Florence Cave-Riant
Overview
Explore the profile of Florence Cave-Riant including associated specialties, affiliations and a list of published articles.
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Snapshot
Articles
6
Citations
156
Followers
0
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Top 10 Co-Authors
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Recent Articles
1.
Ishida C, Sakajiri K, Yoshita M, Joutel A, Cave-Riant F, Yamada M
Intern Med
. 2006 Sep;
45(16):981-5.
PMID: 16974063
We report a 38-year-old Japanese woman who had cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) with a novel mutation (TGT to TAT) at nucleotide position 1241 (C388Y)...
2.
Beauvais K, Cave-Riant F, De Barace C, Tardieu M, Tournier-Lasserve E, Furby A
Eur Neurol
. 2004 Jul;
52(1):58-61.
PMID: 15240985
No abstract available.
3.
Denier C, Labauge P, Brunereau L, Cave-Riant F, Marchelli F, Arnoult M, et al.
Ann Neurol
. 2004 Feb;
55(2):213-20.
PMID: 14755725
Cerebral Cavernous Malformations (CCM/OMIM 604214) are vascular malformations causing seizures and cerebral hemorrhages. They occur as a sporadic and autosomal dominant condition, the latter being characterized by the presence of...
4.
Moog-Lutz C, Cave-Riant F, Guibal F, Breau M, Di Gioia Y, Couraud P, et al.
Blood
. 2003 Jul;
102(9):3371-8.
PMID: 12869515
Retinoic acid induces clinical remission in acute promyelocytic leukemia (APL) by triggering differentiation of leukemia promyelocytes. Here, we have characterized a gene encoding a member of the immunoglobulin superfamily, among...
5.
Cave-Riant F, Denier C, Labauge P, Cecillon M, Maciazek J, Joutel A, et al.
Eur J Hum Genet
. 2002 Oct;
10(11):733-40.
PMID: 12404106
Cerebral Cavernous Malformations (CCM/MIM 604214) are vascular malformations characterised by abnormally enlarged capillary cavities without intervening brain parenchyma. Clinical manifestations include seizures, cerebral haemorrhages and focal neurological deficits. They occur...
6.
Cave-Riant F, Cuillerier B, Beau-Faller M, Martinet N, Alla F, Bronner C, et al.
Am J Respir Cell Mol Biol
. 2002 Oct;
27(4):495-502.
PMID: 12356584
Genetic mechanisms underlying origin and progression of lung cancer are still poorly understood, despite the numerous studies which identified many genomic alterations. Using polymorphic microsatellites, allelic imbalances have been frequently...