Literature DB >> 13545871

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

P E SYLVESTER.   

Abstract

Entities:  

Keywords:  HEREDITARY SPINAL SCLEROSIS/case reports

Mesh：

Year:  1958        PMID： 13545871      PMCID： PMC2012228          DOI： 10.1136/adc.33.169.217

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN： 0003-9888            Impact factor:   3.791


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  2 in total

1.  Suprasegmental lesions in Friedreich's ataxia.

Authors:  H URICH; R M NORMAN; O C LLOYD
Journal:  Confin Neurol       Date:  1957

2.  Familial ataxia, deaf-mutism, and muscular wasting.

Authors:  W B MATTHEWS
Journal:  J Neurol Neurosurg Psychiatry       Date:  1950-11       Impact factor: 10.154
  2 in total
  3 in total

1.  A syndrome of early onset spinocerebellar ataxia with optic atrophy, internuclear ophthalmoplegia, dementia, and startle myoclonus in a Sri Lankan family.

Authors:  N Senanayake
Journal:  J Neurol       Date:  1992-05       Impact factor: 4.849

2.  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

3.  Hypersensitivity to N-methyl-N'-nitro-N-nitrosoguanidine in fibroblasts from patients with Huntington disease, familial dysautonomia, and other primary neuronal degenerations.

Authors:  D A Scudiero; S A Meyer; B E Clatterbuck; R E Tarone; J H Robbins
Journal:  Proc Natl Acad Sci U S A       Date:  1981-10       Impact factor: 11.205
  3 in total

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