Results 11 to 20 of about 1,156,270 (203)

Differential Diagnosis of Lennox-Gastaut Syndrome

open access: yesPediatric Neurology Briefs, 2014
Epileptologists from Children's Hospital, Boston, and UCLA, California, discuss approaches to the differential diagnosis of Lennox Gastaut syndrome (LGS) and identification of a possible underlying etiology.
J Gordon Millichap, John J Millichap
doaj   +2 more sources

Neurocisticercose e síndrome de lennox-gastaut: relato de caso Neurocysticercosis and Lennox-Gastaut syndrome: case report [PDF]

open access: yesArquivos de Neuro-Psiquiatria, 2000
Relata-se o caso de uma menina que, aos 2 anos de idade, apresentou a forma epiléptica, hidrocefálica e encefalítica da neurocisticercose, diagnosticada por exame do líquido cefalorraqueano e tomografia computadorizada de crânio, evolução com crises ...
SVETLANA AGAPEJEV   +3 more
doaj   +2 more sources

Felbamate in Lennox-Gastaut Syndrome

open access: yesPediatric Neurology Briefs, 1993
The Felbamate Study Group report results in 73 patients ages 4 to 36 years with the Lennox-Gastaut syndrome, using a double-blind, placebo- controlled, add-on trial design.
J Gordon Millichap
doaj   +2 more sources

Topiramate in Lennox-Gastaut Syndrome

open access: yesPediatric Neurology Briefs, 1999
The efficacy and safety of topiramate as adjunctive therapy for Lennox-Gastaut syndrome were studied in an 11-week multicenter, double-blind, placebo-controlled trial involving 98 patients, 1-30 years of age, and reported from the New Jersey-Robert Wood ...
J Gordon Millichap
doaj   +2 more sources

Update on the management of Lennox-Gastaut syndrome with a focus on rufinamide

open access: yesNeuropsychiatric Disease and Treatment, 2009
Carl E StafstromSection of Pediatric Neurology, Departments of Neurology and Pediatrics, University of Wisconsin School of Medicine and Public Health, Madison, WI, USAObjective: This review summarizes the treatment of Lennox-Gastaut syndrome, an
Carl E Stafstrom
doaj   +1 more source

Lennox-gastaut syndrome in a pediatric patient with prader-willi syndrome: A case report and review

open access: yesBrain Disorders
Prader-Willi Syndrome is typically caused by paternal deletion of chromosome 15q11-q13. It involves multiple systems and is commonly associated with hypotonia, global developmental delay, and endocrine abnormalities. Seizures are less frequently reported
Raidah Albaradie   +3 more
doaj   +2 more sources

Prevalence of Lennox-Gastaut Syndrome in Atlanta

open access: yesPediatric Neurology Briefs, 1998
The prevalence and epidemiology of Lennox-Gastaut syndrome (LGS) among metropolitan Atlanta children were studied at the University of Kentucky, Lexington, KY, and Centers for Disease Control and Prevention, USPHS, Atlanta, GA, using data from the ...
J Gordon Millichap
doaj   +2 more sources

Effects of barbexaclone on Lennox-Gastaut syndrome

open access: yesArquivos de Neuro-Psiquiatria, 1978
The Lennox-Gastaut syndrome has been a source of interest for many workers both from a clinical and electroencephalographic view point. Treatment has always posed problems.
Clovis Oliveira   +4 more
doaj   +2 more sources

Forced normalization after turning off vagus nerve stimulation in Lennox–Gastaut syndrome

open access: yesEpilepsy and Behavior Case Reports, 2019
Forced normalization is the development of psychiatric symptoms in a patient experiencing remission of seizures. We present a case of Lennox Gastaut syndrome in which forced normalization developed after vagus nerve stimulation was stopped.The patient ...
Sydney Lee   +5 more
doaj   +2 more sources

Demonstration of antibody and cellular immune response to brain extract in West and Lennox-Gastaut syndromes [PDF]

open access: yesArquivos de Neuro-Psiquiatria, 1984
We investigated humoral and cellular immune response to brain tissues in 15 patients with West syndrome, in 9 patients with Lennox-Gastaut syndrome and in 20 healthy children.
Norma G. S. Mota   +3 more
doaj   +2 more sources

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