Co-existence of nemaline and cytoplasmic bodies in muscle of an infant with nemaline myopathy-Reference-Cited by-同舟云学术

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Co-existence of nemaline and cytoplasmic bodies in muscle of an infant with nemaline myopathy

Published:2002-12 Issue:4 Volume:22 Page:294-298
ISSN:0919-6544
Container-title:Neuropathology
language:en
Short-container-title:

Author:

Suwa Kiyotaka,Mizuguchi Masashi,Momoi Mariko Y.,Nakamura Minako,Arima Kunimasa,Komaki Hirofumi,Nonaka Ikuya

Publisher

Wiley

Subject

Neurology (clinical),General Medicine,Pathology and Forensic Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1440-1789.2002.00461.x/fullpdf

Reference20 articles.

1. Nemaline myopathy: a new congenital myopathy;Shy;Brain,1963

2. Nemaline myopathy. Comparative muscle histochemistry in the severe neonatal, moderate congenital, and adult-onset forms;Shimomura;Pediatric Neurol,1989

3. A mutation in the alpha tropomyosin gene TPM3 associated with autosomal dominant nemaline myopathy NEM1;Laing;Nature Genet,1995

4. Mutations in the nebulin gene associated with autosomal recessive nemaline myopathy;Pelin;Proc Natl Acad Sci USA,1999

5. Mutations in the skeletal muscle alpha actin gene in patients with actin myopathy and nemaline myopathy;Nowak;Nature Genet,1999

Cited by 6 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. Severe ACTA1-related nemaline myopathy: intranuclear rods, cytoplasmic bodies, and enlarged perinuclear space as characteristic pathological features on muscle biopsies;Acta Neuropathologica Communications;2022-07-09

2. Cytoplasmic body pathology in severe ACTA1 -related myopathy in the absence of typical nemaline rods;Neuromuscular Disorders;2017-06

3. Congenital (Structural) Myopathies;Emery and Rimoin's Principles and Practice of Medical Genetics;2013

4. Histopathologic Progression and a Novel Mutation in a Child With Nemaline Myopathy;Journal of Child Neurology;2008-07

5. Congenital myopathies;Handbook of Clinical Neurology;2007

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