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Annals of Neurology
|
January 1, 1997
Bilateral parasagittal parietooccipital polymicrogyria and epilepsy
R Guerrini, F Dubeau, O Dulac, et al.
Annals of Neurology
|
May 1, 1997
Periventricular nodular heterotopia and intractable temporal lobe epilepsy: poor outcome after temporal lobe resection
L M Li, F Dubeau, F Andermann, et al.
Neurosurgical Review
|
September 18, 2009
Inherited cavernous malformations of the central nervous system: clinical and genetic features in 19 Swiss families
C Graeni, F Stepper, M Sturzenegger, et al.
Neuropediatrics
|
February 1, 1997
Genetic linkage analysis of a variant of juvenile onset neuronal ceroid lipofuscinosis with granular osmiophilic deposits
A O'Rawe, H M Mitchison, R Williams, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
February 18, 2006
Patterns of hippocampal abnormalities in malformations of cortical development
M A Montenegro, D Kinay, F Cendes, et al.
Neurology
|
June 24, 2004
Posterior quadrantic dysplasia or hemi-hemimegalencephaly: a characteristic brain malformation
M D D'Agostino, A Bastos, C Piras, et al.
Clinical Genetics
|
September 18, 2012
Recurrent mutations in DNAJC5 cause autosomal dominant Kufs disease
M Cadieux-Dion, E Andermann, P Lachance-Touchette, et al.
Brain : a Journal of Neurology
|
June 4, 1999
Surgical outcome in patients with epilepsy and dual pathology
L M Li, F Cendes, F Andermann, et al.
Neurology
|
May 25, 2005
Adult-onset epilepsy in focal cortical dysplasia of Taylor type
A M Siegel, G D Cascino, C E Elger, et al.
American Journal of Human Genetics
|
December 1, 1999
Mapping of a gene determining familial partial epilepsy with variable foci to chromosome 22q11-q12
L Xiong, M Labuda, D S Li, et al.
Page
of 37
Search research articles
Search
Showing results (341-350 of 367) with videos related to
Sort By:
Page
of 37
Annals of Neurology
|
January 1, 1997
Bilateral parasagittal parietooccipital polymicrogyria and epilepsy
R Guerrini, F Dubeau, O Dulac, et al.
Annals of Neurology
|
May 1, 1997
Periventricular nodular heterotopia and intractable temporal lobe epilepsy: poor outcome after temporal lobe resection
L M Li, F Dubeau, F Andermann, et al.
Neurosurgical Review
|
September 18, 2009
Inherited cavernous malformations of the central nervous system: clinical and genetic features in 19 Swiss families
C Graeni, F Stepper, M Sturzenegger, et al.
Neuropediatrics
|
February 1, 1997
Genetic linkage analysis of a variant of juvenile onset neuronal ceroid lipofuscinosis with granular osmiophilic deposits
A O'Rawe, H M Mitchison, R Williams, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
February 18, 2006
Patterns of hippocampal abnormalities in malformations of cortical development
M A Montenegro, D Kinay, F Cendes, et al.
Neurology
|
June 24, 2004
Posterior quadrantic dysplasia or hemi-hemimegalencephaly: a characteristic brain malformation
M D D'Agostino, A Bastos, C Piras, et al.
Clinical Genetics
|
September 18, 2012
Recurrent mutations in DNAJC5 cause autosomal dominant Kufs disease
M Cadieux-Dion, E Andermann, P Lachance-Touchette, et al.
Brain : a Journal of Neurology
|
June 4, 1999
Surgical outcome in patients with epilepsy and dual pathology
L M Li, F Cendes, F Andermann, et al.
Neurology
|
May 25, 2005
Adult-onset epilepsy in focal cortical dysplasia of Taylor type
A M Siegel, G D Cascino, C E Elger, et al.
American Journal of Human Genetics
|
December 1, 1999
Mapping of a gene determining familial partial epilepsy with variable foci to chromosome 22q11-q12
L Xiong, M Labuda, D S Li, et al.
Page
of 37