): 116–118. doi:10.4103/aian.AIAN_182_17. PMC 6073962. PMID 30122835.{{cite journal}}: CS1 սպաս․ չպիտակված ազատ DOI (link)

dx.doi.org

Campbell C., Levin S., Siu V. M., Venance S., Jacob P. Congenital myotonic dystrophy: Canadian population-based surveillance study. // J. Pediatr. — Elsevier BV, 2013. — Vol. 163, Iss. 1. — P. 120—5.e1—3. — ISSN 0022-3476; 1097-6833; 1085-8695 — doi:10.1016/J.JPEDS.2012.12.070 — PMID:23415617
«Construction of a Quality of Life Questionnaire for slowly progressive neuromuscular disease»։ Qual Life Res 24 (11): 2615–23։ November 2015։ PMID 26141500։ doi:10.1007/s11136-015-1013-8

handle.net

hdl.handle.net

Voet NB, van der Kooi EL, Riphagen II, Lindeman E, van Engelen BG, Geurts AC (July 2013). «Strength training and aerobic exercise training for muscle disease». Cochrane Database Syst Rev (7): CD003907. doi:10.1002/14651858.CD003907.pub4. hdl:2066/123481. PMID 23835682.
Voet NB, van der Kooi EL, Riphagen II, Lindeman E, van Engelen BG, Geurts AC (January 2010). «Strength training and aerobic exercise training for muscle disease». Cochrane Database Syst Rev (1): CD003907. doi:10.1002/14651858.CD003907.pub3. hdl:2066/123481. PMID 20091552.

harvard.edu

ui.adsabs.harvard.edu

Mahadevan M, Tsilfidis C, Sabourin L, Shutler G, Amemiya C, Jansen G, Neville C, Narang M, Barceló J, O'Hoy K (March 1992). «Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene». Science. 255 (5049): 1253–5. Bibcode:1992Sci...255.1253M. doi:10.1126/science.1546325. PMID 1546325.

mda.org

«Juvenile-Onset MMD1». Muscular Dystrophy Association. MDA. Արխիվացված է օրիգինալից 2015 թ․ մարտի 8-ին. Վերցված է 2015 թ․ մարտի 17-ին.

myotonic.org

Pandya, S; Eichinger, K. «Role of physical therapy in the assessment and management of individuals with myotonic dystrophy». Myotonic Dystrophy Foundation. Արխիվացված է օրիգինալից 2015 թ․ սեպտեմբերի 26-ին. Վերցված է 2012 թ․ մայիսի 5-ին.

nih.gov

pubmed.ncbi.nlm.nih.gov

Meola, G; Cardani, R (April 2015). «Myotonic dystrophies: An update on clinical aspects, genetic, pathology, and molecular pathomechanisms». Biochimica et Biophysica Acta. 1852 (4): 594–606. doi:10.1016/j.bbadis.2014.05.019. PMID 24882752.
Klein, AF; Dastidar, S; Furling, D; Chuah, MK (2015). «Therapeutic Approaches for Dominant Muscle Diseases: Highlight on Myotonic Dystrophy». Current Gene Therapy. 15 (4): 329–37. doi:10.2174/1566523215666150630120537. PMID 26122101.
Mahadevan M, Tsilfidis C, Sabourin L, Shutler G, Amemiya C, Jansen G, Neville C, Narang M, Barceló J, O'Hoy K (March 1992). «Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene». Science. 255 (5049): 1253–5. Bibcode:1992Sci...255.1253M. doi:10.1126/science.1546325. PMID 1546325.
van der Ven PF, Jansen G, van Kuppevelt TH, Perryman MB, Lupa M, Dunne PW, ter Laak HJ, Jap PH, Veerkamp JH, Epstein HF (November 1993). «Myotonic dystrophy kinase is a component of neuromuscular junctions». Hum. Mol. Genet. 2 (11): 1889–94. doi:10.1093/hmg/2.11.1889. PMID 8281152.
Harley HG, Walsh KV, Rundle S, Brook JD, Sarfarazi M, Koch MC, Floyd JL, Harper PS, Shaw DJ (May 1991). «Localisation of the myotonic dystrophy locus to 19q13.2-19q13.3 and its relationship to twelve polymorphic loci on 19q». Hum. Genet. 87 (1): 73–80. doi:10.1007/BF01213096. PMID 2037285.
Turner C, Hilton-Jones D (April 2010). «The myotonic dystrophies: diagnosis and management». J. Neurol. Neurosurg. Psychiatry. 81 (4): 358–67. doi:10.1136/jnnp.2008.158261. PMID 20176601.
Usdin K, House NC, Freudenreich CH (2015). «Repeat instability during DNA repair: Insights from model systems». Crit. Rev. Biochem. Mol. Biol. 50 (2): 142–67. doi:10.3109/10409238.2014.999192. PMC 4454471. PMID 25608779.
Ho TH, Savkur RS, Poulos MG, Mancini MA, Swanson MS, Cooper TA (July 2005). «Colocalization of muscleblind with RNA foci is separable from mis-regulation of alternative splicing in myotonic dystrophy». J. Cell Sci. 118 (Pt 13): 2923–33. doi:10.1242/jcs.02404. PMID 15961406.
Day JW, Ricker K, Jacobsen JF, Rasmussen LJ, Dick KA, Kress W, Schneider C, Koch MC, Beilman GJ, Harrison AR, Dalton JC, Ranum LP (February 2003). «Myotonic dystrophy type 2: molecular, diagnostic and clinical spectrum». Neurology. 60 (4): 657–64. doi:10.1001/archneur.60.5.657. PMID 12601109.
Dalton, Joline C.; Ranum, Laura PW; Day, John W. (1993 թ․ հունվարի 1). Pagon, Roberta A.; Adam, Margaret P.; Ardinger, Holly H.; Wallace, Stephanie E.; Amemiya, Anne; Bean, Lora JH; Bird, Thomas D.; Fong, Chin-To; Mefford, Heather C. (eds.). Myotonic Dystrophy Type 2. Seattle (WA): University of Washington, Seattle. PMID 20301639. Արխիվացված օրիգինալից 2017 թ․ հունվարի 28-ին.updated 2013
Liquori CL, Ricker K, Moseley ML, Jacobsen JF, Kress W, Naylor SL, Day JW, Ranum LP (August 2001). «Myotonic dystrophy type 2 caused by a CCTG expansion in intron 1 of ZNF9». Science. 293 (5531): 864–7. doi:10.1126/science.1062125. PMID 11486088.
Le Ber I, Martinez M, Campion D, Laquerrière A, Bétard C, Bassez G, Girard C, Saugier-Veber P, Raux G, Sergeant N, Magnier P, Maisonobe T, Eymard B, Duyckaerts C, Delacourte A, Frebourg T, Hannequin D (September 2004). «A non-DM1, non-DM2 multisystem myotonic disorder with frontotemporal dementia: phenotype and suggestive mapping of the DM3 locus to chromosome 15q21-24». Brain. 127 (Pt 9): 1979–92. doi:10.1093/brain/awh216. PMID 15215218.
Udd B, Meola G, Krahe R, Thornton C, Ranum LP, Bassez G, Kress W, Schoser B, Moxley R (June 2006). «140th ENMC International Workshop: Myotonic Dystrophy DM2/PROMM and other myotonic dystrophies with guidelines on management». Neuromuscul. Disord. 16 (6): 403–13. doi:10.1016/j.nmd.2006.03.010. PMID 16684600.
Nakamori M, Taylor K, Mochizuki H, Sobczak K, Takahashi MP (January 2016). «Oral administration of erythromycin decreases RNA toxicity in myotonic dystrophy». Ann Clin Transl Neurol. 3 (1): 42–54. doi:10.1002/acn3.271. PMC 4704483. PMID 26783549.
Rönnblom A, Andersson S, Hellström PM, Danielsson A (August 2002). «Gastric emptying in myotonic dystrophy». Eur. J. Clin. Invest. 32 (8): 570–4. doi:10.1046/j.1365-2362.2002.01028.x. PMID 12190956.
Wheeler TM, Lueck JD, Swanson MS, Dirksen RT, Thornton CA (December 2007). «Correction of ClC-1 splicing eliminates chloride channelopathy and myotonia in mouse models of myotonic dystrophy». J. Clin. Invest. 117 (12): 3952–7. doi:10.1172/JCI33355. PMC 2075481. PMID 18008009.
Voet NB, van der Kooi EL, Riphagen II, Lindeman E, van Engelen BG, Geurts AC (July 2013). «Strength training and aerobic exercise training for muscle disease». Cochrane Database Syst Rev (7): CD003907. doi:10.1002/14651858.CD003907.pub4. hdl:2066/123481. PMID 23835682.
Cup EH, Pieterse AJ, Ten Broek-Pastoor JM, Munneke M, van Engelen BG, Hendricks HT, van der Wilt GJ, Oostendorp RA (November 2007). «Exercise therapy and other types of physical therapy for patients with neuromuscular diseases: a systematic review». Arch Phys Med Rehabil. 88 (11): 1452–64. doi:10.1016/j.apmr.2007.07.024. PMID 17964887.
Orngreen MC, Olsen DB, Vissing J (May 2005). «Aerobic training in patients with myotonic dystrophy type 1». Ann. Neurol. 57 (5): 754–7. doi:10.1002/ana.20460. PMID 15852373.
Voet NB, van der Kooi EL, Riphagen II, Lindeman E, van Engelen BG, Geurts AC (January 2010). «Strength training and aerobic exercise training for muscle disease». Cochrane Database Syst Rev (1): CD003907. doi:10.1002/14651858.CD003907.pub3. hdl:2066/123481. PMID 20091552.
Mishra SK, Singh S, Lee B, Khosa S, Moheb N, Tandon VA (2018). «"Dystrophia Myotonica" and the Legacy of Hans Gustav Wilhelm Steinert». Ann Indian Acad Neurol. 21 (2): 116–118. doi:10.4103/aian.AIAN_182_17. PMC 6073962. PMID 30122835.{{cite journal}}: CS1 սպաս․ չպիտակված ազատ DOI (link)
Olbrych-Karpińska B, Tutaj A (September 1981). «[Case of Curschmann-Batten-Steinert syndrome]». Wiad. Lek. (Polish). 34 (17): 1467–9. ISSN 0043-5147. PMID 7331343.{{cite journal}}: CS1 սպաս․ չճանաչված լեզու (link)

ncbi.nlm.nih.gov

Campbell C., Levin S., Siu V. M., Venance S., Jacob P. Congenital myotonic dystrophy: Canadian population-based surveillance study. // J. Pediatr. — Elsevier BV, 2013. — Vol. 163, Iss. 1. — P. 120—5.e1—3. — ISSN 0022-3476; 1097-6833; 1085-8695 — doi:10.1016/J.JPEDS.2012.12.070 — PMID:23415617
Bird, Thomas D. (1993 թ․ հունվարի 1). «Myotonic Dystrophy Type 1». GeneReviews(®). Արխիվացված օրիգինալից 2017 թ․ հունվարի 18-ին. Վերցված է 2016 թ․ մայիսի 9-ին.update 2015
Usdin K, House NC, Freudenreich CH (2015). «Repeat instability during DNA repair: Insights from model systems». Crit. Rev. Biochem. Mol. Biol. 50 (2): 142–67. doi:10.3109/10409238.2014.999192. PMC 4454471. PMID 25608779.
Dalton, Joline C.; Ranum, Laura PW; Day, John W. (1993 թ․ հունվարի 1). Pagon, Roberta A.; Adam, Margaret P.; Ardinger, Holly H.; Wallace, Stephanie E.; Amemiya, Anne; Bean, Lora JH; Bird, Thomas D.; Fong, Chin-To; Mefford, Heather C. (eds.). Myotonic Dystrophy Type 2. Seattle (WA): University of Washington, Seattle. PMID 20301639. Արխիվացված օրիգինալից 2017 թ․ հունվարի 28-ին.updated 2013
«Construction of a Quality of Life Questionnaire for slowly progressive neuromuscular disease»։ Qual Life Res 24 (11): 2615–23։ November 2015։ PMID 26141500։ doi:10.1007/s11136-015-1013-8
Nakamori M, Taylor K, Mochizuki H, Sobczak K, Takahashi MP (January 2016). «Oral administration of erythromycin decreases RNA toxicity in myotonic dystrophy». Ann Clin Transl Neurol. 3 (1): 42–54. doi:10.1002/acn3.271. PMC 4704483. PMID 26783549.
Wheeler TM, Lueck JD, Swanson MS, Dirksen RT, Thornton CA (December 2007). «Correction of ClC-1 splicing eliminates chloride channelopathy and myotonia in mouse models of myotonic dystrophy». J. Clin. Invest. 117 (12): 3952–7. doi:10.1172/JCI33355. PMC 2075481. PMID 18008009.
Mishra SK, Singh S, Lee B, Khosa S, Moheb N, Tandon VA (2018). «"Dystrophia Myotonica" and the Legacy of Hans Gustav Wilhelm Steinert». Ann Indian Acad Neurol. 21 (2): 116–118. doi:10.4103/aian.AIAN_182_17. PMC 6073962. PMID 30122835.{{cite journal}}: CS1 սպաս․ չպիտակված ազատ DOI (link)

ghr.nlm.nih.gov

«myotonic dystrophy». GHR. 2016 թ․ հոկտեմբերի 11. Արխիվացված օրիգինալից 2016 թ․ հոկտեմբերի 18-ին. Վերցված է 2016 թ․ հոկտեմբերի 16-ին.

uptodate.com

«Myotonic dystrophy: Etiology, clinical features, and diagnosis». Արխիվացված օրիգինալից 2014 թ․ փետրվարի 22-ին. Վերցված է 2014 թ․ փետրվարի 15-ին.

web.archive.org

«myotonic dystrophy». GHR. 2016 թ․ հոկտեմբերի 11. Արխիվացված օրիգինալից 2016 թ․ հոկտեմբերի 18-ին. Վերցված է 2016 թ․ հոկտեմբերի 16-ին.
Bird, Thomas D. (1993 թ․ հունվարի 1). «Myotonic Dystrophy Type 1». GeneReviews(®). Արխիվացված օրիգինալից 2017 թ․ հունվարի 18-ին. Վերցված է 2016 թ․ մայիսի 9-ին.update 2015
Dalton, Joline C.; Ranum, Laura PW; Day, John W. (1993 թ․ հունվարի 1). Pagon, Roberta A.; Adam, Margaret P.; Ardinger, Holly H.; Wallace, Stephanie E.; Amemiya, Anne; Bean, Lora JH; Bird, Thomas D.; Fong, Chin-To; Mefford, Heather C. (eds.). Myotonic Dystrophy Type 2. Seattle (WA): University of Washington, Seattle. PMID 20301639. Արխիվացված օրիգինալից 2017 թ․ հունվարի 28-ին.updated 2013
«Juvenile-Onset MMD1». Muscular Dystrophy Association. MDA. Արխիվացված է օրիգինալից 2015 թ․ մարտի 8-ին. Վերցված է 2015 թ․ մարտի 17-ին.
«Myotonic dystrophy: Etiology, clinical features, and diagnosis». Արխիվացված օրիգինալից 2014 թ․ փետրվարի 22-ին. Վերցված է 2014 թ․ փետրվարի 15-ին.
Pandya, S; Eichinger, K. «Role of physical therapy in the assessment and management of individuals with myotonic dystrophy». Myotonic Dystrophy Foundation. Արխիվացված է օրիգինալից 2015 թ․ սեպտեմբերի 26-ին. Վերցված է 2012 թ․ մայիսի 5-ին.

wikidata.org

Bednařík J., Ambler Z., Růžička E. Klinická neurologie: část speciální — ISBN 978-80-7387-389-9
Campbell C., Levin S., Siu V. M., Venance S., Jacob P. Congenital myotonic dystrophy: Canadian population-based surveillance study. // J. Pediatr. — Elsevier BV, 2013. — Vol. 163, Iss. 1. — P. 120—5.e1—3. — ISSN 0022-3476; 1097-6833; 1085-8695 — doi:10.1016/J.JPEDS.2012.12.070 — PMID:23415617

wikipedia.org

en.wikipedia.org

Campbell C., Levin S., Siu V. M., Venance S., Jacob P. Congenital myotonic dystrophy: Canadian population-based surveillance study. // J. Pediatr. — Elsevier BV, 2013. — Vol. 163, Iss. 1. — P. 120—5.e1—3. — ISSN 0022-3476; 1097-6833; 1085-8695 — doi:10.1016/J.JPEDS.2012.12.070 — PMID:23415617
«Construction of a Quality of Life Questionnaire for slowly progressive neuromuscular disease»։ Qual Life Res 24 (11): 2615–23։ November 2015։ PMID 26141500։ doi:10.1007/s11136-015-1013-8

worldcat.org

Campbell C., Levin S., Siu V. M., Venance S., Jacob P. Congenital myotonic dystrophy: Canadian population-based surveillance study. // J. Pediatr. — Elsevier BV, 2013. — Vol. 163, Iss. 1. — P. 120—5.e1—3. — ISSN 0022-3476; 1097-6833; 1085-8695 — doi:10.1016/J.JPEDS.2012.12.070 — PMID:23415617
Olbrych-Karpińska B, Tutaj A (September 1981). «[Case of Curschmann-Batten-Steinert syndrome]». Wiad. Lek. (Polish). 34 (17): 1467–9. ISSN 0043-5147. PMID 7331343.{{cite journal}}: CS1 սպաս․ չճանաչված լեզու (link)