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Samuel F Berkovic

Showing results (191-200 of 464) with videos related to

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Epilepsia|July 12, 2012
Familial focal epilepsy with variable foci mapped to chromosome 22q12: expansion of the phenotypic spectrumKarl Martin Klein, Terence J O'Brien, Kavita Praveen, et al.
Epilepsia|March 16, 2012
Long-term seizure outcome and risk factors for recurrence after extratemporal epilepsy surgeryAnne M McIntosh, Clare A Averill, Renate M Kalnins, et al.
Epilepsia|April 14, 2010
Familial neonatal seizures with intellectual disability caused by a microduplication of chromosome 2q24.3Sarah E Heron, Ingrid E Scheffer, Bronwyn E Grinton, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|December 21, 2017
Sensitive quantitative detection of somatic mosaic mutation in "double cortex" syndromeJohn A Damiano, Hongdo Do, Ezgi Ozturk, et al.
Epilepsia|July 6, 2018
Evidence of linkage to chromosome 5p13.2-q11.1 in a large inbred family with genetic generalized epilepsyDemet Kinay, Karen L Oliver, Erdem Tüzün, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|July 13, 2004
Temporal lobe dysembryoplastic neuroepithelial tumour: significance of discordant interictal spikesAngelo Labate, Regula S Briellmann, Anthony S Harvey, et al.
Neuroimage|November 9, 2005
Increased serotonin receptor availability in human sleep: evidence from an [18F]MPPF PET study in narcolepsyChristopher Derry, Christopher Benjamin, Peter Bladin, et al.
Epilepsia|January 28, 2016
Seizures as presenting and prominent symptom in chorea-acanthocytosis with c.2343del VPS13A gene mutationFelix Benninger, Zaid Afawi, Amos D Korczyn, et al.
Epilepsia|July 23, 2011
Investigation of the 15q13.3 CNV as a genetic modifier for familial epilepsies with variable phenotypesJohn C Mulley, Ingrid E Scheffer, Tarishi Desai, et al.
Biochemical and Biophysical Research Communications|January 11, 2015
Lysosomal integral membrane protein type-2 (LIMP-2/SCARB2) is a substrate of cathepsin-F, a cysteine protease mutated in type-B-Kufs-diseaseJudith Peters, Andrea Rittger, Rebecca Weisner, et al.
Pageof 47

Showing results (191-200 of 464) with videos related to

Sort By:
Pageof 47
Epilepsia|July 12, 2012
Familial focal epilepsy with variable foci mapped to chromosome 22q12: expansion of the phenotypic spectrumKarl Martin Klein, Terence J O'Brien, Kavita Praveen, et al.
Epilepsia|March 16, 2012
Long-term seizure outcome and risk factors for recurrence after extratemporal epilepsy surgeryAnne M McIntosh, Clare A Averill, Renate M Kalnins, et al.
Epilepsia|April 14, 2010
Familial neonatal seizures with intellectual disability caused by a microduplication of chromosome 2q24.3Sarah E Heron, Ingrid E Scheffer, Bronwyn E Grinton, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|December 21, 2017
Sensitive quantitative detection of somatic mosaic mutation in "double cortex" syndromeJohn A Damiano, Hongdo Do, Ezgi Ozturk, et al.
Epilepsia|July 6, 2018
Evidence of linkage to chromosome 5p13.2-q11.1 in a large inbred family with genetic generalized epilepsyDemet Kinay, Karen L Oliver, Erdem Tüzün, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|July 13, 2004
Temporal lobe dysembryoplastic neuroepithelial tumour: significance of discordant interictal spikesAngelo Labate, Regula S Briellmann, Anthony S Harvey, et al.
Neuroimage|November 9, 2005
Increased serotonin receptor availability in human sleep: evidence from an [18F]MPPF PET study in narcolepsyChristopher Derry, Christopher Benjamin, Peter Bladin, et al.
Epilepsia|January 28, 2016
Seizures as presenting and prominent symptom in chorea-acanthocytosis with c.2343del VPS13A gene mutationFelix Benninger, Zaid Afawi, Amos D Korczyn, et al.
Epilepsia|July 23, 2011
Investigation of the 15q13.3 CNV as a genetic modifier for familial epilepsies with variable phenotypesJohn C Mulley, Ingrid E Scheffer, Tarishi Desai, et al.
Biochemical and Biophysical Research Communications|January 11, 2015
Lysosomal integral membrane protein type-2 (LIMP-2/SCARB2) is a substrate of cathepsin-F, a cysteine protease mutated in type-B-Kufs-diseaseJudith Peters, Andrea Rittger, Rebecca Weisner, et al.
Pageof 47