Progressive myoclonus epilepsy - Open Access .click

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Progressive Myoclonus Epilepsy of Lafora

2012
Abstract Lafora disease is an autosomal recessive form of progressive myoclonus epilepsy characterized by a severe course that leads to death in 5–10 years in most patients. Patients present with myoclonic, absence, and generalized tonic-clonic seizures at onset, typically at around age 14–15 years.
José M. Serratosa +2 more
openaire +1 more source

THALAMOTOMY IN PROGRESSIVE MYOCLONUS EPILEPSY

Acta Neurologica Scandinavica, 2009
openaire +2 more sources

Cognitive functioning in progressive myoclonus epilepsy type 1 (Unverricht-Lundborg Disease, EPM1)

Epilepsy and Behavior, 2021
Jelena Hyppönen, Esa Mervaala, Reetta Kälviäinen +2 more
exaly

IRF2BPL as a novel causative gene for progressive myoclonus epilepsy

Epilepsia, 2023
Elena Gardella +2 more
exaly

Reduced cystatin B activity correlates with enhanced cathepsin activity in progressive myoclonus epilepsy

Annals of Medicine, 2002
Mikko Jarvinen, Anna-Elina Lehesjoki
exaly

The improvement in diagnosis and epilepsy managing in children with progressive myoclonus epilepsy during the last decade — A tertiary center experience in cohort of 51 patients

Epilepsy and Behavior, 2020
Ruzica Kravljanac +2 more
exaly

NEW EMBO MEMBER'S REVIEW: Molecular background of progressive myoclonus epilepsy

EMBO Journal, 2003
Anna-Elina Lehesjoki
exaly