Results 161 to 169 of about 2,714 (169)

Uniparental disomy as a cause of spinal muscular atrophy and progressive myoclonic epilepsy: Phenotypic homogeneity due to the homozygous c.125C>T mutation in ASAH1

Neuromuscular Disorders, 2015
BEATRIZ G Giraldéz, Rosa Guerrero-López, JOSÉ Manuel Pardal-Fernández   +2 more
exaly  

Progressive Myoclonic Epilepsy Type 8 Due to CERS1 Deficiency: A Novel Mutation with Prominent Ataxia

Movement Disorders Clinical Practice, 2018
Thiago Cardoso Vale, Fernando Kok, JOSÉ Luiz Pedroso   +2 more
exaly  

KCTD7‐related progressive myoclonic epilepsy: Report of 42 cases and review of literature

Epilepsia
Sangeetha Yoganathan, Robyn Whitney, Maya Thomas   +2 more
exaly  

The effect of mephenesin on progressive familial myoclonic epilepsy

The Irish Journal of Medical Science, 1957
openaire   +2 more sources

Other Progressive Myoclonic Epilepsies

2012
openaire   +1 more source

Progressive Myoclonic Epilepsies: Overview

2012
openaire   +1 more source

Progressive Myoclonic Epilepsies: Overview

2010
openaire   +1 more source

[PROGRESSIVE MYOCLONIC EPILEPSY AS A THESAURISMOSIS].

Revue neurologique, 1996
openaire   +1 more source

[Discussion of the report on progressive myoclonic epilepsy].

Revue neurologique, 1969
openaire   +1 more source