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Showing results (661-670 of 723) with videos related to

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Epilepsia|February 13, 2008
The three stages of epilepsy in patients with CDKL5 mutationsNadia Bahi-Buisson, Anna Kaminska, Nathalie Boddaert, et al.
Epilepsia|July 3, 2013
Children often present with infantile spasms after herpetic encephalitisGemma Aznar Laín, Georges Dellatolas, Monika Eisermann, et al.
Epilepsy Research|September 28, 2002
No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 5 in families with typical absence seizuresC Windemuth, H Schulz, K Saar, et al.
Neurology|August 1, 1996
X-linked malformations of neuronal migrationW B Dobyns, E Andermann, F Andermann, et al.
Epilepsia|November 23, 2007
Spectrum of epilepsy in terminal 1p36 deletion syndromeNadia Bahi-Buisson, Eva Guttierrez-Delicado, Christine Soufflet, et al.
Nature|February 26, 2025
A hypothalamic circuit underlying the dynamic control of social homeostasisDing Liu, Mostafizur Rahman, Autumn Johnson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 12, 2019
Genetic diversity and pathogenic variants as possible predictors of severity in a French sample of nonsyndromic heritable thoracic aortic aneurysms and dissections (nshTAAD)Pauline Arnaud, Nadine Hanna, Louise Benarroch, et al.
Nature Genetics|October 23, 2012
De novo gain-of-function KCNT1 channel mutations cause malignant migrating partial seizures of infancyGiulia Barcia, Matthew R Fleming, Aline Deligniere, et al.
JACC. Clinical Electrophysiology|March 25, 2022
Incidence, Risk Factors, and Outcomes of Atrial Arrhythmias in Adult Patients With Atrioventricular Septal DefectEtienne Jacquemart, Francis Bessière, Nicolas Combes, et al.
Epilepsy Research|June 21, 2007
Linkage and mutational analysis of CLCN2 in childhood absence epilepsyKate Everett, Barry Chioza, Jean Aicardi, et al.
Pageof 73

Showing results (661-670 of 723) with videos related to

Sort By:
Pageof 73
Epilepsia|February 13, 2008
The three stages of epilepsy in patients with CDKL5 mutationsNadia Bahi-Buisson, Anna Kaminska, Nathalie Boddaert, et al.
Epilepsia|July 3, 2013
Children often present with infantile spasms after herpetic encephalitisGemma Aznar Laín, Georges Dellatolas, Monika Eisermann, et al.
Epilepsy Research|September 28, 2002
No evidence for a susceptibility locus for idiopathic generalized epilepsy on chromosome 5 in families with typical absence seizuresC Windemuth, H Schulz, K Saar, et al.
Neurology|August 1, 1996
X-linked malformations of neuronal migrationW B Dobyns, E Andermann, F Andermann, et al.
Epilepsia|November 23, 2007
Spectrum of epilepsy in terminal 1p36 deletion syndromeNadia Bahi-Buisson, Eva Guttierrez-Delicado, Christine Soufflet, et al.
Nature|February 26, 2025
A hypothalamic circuit underlying the dynamic control of social homeostasisDing Liu, Mostafizur Rahman, Autumn Johnson, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 12, 2019
Genetic diversity and pathogenic variants as possible predictors of severity in a French sample of nonsyndromic heritable thoracic aortic aneurysms and dissections (nshTAAD)Pauline Arnaud, Nadine Hanna, Louise Benarroch, et al.
Nature Genetics|October 23, 2012
De novo gain-of-function KCNT1 channel mutations cause malignant migrating partial seizures of infancyGiulia Barcia, Matthew R Fleming, Aline Deligniere, et al.
JACC. Clinical Electrophysiology|March 25, 2022
Incidence, Risk Factors, and Outcomes of Atrial Arrhythmias in Adult Patients With Atrioventricular Septal DefectEtienne Jacquemart, Francis Bessière, Nicolas Combes, et al.
Epilepsy Research|June 21, 2007
Linkage and mutational analysis of CLCN2 in childhood absence epilepsyKate Everett, Barry Chioza, Jean Aicardi, et al.
Pageof 73