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F Riant

Showing results (1-10 of 17) with videos related to

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Revue Neurologique|April 16, 2011
[Hereditary episodic ataxia]F Riant, K Vahedi, E Tournier-Lasserve
Journal of Neurology, Neurosurgery, and Psychiatry|October 30, 2009
Episodic ataxia type 2: unusual aspects in clinical and genetic presentation. Special emphasis in childhoodP Bertholon, S Chabrier, F Riant, et al.
European Journal of Neurology|February 13, 2013
PRRT2 mutations and paroxysmal disordersA Méneret, C Gaudebout, F Riant, et al.
Neurology|September 10, 2008
Familial cerebral cavernomatous malformations associated with palmar capillary telangiectasiasR Ahdab, F Riant, P Brugières, et al.
Neurology|September 15, 2010
De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraineF Riant, A Ducros, C Ploton, et al.
Cephalalgia : an International Journal of Headache|May 24, 2008
Severe attacks of familial hemiplegic migraine, childhood epilepsy and ATP1A2 mutationA Lebas, L Guyant-Maréchal, D Hannequin, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 18, 2009
Late onset hereditary episodic ataxiaM Damak, F Riant, M Boukobza, et al.
Cephalalgia : an International Journal of Headache|May 15, 2009
The FHM1 mutation S218L: a severe clinical phenotype? A case report and review of the literatureS Debiais, C Hommet, I Bonnaud, et al.
Journal of the Neurological Sciences|February 23, 2015
Occurrence of multiple Cerebral Cavernous Malformations in a patient with Neurofibromatosis type 1K Rerat, F Parker, G Nasser, et al.
Clinical Genetics|November 21, 2013
Deep intronic KRIT1 mutation in a family with clinically silent multiple cerebral cavernous malformationsF Riant, S Odent, M Cecillon, et al.
Pageof 2

Showing results (1-10 of 17) with videos related to

Sort By:
Pageof 2
Revue Neurologique|April 16, 2011
[Hereditary episodic ataxia]F Riant, K Vahedi, E Tournier-Lasserve
Journal of Neurology, Neurosurgery, and Psychiatry|October 30, 2009
Episodic ataxia type 2: unusual aspects in clinical and genetic presentation. Special emphasis in childhoodP Bertholon, S Chabrier, F Riant, et al.
European Journal of Neurology|February 13, 2013
PRRT2 mutations and paroxysmal disordersA Méneret, C Gaudebout, F Riant, et al.
Neurology|September 10, 2008
Familial cerebral cavernomatous malformations associated with palmar capillary telangiectasiasR Ahdab, F Riant, P Brugières, et al.
Neurology|September 15, 2010
De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraineF Riant, A Ducros, C Ploton, et al.
Cephalalgia : an International Journal of Headache|May 24, 2008
Severe attacks of familial hemiplegic migraine, childhood epilepsy and ATP1A2 mutationA Lebas, L Guyant-Maréchal, D Hannequin, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|April 18, 2009
Late onset hereditary episodic ataxiaM Damak, F Riant, M Boukobza, et al.
Cephalalgia : an International Journal of Headache|May 15, 2009
The FHM1 mutation S218L: a severe clinical phenotype? A case report and review of the literatureS Debiais, C Hommet, I Bonnaud, et al.
Journal of the Neurological Sciences|February 23, 2015
Occurrence of multiple Cerebral Cavernous Malformations in a patient with Neurofibromatosis type 1K Rerat, F Parker, G Nasser, et al.
Clinical Genetics|November 21, 2013
Deep intronic KRIT1 mutation in a family with clinically silent multiple cerebral cavernous malformationsF Riant, S Odent, M Cecillon, et al.
Pageof 2