Chewing-induced segmental myoclonus in a patient with Leigh syndrome-Reference-Cited by-同舟云学术

Chewing-induced segmental myoclonus in a patient with Leigh syndrome

Published:2013-06-18 Issue:12 Volume:28 Page:1756-1757
ISSN:0885-3185
Container-title:Movement Disorders
language:en
Short-container-title:Mov Disord.

Author:

Navarro-Otano Judith¹,Valls-Solé Josep²,Guaita Marc²,Santamaria Joan²,Cardellach Francesc³,Muñoz Esteban¹

Affiliation:

1. Parkinson's Disease and Movement Disorders Unit, Neurology Service, Hospital Clínic; Institut d'Investigació Augustí Pi i Sunyer (IDIBAPS); University of Barcelona Catalonia; Barcelona Spain

2. Neurology Service, Hospital Clinic; Institut d'Investigació Augustí Pi i Sunyer (IDIBAPS); University of Barcelona; Catalonia Barcelona Spain

3. Internal Medicine Service, Hospital Clinic, Institut d'Investigació AugustíPi i Sunyer (IDIBAPS), CIBER of Rare Diseases; University of Barcelona; Catalonia Barcelona Spain

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/mds.25516/fullpdf

Reference7 articles.

1. Juvenile Leigh syndrome, optic atrophy, ataxia, dystonia, and epilepsy due to T14487C mutation in the mtDNA-ND6 gene: a mitochondrial syndrome presenting from birth to adolescence;Leshinsky-Silver;J Child Neurol,2011

2. Milestones in myoclonus;Shibasaki;Mov Disord,2011

3. Segmental myoclonus. Clinical and pharmacologic study;Jankovic;Arch Neurol,1986

4. Cervical and facial myoclonus associated with dolichoectasia of the left vertebral artery;Munoz;Mov Disord,1997

5. Eating-induced facial myoclonic dystonia probably due to a putaminal lesion;Gaig;Mov Disord,2007

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1. Síndrome de Leigh de inicio adulto, con epilepsia mioclónica progresiva, asociado a la mutación m.14487T>C: reporte de caso;Neurología Argentina;2023-01

2. Genetics of Mitochondrial Disease with Focus on Movement Disorders;Movement Disorder Genetics;2015