Results 151 to 160 of about 1,335,280 (195)
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Rasmussen?s syndrome

Neurological Sciences, 2003
Rasmussen's encephalitis (RE) is characterized by focal seizures, often associated with epilepsia partialis continua, progressive neurological deterioration, hemispheric atrophy, and inflammatory histopathology. Surgical exclusion of the affected hemisphere is the only treatment that halts progression of the disease.
openaire   +2 more sources

Neuroimaging Findings in Rasmussen's Syndrome

Journal of Neuroimaging, 1997
AbstractRasmussen's syndrome is a progressive childhood disease of unknown cause characterized by severe epilepsy, hemiparesis, mental deterioration, inflammation of one cerebral hemisphere, and brain atrophy. Computed tomography, single‐photon emission computed tomography (SPECT), and magnetic resonance (MR) neuroimaging findings of 8 patients with ...
E M, Yacubian   +5 more
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Treatment of Rasmussen's syndrome with ganciclovir

Neurology, 1996
Since cytomegalovirus (CMV) has been implicated in the pathogenesis of Rasmussen's syndrome, we treated four patients with ganciclovir, a potent anti-CMV drug. A 7-year-old girl with seizures escalating to 60/day over 3 months despite triple antiepileptic drug therapy became seizure-free 5 days after initiation of treatment with no recurrence at 1.5 ...
R S, McLachlan, S, Levin, W T, Blume
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Electrophysiological findings in Rasmussen's syndrome

Epileptic Disorders, 2016
AbstractBackground. Rasmussen syndrome is a rare, inflammatory and probably autoimmune disease presenting with epilepsia partialis continua which is generally in the form of myoclonic jerks and involves the upper extremities with or without head involvement.
Gunduz, Aysegul   +5 more
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Rasmussen Syndrome: An Argentinean Experience in 32 Patients [PDF]

open access: yesSeizure: the Journal of the British Epilepsy Association, 2013
The aim of this study is to analyze the electroclinical features, treatment, and evolution of patients with Rasmussen syndrome (RS).We conducted a retrospective, descriptive study in 32 consecutive patients with RS followed between 1990 and 2012.Twenty boys and 12 girls were included in the study.
Roberto H Caraballo   +2 more
exaly   +3 more sources

Rasmussen’s Syndrome

2011
Rasmussen’s syndrome is a childhood developing syndrome, usually characterized by refractory focal motor seizures (epilepsia partialis continua). Most cases originate between the age of 1 and 10 years, mean age about 5 years. Symptoms are attributed to chronic pathogen-free inflammation of both gray and white matter.
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Double pathology in Rasmussen's syndrome

Neurology, 1998
The syndrome of chronic encephalitis with epilepsy (Rasmussen's syndrome) typically occurs in children and is characterized by the development of intractable focal seizures, progressive hemiparesis and intellectual deterioration. The etiology is unknown, and the pathological abnormalities vary from those of active disease, with numerous microglial ...
Y M, Hart   +5 more
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[Rasmussen syndrome].

Revista de neurologia, 1998
Rasmussen's encephalitis is a neurological disorder probably of immunological origin, characterized by intractable epilepsy, neurological deterioration and the presence of antibodies against R3 glutamate receptors.To present the experience of an Argentinian Paediatric Neurology Service during the past 7 years.We analyzed the clinical histories of 12 ...
R, Caraballo   +6 more
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Rasmussen Syndrome of Chronic Focal Encephalitis

European Journal of Paediatric Neurology, 2002
Rasmussen syndrome of chronic focal encephalitis is a relatively rare disease, which presents with epilepsia partialis continua and hemiparesis in childhood. Though first described in the 1950s it still remains somewhat of an enigma. The immunological process involved in its pathogenesis is better understood now but the exact relationship to viral ...
exaly   +3 more sources

[Rasmussen syndrome].

Orvosi hetilap, 1994
Authors report about a boy with Rasmussen syndrome. This is a chronic localised encephalitis with focal epileptic seizures causing progressive neurologic deficits and mental impairment. The etiology and the clinical features of the syndrome are discussed, and the diagnostic role of the new imaging modalities is emphasized.
I, Velkey, B, Lombay
openaire   +1 more source

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