Literature DB >> 14795246

Familial ataxia, deaf-mutism, and muscular wasting.

W B MATTHEWS.   

Abstract

Entities:  

Keywords:  ATROPHY, MUSCULAR; DEAF-MUTISM

Mesh：

Year:  1950        PMID： 14795246      PMCID： PMC498655          DOI： 10.1136/jnnp.13.4.307

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


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  5 in total

Review 1.  PROFOUND CHILDHOOD DEAFNESS.

Authors:  G R FRASER
Journal:  J Med Genet       Date:  1964-12       Impact factor: 6.318

2.  Some unusual findings in a family with Friedreich's ataxia.

Authors:  P E SYLVESTER
Journal:  Arch Dis Child       Date:  1958-06       Impact factor: 3.791

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.  [Friedreich's ataxia with peripheral nerve involvement resembling peroneal muscular atrophy].

Authors:  H C Hopf; F K Port
Journal:  Dtsch Z Nervenheilkd       Date:  1968

5.  Conductive hearing loss and malformed low-set ears, as a possible recessive syndrome.

Authors:  M C Mengel; B W Konigsmark; C I Berlin; V A McKusick
Journal:  J Med Genet       Date:  1969-03       Impact factor: 6.318
  5 in total

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