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Florence Riant

Showing results (31-40 of 68) with videos related to

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Human Mutation|August 10, 2005
ATP1A2 mutations in 11 families with familial hemiplegic migraineFlorence Riant, Maurizio De Fusco, Paolo Aridon, et al.
Stroke|November 15, 2012
Antithrombotic therapy and bleeding risk in a prospective cohort study of patients with cerebral cavernous malformationsHans-Martin Schneble, Aicha Soumare, Dominique Hervé, et al.
European Journal of Neurology|June 23, 2026
Risk of Clinical Events in Presymptomatic Familial Cerebral Cavernous MalformationsConstantina Rodica Popa, Dominique Hervé, Nassira Alili, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 14, 2013
The multiple faces of the ATP1A3-related dystonic movement disorderAnne Roubergue, Emmanuel Roze, Sandrine Vuillaumier-Barrot, et al.
Stroke|March 20, 2014
Cerebral cavernous malformations arise independent of the heart of glass receptorXiangjian Zheng, Florence Riant, Françoise Bergametti, et al.
Developmental Medicine and Child Neurology|January 28, 2016
Eye movement disorders are an early manifestation of CACNA1A mutations in childrenEsther M Tantsis, Deepak Gill, Lyn Griffiths, et al.
The European Respiratory Journal|October 19, 2013
Pulmonary arterial hypertension in familial hemiplegic migraine with ATP1A2 channelopathyDavid Montani, Barbara Girerd, Sven Günther, et al.
Stroke|March 26, 2019
Clinical and Molecular Features of 5 European Multigenerational Families With Moyamoya AngiopathyLou Grangeon, Stéphanie Guey, Jan Claudius Schwitalla, et al.
Journal of Medical Genetics|January 16, 2020
Novel CCM2 missense variants abrogating the CCM1-CCM2 interaction cause cerebral cavernous malformationsFrançoise Bergametti, Geraldine Viot, Christophe Verny, et al.
European Journal of Medical Genetics|August 25, 2018
Major intra-familial phenotypic heterogeneity and incomplete penetrance due to a CACNA1A pathogenic variantChloé Angelini, Julien Van Gils, Antoine Bigourdan, et al.
Pageof 7

Showing results (31-40 of 68) with videos related to

Sort By:
Pageof 7
Human Mutation|August 10, 2005
ATP1A2 mutations in 11 families with familial hemiplegic migraineFlorence Riant, Maurizio De Fusco, Paolo Aridon, et al.
Stroke|November 15, 2012
Antithrombotic therapy and bleeding risk in a prospective cohort study of patients with cerebral cavernous malformationsHans-Martin Schneble, Aicha Soumare, Dominique Hervé, et al.
European Journal of Neurology|June 23, 2026
Risk of Clinical Events in Presymptomatic Familial Cerebral Cavernous MalformationsConstantina Rodica Popa, Dominique Hervé, Nassira Alili, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|March 14, 2013
The multiple faces of the ATP1A3-related dystonic movement disorderAnne Roubergue, Emmanuel Roze, Sandrine Vuillaumier-Barrot, et al.
Stroke|March 20, 2014
Cerebral cavernous malformations arise independent of the heart of glass receptorXiangjian Zheng, Florence Riant, Françoise Bergametti, et al.
Developmental Medicine and Child Neurology|January 28, 2016
Eye movement disorders are an early manifestation of CACNA1A mutations in childrenEsther M Tantsis, Deepak Gill, Lyn Griffiths, et al.
The European Respiratory Journal|October 19, 2013
Pulmonary arterial hypertension in familial hemiplegic migraine with ATP1A2 channelopathyDavid Montani, Barbara Girerd, Sven Günther, et al.
Stroke|March 26, 2019
Clinical and Molecular Features of 5 European Multigenerational Families With Moyamoya AngiopathyLou Grangeon, Stéphanie Guey, Jan Claudius Schwitalla, et al.
Journal of Medical Genetics|January 16, 2020
Novel CCM2 missense variants abrogating the CCM1-CCM2 interaction cause cerebral cavernous malformationsFrançoise Bergametti, Geraldine Viot, Christophe Verny, et al.
European Journal of Medical Genetics|August 25, 2018
Major intra-familial phenotypic heterogeneity and incomplete penetrance due to a CACNA1A pathogenic variantChloé Angelini, Julien Van Gils, Antoine Bigourdan, et al.
Pageof 7