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The Neuropharmacology of Juvenile Myoclonic Epilepsy
Clinical Neuropharmacology, 1990S R, Resor, L D, Resor
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[Juvenile myoclonic epilepsy].
Revista de neurologia, 2003In 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
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[Juvenile myoclonic epilepsy].
Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova, 1995Juvenile 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
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Juvenile myoclonic epilepsy: Long-term prognosis and risk factors
Brain and Development, 2021Federico Vigevano +2 more
exaly
Prognosis of juvenile myoclonic epilepsy is related to endophenotypes
Seizure: the Journal of the British Epilepsy Association, 2011Laura Guilhoto, Katia Lin
exaly
Video-Polygraphic Analysis of Myoclonic Seizures in Juvenile Myoclonic Epilepsy
Epilepsia, 1994Hirokazu Oguni
exaly
Subcortical gray matter changes in pediatric patients with new-onset juvenile myoclonic epilepsy
Epilepsy and Behavior, 2020Zeynep ÖZTÜRK
exaly

