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Robert Robinson

Showing results (61-70 of 70) with videos related to

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Epilepsy Research|October 20, 2009
Genome wide high density SNP-based linkage analysis of childhood absence epilepsy identifies a susceptibility locus on chromosome 3p23-p14Barry A Chioza, Jean Aicardi, Harald Aschauer, et al.
Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance|March 15, 2019
Automated quality control in image segmentation: application to the UK Biobank cardiovascular magnetic resonance imaging studyRobert Robinson, Vanya V Valindria, Wenjia Bai, et al.
European Journal of Human Genetics : EJHG|February 1, 2007
Linkage and association analysis of CACNG3 in childhood absence epilepsyKate V Everett, Barry Chioza, Jean Aicardi, et al.
Epilepsia|October 24, 2006
Exploration of the genetic architecture of idiopathic generalized epilepsiesAnne Hempelmann, Kirsten P Taylor, Armin Heils, et al.
Neurology|April 1, 2016
Delineation of the movement disorders associated with FOXG1 mutationsApostolos Papandreou, Ruth B Schneider, Erika F Augustine, et al.
Epilepsia|February 13, 2003
Exploration of a putative susceptibility locus for idiopathic generalized epilepsy on chromosome 8p12Thomas Sander, Christine Windemuth, Herbert Schulz, et al.
Epilepsia|May 30, 2020
Phenotypic and genetic spectrum of epilepsy with myoclonic atonic seizuresShan Tang, Laura Addis, Anna Smith, et al.
Human Molecular Genetics|September 6, 2022
Germline homozygous missense DEPDC5 variants cause severe refractory early-onset epilepsy, macrocephaly and bilateral polymicrogyriaAthina Ververi, Sara Zagaglia, Lara Menzies, et al.
Human Molecular Genetics|June 18, 2015
Adaptor protein-2 sigma subunit mutations causing familial hypocalciuric hypercalcaemia type 3 (FHH3) demonstrate genotype-phenotype correlations, codon bias and dominant-negative effectsFadil M Hannan, Sarah A Howles, Angela Rogers, et al.
Brain : a Journal of Neurology|August 14, 2025
Molecular and clinical spectrum of epilepsy-dyskinesia syndromes: a cross-sectional study of 609 patientsVicente Quiroz, Julian E Alecu, Umar Zubair, et al.
Pageof 7

Showing results (61-70 of 70) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 70 results.
Epilepsy Research|October 20, 2009
Genome wide high density SNP-based linkage analysis of childhood absence epilepsy identifies a susceptibility locus on chromosome 3p23-p14Barry A Chioza, Jean Aicardi, Harald Aschauer, et al.
Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance|March 15, 2019
Automated quality control in image segmentation: application to the UK Biobank cardiovascular magnetic resonance imaging studyRobert Robinson, Vanya V Valindria, Wenjia Bai, et al.
European Journal of Human Genetics : EJHG|February 1, 2007
Linkage and association analysis of CACNG3 in childhood absence epilepsyKate V Everett, Barry Chioza, Jean Aicardi, et al.
Epilepsia|October 24, 2006
Exploration of the genetic architecture of idiopathic generalized epilepsiesAnne Hempelmann, Kirsten P Taylor, Armin Heils, et al.
Neurology|April 1, 2016
Delineation of the movement disorders associated with FOXG1 mutationsApostolos Papandreou, Ruth B Schneider, Erika F Augustine, et al.
Epilepsia|February 13, 2003
Exploration of a putative susceptibility locus for idiopathic generalized epilepsy on chromosome 8p12Thomas Sander, Christine Windemuth, Herbert Schulz, et al.
Epilepsia|May 30, 2020
Phenotypic and genetic spectrum of epilepsy with myoclonic atonic seizuresShan Tang, Laura Addis, Anna Smith, et al.
Human Molecular Genetics|September 6, 2022
Germline homozygous missense DEPDC5 variants cause severe refractory early-onset epilepsy, macrocephaly and bilateral polymicrogyriaAthina Ververi, Sara Zagaglia, Lara Menzies, et al.
Human Molecular Genetics|June 18, 2015
Adaptor protein-2 sigma subunit mutations causing familial hypocalciuric hypercalcaemia type 3 (FHH3) demonstrate genotype-phenotype correlations, codon bias and dominant-negative effectsFadil M Hannan, Sarah A Howles, Angela Rogers, et al.
Brain : a Journal of Neurology|August 14, 2025
Molecular and clinical spectrum of epilepsy-dyskinesia syndromes: a cross-sectional study of 609 patientsVicente Quiroz, Julian E Alecu, Umar Zubair, et al.
Pageof 7