Riant F - Search Results

1

Hemiplegic Migraine Associated With PRRT2 Variations: A Clinical and Genetic Study.

Riant F, Roos C, Roubertie A, Barbance C, Hadjadj J, Auvin S, Baille G, Beltramone M, Boulanger C, Cahn A, Cata F, Cheuret E, Cuvellier JC, Defo A, Demarquay G, Donnet A, Gaillard N, Massardier E, Guy N, Lamoureux S, Le Moigno L, Lucas C, Ratiu D, Redon S, Rey C, Thauvin C, Viallet F, Tournier-Lasserve E, Ducros A. Riant F, et al. Neurology. 2022 Jan 4;98(1):e51-e61. doi: 10.1212/WNL.0000000000012947. Epub 2021 Oct 14. Neurology. 2022. PMID: 34649875

2

Hereditary infantile hemiparesis, retinal arteriolar tortuosity, and leukoencephalopathy.

Vahedi K, Massin P, Guichard JP, Miocque S, Polivka M, Goutières F, Dress D, Chapon F, Ruchoux MM, Riant F, Joutel A, Gaudric A, Bousser MG, Tournier-Lasserve E. Vahedi K, et al. Among authors: riant f. Neurology. 2003 Jan 14;60(1):57-63. doi: 10.1212/wnl.60.1.57. Neurology. 2003. PMID: 12525718

3

Pathogenic mutations associated with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy differently affect Jagged1 binding and Notch3 activity via the RBP/JK signaling Pathway.

Joutel A, Monet M, Domenga V, Riant F, Tournier-Lasserve E. Joutel A, et al. Among authors: riant f. Am J Hum Genet. 2004 Feb;74(2):338-47. doi: 10.1086/381506. Epub 2004 Jan 8. Am J Hum Genet. 2004. PMID: 14714274 Free PMC article.

4

ATP1A2 mutations in 11 families with familial hemiplegic migraine.

Riant F, De Fusco M, Aridon P, Ducros A, Ploton C, Marchelli F, Maciazek J, Bousser MG, Casari G, Tournier-Lasserve E. Riant F, et al. Hum Mutat. 2005 Sep;26(3):281. doi: 10.1002/humu.9361. Hum Mutat. 2005. PMID: 16088919

5

Activating NOTCH3 mutation in a patient with small-vessel-disease of the brain.

Fouillade C, Chabriat H, Riant F, Mine M, Arnoud M, Magy L, Bousser MG, Tournier-Lasserve E, Joutel A. Fouillade C, et al. Among authors: riant f. Hum Mutat. 2008 Mar;29(3):452. doi: 10.1002/humu.9527. Hum Mutat. 2008. PMID: 18273901

6

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. Lebas A, et al. Among authors: riant f. Cephalalgia. 2008 Jul;28(7):774-7. doi: 10.1111/j.1468-2982.2008.01603.x. Epub 2008 May 21. Cephalalgia. 2008. PMID: 18498390

7

Large CACNA1A deletion in a family with episodic ataxia type 2.

Riant F, Mourtada R, Saugier-Veber P, Tournier-Lasserve E. Riant F, et al. Arch Neurol. 2008 Jun;65(6):817-20. doi: 10.1001/archneur.65.6.817. Arch Neurol. 2008. PMID: 18541804

8

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. Roubertie A, et al. Among authors: riant f. J Neurol. 2008 Oct;255(10):1600-2. doi: 10.1007/s00415-008-0982-8. Epub 2008 Sep 3. J Neurol. 2008. PMID: 18758887 No abstract available.

9

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 MA, Leguern E, Tournier-Lasserve E, Bousser MG. Vahedi K, et al. Among authors: riant f. Neurology. 2009 Mar 31;72(13):1178-83. doi: 10.1212/01.wnl.0000345393.53132.8c. Neurology. 2009. PMID: 19332696 Review.

10

Late onset hereditary episodic ataxia.

Damak M, Riant F, Boukobza M, Tournier-Lasserve E, Bousser MG, Vahedi K. Damak M, et al. Among authors: riant f. J Neurol Neurosurg Psychiatry. 2009 May;80(5):566-8. doi: 10.1136/jnnp.2008.150615. J Neurol Neurosurg Psychiatry. 2009. PMID: 19372292

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