Results 151 to 160 of about 4,695 (177)
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The Neuropharmacology of Juvenile Myoclonic Epilepsy

Clinical Neuropharmacology, 1990
S R, Resor, L D, Resor
openaire   +2 more sources

[Juvenile myoclonic epilepsy].

Revista de neurologia, 2003
In this paper we review the history of juvenile myoclonic epilepsy (JME) since the description by Herpin in 1852 and 1857 of the seizures of some epileptic patients which he called impulsions . Credit is due to Janz and Christian who in 1957 gave a detailed description of the condition which they called impulsive Petit mal and we know today as JME ...
J, Salas-Puig   +3 more
openaire   +1 more source

[Juvenile myoclonic epilepsy].

Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova, 1995
Juvenile myoclonic epilepsy (JME) is an idiopathic primary generalized epilepsy of teenagers, characterized by massive myoclonic seizures. 18 patients were investigated. Myoclonic seizures first appeared at the mean age of 14 years and were characterized by short rapid abrupt involuntary jerks of extremities with the preserved consciousness. There were
K Iu, Mukhin   +2 more
openaire   +1 more source

Juvenile myoclonic epilepsy: Long-term prognosis and risk factors

Brain and Development, 2021
Federico Vigevano   +2 more
exaly  

Prognosis of juvenile myoclonic epilepsy is related to endophenotypes

Seizure: the Journal of the British Epilepsy Association, 2011
Laura Guilhoto, Katia Lin
exaly  

Clinical heterogeneity of juvenile myoclonic epilepsy: Follow-up after an interval of more than 20 years

Seizure: the Journal of the British Epilepsy Association, 2014
Eylert Brodtkorb
exaly  

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