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Epilepsy Research
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November 1, 1995
Genetic linkage studies in familial frontal epilepsy: exclusion of the human chromosome regions homologous to the El-1 mouse locus
I Lopes-Cendes, H A Phillips, I E Scheffer, et al.
Brain : a Journal of Neurology
|
February 1, 1995
Autosomal dominant nocturnal frontal lobe epilepsy. A distinctive clinical disorder
I E Scheffer, K P Bhatia, I Lopes-Cendes, et al.
Neurology
|
February 1, 1997
Chronic encephalitis and epilepsy in adults and adolescents: a variant of Rasmussen's syndrome?
Y M Hart, F Andermann, D R Fish, et al.
Neurology
|
March 23, 2007
Familial mesial temporal lobe epilepsy maps to chromosome 4q13.2-q21.3
P Hedera, M A Blair, E Andermann, et al.
Lancet (London, England)
|
February 26, 1994
Autosomal dominant frontal epilepsy misdiagnosed as sleep disorder
I E Scheffer, K P Bhatia, I Lopes-Cendes, et al.
American Journal of Human Genetics
|
January 1, 1996
The gene responsible for a severe form of peripheral neuropathy and agenesis of the corpus callosum maps to chromosome 15q
L K Casaubon, M Melanson, I Lopes-Cendes, et al.
Neurology
|
April 1, 1993
Gelastic seizures and hypothalamic hamartomas: evaluation of patients undergoing chronic intracranial EEG monitoring and outcome of surgical treatment
G D Cascino, F Andermann, S F Berkovic, et al.
Neurology
|
November 18, 1998
Surgical treatment of epilepsy in tuberous sclerosis: strategies and results in 18 patients
M M Guerreiro, F Andermann, E Andermann, et al.
Epilepsia
|
August 8, 2001
Severe myoclonic epilepsy of infancy: extended spectrum of GEFS+?
R Singh, E Andermann, W P Whitehouse, et al.
Journal of Medical Genetics
|
September 10, 2003
Genetic mapping of a new Lafora progressive myoclonus epilepsy locus (EPM2B) on 6p22
E M Chan, D E Bulman, A D Paterson, et al.
Page
of 37
Search research articles
Search
Showing results (331-340 of 367) with videos related to
Sort By:
Page
of 37
Epilepsy Research
|
November 1, 1995
Genetic linkage studies in familial frontal epilepsy: exclusion of the human chromosome regions homologous to the El-1 mouse locus
I Lopes-Cendes, H A Phillips, I E Scheffer, et al.
Brain : a Journal of Neurology
|
February 1, 1995
Autosomal dominant nocturnal frontal lobe epilepsy. A distinctive clinical disorder
I E Scheffer, K P Bhatia, I Lopes-Cendes, et al.
Neurology
|
February 1, 1997
Chronic encephalitis and epilepsy in adults and adolescents: a variant of Rasmussen's syndrome?
Y M Hart, F Andermann, D R Fish, et al.
Neurology
|
March 23, 2007
Familial mesial temporal lobe epilepsy maps to chromosome 4q13.2-q21.3
P Hedera, M A Blair, E Andermann, et al.
Lancet (London, England)
|
February 26, 1994
Autosomal dominant frontal epilepsy misdiagnosed as sleep disorder
I E Scheffer, K P Bhatia, I Lopes-Cendes, et al.
American Journal of Human Genetics
|
January 1, 1996
The gene responsible for a severe form of peripheral neuropathy and agenesis of the corpus callosum maps to chromosome 15q
L K Casaubon, M Melanson, I Lopes-Cendes, et al.
Neurology
|
April 1, 1993
Gelastic seizures and hypothalamic hamartomas: evaluation of patients undergoing chronic intracranial EEG monitoring and outcome of surgical treatment
G D Cascino, F Andermann, S F Berkovic, et al.
Neurology
|
November 18, 1998
Surgical treatment of epilepsy in tuberous sclerosis: strategies and results in 18 patients
M M Guerreiro, F Andermann, E Andermann, et al.
Epilepsia
|
August 8, 2001
Severe myoclonic epilepsy of infancy: extended spectrum of GEFS+?
R Singh, E Andermann, W P Whitehouse, et al.
Journal of Medical Genetics
|
September 10, 2003
Genetic mapping of a new Lafora progressive myoclonus epilepsy locus (EPM2B) on 6p22
E M Chan, D E Bulman, A D Paterson, et al.
Page
of 37