Literature DB >> 5037445

Centronuclear myopathy: disease entity or a syndrome? Light- and electron-microscopic study of two cases and review of the literature.

S S Schochet, H Zellweger, V Ionasescu, W F McCormick.   

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Year:  1972        PMID: 5037445     DOI: 10.1016/0022-510x(72)90091-3

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN: 0022-510X            Impact factor:   3.181


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  6 in total

1.  Centronuclear myopathy.

Authors:  P L Bill; G Cole; N S Proctor
Journal:  J Neurol Neurosurg Psychiatry       Date:  1979-06       Impact factor: 10.154

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

Authors:  J R Ricoy; A Cabello
Journal:  J Neurol Neurosurg Psychiatry       Date:  1985-02       Impact factor: 10.154

3.  Teaching monograph: pathology of skeletal muscle diseases.

Authors:  U U DeGirolami; T W Smith
Journal:  Am J Pathol       Date:  1982-05       Impact factor: 4.307

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

Authors:  W Mortier; E Michaelis; J Becker; L Gerhard
Journal:  Humangenetik       Date:  1975

Review 5.  The myotubular myopathies: differential diagnosis of the X linked recessive, autosomal dominant, and autosomal recessive forms and present state of DNA studies.

Authors:  C Wallgren-Pettersson; A Clarke; F Samson; M Fardeau; V Dubowitz; H Moser; T Grimm; R J Barohn; P G Barth
Journal:  J Med Genet       Date:  1995-09       Impact factor: 6.318

Review 6.  Centronuclear (myotubular) myopathy.

Authors:  Heinz Jungbluth; Carina Wallgren-Pettersson; Jocelyn Laporte
Journal:  Orphanet J Rare Dis       Date:  2008-09-25       Impact factor: 4.123

  6 in total

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