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Florence Riant

Showing results (21-30 of 68) with videos related to

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Human Mutation|February 15, 2008
Activating NOTCH3 mutation in a patient with small-vessel-disease of the brainCharles Fouillade, Hugues Chabriat, Florence Riant, et al.
Annals of Clinical and Translational Neurology|March 13, 2020
FGF14-related episodic ataxia: delineating the phenotype of Episodic Ataxia type 9Julie Piarroux, Florence Riant, Véronique Humbertclaude, et al.
Journal of Neurology|September 11, 2010
Excellent response to acetazolamide in a case of paroxysmal dyskinesias due to GLUT1-deficiencyMathieu Anheim, Elisabeth Maillart, Sandrine Vuillaumier-Barrot, et al.
Annals of Neurology|October 17, 2006
Genotype-phenotype correlations in cerebral cavernous malformations patientsChristian Denier, Pierre Labauge, Françoise Bergametti, et al.
Neuropediatrics|June 22, 2019
Infantile-Onset Paroxysmal Movement Disorder and Episodic Ataxia Associated with a TBC1D24 MutationVincent Zimmern, Florence Riant, Emmanuel Roze, et al.
Annals of Neurology|January 13, 2006
A novel hereditary small vessel disease of the brainSteve Verreault, Anne Joutel, Florence Riant, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 14, 2023
Autosomal recessive systemic microangiopathy associated with <i>FANCL</i> Fanconi anaemiaLouis Cousyn, Sophie Demeret, Anne Philippi, et al.
Neurology|October 19, 2012
PRRT2 mutations cause hemiplegic migraineFlorence Riant, Emmanuel Roze, Cecile Barbance, et al.
Epilepsia|June 22, 2010
Familial form of typical childhood absence epilepsy in a consanguineous contextHanen Abouda, Yosr Hizem, Amina Gargouri, et al.
The Neuroradiology Journal|August 7, 2015
Cerebral cavernous malformations associated to meningioma: High penetrance in a novel family mutated in the PDCD10 geneFrancesco Garaci, Luisa Marsili, Florence Riant, et al.
Pageof 7

Showing results (21-30 of 68) with videos related to

Sort By:
Pageof 7
Human Mutation|February 15, 2008
Activating NOTCH3 mutation in a patient with small-vessel-disease of the brainCharles Fouillade, Hugues Chabriat, Florence Riant, et al.
Annals of Clinical and Translational Neurology|March 13, 2020
FGF14-related episodic ataxia: delineating the phenotype of Episodic Ataxia type 9Julie Piarroux, Florence Riant, Véronique Humbertclaude, et al.
Journal of Neurology|September 11, 2010
Excellent response to acetazolamide in a case of paroxysmal dyskinesias due to GLUT1-deficiencyMathieu Anheim, Elisabeth Maillart, Sandrine Vuillaumier-Barrot, et al.
Annals of Neurology|October 17, 2006
Genotype-phenotype correlations in cerebral cavernous malformations patientsChristian Denier, Pierre Labauge, Françoise Bergametti, et al.
Neuropediatrics|June 22, 2019
Infantile-Onset Paroxysmal Movement Disorder and Episodic Ataxia Associated with a TBC1D24 MutationVincent Zimmern, Florence Riant, Emmanuel Roze, et al.
Annals of Neurology|January 13, 2006
A novel hereditary small vessel disease of the brainSteve Verreault, Anne Joutel, Florence Riant, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|July 14, 2023
Autosomal recessive systemic microangiopathy associated with <i>FANCL</i> Fanconi anaemiaLouis Cousyn, Sophie Demeret, Anne Philippi, et al.
Neurology|October 19, 2012
PRRT2 mutations cause hemiplegic migraineFlorence Riant, Emmanuel Roze, Cecile Barbance, et al.
Epilepsia|June 22, 2010
Familial form of typical childhood absence epilepsy in a consanguineous contextHanen Abouda, Yosr Hizem, Amina Gargouri, et al.
The Neuroradiology Journal|August 7, 2015
Cerebral cavernous malformations associated to meningioma: High penetrance in a novel family mutated in the PDCD10 geneFrancesco Garaci, Luisa Marsili, Florence Riant, et al.
Pageof 7