Cardiomyopathy in Patients With Hereditary Motor and Sensory Neuropathy-Reference-Cited by-同舟云学术

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Cardiomyopathy in Patients With Hereditary Motor and Sensory Neuropathy

Published:1987-08 Issue:8 Volume:62 Page:672-675
ISSN:0025-6196
Container-title:Mayo Clinic Proceedings
language:en
Short-container-title:Mayo Clinic Proceedings

Author:

DYCK PETER JAMES,SWANSON CAROL J.,NISHIMURA RICK A.,KAZMIER FRANCIS J.,LIE J.T.

Publisher

Elsevier BV

Subject

General Medicine

Reference11 articles.

1. Paroxysmal atrial flutter in peroneal muscular atrophy;Leak;Br Heart J,1961

2. Hereditary polyneuropathy of Roussy-Lévy type with associated cardiomyopathy;Lascelles;Guy's Hosp Rep,1970

3. Heart block and peroneal muscular atrophy: a family study;Littler;Q J Med,1970

4. Ultrastructure of myocardium in familial heart block and peroneal muscular atrophy;Kay;Br Heart J,1972

5. Charcot-Marie-Tooth disease, Wolff-Parkinson-White syndrome, and abnormal intracardiac conduction;Bowers;Am Heart J,1973

Cited by 11 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. Kidney Function in Patients With Neuromuscular Disease: Creatinine Versus Cystatin C;Frontiers in Neurology;2021-09-24

2. Left Ventricular Hypertrabeculation/Noncompaction with PMP22 Duplication-Based Charcot-Marie-Tooth Disease Type 1A;Cardiology;2006

3. A new mutation of the lamin A/C gene leading to autosomal dominant axonal neuropathy, muscular dystrophy, cardiac disease, and leuconychia;Journal of Medical Genetics;2004-03-01

4. Phenotypic variability in autosomal recessive axonal Charcot-Marie-Tooth disease due to the R298C mutation in lamin A/C;Brain;2004-01-01

5. The phenotypic manifestations of autosomal recessive axonalCharcot–Marie–Tooth due to a mutation in Lamin A/C gene;Neuromuscular Disorders;2003-01

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