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E Andermann

Showing results (71-80 of 159) with videos related to

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American Journal of Medical Genetics. Supplement|January 1, 1988
The Newfoundland aggregate of neuronal ceroid-lipofuscinosisE Andermann, J C Jacob, F Andermann, et al.
Neurology|October 1, 1996
Exquisite sensitivity of paroxysmal kinesigenic choreoathetosis to carbamazepineT Wein, F Andermann, K Silver, et al.
Canadian Association of Radiologists Journal = Journal L'Association Canadienne Des Radiologistes|June 1, 1993
Magnetic resonance imaging in the diagnosis of dominantly inherited cerebello-olivary atrophy: a clinicopathologic studyA Bonni, R del Carpio-O'Donovan, Y Robitaille, et al.
Neurology|April 13, 2005
Intrinsic epileptogenicity in polymicrogyric cortex suggested by EEG-fMRI BOLD responsesE Kobayashi, A P Bagshaw, A Jansen, et al.
Epilepsy Research|December 1, 1993
Increased neocortical spiking and surgical outcome after selective amygdalo-hippocampectomyF Cendes, F Dubeau, A Olivier, et al.
Advances in Neurology|January 1, 1986
Action myoclonus-renal failure syndrome: a previously unrecognized neurological disorder unmasked by advances in nephrologyE Andermann, F Andermann, S Carpenter, et al.
Transactions of the American Neurological Association|January 1, 1973
Tay-Sachs disease in Quebec: evidence for a geographic aggregate in the French-Canadian population and identification of a new retardation syndrome with possible linkage to the Tay-Sachs geneE Andermann, F Andermann, G Patry, et al.
American Journal of Human Genetics|March 21, 2000
A new locus for generalized epilepsy with febrile seizures plus maps to chromosome 2I Lopes-Cendes, I E Scheffer, S F Berkovic, et al.
Annals of Neurology|March 1, 1986
Urinary sediment dolichols in the diagnosis of neuronal ceroid-lipofuscinosisL S Wolfe, J Palo, P Santavuori, et al.
Neurology|December 1, 1994
Sweat gland vacuoles in Unverricht-Lundborg disease: a clue to diagnosis?J Cochius, S Carpenter, E Andermann, et al.
Pageof 16

Showing results (71-80 of 159) with videos related to

Sort By:
Pageof 16
American Journal of Medical Genetics. Supplement|January 1, 1988
The Newfoundland aggregate of neuronal ceroid-lipofuscinosisE Andermann, J C Jacob, F Andermann, et al.
Neurology|October 1, 1996
Exquisite sensitivity of paroxysmal kinesigenic choreoathetosis to carbamazepineT Wein, F Andermann, K Silver, et al.
Canadian Association of Radiologists Journal = Journal L'Association Canadienne Des Radiologistes|June 1, 1993
Magnetic resonance imaging in the diagnosis of dominantly inherited cerebello-olivary atrophy: a clinicopathologic studyA Bonni, R del Carpio-O'Donovan, Y Robitaille, et al.
Neurology|April 13, 2005
Intrinsic epileptogenicity in polymicrogyric cortex suggested by EEG-fMRI BOLD responsesE Kobayashi, A P Bagshaw, A Jansen, et al.
Epilepsy Research|December 1, 1993
Increased neocortical spiking and surgical outcome after selective amygdalo-hippocampectomyF Cendes, F Dubeau, A Olivier, et al.
Advances in Neurology|January 1, 1986
Action myoclonus-renal failure syndrome: a previously unrecognized neurological disorder unmasked by advances in nephrologyE Andermann, F Andermann, S Carpenter, et al.
Transactions of the American Neurological Association|January 1, 1973
Tay-Sachs disease in Quebec: evidence for a geographic aggregate in the French-Canadian population and identification of a new retardation syndrome with possible linkage to the Tay-Sachs geneE Andermann, F Andermann, G Patry, et al.
American Journal of Human Genetics|March 21, 2000
A new locus for generalized epilepsy with febrile seizures plus maps to chromosome 2I Lopes-Cendes, I E Scheffer, S F Berkovic, et al.
Annals of Neurology|March 1, 1986
Urinary sediment dolichols in the diagnosis of neuronal ceroid-lipofuscinosisL S Wolfe, J Palo, P Santavuori, et al.
Neurology|December 1, 1994
Sweat gland vacuoles in Unverricht-Lundborg disease: a clue to diagnosis?J Cochius, S Carpenter, E Andermann, et al.
Pageof 16