PRRT2 mutations and paroxysmal disorders
Méneret, A., Gaudebout, C., Riant, F., Vidailhet, M., Depienne, C., Roze, E.
Published in European journal of neurology (01.06.2013)
Published in European journal of neurology (01.06.2013)
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Journal Article
De novo mutations in ATP1A2 and CACNA1A are frequent in early-onset sporadic hemiplegic migraine
Riant, F, Ducros, A, Ploton, C, Barbance, C, Depienne, C, Tournier-Lasserve, E
Published in Neurology (14.09.2010)
Published in Neurology (14.09.2010)
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Journal Article
Leukoencephalopathy with calcifications and cysts (LCC): 5 cases and literature review
Osman, O., Labrune, P., Reiner, P., Sarov, M., Nasser, G., Riant, F., Tournier-lasserve, E., Chabriat, H., Denier, C.
Published in Revue neurologique (01.03.2020)
Published in Revue neurologique (01.03.2020)
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Journal Article
Elicited repetitive daily blindness: a new phenotype associated with hemiplegic migraine and SCN1A mutations
Vahedi, K, Depienne, C, Le Fort, D, Riant, F, Chaine, P, Trouillard, O, Gaudric, A, Morris, M A, Leguern, E, Tournier-Lasserve, E, Bousser, M-G
Published in Neurology (31.03.2009)
Published in Neurology (31.03.2009)
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Journal Article
Occurrence of multiple Cerebral Cavernous Malformations in a patient with Neurofibromatosis type 1
Rerat, K, Parker, F, Nasser, G, Vidaud, D, Riant, F, Tournier-Lasserve, E, Denier, C
Published in Journal of the neurological sciences (15.03.2015)
Published in Journal of the neurological sciences (15.03.2015)
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Journal Article
CCM3 Mutations Are Associated with Early-Onset Cerebral Hemorrhage and Multiple Meningiomas
Riant, F., Bergametti, F., Fournier, H.-D., Chapon, F., Michalak-Provost, S., Cecillon, M., Lejeune, P., Hosseini, H., Choe, C., Orth, M., Bernreuther, C., Boulday, G., Denier, C., Labauge, P., Tournier-Lasserve, E.
Published in Molecular syndromology (01.04.2013)
Published in Molecular syndromology (01.04.2013)
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Journal Article
Deep intronic KRIT1 mutation in a family with clinically silent multiple cerebral cavernous malformations
Riant, F., Odent, S., Cecillon, M., Pasquier, L., de Baracé, C., Carney, M.P., Tournier-Lasserve, E.
Published in Clinical genetics (01.12.2014)
Published in Clinical genetics (01.12.2014)
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Journal Article
A novel large deletion in CCM1 gene in a Tunisian family
Tinsa, F., Bel Hadj, I., Riant, F., Ben Romdhane, M., Brini, I., Tournier-Lasserve, E., Louati, H., Abdelhak, S., Hamouda, S., Boussetta, K.
Published in Revue neurologique (01.03.2019)
Published in Revue neurologique (01.03.2019)
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Journal Article
Benign paroxysmal tonic upgaze, benign paroxysmal torticollis, episodic ataxia and CACNA1A mutation in a family
Roubertie, A., Echenne, B., Leydet, J., Soete, S., Krams, B., Rivier, F., Riant, F., Tournier-Lasserve, E.
Published in Journal of neurology (01.10.2008)
Published in Journal of neurology (01.10.2008)
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Journal Article
Severe Attacks of Familial Hemiplegic Migraine, Childhood Epilepsy and ATP1A2 Mutation
Lebas, A, Guyant-Maréchal, L, Hannequin, D, Riant, F, Tournier-Lasserve, E, Parain, D
Published in Cephalalgia (01.07.2008)
Published in Cephalalgia (01.07.2008)
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Journal Article
Cerebro-retinal microangiopathy with calcifications and cysts due to recessive mutations in the CTC1 gene
Bisserbe, A., Tertian, G., Buffet, C., Turhan, A., Lambotte, O., Nasser, G., Alvin, P., Tardieu, M., Riant, F., Bergametti, F., Tournier-Lasserve, E., Denier, C.
Published in Revue neurologique (01.05.2015)
Published in Revue neurologique (01.05.2015)
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Journal Article
The FHM1 Mutation S218L: A Severe Clinical Phenotype? A Case Report and Review of the Literature
Debiais, S, Hommet, C, Bonnaud, I, Barthez, MA, Rimbaux, S, Riant, F, Autret, A
Published in Cephalalgia (01.12.2009)
Published in Cephalalgia (01.12.2009)
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Journal Article
Multiple dural lesions mimicking meningiomas in patients with CCM3/PDCD10 mutations
Labauge, P, Fontaine, B, Neau, J-P, Bergametti, F, Riant, F, Blecon, A, Marchelli, F, Arnoult, M, Lannuzel, A, Clanet, M, Olschwang, S, Denier, C, Tournier-Lasserve, E
Published in Neurology (09.06.2009)
Published in Neurology (09.06.2009)
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Journal Article
Late onset hereditary episodic ataxia
Damak, M, Riant, F, Boukobza, M, Tournier-Lasserve, E, Bousser, M-G, Vahedi, K
Published in Journal of neurology, neurosurgery and psychiatry (01.05.2009)
Published in Journal of neurology, neurosurgery and psychiatry (01.05.2009)
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Journal Article
Hereditary infantile hemiparesis, retinal arteriolar tortuosity, and leukoencephalopathy
Vahedi, K, Massin, P, Guichard, J-P, Miocque, S, Polivka, M, Goutières, F, Dress, D, Chapon, F, Ruchoux, M-M, Riant, F, Joutel, A, Gaudric, A, Bousser, M-G, Tournier-Lasserve, E
Published in Neurology (14.01.2003)
Published in Neurology (14.01.2003)
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Journal Article
Familial cerebral cavernomatous malformations associated with palmar capillary telangiectasias
Ahdab, R, Riant, F, Brugières, P, Roujeau, J-C, Hodel, J, Hosseini, H
Published in Neurology (09.09.2008)
Published in Neurology (09.09.2008)
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Journal Article
PRAM-1 Is a Novel Adaptor Protein Regulated by Retinoic Acid (RA) and Promyelocytic Leukemia (PML)-RA Receptor α in Acute Promyelocytic Leukemia Cells
Moog-Lutz, Christel, Peterson, Erik J., Lutz, Pierre G., Eliason, Steve, Cavé-Riant, Florence, Singer, Andrew, Di Gioia, Yolande, Dmowski, Sally, Kamens, Joanne, Cayre, Yvon E., Koretzky, Gary
Published in The Journal of biological chemistry (22.06.2001)
Published in The Journal of biological chemistry (22.06.2001)
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Journal Article
PRRT2 mutations cause hemiplegic migraine
Riant, Florence, Roze, Emmanuel, Barbance, Cecile, Méneret, Aurélie, Guyant-Maréchal, Lucie, Lucas, Christian, Sabouraud, Pascal, Trébuchon, Agnes, Depienne, Christel, Tournier-Lasserve, Elisabeth
Published in Neurology (20.11.2012)
Published in Neurology (20.11.2012)
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