Literature DB >> 4833925

Letter: Hereditary ataxia and HL-A genotypes.

H Yakura, A Wakisaka, S Fujimoto, K Itakura.   

Abstract

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Year:  1974        PMID： 4833925     DOI： 10.1056/NEJM197407182910314

Source DB:  PubMed          Journal:  N Engl J Med        ISSN： 0028-4793            Impact factor:   91.245


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  32 in total

Review 1.  Modifiers and mechanisms of multi-system polyglutamine neurodegenerative disorders: lessons from fly models.

Authors:  Moushami Mallik; Subhash C Lakhotia
Journal:  J Genet       Date:  2010-12       Impact factor: 1.166

2.  Unexpected clinicopathological phenotype linked to small elongation of CAG repeat in SCA1 gene.

Authors:  T Uchihara; Y Takeda; T Kobayashi; T Kasuga; K Ishikawa; K Kirei; H Mizusawa; T Endo; K Hirokawa; T Kuroiwa
Journal:  J Neurol       Date:  2005-11-29       Impact factor: 4.849

3.  Autosomal dominant cerebellar ataxia type I in Martinique (French West Indies): genetic analysis of three unrelated SCA2 families.

Authors:  A Lezin; G Cancel; G Stevanin; D Smadja; J C Vernant; A Dürr; J Martial; G G Buisson; R Bellance; H Chneiweiss; Y Agid; A Brice
Journal:  Hum Genet       Date:  1996-05       Impact factor: 4.132

Review 4.  SCA1-phosphorylation, a regulator of Ataxin-1 function and pathogenesis.

Authors:  Harry T Orr
Journal:  Prog Neurobiol       Date:  2012-04-16       Impact factor: 11.685

Review 5.  Immunology of amyotrophic lateral sclerosis.

Authors:  N R Cashman; M E Gurney; J P Antel
Journal:  Springer Semin Immunopathol       Date:  1985

Review 6.  The inherited ataxias and the new genetics.

Authors:  S R Hammans
Journal:  J Neurol Neurosurg Psychiatry       Date:  1996-10       Impact factor: 10.154

7.  Spinocerebellar ataxia 1 (SCA1) in the Japanese in Hokkaido may derive from a single common ancestry.

Authors:  A Wakisaka; H Sasaki; A Takada; T Fukazawa; Y Suzuki; T Hamada; K Iwabuchi; K Tashiro; T Yoshiki
Journal:  J Med Genet       Date:  1995-08       Impact factor: 6.318

8.  Molecular and clinical correlations in spinocerebellar ataxia type I: evidence for familial effects on the age at onset.

Authors:  L P Ranum; M Y Chung; S Banfi; A Bryer; L J Schut; R Ramesar; L A Duvick; A McCall; S H Subramony; L Goldfarb
Journal:  Am J Hum Genet       Date:  1994-08       Impact factor: 11.025

9.  Relations between genotype and phenotype in German patients with the Machado-Joseph disease mutation.

Authors:  L Schöls; G Amoiridis; J T Epplen; M Langkafel; H Przuntek; O Riess
Journal:  J Neurol Neurosurg Psychiatry       Date:  1996-11       Impact factor: 10.154

10.  The gene for autosomal dominant spinocerebellar ataxia (SCA1) maps centromeric to D6S89 and shows no recombination, in nine large kindreds, with a dinucleotide repeat at the AM10 locus.

Authors:  T J Kwiatkowski; H T Orr; S Banfi; A E McCall; C Jodice; F Persichetti; A Novelletto; F LeBorgne-DeMarquoy; L A Duvick; M Frontali
Journal:  Am J Hum Genet       Date:  1993-08       Impact factor: 11.025
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