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Jean Aicardi

Showing results (1-10 of 12) with videos related to

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Brain & Development|March 2, 2005
Aicardi syndromeJean Aicardi
Journal of Clinical Neurophysiology : Official Publication of the American Electroencephalographic Society|January 22, 2004
Epileptic encephalopathies with myoclonic seizures in infants and children (severe myoclonic epilepsy and myoclonic-astatic epilepsy)Renzo Guerrini, Jean Aicardi
Epileptic Disorders : International Epilepsy Journal with Videotape|May 30, 2003
Benign idiopathic occipital epilepsy: report of a case of the late (Gastaut) type [corrected]Pierre Thomas, Alexis Arzimanoglou, Jean Aicardi
Epileptic Disorders : International Epilepsy Journal with Videotape|February 21, 2004
Hypothalamic hamartoma and epilepsy in children: illustrative cases of possible evolutionsAlexis A Arzimanoglou, Edouard Hirsch, Jean Aicardi
Clinical Dysmorphology|September 15, 2004
Aicardi syndrome in a girl with mild developmental delay, absence of epilepsy and normal EEGArpad Matlary, Trine Prescott, Bjørn Tvedt, et al.
Epilepsy Research|March 21, 2002
Linkage analysis between childhood absence epilepsy and genes encoding GABAA and GABAB receptors, voltage-dependent calcium channels, and the ECA1 region on chromosome 8qRobert Robinson, Nichole Taske, Thomas Sander, et al.
Epilepsy Research|June 21, 2007
Linkage and mutational analysis of CLCN2 in childhood absence epilepsyKate Everett, Barry Chioza, Jean Aicardi, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|September 16, 2005
Nonconvulsive status epilepticus: Epilepsy Research Foundation workshop reportsMatthew Walker, Helen Cross, Shelagh Smith, et al.
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.
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.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Brain & Development|March 2, 2005
Aicardi syndromeJean Aicardi
Journal of Clinical Neurophysiology : Official Publication of the American Electroencephalographic Society|January 22, 2004
Epileptic encephalopathies with myoclonic seizures in infants and children (severe myoclonic epilepsy and myoclonic-astatic epilepsy)Renzo Guerrini, Jean Aicardi
Epileptic Disorders : International Epilepsy Journal with Videotape|May 30, 2003
Benign idiopathic occipital epilepsy: report of a case of the late (Gastaut) type [corrected]Pierre Thomas, Alexis Arzimanoglou, Jean Aicardi
Epileptic Disorders : International Epilepsy Journal with Videotape|February 21, 2004
Hypothalamic hamartoma and epilepsy in children: illustrative cases of possible evolutionsAlexis A Arzimanoglou, Edouard Hirsch, Jean Aicardi
Clinical Dysmorphology|September 15, 2004
Aicardi syndrome in a girl with mild developmental delay, absence of epilepsy and normal EEGArpad Matlary, Trine Prescott, Bjørn Tvedt, et al.
Epilepsy Research|March 21, 2002
Linkage analysis between childhood absence epilepsy and genes encoding GABAA and GABAB receptors, voltage-dependent calcium channels, and the ECA1 region on chromosome 8qRobert Robinson, Nichole Taske, Thomas Sander, et al.
Epilepsy Research|June 21, 2007
Linkage and mutational analysis of CLCN2 in childhood absence epilepsyKate Everett, Barry Chioza, Jean Aicardi, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|September 16, 2005
Nonconvulsive status epilepticus: Epilepsy Research Foundation workshop reportsMatthew Walker, Helen Cross, Shelagh Smith, et al.
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.
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.
Pageof 2