Acetylcholine receptor antibodies in patients with genetic myopathies: Clinical and biological significance-Reference-Cited by-同舟云学术

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Acetylcholine receptor antibodies in patients with genetic myopathies: Clinical and biological significance

Published:2012-02 Issue:2 Volume:22 Page:122-128
ISSN:0960-8966
Container-title:Neuromuscular Disorders
language:en
Short-container-title:Neuromuscular Disorders

Author:

Lane Russell J.M.,Roncaroli Federico,Charles Peter,McGonagle Dennis G.,Orrell Richard W.

Publisher

Elsevier BV

Subject

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

Reference44 articles.

1. The coexistence of myasthenia gravis and myotonic dystrophy in one family;Maytal;Neuropediatrics,1987

2. Concurrence of limb girdle muscular dystrophy and myasthenia gravis;Husain;Arch Neurol,1989

3. A patient with facioscapulohumeral muscular dystrophy accompanied by myasthenia gravis;Sakuma;Rinsho Shinkeigaku,2001

4. Facioscapulohumeral muscular dystrophy and myasthenia gravis co-existing in the same patient: a case report;McGonigal;J Neurol,2002

5. Concurrence of facioscapulohumeral muscular dystrophy and myasthenia gravis;Sansone;Muscle Nerve,2004

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1. AChR-seropositive myasthenia gravis in muscular dystrophy: diagnostic pitfalls and clinical management challenges;Neurological Sciences;2024-07-05

2. Oculopharyngeal muscular dystrophy coexisting with myasthenia gravis;Practical Neurology;2022-05-09

3. c.3G>A mutation in the CRYAB gene that causes fatal infantile hypertonic myofibrillar myopathy in the Chinese population;Journal of Integrative Neuroscience;2021

4. Congenital myasthenic syndrome with novel pathogenic variants in the COLQ gene associated with the presence of antibodies to acetylcholine receptors;Journal of Clinical Neuroscience;2020-02

5. Toxic and Drug-Induced Myopathies;Muscle Biopsy;2020

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