Body composition in patients with congenital myotonic dystrophy-Reference-Cited by-同舟云学术

Body composition in patients with congenital myotonic dystrophy

Published:2019-06-10 Issue:2 Volume:60 Page:176-179
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle Nerve

Author:

Ceballos‐Sáenz Delia¹,Zapata‐Aldana Eugenio²,Singeris Stephanie¹,Hicks Rhiannon¹,Johnson Nicholas³^ORCID,Campbell Craig¹⁴

Affiliation:

1. Paediatric Neurology DepartmentChildren's Hospital, London Health Science Centre 800 Commissioners Road East, PO Box 5012, London Ontario Canada N6A 5W9

2. Department of Pediatrics and Child Health, Max Rady College of Medicine, Rady Faculty of Health SciencesUniversity of Manitoba Winnipeg Manitoba Canada

3. Department of NeurologyVirginia Commonwealth University Richmond Virginia USA

4. Department of Paediatrics, Clinical Neurological Sciences and EpidemiologySchulich School of Medicine and Dentistry, Western University London Ontario Canada

Publisher

Wiley

Subject

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

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mus.26509

Reference17 articles.

1. The myotonic dystrophies: molecular, clinical, and therapeutic challenges

2. Congenital Myotonic Dystrophy: Canadian Population-Based Surveillance Study

3. Physical function and mobility in children with congenital myotonic dystrophy

4. Developmental Milestones and Quality of Life Assessment in a Congenital Myotonic Dystrophy Cohort

5. Immaturity of muscle fibers in the congenital form of myotonic dystrophy: Its consequences and its origin

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