Literature DB >> 5417642

Optic atrophy, neural deafness, and distal neurogenic amyotrophy; report of a family with two affected siblings.

H Iwashita, N Inoue, S Araki, Y Kuroiwa.   

Abstract

Entities:  

Mesh：

Year:  1970        PMID： 5417642     DOI： 10.1001/archneur.1970.00480220071010

Source DB:  PubMed          Journal:  Arch Neurol        ISSN： 0003-9942


× No keyword cloud information.
  5 in total

1.  Hereditary motor and sensory neuropathy (HMSN) and optic atrophy (HMSN type VI, Vizioli).

Authors:  C Weiller; A Ferbert
Journal:  Eur Arch Psychiatry Clin Neurosci       Date:  1991       Impact factor: 5.270

Review 2.  Clinical features, molecular genetics, and pathophysiology of dominant optic atrophy.

Authors:  M Votruba; A T Moore; S S Bhattacharya
Journal:  J Med Genet       Date:  1998-10       Impact factor: 6.318

3.  Cerebellar ataxia, areflexia, pes cavus, optic atrophy, and sensorineural hearing loss (CAPOS): a new syndrome.

Authors:  P Nicolaides; R E Appleton; A Fryer
Journal:  J Med Genet       Date:  1996-05       Impact factor: 6.318

4.  Optico-acoustic atrophy in distal spinal muscular atrophy.

Authors:  N Chalmers; J D Mitchell
Journal:  J Neurol Neurosurg Psychiatry       Date:  1987-02       Impact factor: 10.154

5.  Autosomal recessive hereditary motor and sensory neuropathy with mental retardation, optic atrophy and pyramidal signs.

Authors:  K D MacDermot; R W Walker
Journal:  J Neurol Neurosurg Psychiatry       Date:  1987-10       Impact factor: 10.154
  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.