Respiratory dysfunction in myotonic dystrophy type 1: A systematic review-Reference-Cited by-同舟云学术

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Respiratory dysfunction in myotonic dystrophy type 1: A systematic review

Published:2019-03 Issue:3 Volume:29 Page:198-212
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Hawkins A.M.,Hawkins C.L.,Abdul Razak K.,Khoo T.K.,Tran K.,Jackson R.V.

Publisher

Elsevier BV

Subject

Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health

Reference76 articles.

1. Myotonic dystrophy, 3rd ed;Harper,2001

2. 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

3. Towards an integrative approach to the management of myotonic dystrophy type 1;Gagnon;J Neurol Neurosurg Psychiatry,2007

4. A 10-year study of mortality in a cohort of patients with myotonic dystrophy;Mathieu;Neurology,1999

5. Respiratory function, electrocardiography and quality of life in individuals with muscular dystrophy;Ahlström;Chest,1994

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