Results 311 to 320 of about 2,272,583 (371)
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Annals of Neurology, 1988
Detailed study of 4 patients and review of the literature allowed us to delineate further the epileptic syndrome associated with hypothalamic hamartomas, which characteristically begins in infancy with laughing seizures.
MD S. F. Berkovic+8 more
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Detailed study of 4 patients and review of the literature allowed us to delineate further the epileptic syndrome associated with hypothalamic hamartomas, which characteristically begins in infancy with laughing seizures.
MD S. F. Berkovic+8 more
semanticscholar +1 more source
An epileptic syndrome caused by mesial frontal lobe seizure foci
Neurology, 1987We describe an epileptic syndrome of bilaterally coordinated limb movements, axial movements, vocalization, and nonmasticatory oral activity. EEG and physiologic evidence indicates the syndrome is caused by ictal discharge in the mesial frontal lobes ...
K. Waterman+4 more
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Journal of Neurophysiology, 1989
1. Minute doses of tetanus toxin were injected into the hippocampi of rats, under pentobarbitone anesthesia, to induce a chronic experimental epilepsy.
John Gordon Ralph Jefferys
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1. Minute doses of tetanus toxin were injected into the hippocampi of rats, under pentobarbitone anesthesia, to induce a chronic experimental epilepsy.
John Gordon Ralph Jefferys
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Drop Attacks and Epileptic Syndromes
Psychiatry and Clinical Neurosciences, 19931. In addition to 4 types of drop attacks previously described by Ikeno et al., we could ascertain the falls of the myoclonic-tonic type in genuine drop attacks. The genuine drop attacks were seen in Lennox-Gastaut syndrome, epilepsy with myoclonic-astatic seizures and other symptomatic generalized epilepsies, and never in partial epilepsies. 2.
Masakazu Seino+3 more
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Neuropathology and Applied Neurobiology, 1992
A few nanograms of tetanus toxin injected into a rat hippocampus causes a chronic epileptic syndrome characterized by brief seizures that recur intermittently for about 6 weeks.
John Gordon Ralph Jefferys+3 more
semanticscholar +1 more source
A few nanograms of tetanus toxin injected into a rat hippocampus causes a chronic epileptic syndrome characterized by brief seizures that recur intermittently for about 6 weeks.
John Gordon Ralph Jefferys+3 more
semanticscholar +1 more source
Neuropsychobiology, 1994
Sex steroid peripheral pattern, pulsatile luteinizing hormone (LH) secretion, gonadotropin and prolactin responses to LH-releasing hormone (LHRH) and thyrotropin-releasing hormone (TRH) were studied in 35 male epileptics treated with phenobarbital (PB ...
G. Murialdo+9 more
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Sex steroid peripheral pattern, pulsatile luteinizing hormone (LH) secretion, gonadotropin and prolactin responses to LH-releasing hormone (LHRH) and thyrotropin-releasing hormone (TRH) were studied in 35 male epileptics treated with phenobarbital (PB ...
G. Murialdo+9 more
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Seizure Types and Epileptic Syndromes
European Neurology, 1994The main epileptic syndromes occurring during brain maturation, i.e. during the neonatal period, infancy, childhood and adolescence, are reviewed. The concept of epileptic syndromes is of pragmatic significance and helps the physician to select appropriate modes of investigation, to predict the outcome and to choose the treatment of first choice.
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Epilepsia, 1993
Summary: In the pediatric age period, three idiopathic partial epileptic syndromes are recognized: benign childhood epilepsy with centrotemporal spikes, childhood epilepsy with occipital paroxysms, and primary reading epilepsy.
F. Vigevano, L. Fusco
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Summary: In the pediatric age period, three idiopathic partial epileptic syndromes are recognized: benign childhood epilepsy with centrotemporal spikes, childhood epilepsy with occipital paroxysms, and primary reading epilepsy.
F. Vigevano, L. Fusco
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Epileptic Syndromes and Their Classification
2017The recognition of epileptic syndromes is the most important milestone in modern epileptology because it allows accurate diagnosis and management of epilepsy. An epileptic syndrome, is a complex of clinical features, signs, and symptoms that together define a distinctive, recognizable clinical disorder. There are many types of epileptic syndromes which
Thalia Valeta, Thalia Valeta
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Perioral myoclonia with absence seizures: a rare epileptic syndrome.
Epileptic disorders, 2001We present the clinical and video-EEG data on an epileptic boy whose absence seizures with marked perioral movements had started at the age of 1.5 years.
B. Bilgiç+3 more
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