Search Results - "Cersosimo, Ricardo Oscar"
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Ketogenic Diet in Patients with Dravet Syndrome
Published in Epilepsia (Copenhagen) (01-09-2005)“…Purpose: The ketogenic diet (KD) has been used as a therapeutic alternative to antiepileptic drugs (AEDs) for refractory epilepsy. Severe myoclonic epilepsy in…”
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2
Electroclinical overlap of two types of epileptic encephalopathy occurring in the same children in a certain age period?
Published in Epilepsy research (01-08-2012)“…Summary In this study, we describe three patients who each had an electroclinical overlap of two different epileptic encephalopathies (EE), with onset in a…”
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3
Congenital hemiparesis, unilateral polymicrogyria and epilepsy with or without status epilepticus during sleep: a study of 66 patients with long-term follow-up
Published in Epileptic disorders (01-12-2013)“…Aim We retrospectively analysed the electroclinical features, treatment, and outcome in patients with unilateral polymicrogyria (PMG), focussing on epileptic…”
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4
Myoclonic Status in Nonprogressive Encephalopathies: Study of 29 Cases
Published in Epilepsia (Copenhagen) (01-01-2007)“…Purpose: Myoclonic status in nonprogressive encephalopaties (MSNE) is characterized by recurrence of long‐lasting myoclonic status appearing in infants and…”
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5
Childhood occipital epilepsy of Gastaut: A study of 33 patients
Published in Epilepsia (Copenhagen) (01-02-2008)“…Summary Purpose: To characterize the electroclinical features and evolution of childhood occipital epilepsy of Gastaut (COE‐G). Methods: Children with…”
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6
Ketogenic diet in patients with myoclonic-astatic epilepsy
Published in Epileptic disorders (01-06-2006)“…For more than 80 years, the ketogenic diet has been used as an alternative to antiepileptic drugs for patients with refractory epilepsy. Myoclonic-astatic…”
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7
Bilateral posterior agyria–pachygyria and epilepsy
Published in Brain & development (Tokyo. 1979) (01-03-2003)“…We analyzed the electroclinical findings in two patients with bilateral posterior agyria–pachygyria. Both patients presented with mental retardation, mild…”
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8
Unilateral closed-lip schizencephaly and epilepsy: a comparison with cases of unilateral polymicrogyria
Published in Brain & development (Tokyo. 1979) (01-04-2004)“…We compared the electroclinical features and evolution of patients with two different types of abnormal cortical organization: unilateral closed-lip…”
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9
Benign Focal Seizures of Adolescence: A Prospective Study
Published in Epilepsia (Copenhagen) (01-12-2004)“…Purpose: To characterize the clinical and EEG findings and evolution of the syndrome of benign focal seizures of adolescence (BFSA), as described by Loiseau et…”
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10
Benign familial and non‐familial infantile seizures: a study of 64 patients
Published in Epileptic disorders (01-03-2003)“…ABSTRACT Introduction The recently proposed diagnostic scheme for people with epileptic seizures and with epilepsy (Epilepsia 2001) includes two idiopathic…”
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11
Congenital hemiparesis, unilateral polymicrogyria and epilepsy with or without status epilepticus during sleep: a study of 66 patients with long-term follow-up
Published in Epileptic disorders (01-12-2013)“…Aim. We retrospectively analysed the electroclinical features, treatment, and outcome in patients with unilateral polymicrogyria (PMG), focussing on epileptic…”
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12
Late-onset, "Gastaut type", childhood occipital epilepsy: an unusual evolution
Published in Epileptic disorders (01-12-2005)“…We report on two girls and one boy with clinical and electroencephalographic features of late-onset childhood epilepsy with occipital paroxysms of the "Gastaut…”
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13
Benign Familial Infantile Seizures: Further Delineation of the Syndrome
Published in Journal of child neurology (01-09-2002)“…Benign familial infantile seizures are an autosomal dominant epilepsy disorder that is characterized by convulsions, with onset at age 3 to 12 months and a…”
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14
Focal polymicrogyria in mother and son
Published in Brain & development (Tokyo. 1979) (01-08-2000)“…This 9-year-old boy was admitted at the age of 2 with a diagnosis of congenital hemiparesis while the rest of physical and neurological examination was normal…”
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