Literature DB >> 13716305

Charcot-Marie-Tooth disease with primary optic atrophy; report of a case.

W F HOYT.   

Abstract

Entities:  

Keywords:  EYE/diseases; MUSCULAR ATROPHY/case reports

Mesh：

Year:  1960        PMID： 13716305     DOI： 10.1001/archopht.1960.01840010927014

Source DB:  PubMed          Journal:  Arch Ophthalmol        ISSN： 0003-9950


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  6 in total

1.  Charcot's Patient.

Authors: 
Journal:  Br Med J       Date:  1968-02-10

2.  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

3.  Autosomal dominant optic atrophy with asymptomatic peripheral neuropathy.

Authors:  R M Chalmers; A C Bird; A E Harding
Journal:  J Neurol Neurosurg Psychiatry       Date:  1996-02       Impact factor: 10.154

4.  Pathology of the optic nerves. I. Histopathological changes in the intracranial portions, associated with arteriosclerotic and hypertensive cardiovascular diseases and with liver parenchymal damage.

Authors:  Y Doron; A Behar
Journal:  Acta Neuropathol       Date:  1968-06-07       Impact factor: 17.088

5.  Strachan's syndrome: variation on a theme.

Authors:  O C Cockerell; I E Ormerod
Journal:  J Neurol       Date:  1993-05       Impact factor: 4.849

6.  Autosomal recessive inheritance of hereditary motor and sensory neuropathy with optic atrophy.

Authors:  R M Chalmers; P Riordan-Eva; N W Wood
Journal:  J Neurol Neurosurg Psychiatry       Date:  1997-04       Impact factor: 10.154
  6 in total

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