Literature DB >> 4154794

Optic and cochleovestibular degenerations in the hereditary ataxias. I. Clinico-pathological and genetic aspects.

L van Bogaert, L Martin.   

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Year:  1974        PMID: 4154794     DOI: 10.1093/brain/97.1.15

Source DB:  PubMed          Journal:  Brain        ISSN: 0006-8950            Impact factor:   13.501


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  5 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.  CT scan and threshold vibrometry in the diagnosis of spinocerebellar degenerations.

Authors:  N Uzunov; M Kutchoukov; C Kolchev
Journal:  Ital J Neurol Sci       Date:  1991-04

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.  Hereditary cerebellar atrophy (Holmes type) with optic atrophy: a clinico-pathological study of four generations in a family.

Authors:  H Budka; D Seemann; W Danielczyk
Journal:  Arch Psychiatr Nervenkr (1970)       Date:  1979-04-12

5.  The Pathology of the Vestibular System in CANVAS.

Authors:  Reuven Ishai; Mohammad Seyyedi; Andrew M Chancellor; Catriona A McLean; Michael L Rodriguez; Gabor Michael Halmagyi; Joseph B Nadol; David J Szmulewicz; Alicia M Quesnel
Journal:  Otol Neurotol       Date:  2021-03-01       Impact factor: 2.619

  5 in total

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