Centronuclear myopathy with autosomal dominant inheritance

Journal of the Neurological Sciences

Volumn 15, Issue 4, 1972, Pages 375-387

  McLeod, J G ^a   De C Baker, W ^a   Lethlean, A K ^a   Shorey, C D ^a  

^a ROYAL PRINCE ALFRED HOSPITAL   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; AGED; ARTICLE; CELL NUCLEUS; DOMINANT GENE; ELECTROMYOGRAPHY; ELECTRON MICROSCOPY; FEMALE; GENETICS; HUMAN; MALE; MUSCLE; MUSCLE DISEASE; PATHOLOGY; PATHOPHYSIOLOGY; PEDIGREE; PTOSIS;

ADULT; AGED; BLEPHAROPTOSIS; CELL NUCLEUS; ELECTROMYOGRAPHY; FEMALE; GENES, DOMINANT; HUMAN; MALE; MICROSCOPY, ELECTRON; MIDDLE AGE; MUSCLES; MUSCULAR DISEASES; PEDIGREE;

EID: 0015318837     PISSN: 0022510X     EISSN: None     Source Type: Journal    
DOI: 10.1016/0022-510X(72)90166-9     Document Type: Article

References (19)

1. Myotubular myopathy
2. Centronuclear myopathy
3. Neuromuscular disease with Type I fiber atrophy, central nuclei, and myotube-like structures
4. Centronuclear myopathy with Type I fibre atrophy and “myotubes”
5. Familial centronculear myopathy
6. Myotubular, centronuclear, or pericentronuclear myopathy?
7. Reversal of the ATP-ase reaction in muscle fibres by EDTA
8. Rapid examination of muscle tissue
9. Type I fiber hypotrophy and central nuclei
10. Type I muscle fibre atrophy and centrla nuclei
11. Myotubular myopathy
12. Centronuclear (“myotubular”) myopathy
13. Factors affecting activity of adenosine triphosphatase and other phosphatases as measured by histochemical techniques
14. The use of lead acetate at high pH as an electron opaque stain in electron microscopy
15. Familial centronuclear myopathy: A clinical and pathological study
16. Myotubular myopathy
17. Familiar “myotubular” myopathy