Literature DB >> 8648347

Clinical and genetic evaluation of Japanese autosomal dominant cerebellar ataxias; is Machado-Joseph disease common in the Japanese?

K Inoue, T Hanihara, Y Yamada, K Kosaka, T Katsuragi, K Iwabuchi.   

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Year:  1996        PMID： 8648347      PMCID： PMC1073964          DOI： 10.1136/jnnp.60.6.697

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


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  4 in total

Review 1.  Clinical features and classification of inherited ataxias.

Authors:  A E Harding
Journal:  Adv Neurol       Date:  1993

2.  CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1.

Authors:  Y Kawaguchi; T Okamoto; M Taniwaki; M Aizawa; M Inoue; S Katayama; H Kawakami; S Nakamura; M Nishimura; I Akiguchi
Journal:  Nat Genet       Date:  1994-11       Impact factor: 38.330

3.  Spinocerebellar degenerations in Japan: a nationwide epidemiological and clinical study.

Authors:  K Hirayama; T Takayanagi; R Nakamura; N Yanagisawa; T Hattori; K Kita; S Yanagimoto; M Fujita; M Nagaoka; Y Satomura
Journal:  Acta Neurol Scand Suppl       Date:  1994

4.  Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA).

Authors:  R Koide; T Ikeuchi; O Onodera; H Tanaka; S Igarashi; K Endo; H Takahashi; R Kondo; A Ishikawa; T Hayashi
Journal:  Nat Genet       Date:  1994-01       Impact factor: 38.330
  4 in total

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