Juvenile myoclonic epilepsy subsyndromes: family studies and long-term follow-up.
about
Advances in genetics of juvenile myoclonic epilepsiesThe prognosis of idiopathic generalized epilepsyEfhc1 deficiency causes spontaneous myoclonus and increased seizure susceptibility.The developmental evolution of the seizure phenotype and cortical inhibition in mouse models of juvenile myoclonic epilepsy.Accuracy of claims-based algorithms for epilepsy research: Revealing the unseen performance of claims-based studies.Genetic susceptibility in Juvenile Myoclonic Epilepsy: Systematic review of genetic association studies.Animal models of absence epilepsies: what do they model and do sex and sex hormones matter?Mutational analysis of EFHC1 gene in Italian families with juvenile myoclonic epilepsy.Long-term outcome in adolescent-onset generalized genetic epilepsies.Epidemiology and characterization of seizures in a pedigreed baboon colony.Chromosome loci vary by juvenile myoclonic epilepsy subsyndromes: linkage and haplotype analysis applied to epilepsy and EEG 3.5-6.0 Hz polyspike waves.Juvenile myoclonic epilepsy: when will it endPredictors for long-term seizure outcome in juvenile myoclonic epilepsy: 25-63 years of follow-up.Clinical predictors of the long-term social outcome and quality of life in juvenile myoclonic epilepsy: 20-65 years of follow-up.Concepts and controversies of juvenile myoclonic epilepsy: still an enigmatic epilepsy.Epidemiologic aspects: lost in transition.Cessation of epilepsy therapy in children.Predicting antiepileptic drug response in children with epilepsy.Dynamics of sensorimotor cortex activation during absence and myoclonic seizures in a mouse model of juvenile myoclonic epilepsy.High-dose versus low-dose valproate for the treatment of juvenile myoclonic epilepsy: Going from low to high.Juvenile myoclonic epilepsy: more trials are needed to guide therapy.Proton spectroscopy of the thalamus in a homogeneous sample of patients with easy-to-control juvenile myoclonic epilepsy.Brain morphology in juvenile myoclonic epilepsy and absence seizures.Exploration of the genetic architecture of idiopathic generalized epilepsies.A Multicenter Study of BRD2 as a Risk Factor for Juvenile Myoclonic Epilepsy
P2860
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P2860
Juvenile myoclonic epilepsy subsyndromes: family studies and long-term follow-up.
description
2006 nî lūn-bûn
@nan
2006年の論文
@ja
2006年学术文章
@wuu
2006年学术文章
@zh
2006年学术文章
@zh-cn
2006年学术文章
@zh-hans
2006年学术文章
@zh-my
2006年学术文章
@zh-sg
2006年學術文章
@yue
2006年學術文章
@zh-hant
name
Juvenile myoclonic epilepsy subsyndromes: family studies and long-term follow-up.
@en
Juvenile myoclonic epilepsy subsyndromes: family studies and long-term follow-up.
@nl
type
label
Juvenile myoclonic epilepsy subsyndromes: family studies and long-term follow-up.
@en
Juvenile myoclonic epilepsy subsyndromes: family studies and long-term follow-up.
@nl
prefLabel
Juvenile myoclonic epilepsy subsyndromes: family studies and long-term follow-up.
@en
Juvenile myoclonic epilepsy subsyndromes: family studies and long-term follow-up.
@nl
P2093
P356
P1433
P1476
Juvenile myoclonic epilepsy subsyndromes: family studies and long-term follow-up.
@en
P2093
Antonio V Delgado-Escueta
Gregorio Pineda
Ignacio Pascual Castroviejo
Jesús Machado-Salas
Julia N Bailey
Katerina Perez-Gosiengfiao
Lizardo Mija
Lourdes León
Marco T Medina
María Elisa Alonso
P304
P356
10.1093/BRAIN/AWL048
P407
P577
2006-03-06T00:00:00Z