Riant F - Search Results

1

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.

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

A novel hereditary small vessel disease of the brain.

Verreault S, Joutel A, Riant F, Neves G, Rui Silva M, Maciazek J, Tournier-Lasserve E, Bousser MG, Chabriat H. Verreault S, et al. Among authors: riant f. Ann Neurol. 2006 Feb;59(2):353-7. doi: 10.1002/ana.20775. Ann Neurol. 2006. PMID: 16404745

6

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.

7

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. Denier C, et al. Among authors: riant f. Ann Neurol. 2006 Nov;60(5):550-556. doi: 10.1002/ana.20947. Ann Neurol. 2006. PMID: 17041941

8

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

9

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.

10

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.

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