Long-term disease progression in spinocerebellar ataxia types 1, 2, 3, and 6: a longitudinal cohort study-Reference-Cited by-同舟云学术

Long-term disease progression in spinocerebellar ataxia types 1, 2, 3, and 6: a longitudinal cohort study

Published:2015-11 Issue:11 Volume:14 Page:1101-1108
ISSN:1474-4422
Container-title:The Lancet Neurology
language:en
Short-container-title:The Lancet Neurology

Author:

Jacobi Heike,du Montcel Sophie Tezenas,Bauer Peter,Giunti Paola,Cook Arron,Labrum Robyn,Parkinson Michael H,Durr Alexandra,Brice Alexis,Charles Perrine,Marelli Cecilia,Mariotti Caterina,Nanetti Lorenzo,Panzeri Marta,Rakowicz Maria,Sulek Anna,Sobanska Anna,Schmitz-Hübsch Tanja,Schöls Ludger,Hengel Holger,Baliko Laszlo,Melegh Bela,Filla Alessandro,Antenora Antonella,Infante Jon,Berciano José,van de Warrenburg Bart P,Timmann Dagmar,Szymanski Sandra,Boesch Sylvia,Kang Jun-Suk,Pandolfo Massimo,Schulz Jörg B,Molho Sonia,Diallo Alhassane,Klockgether Thomas

Publisher

Elsevier BV

Subject

Clinical Neurology

Reference24 articles.

1. Autosomal dominant cerebellar ataxias: polyglutamine expansions and beyond;Durr;Lancet Neurol,2010

2. Spinocerebellar ataxia types 1, 2, 3, and 6: disease severity and nonataxia symptoms;Schmitz-Hübsch;Neurology,2008

3. The natural history of spinocerebellar ataxia type 1, 2, 3, and 6: a 2-year follow-up study;Jacobi;Neurology,2011

4. Scale for the assessment and rating of ataxia: development of a new clinical scale;Schmitz-Hübsch;Neurology,2006

5. Inventory of Non-Ataxia Signs (INAS): validation of a new clinical assessment instrument;Jacobi;Cerebellum,2013

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