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Isabelle An

Showing results (11-20 of 23) with videos related to

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Epileptic Disorders : International Epilepsy Journal with Videotape|December 12, 2018
Early and long-term electroclinical features of patients with epilepsy and PCDH19 mutationNicole Chemaly, Emma Losito, Jean Marc Pinard, et al.
Molecular Genetics and Metabolism|July 17, 2017
Severe neuroimaging anomalies are usually associated with random X inactivation in leucocytes circulating DNA in X-linked dominant Incontinentia PigmentiVolodia Dangouloff-Ros, Smail Hadj-Rabia, Judite Oliveira Santos, et al.
Child and Adolescent Psychiatry and Mental Health|May 17, 2011
Malignant catatonia due to anti-NMDA-receptor encephalitis in a 17-year-old girl: case reportAngèle Consoli, Karine Ronen, Isabelle An-Gourfinkel, et al.
Annals of Neurology|October 25, 2021
Cardiac Investigations in Sudden Unexpected Death in DEPDC5-Related EpilepsyAlexandre Bacq, Delphine Roussel, Thomas Bonduelle, et al.
Neurology. Genetics|April 12, 2016
Novel GABRG2 mutations cause familial febrile seizuresMorgane Boillot, Mélanie Morin-Brureau, Fabienne Picard, et al.
Epilepsia|July 3, 2013
Children often present with infantile spasms after herpetic encephalitisGemma Aznar Laín, Georges Dellatolas, Monika Eisermann, et al.
Epilepsia|May 14, 2016
Involvement of GATOR complex genes in familial focal epilepsies and focal cortical dysplasiaSarah Weckhuysen, Elise Marsan, Virginie Lambrecq, et al.
Brain : a Journal of Neurology|October 9, 2010
GPR56-related bilateral frontoparietal polymicrogyria: further evidence for an overlap with the cobblestone complexNadia Bahi-Buisson, Karine Poirier, Nathalie Boddaert, et al.
Neurology|May 13, 2014
DEPDC5 mutations in families presenting as autosomal dominant nocturnal frontal lobe epilepsyFabienne Picard, Periklis Makrythanasis, Vincent Navarro, et al.
Orphanet Journal of Rare Diseases|May 23, 2013
Similar early characteristics but variable neurological outcome of patients with a de novo mutation of KCNQ2Mathieu Milh, Nadia Boutry-Kryza, Julie Sutera-Sardo, et al.
Pageof 3

Showing results (11-20 of 23) with videos related to

Sort By:
Pageof 3
Epileptic Disorders : International Epilepsy Journal with Videotape|December 12, 2018
Early and long-term electroclinical features of patients with epilepsy and PCDH19 mutationNicole Chemaly, Emma Losito, Jean Marc Pinard, et al.
Molecular Genetics and Metabolism|July 17, 2017
Severe neuroimaging anomalies are usually associated with random X inactivation in leucocytes circulating DNA in X-linked dominant Incontinentia PigmentiVolodia Dangouloff-Ros, Smail Hadj-Rabia, Judite Oliveira Santos, et al.
Child and Adolescent Psychiatry and Mental Health|May 17, 2011
Malignant catatonia due to anti-NMDA-receptor encephalitis in a 17-year-old girl: case reportAngèle Consoli, Karine Ronen, Isabelle An-Gourfinkel, et al.
Annals of Neurology|October 25, 2021
Cardiac Investigations in Sudden Unexpected Death in DEPDC5-Related EpilepsyAlexandre Bacq, Delphine Roussel, Thomas Bonduelle, et al.
Neurology. Genetics|April 12, 2016
Novel GABRG2 mutations cause familial febrile seizuresMorgane Boillot, Mélanie Morin-Brureau, Fabienne Picard, et al.
Epilepsia|July 3, 2013
Children often present with infantile spasms after herpetic encephalitisGemma Aznar Laín, Georges Dellatolas, Monika Eisermann, et al.
Epilepsia|May 14, 2016
Involvement of GATOR complex genes in familial focal epilepsies and focal cortical dysplasiaSarah Weckhuysen, Elise Marsan, Virginie Lambrecq, et al.
Brain : a Journal of Neurology|October 9, 2010
GPR56-related bilateral frontoparietal polymicrogyria: further evidence for an overlap with the cobblestone complexNadia Bahi-Buisson, Karine Poirier, Nathalie Boddaert, et al.
Neurology|May 13, 2014
DEPDC5 mutations in families presenting as autosomal dominant nocturnal frontal lobe epilepsyFabienne Picard, Periklis Makrythanasis, Vincent Navarro, et al.
Orphanet Journal of Rare Diseases|May 23, 2013
Similar early characteristics but variable neurological outcome of patients with a de novo mutation of KCNQ2Mathieu Milh, Nadia Boutry-Kryza, Julie Sutera-Sardo, et al.
Pageof 3