Hyper-CK-emia as the sole manifestation of myotonic dystrophy type 2-Reference-Cited by-同舟云学术

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Hyper-CK-emia as the sole manifestation of myotonic dystrophy type 2

Published:2005 Issue:6 Volume:31 Page:764-767
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle Nerve

Author:

Merlini Luciano,Sabatelli Patrizia,Columbaro Marta,Bonifazi Emanuela,Pisani Valerio,Massa Roberto,Novelli Giuseppe

Publisher

Wiley

Subject

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

Reference15 articles.

1. Idiopathic HyperCKemia Revisited

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

3. Pathological reactions of skeletal muscle. In: editors. Skeletal muscle pathology. New York: Churchill Livingstone; 1992. p 123-184.

4. Myotonic dystrophy type 2

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1. Myotonic Dystrophies;Current Clinical Neurology;2023

2. The etiology of rhabdomyolysis: an interaction between genetic susceptibility and external triggers;European Journal of Neurology;2020-10-25

3. Asymptomatic HyperCKemia;Managing Myositis;2019-12-15

4. Significance of Asymptomatic Hyper Creatine-Kinase Emia;Journal of Clinical Neuromuscular Disease;2019-12

5. Marathoning with myotonic dystrophy type 2 (proximal myotonic myopathy) and leukopenia;SAGE Open Medical Case Reports;2017-01-01

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