Myopathy with respiratory failure and typical myofibrillar lesions-Reference-Cited by-同舟云学术

Myopathy with respiratory failure and typical myofibrillar lesions

Published:1990-05 Issue:2-3 Volume:96 Page:211-228
ISSN:0022-510X
Container-title:Journal of the Neurological Sciences
language:en
Short-container-title:Journal of the Neurological Sciences

Author:

Edström Lars,Thornell Lars-Eric,Albo Jaan,Landin Sven,Samuelsson Margareta

Publisher

Elsevier BV

Subject

Clinical Neurology,Neurology

Reference49 articles.

1. Immunostaining of skeletal and cardiac muscle surface membrane with antibody against Duchenne muscular dystrophy peptide;Arahata;Nature,1988

2. The congenital myopathies;Banker,1986

3. Muscle fibre types;Brooke;Arch. Neurol.,1970

4. Cap Z (3632), a barbed and actin-capping protein, is a component of the Z-line of skeletal muscle;Casella;J. Cell Biol.,1978

5. Autosomal dominant myofibrillar inclusion body myopathy: clinical, histologic, histochemical, and ultrastructural characteristics;Clark;Neurology,1978

Cited by 81 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

2. Protein Quality Control at the Sarcomere: Titin Protection and Turnover and Implications for Disease Development;Frontiers in Physiology;2022-06-30

3. SRF: a seriously responsible factor in cardiac development and disease;Journal of Biomedical Science;2022-06-09

4. A Japanese Patient with Hereditary Myopathy with Early Respiratory Failure Due to the p.P31732L Mutation of Titin;Internal Medicine;2022

5. Sibling cases of <i>four and a half LIM domains 1</i> (<i>FHL1</i>) myopathy who developed respiratory failure without apparent limb weakness;Rinsho Shinkeigaku;2022