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Ingrid E Scheffer

Showing results (171-180 of 586) with videos related to

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Annals of Neurology|March 30, 2004
Genetic variation of CACNA1H in idiopathic generalized epilepsySarah E Heron, Hilary A Phillips, John C Mulley, et al.
Epilepsia|May 1, 2022
International consensus on diagnosis and management of Dravet syndromeElaine C Wirrell, Veronica Hood, Kelly G Knupp, et al.
Nature Communications|July 21, 2022
Heterogeneous nuclear ribonucleoprotein U (HNRNPU) safeguards the developing mouse cortexTamar Sapir, Aditya Kshirsagar, Anna Gorelik, et al.
Neurology|June 11, 2013
Etiology of hippocampal sclerosis: evidence for a predisposing familial morphologic anomalyMeng-Han Tsai, Heath R Pardoe, Yuliya Perchyonok, et al.
Epilepsy Research|March 26, 2013
Genetics of febrile seizure subtypes and syndromes: a twin studyJazmin Eckhaus, Kate M Lawrence, Ingo Helbig, et al.
American Journal of Medical Genetics. Part A|November 22, 2017
Mosaic uniparental disomy results in GM1 gangliosidosis with normal enzyme assayKenneth A Myers, Mark F Bennett, Chung W Chow, et al.
Epilepsia|December 22, 2017
ADGRV1 is implicated in myoclonic epilepsyKenneth A Myers, Steven Nasioulas, Amber Boys, et al.
Annals of Neurology|July 6, 2004
Is benign rolandic epilepsy genetically determined?Lata Vadlamudi, A Simon Harvey, Mary M Connellan, et al.
American Journal of Medical Genetics. Part A|December 29, 2015
A mutation in COL4A2 causes autosomal dominant porencephaly with cataractsThuong T Ha, Lynette G Sadleir, Simone A Mandelstam, et al.
Neurology. Genetics|May 16, 2019
Double somatic mosaicism in a child with Dravet syndromeAlison M Muir, Chontelle King, Amy L Schneider, et al.
Pageof 59

Showing results (171-180 of 586) with videos related to

Sort By:
Pageof 59
Annals of Neurology|March 30, 2004
Genetic variation of CACNA1H in idiopathic generalized epilepsySarah E Heron, Hilary A Phillips, John C Mulley, et al.
Epilepsia|May 1, 2022
International consensus on diagnosis and management of Dravet syndromeElaine C Wirrell, Veronica Hood, Kelly G Knupp, et al.
Nature Communications|July 21, 2022
Heterogeneous nuclear ribonucleoprotein U (HNRNPU) safeguards the developing mouse cortexTamar Sapir, Aditya Kshirsagar, Anna Gorelik, et al.
Neurology|June 11, 2013
Etiology of hippocampal sclerosis: evidence for a predisposing familial morphologic anomalyMeng-Han Tsai, Heath R Pardoe, Yuliya Perchyonok, et al.
Epilepsy Research|March 26, 2013
Genetics of febrile seizure subtypes and syndromes: a twin studyJazmin Eckhaus, Kate M Lawrence, Ingo Helbig, et al.
American Journal of Medical Genetics. Part A|November 22, 2017
Mosaic uniparental disomy results in GM1 gangliosidosis with normal enzyme assayKenneth A Myers, Mark F Bennett, Chung W Chow, et al.
Epilepsia|December 22, 2017
ADGRV1 is implicated in myoclonic epilepsyKenneth A Myers, Steven Nasioulas, Amber Boys, et al.
Annals of Neurology|July 6, 2004
Is benign rolandic epilepsy genetically determined?Lata Vadlamudi, A Simon Harvey, Mary M Connellan, et al.
American Journal of Medical Genetics. Part A|December 29, 2015
A mutation in COL4A2 causes autosomal dominant porencephaly with cataractsThuong T Ha, Lynette G Sadleir, Simone A Mandelstam, et al.
Neurology. Genetics|May 16, 2019
Double somatic mosaicism in a child with Dravet syndromeAlison M Muir, Chontelle King, Amy L Schneider, et al.
Pageof 59