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E Andermann

Showing results (111-120 of 159) with videos related to

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American Journal of Human Genetics|November 1, 1990
More than one mutant allele causes infantile Tay-Sachs disease in French-CanadiansP Hechtman, F Kaplan, J Bayleran, et al.
Annals of Neurology|December 1, 1993
Atrophy of mesial structures in patients with temporal lobe epilepsy: cause or consequence of repeated seizures?F Cendes, F Andermann, P Gloor, et al.
Neurology|June 1, 1993
Early childhood prolonged febrile convulsions, atrophy and sclerosis of mesial structures, and temporal lobe epilepsy: an MRI volumetric studyF Cendes, F Andermann, F Dubeau, et al.
Annals of Neurology|April 1, 1995
Intrinsic epileptogenicity of human dysplastic cortex as suggested by corticography and surgical resultsA Palmini, A Gambardella, F Andermann, et al.
Annals of the New York Academy of Sciences|January 1, 1991
Clinical findings and linkage studies in familial tuberous sclerosisM P Short, J Haines, A Jewell, et al.
Neurology|June 1, 1996
Genetic mapping of the spinocerebellar ataxia type 2 gene on human chromosome 12A Nechiporuk, I Lopes-Cendes, T Nechiporuk, et al.
Neurology|November 14, 2001
Localizing value of alpha-methyl-L-tryptophan PET in intractable epilepsy of neocortical originM Fedi, D Reutens, H Okazawa, et al.
Human Molecular Genetics|July 21, 1998
Human doublecortin (DCX) and the homologous gene in mouse encode a putative Ca2+-dependent signaling protein which is mutated in human X-linked neuronal migration defectsK Sossey-Alaoui, A J Hartung, R Guerrini, et al.
American Journal of Human Genetics|October 1, 1991
Localization of one gene for tuberous sclerosis within 9q32-9q34, and further evidence for heterogeneityJ L Haines, M P Short, D J Kwiatkowski, et al.
Annals of Neurology|October 1, 1988
Encephalitis among Cree children in northern QuebecD N Black, G V Watters, E Andermann, et al.
Pageof 16

Showing results (111-120 of 159) with videos related to

Sort By:
Pageof 16
American Journal of Human Genetics|November 1, 1990
More than one mutant allele causes infantile Tay-Sachs disease in French-CanadiansP Hechtman, F Kaplan, J Bayleran, et al.
Annals of Neurology|December 1, 1993
Atrophy of mesial structures in patients with temporal lobe epilepsy: cause or consequence of repeated seizures?F Cendes, F Andermann, P Gloor, et al.
Neurology|June 1, 1993
Early childhood prolonged febrile convulsions, atrophy and sclerosis of mesial structures, and temporal lobe epilepsy: an MRI volumetric studyF Cendes, F Andermann, F Dubeau, et al.
Annals of Neurology|April 1, 1995
Intrinsic epileptogenicity of human dysplastic cortex as suggested by corticography and surgical resultsA Palmini, A Gambardella, F Andermann, et al.
Annals of the New York Academy of Sciences|January 1, 1991
Clinical findings and linkage studies in familial tuberous sclerosisM P Short, J Haines, A Jewell, et al.
Neurology|June 1, 1996
Genetic mapping of the spinocerebellar ataxia type 2 gene on human chromosome 12A Nechiporuk, I Lopes-Cendes, T Nechiporuk, et al.
Neurology|November 14, 2001
Localizing value of alpha-methyl-L-tryptophan PET in intractable epilepsy of neocortical originM Fedi, D Reutens, H Okazawa, et al.
Human Molecular Genetics|July 21, 1998
Human doublecortin (DCX) and the homologous gene in mouse encode a putative Ca2+-dependent signaling protein which is mutated in human X-linked neuronal migration defectsK Sossey-Alaoui, A J Hartung, R Guerrini, et al.
American Journal of Human Genetics|October 1, 1991
Localization of one gene for tuberous sclerosis within 9q32-9q34, and further evidence for heterogeneityJ L Haines, M P Short, D J Kwiatkowski, et al.
Annals of Neurology|October 1, 1988
Encephalitis among Cree children in northern QuebecD N Black, G V Watters, E Andermann, et al.
Pageof 16