Huntington's disease‐like presentation in Spinocerebellar ataxia type 12-Reference-Cited by-同舟云学术

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Huntington's disease‐like presentation in Spinocerebellar ataxia type 12

Published:2016-06 Issue:8 Volume:31 Page:1248-1249
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

Groppo Elisabetta¹,Armaroli Annarita²,Selvatici Rita²,Gualandi Francesca²,Sensi Mariachiara³

Affiliation:

1. Department of Biomedical and Specialistic Surgical SciencesUniversity of Ferrara, University‐Hospital Arcispedale S. AnnaFerrara Italy

2. Department of Medical Sciences & Department of Reproduction and GrowthUOL of Medical Genetics Unit, University‐Hospital S. AnnaFerrara Italy

3. Neurological Unit, Neuroscience Department, University‐Hospital Arcispedale S. AnnaCona Italy

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/mds.26679

Reference5 articles.

1. Why is SCA12 different from other SCAs?

2. SCA-12: Tremor with cerebellar and cortical atrophy is associated with a CAG repeat expansion

3. SCA12 is a rare locus for autosomal dominant cerebellar ataxia: A study of an Indian family

4. Spinocerebellar ataxia type 12 identified in two Italian families may mimic sporadic ataxia

5. Expansion of a novel CAG trinucleotide repeat in the 5′ region of PPP2R2B is associated with SCA12

Cited by 7 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. Clinical, Radiological, and Genetic Profile of Spinocerebellar Ataxia 12: A Hospital-Based Cohort Analysis;Tremor and Other Hyperkinetic Movements;2022

2. Monochorea of the Upper Limb in a Patient with Spinocerebellar Ataxia Type 12;Movement Disorders Clinical Practice;2021-08

3. Degenerative dementias: a question of syndrome or disease?;Neurología (English Edition);2021-05

4. Huntington’s disease: lessons from prion disorders;Journal of Neurology;2021-02-24

5. Review of Hereditary and Acquired Rare Choreas;Tremor and Other Hyperkinetic Movements;2020

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