CAG Repeat Expansion in an Italian Family with Spinocerebellar Ataxia Type 2 (SCA2): A Clinical and Genetic Study-Reference-Cited by-同舟云学术

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CAG Repeat Expansion in an Italian Family with Spinocerebellar Ataxia Type 2 (SCA2): A Clinical and Genetic Study

Published:1998 Issue:3 Volume:40 Page:164-168
ISSN:0014-3022
Container-title:European Neurology
language:en
Short-container-title:Eur Neurol

Author:

Malandrini Alessandro,Galli Lucia,Villanova Marcello,Palmeri Silvia,Parrotta Emma,DeFalco Danilo,Cappelli Michela,Salvatore Grieco Gaetano,Renieri Alessandra,Guazzi Giancarlo

Publisher

S. Karger AG

Subject

Clinical Neurology,Neurology

Cited by 15 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Neurophysiological features in spinocerebellar ataxia type 2: Prospects for novel biomarkers;Clinical Neurophysiology;2022-03

2. Phenotypic and molecular diversities of spinocerebellar ataxia type 2 in Japan;Journal of Neurology;2021-02-24

3. Peripheral Neuropathy in Spinocerebellar Ataxia Type 1, 2, 3, and 6;The Cerebellum;2015-06-09

4. Intermediate-length polyglutamine in ATXN2 is a possible risk factor among Eastern Chinese patients with amyotrophic lateral sclerosis;Neurobiology of Aging;2015-03

5. Neuropathological Staging of Spinocerebellar Ataxia Type 2 by Semiquantitative 1C2-Positive Neuron Typing. Nuclear Translocation of Cytoplasmic 1C2 Underlies Disease Progression of Spinocerebellar Ataxia Type 2;Brain Pathology;2014-05-28

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