Literature DB >> 2614456

Autosomal dominant cerebellar ataxia with deafness, myoclonus and amyotrophy.

T P Melo, J M Ferro.   

Abstract

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Year:  1989        PMID： 2614456      PMCID： PMC1031620          DOI： 10.1136/jnnp.52.12.1448

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


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  4 in total

Review 1.  The Ramsay Hunt syndrome is no longer a useful diagnostic category.

Authors:  F Andermann; S Berkovic; S Carpenter; E Andermann
Journal:  Mov Disord       Date:  1989       Impact factor: 10.338

2.  Familial myoclonus, cerebellar ataxia, and deafness. Specific genetically-determined disease.

Authors:  D L May; H H White
Journal:  Arch Neurol       Date:  1968-09

3.  The clinical features of mitochondrial myopathy.

Authors:  R K Petty; A E Harding; J A Morgan-Hughes
Journal:  Brain       Date:  1986-10       Impact factor: 13.501

Review 4.  Mitochondrial diseases.

Authors:  M Zeviani; E Bonilla; D C DeVivo; S DiMauro
Journal:  Neurol Clin       Date:  1989-02       Impact factor: 3.806
  4 in total
  1 in total

1.  Abnormal muscle and skin mitochondria in family with myoclonus, ataxia, and deafness (May and White syndrome).

Authors:  J Vaamonde; J Muruzabal; T Tuñón; N Perez; J Artieda; M Rodriguez; J A Obeso
Journal:  J Neurol Neurosurg Psychiatry       Date:  1992-02       Impact factor: 10.154
  1 in total

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