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European Journal of Medical Genetics
|
October 8, 2013
A novel mutation in STXBP1 causing epileptic encephalopathy (late onset infantile spasms) with partial respiratory chain complex IV deficiency
G Barcia, C Barnerias, M Rio, et al.
American Journal of Human Genetics
|
September 9, 2000
A gene for pyridoxine-dependent epilepsy maps to chromosome 5q31
V Cormier-Daire, N Dagoneau, R Nabbout, et al.
Epilepsy Research
|
December 4, 2003
Absence of mutations in major GEFS+ genes in myoclonic astatic epilepsy
R Nabbout, A Kozlovski, E Gennaro, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
December 14, 2005
[Neonatal epilepsy and inborn errors of metabolism]
N Bahi-Buisson, K Mention, P L Léger, et al.
Experimental Neurology
|
June 2, 2016
Dynamic changes of depolarizing GABA in a computational model of epileptogenic brain: Insight for Dravet syndrome
P Kurbatova, F Wendling, A Kaminska, et al.
AJNR. American Journal of Neuroradiology
|
September 22, 2022
Arterial Spin-Labeling Perfusion Imaging in the Early Stage of Sturge-Weber Syndrome
G Pouliquen, L Fillon, V Dangouloff-Ros, et al.
Neuropediatrics
|
March 17, 2006
Molar tooth sign and superior vermian dysplasia: a radiological, clinical, and genetic study
S Romano, N Boddaert, I Desguerre, et al.
Clinical Genetics
|
April 8, 2017
Comprehensive molecular screening strategy of OCLN in band-like calcification with simplified gyration and polymicrogyria
E M Jenkinson, J H Livingston, M C O'Driscoll, et al.
Journal of Medical Genetics
|
October 22, 2008
Spectrum of SCN1A gene mutations associated with Dravet syndrome: analysis of 333 patients
C Depienne, O Trouillard, C Saint-Martin, et al.
Epilepsy & Behavior : E&B
|
March 4, 2017
Outcome of childhood-onset epilepsy from adolescence to adulthood: Transition issues
R Nabbout, D M Andrade, N Bahi-Buisson, et al.
Page
of 5
Search research articles
Search
Showing results (31-40 of 43) with videos related to
Sort By:
Page
of 5
European Journal of Medical Genetics
|
October 8, 2013
A novel mutation in STXBP1 causing epileptic encephalopathy (late onset infantile spasms) with partial respiratory chain complex IV deficiency
G Barcia, C Barnerias, M Rio, et al.
American Journal of Human Genetics
|
September 9, 2000
A gene for pyridoxine-dependent epilepsy maps to chromosome 5q31
V Cormier-Daire, N Dagoneau, R Nabbout, et al.
Epilepsy Research
|
December 4, 2003
Absence of mutations in major GEFS+ genes in myoclonic astatic epilepsy
R Nabbout, A Kozlovski, E Gennaro, et al.
Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie
|
December 14, 2005
[Neonatal epilepsy and inborn errors of metabolism]
N Bahi-Buisson, K Mention, P L Léger, et al.
Experimental Neurology
|
June 2, 2016
Dynamic changes of depolarizing GABA in a computational model of epileptogenic brain: Insight for Dravet syndrome
P Kurbatova, F Wendling, A Kaminska, et al.
AJNR. American Journal of Neuroradiology
|
September 22, 2022
Arterial Spin-Labeling Perfusion Imaging in the Early Stage of Sturge-Weber Syndrome
G Pouliquen, L Fillon, V Dangouloff-Ros, et al.
Neuropediatrics
|
March 17, 2006
Molar tooth sign and superior vermian dysplasia: a radiological, clinical, and genetic study
S Romano, N Boddaert, I Desguerre, et al.
Clinical Genetics
|
April 8, 2017
Comprehensive molecular screening strategy of OCLN in band-like calcification with simplified gyration and polymicrogyria
E M Jenkinson, J H Livingston, M C O'Driscoll, et al.
Journal of Medical Genetics
|
October 22, 2008
Spectrum of SCN1A gene mutations associated with Dravet syndrome: analysis of 333 patients
C Depienne, O Trouillard, C Saint-Martin, et al.
Epilepsy & Behavior : E&B
|
March 4, 2017
Outcome of childhood-onset epilepsy from adolescence to adulthood: Transition issues
R Nabbout, D M Andrade, N Bahi-Buisson, et al.
Page
of 5