Early onset autosomal dominant spinocerebellar ataxia with miosis: Four cases-Reference-Cited by-同舟云学术

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Early onset autosomal dominant spinocerebellar ataxia with miosis: Four cases

Published:2008-01 Issue:1 Volume:12 Page:38-40
ISSN:1090-3798
Container-title:European Journal of Paediatric Neurology
language:en
Short-container-title:European Journal of Paediatric Neurology

Author:

Timby Niklas,Stattin Eva-Lena,Kristiansen Ingela,Eriksson Urban,Erikson Anders

Publisher

Elsevier BV

Subject

Neurology (clinical),General Medicine,Pediatrics, Perinatology and Child Health

Reference5 articles.

1. Gene table: paediatric and adult ataxias (update 5);Morrison;Eur J Ped Neurol,2006

2. Molecular pathogenesis of spinocerebellar ataxias;Dueñas;Brain,2006

3. Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis;Schöls;Lancet Neurol,2004

4. On hereditary ataxia with a series of twenty-one cases;Brown;Brain,1892

5. Hereditary spastic ataxia with congenital miosis: four cases in one family;Dick;Brit J Ophtal,1983

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1. ITPR1: The missing gene in miosis–ataxia syndrome?;American Journal of Medical Genetics Part A;2024-05-06

2. A Diagnostic Approach to Spastic ataxia Syndromes;The Cerebellum;2021-11-15

3. Clinical overview and phenomenology of movement disorders;Principles and Practice of Movement Disorders;2021

4. Spastic ataxias;The Cerebellum: Disorders and Treatment;2018

5. Paediatric and adult autosomal dominant ataxias (update 6);European Journal of Paediatric Neurology;2010-05

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