Familial idiopathic hyper-CK-emia: An underrecognized condition-Reference-Cited by-同舟云学术

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Familial idiopathic hyper-CK-emia: An underrecognized condition

Published:2006 Issue:6 Volume:33 Page:760-765
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle Nerve

Author:

Capasso Margherita,De Angelis Maria Vittoria,Di Muzio Antonio,Scarciolla Oronzo,Pace Marta,Stuppia Liborio,Comi Giacomo Pietro,Uncini Antonino

Publisher

Wiley

Subject

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

Reference26 articles.

1. Idiopathic HyperCKemia Revisited

2. A novel mutation in the caveolin-3 gene causing familial isolated hyperCKaemia

3. Persistent hyperCKemia: fourteen patients studied in retrospect

4. HyperCKemia as the Only Sign of McArdle's Disease in a Child

5. Immunohistochemical study of caveolin-3 in idiopathic hyperCKaemia

Cited by 33 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Causes of HyperCKemia in Children: A Retrospective Cohort Study;Journal of Child Neurology;2022-12-25

2. A novel 1-bp deletion variant in DAG1 in Japanese familial asymptomatic hyper-CK-emia;Human Genome Variation;2022-01-27

3. Erhöhte Kreatinkinase-Serumaktivität (Hyper-CK-Ämie);DGNeurologie;2020-12-17

4. Muscle Toxicity of Drugs: When Drugs Turn Physiology into Pathophysiology;Physiological Reviews;2020-04-01

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

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