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E Andermann

Showing results (51-60 of 159) with videos related to

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Birth Defects Original Article Series|January 1, 1975
Three familial midline malformtion syndromes of the central nervous system: agenesis of the corpus callosum and anterior horn-cell disease; agenesis of cerebellar vermis; and atrophy of the cerebellar vermisE Andermann, F Andermann, M Joubert, et al.
Brain : a Journal of Neurology|February 1, 1988
Kufs' disease: a critical reappraisalS F Berkovic, S Carpenter, F Andermann, et al.
Epilepsia|September 1, 1993
Temporal lobe epilepsy after prolonged febrile convulsions: excellent outcome after surgical treatmentB Abou-Khalil, E Andermann, F Andermann, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|November 1, 1980
Friedreich's ataxia and oral glucose tolerance: II. The effect of ingested glucose on serum growth hormone in homozygotes, obligate heterozygotes and potential carriers of the Friedreich's ataxia geneG Tolis, A Mehta, C Harvey, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|November 1, 1980
Hypertrophic cardiomyopathy in Friedreich's ataxia: symmetric or asymmetric?A Pasternac, R Król, R Petitclerc, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|February 1, 1990
Association between Alzheimer disease and amyotrophic lateral sclerosis?M F Frecker, F C Fraser, E Andermann, et al.
Archives of Neurology|May 18, 2001
Long-term efficacy and safety of piracetam in the treatment of progressive myoclonus epilepsyM Fedi, D Reutens, F Dubeau, et al.
Progress in Clinical and Biological Research|January 1, 1977
Genetic variants of Tay-Sachs disease: Tay-Sachs disease and Sandhoff's disease in French Canadians, juvenile Tay-Sachs disease in Lebanese Canadians, and a Tay-Sachs screening program in the French-Canadian populationE Andermann, C R Scriver, L S Wolfe, et al.
Neurology|June 20, 1998
Nocturnal temporal lobe epilepsyA Bernasconi, F Andermann, F Cendes, et al.
Brain : a Journal of Neurology|October 1, 1988
Familial myopathy with changes resembling inclusion body myositis and periventricular leucoencephalopathy. A new syndromeA J Cole, R Kuzniecky, G Karpati, et al.
Pageof 16

Showing results (51-60 of 159) with videos related to

Sort By:
Pageof 16
Birth Defects Original Article Series|January 1, 1975
Three familial midline malformtion syndromes of the central nervous system: agenesis of the corpus callosum and anterior horn-cell disease; agenesis of cerebellar vermis; and atrophy of the cerebellar vermisE Andermann, F Andermann, M Joubert, et al.
Brain : a Journal of Neurology|February 1, 1988
Kufs' disease: a critical reappraisalS F Berkovic, S Carpenter, F Andermann, et al.
Epilepsia|September 1, 1993
Temporal lobe epilepsy after prolonged febrile convulsions: excellent outcome after surgical treatmentB Abou-Khalil, E Andermann, F Andermann, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|November 1, 1980
Friedreich's ataxia and oral glucose tolerance: II. The effect of ingested glucose on serum growth hormone in homozygotes, obligate heterozygotes and potential carriers of the Friedreich's ataxia geneG Tolis, A Mehta, C Harvey, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|November 1, 1980
Hypertrophic cardiomyopathy in Friedreich's ataxia: symmetric or asymmetric?A Pasternac, R Król, R Petitclerc, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|February 1, 1990
Association between Alzheimer disease and amyotrophic lateral sclerosis?M F Frecker, F C Fraser, E Andermann, et al.
Archives of Neurology|May 18, 2001
Long-term efficacy and safety of piracetam in the treatment of progressive myoclonus epilepsyM Fedi, D Reutens, F Dubeau, et al.
Progress in Clinical and Biological Research|January 1, 1977
Genetic variants of Tay-Sachs disease: Tay-Sachs disease and Sandhoff's disease in French Canadians, juvenile Tay-Sachs disease in Lebanese Canadians, and a Tay-Sachs screening program in the French-Canadian populationE Andermann, C R Scriver, L S Wolfe, et al.
Neurology|June 20, 1998
Nocturnal temporal lobe epilepsyA Bernasconi, F Andermann, F Cendes, et al.
Brain : a Journal of Neurology|October 1, 1988
Familial myopathy with changes resembling inclusion body myositis and periventricular leucoencephalopathy. A new syndromeA J Cole, R Kuzniecky, G Karpati, et al.
Pageof 16