Literature DB >> 11914424

Spinocerebellar ataxia type 10 is rare in populations other than Mexicans.

T Matsuura1, L P W Ranum, V Volpini, M Pandolfo, H Sasaki, K Tashiro, K Watase, H Y Zoghbi, T Ashizawa.   

Abstract

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Year:  2002        PMID： 11914424     DOI： 10.1212/wnl.58.6.983

Source DB:  PubMed          Journal:  Neurology        ISSN： 0028-3878            Impact factor:   9.910


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  15 in total

Review 1.  Clinical, psychological, and genetic characteristics of spinocerebellar ataxia type 19 (SCA19).

Authors:  H Jurgen Schelhaas; Bart P C van de Warrenburg
Journal:  Cerebellum       Date:  2005       Impact factor: 3.847

2.  A Comparative Optical Coherence Tomography Study of Spinocerebellar Ataxia Types 3 and 10.

Authors:  Fernando Spina Tensini; Mario T Sato; Naoye Shiokawa; Tetsuo Ashizawa; Hélio A G Teive
Journal:  Cerebellum       Date:  2017-08       Impact factor: 3.847

3.  Spinocerebellar ataxia type 10: Frequency of epilepsy in a large sample of Brazilian patients.

Authors:  Hélio A G Teive; Renato P Munhoz; Salmo Raskin; Walter O Arruda; Luciano de Paola; Lineu C Werneck; Tetsuo Ashizawa
Journal:  Mov Disord       Date:  2010-12-15       Impact factor: 10.338

Review 4.  Recent progress in spinocerebellar ataxia type-10 (SCA10).

Authors:  Xi Lin; Tetsuo Ashizawa
Journal:  Cerebellum       Date:  2005       Impact factor: 3.847

5.  Heterozygosity for a protein truncation mutation of sodium channel SCN8A in a patient with cerebellar atrophy, ataxia, and mental retardation.

Authors:  M M Trudeau; J C Dalton; J W Day; L P W Ranum; M H Meisler
Journal:  J Med Genet       Date:  2005-10-19       Impact factor: 6.318

6.  Lack of variation of ATTCT pentanucleotide repeats at ATXN10 gene between clinically diagnosed ataxia patients and normal individuals originated from Chinese Han.

Authors:  Jun-Ling Wang; Hong Jiang; Shen Zhang; Qian Xu; Ya-Fang Zhou; Shu-Sheng Liao; Lu Shen; Xin-Xiang Yan; Huai-Xu Zhu; Qian Pan; Kun Xia; Bei-Sha Tang
Journal:  J Genet       Date:  2008-12       Impact factor: 1.166

7.  Haplotype Study in SCA10 Families Provides Further Evidence for a Common Ancestral Origin of the Mutation.

Authors:  Giovana B Bampi; Rafael Bisso-Machado; Tábita Hünemeier; Tailise C Gheno; Gabriel V Furtado; Diego Veliz-Otani; Mario Cornejo-Olivas; Pillar Mazzeti; Maria Cátira Bortolini; Laura B Jardim; Maria Luiza Saraiva-Pereira
Journal:  Neuromolecular Med       Date:  2017-09-13       Impact factor: 3.843

8.  ATXN10 Microsatellite Distribution in a Peruvian Amerindian Population.

Authors:  Diego Véliz-Otani; Miguel Inca-Martinez; Giovana B Bampi; Olimpio Ortega; Laura B Jardim; Maria Luiza Saraiva-Pereira; Pilar Mazzetti; Mario Cornejo-Olivas
Journal:  Cerebellum       Date:  2019-10       Impact factor: 3.847

9.  Spinocerebellar ataxias: genotype-phenotype correlations in 104 Brazilian families.

Authors:  Hélio A G Teive; Renato P Munhoz; Walter O Arruda; Iscia Lopes-Cendes; Salmo Raskin; Lineu C Werneck; Tetsuo Ashizawa
Journal:  Clinics (Sao Paulo)       Date:  2012       Impact factor: 2.365

10.  Ancestral origin of the ATTCT repeat expansion in spinocerebellar ataxia type 10 (SCA10).

Authors:  Teresa Almeida; Isabel Alonso; Sandra Martins; Eliana Marisa Ramos; Luísa Azevedo; Kinji Ohno; António Amorim; Maria Luiza Saraiva-Pereira; Laura Bannach Jardim; Tohru Matsuura; Jorge Sequeiros; Isabel Silveira
Journal:  PLoS One       Date:  2009-02-23       Impact factor: 3.240
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