Complex phenotypes in an Indian family with homozygous SCA2 mutations-Reference-Cited by-同舟云学术

Complex phenotypes in an Indian family with homozygous SCA2 mutations

Published:2003 Issue:1 Volume:55 Page:130-133
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Ragothaman Mona,Sarangmath Nagaraja,Chaudhary Shashi,Khare Vishwamohini,Mittal Uma,Sharma Sangeeta,Komatireddy Sreelatha,Chakrabarti Subhabrata,Mukerji Mitali,Juyal Ramesh C.,Thelma B. K.,Muthane Uday B.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Reference19 articles.

1. Spinocerebellar ataxia type 2 presenting as familial levodopa-responsive parkinsonism

2. Dopa-responsive parkinsonism phenotype of spinocerebellar ataxia type 2

3. SCA-2 presenting as parkinsonism in an Alberta family: Clinical, genetic, and PET findings

4. Dominantly inherited olivopontocerebellar atrophy from eastern Cuba

5. A clinicogenetic analysis of six Indian spinocerebellar ataxia (SCA2) pedigrees. The significance of slow saccades in diagnosis

Cited by 27 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. Modeling amyotrophic lateral sclerosis through Ataxin-2 pathology;Handbook of Animal Models in Neurological Disorders;2023

2. Neurogenetic motor disorders;Motor System Disorders, Part I: Normal Physiology and Function and Neuromuscular Disorders;2023

3. Unraveling movement disorders in spinocerebellar ataxia;Annals of Movement Disorders;2022-05

4. Clinical features and genetic characteristics of homozygous spinocerebellar ataxia type 3;Molecular Genetics & Genomic Medicine;2020-07-09

5. Amyotrophic lateral sclerosis;Rosenberg's Molecular and Genetic Basis of Neurological and Psychiatric Disease;2020