Dystonia with aphonia, slow horizontal saccades, epilepsy and photic myoclonus: A novel syndrome?-Reference-Cited by-同舟云学术

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Dystonia with aphonia, slow horizontal saccades, epilepsy and photic myoclonus: A novel syndrome?

Published:2014-03 Issue:3 Volume:20 Page:328-331
ISSN:1353-8020
Container-title:Parkinsonism & Related Disorders
language:en
Short-container-title:Parkinsonism & Related Disorders

Author:

Ganos Christos,Biskup Saskia,Krüger Stefanie,Meyer-Osores Aracelli,Hodecker Sibylle,Hagel Christian,Schöls Ludger,Bhatia Kailash P.,Münchau Alexander

Publisher

Elsevier BV

Subject

Clinical Neurology,Geriatrics and Gerontology,Neurology

Reference13 articles.

1. Phenomenology and classification of dystonia: a consensus update;Albanese;Mov Disord,2013

2. Severe tongue protrusion dystonia: clinical syndromes and possible treatment;Schneider;Neurology,2006

3. The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATP1A3 gene;Brashear;Brain,2007

4. Clinical features and natural history of neuroferritinopathy caused by the FTL1 460InsA mutation;Chinnery;Brain,2007

5. Speech disturbances in patients with dystonia or chorea due to neurometabolic disorders;Flamand-Rouviere;Mov Disord,2010

Cited by 5 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. Expanding the phenotype of NEDAMSS with a psychiatric perspective: analysis of a new case, and a systematic review of the literature;European Child & Adolescent Psychiatry;2024-07-20

2. Neurological Phenotypes of IRF2BPL Gene Variants: A Report of Four Novel Variants;Journal of Central Nervous System Disease;2023-06-13

3. IRF2BPL as a novel causative gene for progressive myoclonus epilepsy;Epilepsia;2023-06-08

4. IRF2BPL mutations cause autosomal dominant dystonia with anarthria, slow saccades and seizures;Parkinsonism & Related Disorders;2019-11

5. The clinical syndrome of dystonia with anarthria/aphonia;Parkinsonism & Related Disorders;2016-03

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