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Literature DB >> 5478951

Familial centronuclear myopathy.

Abstract

The clinical and histological features of two Negro brothers with a centronuclear myopathy are described. They bring to 19 the number of cases now reported with this constellation of physical signs and pathological changes in the muscles. A review of these patients suggests the existence of several different diseases causing this picture, though presumably the underlying biochemical defects are closely related. It is concluded that these myopathies are degenerative rather than due to arrest of foetal muscle maturation.

Entities: Disease Species

Mesh：

Year: 1970 PMID： 5478951 PMCID： PMC493550 DOI： 10.1136/jnnp.33.5.687

Source DB: PubMed Journal: J Neurol Neurosurg Psychiatry ISSN： 0022-3050 Impact factor: 10.154

12 in total

1. Familial centronuclear myopathy: a clinical and pathological study.

Authors: J H Sher; A B Rimalovski; T J Athanassiades; S M Aronson
Journal: Neurology Date: 1967-08 Impact factor: 9.910

2. Type I fiber hypotrophy and central nuclei. A rare congenital muscle abnormality with a possible experimental model.

Authors: W K Engel; G N Gold; G Karpati
Journal: Arch Neurol Date: 1968-04

3. Myotubular myopathy.

Authors: M Kinoshita; T E Cadman
Journal: Arch Neurol Date: 1968-03

4. Myotubular myopathy.

Authors: B Badurska; A Fidziańska; Z Kamieniecka; J Prot; H Strugalska
Journal: J Neurol Sci Date: 1969 May-Jun Impact factor: 3.181

5. Myotubular myopathy. Persistence of fetal muscle in an adolescent boy.

Authors: A J Spiro; G M Shy; N K Gonatas
Journal: Arch Neurol Date: 1966-01

6. Centronuclear myopathy.

Authors: J Bethlem; A E Meijer; J P Schellens; J J Vroom
Journal: Eur Neurol Date: 1968 Impact factor: 1.710

7. Familial "myotubular" myopathy.

Authors: G K van Wijngaarden; P Fleury; J Bethlem; A E Meijer
Journal: Neurology Date: 1969-09 Impact factor: 9.910

8. Neuromuscular disease with type I fiber atrophy, central nuclei, and myotube-like structures.

Authors: J Bethlem; G K van Wijngaarden; A E Meijer; W C Hülsmann
Journal: Neurology Date: 1969-07 Impact factor: 9.910

9. Myotubular, centronuclear or Peri-Centronuclear myopathy?

Authors: M J Campbell; J J Rebeiz; J N Walton
Journal: J Neurol Sci Date: 1969 May-Jun Impact factor: 3.181

10. Selective and nonselective susceptibility of muscle fiber types. A new approach to human neuromuscular diseases.

Authors: W K Engel
Journal: Arch Neurol Date: 1970-02

11 in total

1. Endplate structure and parameters of neuromuscular transmission in sporadic centronuclear myopathy associated with myasthenia.

Authors: Teerin Liewluck; Xin-Ming Shen; Margherita Milone; Andrew G Engel
Journal: Neuromuscul Disord Date: 2011-04-08 Impact factor: 4.296

Familial centronuclear myopathy.

1. Familial centronuclear myopathy: a clinical and pathological study.

2. Type I fiber hypotrophy and central nuclei. A rare congenital muscle abnormality with a possible experimental model.

3. Myotubular myopathy.

4. Myotubular myopathy.

5. Myotubular myopathy. Persistence of fetal muscle in an adolescent boy.

6. Centronuclear myopathy.

7. Familial "myotubular" myopathy.

8. Neuromuscular disease with type I fiber atrophy, central nuclei, and myotube-like structures.

9. Myotubular, centronuclear or Peri-Centronuclear myopathy?

10. Selective and nonselective susceptibility of muscle fiber types. A new approach to human neuromuscular diseases.

1. Endplate structure and parameters of neuromuscular transmission in sporadic centronuclear myopathy associated with myasthenia.

2. Centronuclear myopathy.

3. A case of centronuclear myopathy.

4. The syndrome of myosclerosis.

5. Hypotrophy of type I fibres with central nuclei: recovery 4 years after diagnosis.

6. Adult onset centronuclear myopathy with peripheral nerve involvement.

7. Teaching monograph: pathology of skeletal muscle diseases.

8. [Centronuclear myopathy with autosomal dominant inheritance(author's transl)].

9. Congenital neuromuscular disease with type I fibre hypotrophy, ophthalmoplegia and myofibril degeneration.

10. Myotubular myopathy associated with cataract and electrical myotonia.