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Photosensitivity in juvenile myoclonic epilepsy [PDF]
Seizure, 1998 Photosensitivity is reported to occur in approximately 40% of patients with juvenile myoclonic epilepsy. Our experience suggests that the prevalence is higher and may be related to both the duration of intermittent photic stimulation and also the age at which the procedure is undertaken. A two-year retrospective review of all EEGs was undertaken on all
Beirne, Margaret +2 more
openaire +3 more sources
CLINICAL AND GENETIC HETEROGENITY OF JUVENILE MYOCLONIC EPILEPSY [PDF]
Эпилепсия и пароксизмальные состояния, 2016 The idiopathic generalized epilepsies constitute roughly one-third of all epilepsies. Juvenile myoclonic epilepsy (Janz syndrome) is characterized by myoclonic jerks on awakening, generalized tonic-clonic seizures, and typical absences, with the latter ...
N. A. Shnayder +4 more
doaj +2 more sources
Diagnosis of Juvenile Myoclonic Epilepsy [PDF]
Pediatric Neurology Briefs, 1991 Factors contributing to the misdiagnosis of juvenile myoclonic epilepsy (JME) in an epilepsy clinic have been examined in 70 patients at the Division of Neurology, King Khalid University Hospital, Riyadh, Saudi Arabia.
J Gordon Millichap
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Long-Term Outcome in Juvenile Myoclonic Epilepsy [PDF]
Pediatric Neurology Briefs, 2012 Researchers at University of Greifswald, Germany; and Cleveland Clinic, OH, studied the long-term seizure outcome in patients with juvenile myoclonic epilepsy (JME) and identified factors predictive of seizure remission.
J Gordon Millichap
doaj +2 more sources
Long-Term Outcome of Juvenile Myoclonic Epilepsy [PDF]
Pediatric Neurology Briefs, 2014 Investigators at Epilepsy Centers in Berlin, Germany, performed a retrospective study of seizure outcome in 66 patients with juvenile myoclonic epilepsy (JME) after a mean follow-up time of 44.6 years (20-69 years); 59.1% of patients remained seizure ...
J Gordon Millichap
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Long-Term Follow-Up of Juvenile Myoclonic Epilepsy [PDF]
Pediatric Neurology Briefs, 2006 A population of 257 juvenile myoclonic epilepsy (JME) patients and family members was prospectively evaluated in a study at UCLA School of Medicine and international centers.
J Gordon Millichap
doaj +4 more sources
Long-Term Outcome of Juvenile Myoclonic Epilepsy [PDF]
Pediatric Neurology Briefs, 2009 All patients developing juvenile myoclonic epilepsy (JME) by 16 years of age in Nova Scotia between 1977 and 1985 were contacted in 2006-2008 to determine long-term seizure and social outcome, in a study at Dalhousie University, Halifax, Canada.
J Gordon Millichap
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Treatment of myoclonic seizures in patients with juvenile myoclonic epilepsy [PDF]
Neuropsychiatric Disease and Treatment, 2007 Stéphane AuvinDepartment of Pediatric Neurology, Lille University Hospital, Lille, France; Pharmacology Laboratory, Lille Medical School, Lille, FranceAbstract: Drug treatment of Juvenile myoclonic epilepsy (JME) is mainly based on clinical ...
Stéphane Auvin
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Lifetime prognosis of juvenile myoclonic epilepsy [PDF]
, 2021 Juvenile myoclonic epilepsy (JME) is among the most common types of genetic epilepsies, displaying a good prognosis when treated with appropriate drugs, but with a well-known tendency to relapse after withdrawal.
Camfield, Peter R. +4 more
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Juvenile myoclonic epilepsy as a spectrum disorder: A focused review [PDF]
, 2021 In consequence of newer research juvenile myoclonic epilepsy (JME) is no longer seen as a homogeneous disease. The causes of the existing variance are only partially known yet.
Wolf, Peter, Baykan, BETÜL
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