Literature DB >> 4341505

Nemaline (neuro) myopathy. Rod-like bodies and type I fibre atrophy in a case of congenital hypotonia with denervation.

H Radu, V Ionescu.   

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Year:  1972        PMID： 4341505     DOI： 10.1016/0022-510x(72)90022-6

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


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  4 in total

1.  Progression in nemaline myopathy.

Authors:  I Nonaka; S Ishiura; K Arahata; H Ishibashi-Ueda; T Maruyama; K Ii
Journal:  Acta Neuropathol       Date:  1989       Impact factor: 17.088

2.  Nemaline myopathy: histological, histochemical and ultrastructural studies.

Authors:  N Fukuhara; T Yuasa; T Tsubaki; S Kushiro; N Takasawa
Journal:  Acta Neuropathol       Date:  1978-04-26       Impact factor: 17.088

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

Authors:  H Sugie; R Hanson; G Rasmussen; M A Verity
Journal:  J Neurol Neurosurg Psychiatry       Date:  1982-06       Impact factor: 10.154

4.  Adult-onset mixed myopathy with nemaline rods, minicores, and central cores: a muscle disorder mimicking polymyositis.

Authors:  R J Seitz; K V Toyka; W Wechsler
Journal:  J Neurol       Date:  1984       Impact factor: 4.849
  4 in total

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