Literature DB >> 27245258

Huntington's disease-like presentation in Spinocerebellar ataxia type 12.

Elisabetta Groppo1, Annarita Armaroli2, Rita Selvatici2, Francesca Gualandi2, Mariachiara Sensi3.   

Abstract

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Year:  2016        PMID： 27245258     DOI： 10.1002/mds.26679

Source DB:  PubMed          Journal:  Mov Disord        ISSN： 0885-3185            Impact factor:   10.338


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  4 in total

1.  Huntington's disease: lessons from prion disorders.

Authors:  Melanie Alpaugh; Francesca Cicchetti
Journal:  J Neurol       Date:  2021-02-24       Impact factor: 4.849

2.  Monochorea of the Upper Limb in a Patient with Spinocerebellar Ataxia Type 12.

Authors:  Sonali Bhattad; Chandra S Rawat; Sanjay Pandey
Journal:  Mov Disord Clin Pract       Date:  2021-09-03

3.  Clinical, Radiological, and Genetic Profile of Spinocerebellar Ataxia 12: A Hospital-Based Cohort Analysis.

Authors:  Valakunja Harikrishna Ganaraja; Vikram V Holla; Albert Stezin; Nitish Kamble; Ravi Yadav; Meera Purushottam; Sanjeev Jain; Pramod Kumar Pal
Journal:  Tremor Other Hyperkinet Mov (N Y)       Date:  2022-04-21

Review 4.  Review of Hereditary and Acquired Rare Choreas.

Authors:  Daniel Martinez-Ramirez; Ruth H Walker; Mayela Rodríguez-Violante; Emilia M Gatto
Journal:  Tremor Other Hyperkinet Mov (N Y)       Date:  2020-08-06
  4 in total

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