Myotonic dystrophy health index: Correlations with clinical tests and patient function-Reference-Cited by-同舟云学术

Myotonic dystrophy health index: Correlations with clinical tests and patient function

Published:2015-12-29 Issue:2 Volume:53 Page:183-190
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle Nerve

Author:

Heatwole Chad¹,Bode Rita²,Johnson Nicholas E.³,Dekdebrun Jeanne¹,Dilek Nuran¹,Eichinger Katy¹,Hilbert James E.¹,Logigian Eric¹,Luebbe Elizabeth¹,Martens William¹,Mcdermott Michael P.¹⁴,Pandya Shree¹,Puwanant Araya⁵,Rothrock Nan⁶,Thornton Charles¹,Vickrey Barbara G.⁷⁸,Victorson David⁶,Moxley Richard T.¹

Affiliation:

1. The University of Rochester Medical Center, Department of Neurology; 601 Elmwood Avenue, Box 673 Rochester New York 14642 USA

2. Psychometric Consultant; Chicago Illinois USA

3. The University of Utah; Salt Lake City Utah USA

4. The University of Rochester Medical Center, Department of Biostatistics and Computational Biology; Rochester New York USA

5. The University of Pittsburgh School of Medicine; Pittsburgh Pennsylvania USA

6. Northwestern University Feinberg School of Medicine; Chicago Illinois USA

7. Greater Los Angeles VA HealthCare System; Los Angeles California USA

8. David Geffen School of Medicine, UCLA Medical Center; Los Angeles California USA

Funder

Wellstone Muscular Dystrophy Cooperative Research Center

University of Rochester CTSA

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Clinical Neurology,Physiology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/mus.24725/fullpdf

Reference47 articles.

1. Molecular basis of myotonic dystrophy: expansion of a trinucleotide (CTG) repeat at the 3' end of a transcript encoding a protein kinase family member;Brook;Cell,1992

2. An unstable triplet repeat in a gene related to myotonic muscular dystrophy;Fu;Science,1992

3. Myotonic dystrophy mutation: an unstable CTG repeat in the 3' untranslated region of the gene;Mahadevan;Science,1992

4. Patient-reported impact of symptoms in myotonic dystrophy type 1 (PRISM-1);Heatwole;Neurology,2012

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