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Showing results (691-700 of 723) with videos related to

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Circulation|August 18, 2012
Parental electrocardiographic screening identifies a high degree of inheritance for congenital and childhood nonimmune isolated atrioventricular blockAlban-Elouen Baruteau, Albin Behaghel, Swanny Fouchard, et al.
Circulation. Arrhythmia and Electrophysiology|May 12, 2023
Systematic Electrophysiological Study Prior to Pulmonary Valve Replacement in Tetralogy of Fallot: A Prospective Multicenter StudyVictor Waldmann, Francis Bessière, Kevin Gardey, et al.
Neurology|June 25, 2003
Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancyR Nabbout, E Gennaro, B Dalla Bernardina, et al.
Epilepsia|July 11, 2006
Linkage analysis and disease models in benign familial infantile seizures: a study of 16 familiesPasquale Striano, Maria Luisa Lispi, Elena Gennaro, et al.
Brain : a Journal of Neurology|June 18, 2010
Genotypic and phenotypic spectrum of pyridoxine-dependent epilepsy (ALDH7A1 deficiency)Philippa B Mills, Emma J Footitt, Kevin A Mills, et al.
European Journal of Cardiovascular Nursing|April 29, 2026
Remote Sophrology in Congenital Heart Disease: The SOPHROCARE Randomized Controlled TrialJohan Moreau, Caroline Neyraud, Helena Huguet, et al.
Epilepsia|April 27, 2019
Clinical study of 19 patients with SCN8A-related epilepsy: Two modes of onset regarding EEG and seizuresJulien Denis, Nathalie Villeneuve, Pierre Cacciagli, et al.
Science (New York, N.Y.)|September 16, 2006
Herpes simplex virus encephalitis in human UNC-93B deficiencyArmanda Casrouge, Shen-Ying Zhang, Céline Eidenschenk, et al.
Epilepsia|April 30, 2009
SCN1A duplications and deletions detected in Dravet syndrome: implications for molecular diagnosisCarla Marini, Ingrid E Scheffer, Rima Nabbout, et al.
American Journal of Human Genetics|March 25, 2014
Mutations in QARS, encoding glutaminyl-tRNA synthetase, cause progressive microcephaly, cerebral-cerebellar atrophy, and intractable seizuresXiaochang Zhang, Jiqiang Ling, Giulia Barcia, et al.
Pageof 73

Showing results (691-700 of 723) with videos related to

Sort By:
Pageof 73
Circulation|August 18, 2012
Parental electrocardiographic screening identifies a high degree of inheritance for congenital and childhood nonimmune isolated atrioventricular blockAlban-Elouen Baruteau, Albin Behaghel, Swanny Fouchard, et al.
Circulation. Arrhythmia and Electrophysiology|May 12, 2023
Systematic Electrophysiological Study Prior to Pulmonary Valve Replacement in Tetralogy of Fallot: A Prospective Multicenter StudyVictor Waldmann, Francis Bessière, Kevin Gardey, et al.
Neurology|June 25, 2003
Spectrum of SCN1A mutations in severe myoclonic epilepsy of infancyR Nabbout, E Gennaro, B Dalla Bernardina, et al.
Epilepsia|July 11, 2006
Linkage analysis and disease models in benign familial infantile seizures: a study of 16 familiesPasquale Striano, Maria Luisa Lispi, Elena Gennaro, et al.
Brain : a Journal of Neurology|June 18, 2010
Genotypic and phenotypic spectrum of pyridoxine-dependent epilepsy (ALDH7A1 deficiency)Philippa B Mills, Emma J Footitt, Kevin A Mills, et al.
European Journal of Cardiovascular Nursing|April 29, 2026
Remote Sophrology in Congenital Heart Disease: The SOPHROCARE Randomized Controlled TrialJohan Moreau, Caroline Neyraud, Helena Huguet, et al.
Epilepsia|April 27, 2019
Clinical study of 19 patients with SCN8A-related epilepsy: Two modes of onset regarding EEG and seizuresJulien Denis, Nathalie Villeneuve, Pierre Cacciagli, et al.
Science (New York, N.Y.)|September 16, 2006
Herpes simplex virus encephalitis in human UNC-93B deficiencyArmanda Casrouge, Shen-Ying Zhang, Céline Eidenschenk, et al.
Epilepsia|April 30, 2009
SCN1A duplications and deletions detected in Dravet syndrome: implications for molecular diagnosisCarla Marini, Ingrid E Scheffer, Rima Nabbout, et al.
American Journal of Human Genetics|March 25, 2014
Mutations in QARS, encoding glutaminyl-tRNA synthetase, cause progressive microcephaly, cerebral-cerebellar atrophy, and intractable seizuresXiaochang Zhang, Jiqiang Ling, Giulia Barcia, et al.
Pageof 73