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Samuel F Berkovic

Showing results (141-150 of 464) with videos related to

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Epilepsia|March 14, 2025
Sleep-related hypermotor epilepsy-No longer controversialFrancesca Bisulli, Samuel F Berkovic, Ingrid E Scheffer, et al.
American Journal of Medical Genetics. Part A|May 31, 2019
Splice variant in ARX leading to loss of C-terminal region in a boy with intellectual disability and infantile onset developmental and epileptic encephalopathyCheryl Shoubridge, Matilda Jackson, Bronwyn Grinton, et al.
Human Genetics|January 11, 2014
Does variation in NIPA2 contribute to genetic generalized epilepsy?Michael S Hildebrand, John A Damiano, Saul A Mullen, et al.
Neurology|August 22, 2014
Rasmussen encephalitis and comorbid autoimmune diseases: A window into disease mechanism?Dina Amrom, Demet Kinay, Yvonne Hart, et al.
Brain : a Journal of Neurology|June 27, 2025
Twins with temporal lobe epilepsy: genetic contributions to hippocampal sclerosis and other subtypesYew Li Dang, Kate Esnault, Gregory Fitt, et al.
Brain : a Journal of Neurology|June 25, 2004
Temporal lobectomy: long-term seizure outcome, late recurrence and risks for seizure recurrenceAnne M McIntosh, Renate M Kalnins, L Anne Mitchell, et al.
Epilepsia|March 28, 2007
SCN2A mutations and benign familial neonatal-infantile seizures: the phenotypic spectrumEric Herlenius, Sarah E Heron, Bronwyn E Grinton, et al.
Epilepsia|February 14, 2007
Hippocampal sclerosis: MR prediction of seizure intractabilityRegula S Briellmann, R Mark Wellard, Richard A J Masterton, et al.
Archives of Neurology|May 10, 2006
Distinguishing sleep disorders from seizures: diagnosing bumps in the nightChristopher Paul Derry, Margot Davey, Murray Johns, et al.
European Journal of Human Genetics : EJHG|January 16, 2022
Bi-allelic SMO variants in hypothalamic hamartoma: a recessive cause of Pallister-Hall syndromeTimothy E Green, Mareike Schimmel, Susanna Schubert, et al.
Pageof 47

Showing results (141-150 of 464) with videos related to

Sort By:
Pageof 47
Epilepsia|March 14, 2025
Sleep-related hypermotor epilepsy-No longer controversialFrancesca Bisulli, Samuel F Berkovic, Ingrid E Scheffer, et al.
American Journal of Medical Genetics. Part A|May 31, 2019
Splice variant in ARX leading to loss of C-terminal region in a boy with intellectual disability and infantile onset developmental and epileptic encephalopathyCheryl Shoubridge, Matilda Jackson, Bronwyn Grinton, et al.
Human Genetics|January 11, 2014
Does variation in NIPA2 contribute to genetic generalized epilepsy?Michael S Hildebrand, John A Damiano, Saul A Mullen, et al.
Neurology|August 22, 2014
Rasmussen encephalitis and comorbid autoimmune diseases: A window into disease mechanism?Dina Amrom, Demet Kinay, Yvonne Hart, et al.
Brain : a Journal of Neurology|June 27, 2025
Twins with temporal lobe epilepsy: genetic contributions to hippocampal sclerosis and other subtypesYew Li Dang, Kate Esnault, Gregory Fitt, et al.
Brain : a Journal of Neurology|June 25, 2004
Temporal lobectomy: long-term seizure outcome, late recurrence and risks for seizure recurrenceAnne M McIntosh, Renate M Kalnins, L Anne Mitchell, et al.
Epilepsia|March 28, 2007
SCN2A mutations and benign familial neonatal-infantile seizures: the phenotypic spectrumEric Herlenius, Sarah E Heron, Bronwyn E Grinton, et al.
Epilepsia|February 14, 2007
Hippocampal sclerosis: MR prediction of seizure intractabilityRegula S Briellmann, R Mark Wellard, Richard A J Masterton, et al.
Archives of Neurology|May 10, 2006
Distinguishing sleep disorders from seizures: diagnosing bumps in the nightChristopher Paul Derry, Margot Davey, Murray Johns, et al.
European Journal of Human Genetics : EJHG|January 16, 2022
Bi-allelic SMO variants in hypothalamic hamartoma: a recessive cause of Pallister-Hall syndromeTimothy E Green, Mareike Schimmel, Susanna Schubert, et al.
Pageof 47