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Electrocardiographic abnormalities in very young Duchenne muscular dystrophy patients precede the onset of cardiac dysfunction

J James, K Kinnett, Y Wang, RF Ittenbach… - Neuromuscular …, 2011 - Elsevier
... Permissions & Reprints. Electrocardiographic abnormalities in very young Duchenne muscular
dystrophy patients precede the onset of cardiac dysfunction. ... Abstract. Overt cardiac involvement
in Duchenne muscular dystrophy (DMD) typically occurs later in the disease. ...
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[HTML] Prevalence and distribution of regional scar in dysfunctional myocardial segments in Duchenne muscular dystrophy

[HTML] from nih.govKC Bilchick, M Salerno, D Plitt, Y Dori… - Journal of …, 2011 - ncbi.nlm.nih.gov
... [PMC free article] [PubMed] [Cross Ref]; Gilroy J, Calahan JL, Berman R, Newman M. Cardiac
and pulmonary complications in Duchenne's progressive muscular dystrophy. Circulation. ... The
pathology of the heart in progressive muscular dystrophy: epimyocardial fibrosis. ...
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Progressive dysphagia in limb‐girdle muscular dystrophy type 2B

R Walsh, F Hill, N Breslin, S Connolly… - Muscle & …, 2011 - Wiley Online Library
A 40-year-old, right-handed woman had been initially referred to the neurology service at our
hospital at age 36 for further assessment. She had a background history of asthma,
migraine, and mild vitamin B 12 deficiency (vitamin B 12 level: 118 pg/ml, normal range: ...
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Dysferlin, Annexin A1, and Mitsugumin 53 Are Upregulated in Muscular Dystrophy and Localize to Longitudinal Tubules of the T-System With Stretch

LB Waddell, FA Lemckert, XF Zheng… - … of Neuropathology & …, 2011 - journals.lww.com
... newly identified protein mitsugumin 53 (MG53). Mitsugumin 53 accumulates at sites
of membrane damage, and MG53-knockout mice display a progressive muscular
dystrophy. This study explored the expression and localization ...
Cited by 2 - Related articles - All 3 versions

A founder mutation in Anoctamin 5 is a major cause of limb-girdle muscular dystrophy

D Hicks, A Sarkozy, N Muelas, K Koehler… - Brain, 2011 - Oxford Univ Press
... We have further defined the clinical phenotype of ANO5-associated muscular dystrophy. ...
Onset varies from the early 20 s to 50 s and the weakness is generally slowly progressive,
with most patients remaining ambulant for several decades. ...
Cited by 6 - Related articles - All 4 versions

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