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E Andermann

Showing results (61-70 of 159) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|August 1, 1994
Subcortical laminar heterotopia and lissencephaly in two families: a single X linked dominant geneJ M Pinard, J Motte, C Chiron, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 1, 1995
Alternating paroxysmal dystonia and hemiplegia in childhood as a symptom of basal ganglia diseaseY M Hart, D Tampieri, E Andermann, et al.
Annals of Neurology|September 1, 1993
Cortical vascular abnormalities in the syndrome of celiac disease, epilepsy, bilateral occipital calcifications, and folate deficiencyA M Bye, F Andermann, Y Robitaille, et al.
Acta Neurologica Scandinavica|December 1, 1986
Immunological and genetic studies in primary generalized corticoreticular epilepsyO Eeg-Olofsson, N A Janjua, E Andermann, et al.
Acta Neurologica Scandinavica|February 7, 2004
Herpesviral DNA in brain tissue from patients with temporal lobe epilepsyO Eeg-Olofsson, T Bergström, F Andermann, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|November 1, 1976
Genetic and family studies in Friedreich's ataxiaE Andermann, G M Remillard, C Goyer, et al.
Annals of Neurology|December 1, 1991
Focal neuronal migration disorders and intractable partial epilepsy: a study of 30 patientsA Palmini, F Andermann, A Olivier, et al.
Journal of Child Neurology|May 1, 1996
Evidence of a third locus for benign familial convulsionsT B Lewis, M I Shevell, E Andermann, et al.
Neurology|February 21, 2008
Levetiracetam for the treatment of idiopathic generalized epilepsy with myoclonic seizuresS Noachtar, E Andermann, P Meyvisch, et al.
Lancet (London, England)|August 17, 1991
Clinical spectrum of mitochondrial DNA mutation at base pair 8344S F Berkovic, E A Shoubridge, F Andermann, et al.
Pageof 16

Showing results (61-70 of 159) with videos related to

Sort By:
Pageof 16
Journal of Neurology, Neurosurgery, and Psychiatry|August 1, 1994
Subcortical laminar heterotopia and lissencephaly in two families: a single X linked dominant geneJ M Pinard, J Motte, C Chiron, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 1, 1995
Alternating paroxysmal dystonia and hemiplegia in childhood as a symptom of basal ganglia diseaseY M Hart, D Tampieri, E Andermann, et al.
Annals of Neurology|September 1, 1993
Cortical vascular abnormalities in the syndrome of celiac disease, epilepsy, bilateral occipital calcifications, and folate deficiencyA M Bye, F Andermann, Y Robitaille, et al.
Acta Neurologica Scandinavica|December 1, 1986
Immunological and genetic studies in primary generalized corticoreticular epilepsyO Eeg-Olofsson, N A Janjua, E Andermann, et al.
Acta Neurologica Scandinavica|February 7, 2004
Herpesviral DNA in brain tissue from patients with temporal lobe epilepsyO Eeg-Olofsson, T Bergström, F Andermann, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|November 1, 1976
Genetic and family studies in Friedreich's ataxiaE Andermann, G M Remillard, C Goyer, et al.
Annals of Neurology|December 1, 1991
Focal neuronal migration disorders and intractable partial epilepsy: a study of 30 patientsA Palmini, F Andermann, A Olivier, et al.
Journal of Child Neurology|May 1, 1996
Evidence of a third locus for benign familial convulsionsT B Lewis, M I Shevell, E Andermann, et al.
Neurology|February 21, 2008
Levetiracetam for the treatment of idiopathic generalized epilepsy with myoclonic seizuresS Noachtar, E Andermann, P Meyvisch, et al.
Lancet (London, England)|August 17, 1991
Clinical spectrum of mitochondrial DNA mutation at base pair 8344S F Berkovic, E A Shoubridge, F Andermann, et al.
Pageof 16