Literature DB >> 26033715

When should we test patients with familial ataxias for SCA31? A misdiagnosed condition outside Japan?

José Luiz Pedroso1, Agessandro Abrahao2, Kinya Ishikawa3, Salmo Raskin4, Paulo Victor Sgobbi de Souza2, Wladimir Bocca Vieira de Rezende Pinto2, Pedro Braga-Neto5, Marcus Vinicius Cristino de Albuquerque2, Hidehiro Mizusawa3, Orlando G P Barsottini2.   

Abstract

Entities:  

Mesh：

Year:  2015        PMID： 26033715     DOI： 10.1016/j.jns.2015.05.016

Source DB:  PubMed          Journal:  J Neurol Sci        ISSN： 0022-510X            Impact factor:   3.181


× No keyword cloud information.
  4 in total

Review 1.  Deafness and Vestibulopathy in Cerebellar Diseases: a Practical Approach.

Authors:  Orlando G Barsottini; José Luiz Pedroso; Carlos Roberto Martins; Marcondes Cavalcante França; Pedro Mangabeira Albernaz
Journal:  Cerebellum       Date:  2019-12       Impact factor: 3.847

2.  Natural History of Spinocerebellar Ataxia Type 31: a 4-Year Prospective Study.

Authors:  Katsuya Nakamura; Kunihiro Yoshida; Akira Matsushima; Yusaku Shimizu; Shunichi Sato; Hiroyuki Yahikozawa; Shinji Ohara; Masanobu Yazawa; Masao Ushiyama; Mitsuto Sato; Hiroshi Morita; Atsushi Inoue; Shu-Ichi Ikeda
Journal:  Cerebellum       Date:  2017-04       Impact factor: 3.847

Review 3.  Mechanistic and Therapeutic Insights into Ataxic Disorders with Pentanucleotide Expansions.

Authors:  Nan Zhang; Tetsuo Ashizawa
Journal:  Cells       Date:  2022-05-06       Impact factor: 7.666

Review 4.  The Geographic Diversity of Spinocerebellar Ataxias (SCAs) in the Americas: A Systematic Review.

Authors:  Hélio A G Teive; Alex T Meira; Carlos Henrique F Camargo; Renato P Munhoz
Journal:  Mov Disord Clin Pract       Date:  2019-08-16
  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.