Riant F - Search Results

1

PRRT2 mutations and paroxysmal disorders.

Méneret A, Gaudebout C, Riant F, Vidailhet M, Depienne C, Roze E. Méneret A, et al. Among authors: riant f. Eur J Neurol. 2013 Jun;20(6):872-8. doi: 10.1111/ene.12104. Epub 2013 Feb 9. Eur J Neurol. 2013. PMID: 23398397 Review.

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

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

4

Long-term improvement of paroxysmal dystonic choreathetosis with acetazolamide.

Michel V, Riant F, Tournier-Lasserve E, Guehl D, Lagueny A, Bioulac B, Burbaud P. Michel V, et al. Among authors: riant f. J Neurol. 2006 Oct;253(10):1362-4. doi: 10.1007/s00415-006-0206-z. Epub 2006 Apr 28. J Neurol. 2006. PMID: 16649095 No abstract available.

5

Genotype-phenotype correlations in cerebral cavernous malformations patients.

Denier C, Labauge P, Bergametti F, Marchelli F, Riant F, Arnoult M, Maciazek J, Vicaut E, Brunereau L, Tournier-Lasserve E; Société Française de Neurochirurgie. Denier C, et al. Among authors: riant f. Ann Neurol. 2006 Nov;60(5):550-6. doi: 10.1002/ana.20947. Ann Neurol. 2006. PMID: 17041941

6

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.

7

Familial cerebral cavernomatous malformations associated with palmar capillary telangiectasias.

Ahdab R, Riant F, Brugières P, Roujeau JC, Hodel J, Hosseini H. Ahdab R, et al. Among authors: riant f. Neurology. 2008 Sep 9;71(11):861-2. doi: 10.1212/01.wnl.0000325474.61048.ae. Neurology. 2008. PMID: 18779516 No abstract available.

8

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.

9

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

10

Multiple dural lesions mimicking meningiomas in patients with CCM3/PDCD10 mutations.

Labauge P, Fontaine B, Neau JP, Bergametti F, Riant F, Blecon A, Marchelli F, Arnoult M, Lannuzel A, Clanet M, Olschwang S, Denier C, Tournier-Lasserve E. Labauge P, et al. Among authors: riant f. Neurology. 2009 Jun 9;72(23):2044-6. doi: 10.1212/WNL.0b013e3181a92b13. Neurology. 2009. PMID: 19506228 No abstract available.

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