Literature DB >> 14467082

Charcot-Marie-Tooth disease with associated myopathy. A report of a family.

G J LUCAS, F M FORSTER.   

Abstract

Entities:  

Keywords:  MUSCULAR ATROPHY/genetics

Mesh：

Year:  1962        PMID： 14467082     DOI： 10.1212/wnl.12.9.629

Source DB:  PubMed          Journal:  Neurology        ISSN： 0028-3878            Impact factor:   9.910


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  5 in total

1.  Electron microscopic and enzyme histochemical studies of cerebellum, ocular and skeletal muscles in chronic progressive ophthalmoplegia with cerebellar ataxia.

Authors:  M Adachi; J Torii; B W Volk; P Briet; A Wolintz; L Schneck
Journal:  Acta Neuropathol       Date:  1973       Impact factor: 17.088

2.  Mitochondrial abnormalities of late motor neuron degeneration following poliomyelitis and other neurogenic muscular atrophies.

Authors:  D Schiffer; L Palmucci; A Bertolotto; G Monga
Journal:  J Neurol       Date:  1979-09       Impact factor: 4.849

3.  Charcot-Marie-Tooth disease and nephritis.

Authors:  G Lemieux; J A Neemeh
Journal:  Can Med Assoc J       Date:  1967-11-11       Impact factor: 8.262

4.  [Mitochondrial changes of the skeletal muscle in the peroneal muscular atrophy (Charcot-Marie-Tooth disease). Histological and electron microscopic studies (author's transl)].

Authors:  G Spalke; R Heene; D Herold
Journal:  J Neurol       Date:  1975       Impact factor: 4.849

5.  Oculopharyngeal involvement in familial neurogenic muscular atrophy.

Authors:  M Matsunaga; T Inokuchi; A Onishi; Y Kuroiwa
Journal:  J Neurol Neurosurg Psychiatry       Date:  1973-02       Impact factor: 10.154
  5 in total

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