Vidaud D - Search Results

1

Natural history of NF1 c.2970_2972del p.(Met992del): confirmation of a low risk of complications in a longitudinal study.

Forde C, Burkitt-Wright E, Turnpenny PD, Haan E, Ealing J, Mansour S, Holder M, Lahiri N, Dixit A, Procter A, Pacot L, Vidaud D, Capri Y, Gerard M, Dollfus H, Schaefer E, Quelin C, Sigaudy S, Busa T, Vera G, Damaj L, Messiaen L, Stevenson DA, Davies P, Palmer-Smith S, Callaway A, Wolkenstein P, Pasmant E, Upadhyaya M. Forde C, et al. Among authors: vidaud d. Eur J Hum Genet. 2022 Mar;30(3):291-297. doi: 10.1038/s41431-021-01015-4. Epub 2021 Dec 13. Eur J Hum Genet. 2022. PMID: 34897289 Free PMC article.

2

[Exclusive nodular plexiform neurofibroma. An unusual case of neurofibromatosis type 1].

Benchikhi H, Zeller J, Wolkenstein P, Wechsler J, Vidaud D, Revuz J. Benchikhi H, et al. Among authors: vidaud d. Ann Dermatol Venereol. 1995;122(9):601-3. Ann Dermatol Venereol. 1995. PMID: 8745684 French.

3

NF1 gene analysis focused on CpG-rich exons in a cohort of 93 patients with neurofibromatosis type 1.

Girodon-Boulandet E, Pantel J, Cazeneuve C, Gijn MV, Vidaud D, Lemay S, Martin J, Zeller J, Revuz J, Goossens M, Amselem S, Wolkenstein P. Girodon-Boulandet E, et al. Among authors: vidaud d. Hum Mutat. 2000 Sep;16(3):274-5. doi: 10.1002/1098-1004(200009)16:3<274::aid-humu21>3.3.co;2-6. Hum Mutat. 2000. PMID: 10980545

4

Elevated risk for MPNST in NF1 microdeletion patients.

De Raedt T, Brems H, Wolkenstein P, Vidaud D, Pilotti S, Perrone F, Mautner V, Frahm S, Sciot R, Legius E. De Raedt T, et al. Among authors: vidaud d. Am J Hum Genet. 2003 May;72(5):1288-92. doi: 10.1086/374821. Epub 2003 Mar 26. Am J Hum Genet. 2003. PMID: 12660952 Free PMC article.

5

Molecular profiles of neurofibromatosis type 1-associated plexiform neurofibromas: identification of a gene expression signature of poor prognosis.

Lévy P, Bièche I, Leroy K, Parfait B, Wechsler J, Laurendeau I, Wolkenstein P, Vidaud M, Vidaud D. Lévy P, et al. Among authors: vidaud m, vidaud d. Clin Cancer Res. 2004 Jun 1;10(11):3763-71. doi: 10.1158/1078-0432.CCR-03-0712. Clin Cancer Res. 2004. PMID: 15173083

6

Conservation of hotspots for recombination in low-copy repeats associated with the NF1 microdeletion.

Raedt TD, Stephens M, Heyns I, Brems H, Thijs D, Messiaen L, Stephens K, Lazaro C, Wimmer K, Kehrer-Sawatzki H, Vidaud D, Kluwe L, Marynen P, Legius E. Raedt TD, et al. Among authors: vidaud d. Nat Genet. 2006 Dec;38(12):1419-23. doi: 10.1038/ng1920. Epub 2006 Nov 19. Nat Genet. 2006. PMID: 17115058

7

Characterization of a germ-line deletion, including the entire INK4/ARF locus, in a melanoma-neural system tumor family: identification of ANRIL, an antisense noncoding RNA whose expression coclusters with ARF.

Pasmant E, Laurendeau I, Héron D, Vidaud M, Vidaud D, Bièche I. Pasmant E, et al. Among authors: vidaud m, vidaud d. Cancer Res. 2007 Apr 15;67(8):3963-9. doi: 10.1158/0008-5472.CAN-06-2004. Cancer Res. 2007. PMID: 17440112

8

Neurofibromatosis 1: analysis of the demand for prenatal diagnosis in a French cohort of 361 patients.

Farhi D, Bastuji-Garin S, Khosrotehrani K, Vidaud D, Bellane C, Revuz J, Wolkenstein P. Farhi D, et al. Among authors: vidaud d. Am J Med Genet A. 2008 Jan 15;146A(2):159-65. doi: 10.1002/ajmg.a.32066. Am J Med Genet A. 2008. PMID: 18076113

9

Characterization of a 7.6-Mb germline deletion encompassing the NF1 locus and about a hundred genes in an NF1 contiguous gene syndrome patient.

Pasmant E, de Saint-Trivier A, Laurendeau I, Dieux-Coeslier A, Parfait B, Vidaud M, Vidaud D, Bièche I. Pasmant E, et al. Among authors: vidaud m, vidaud d. Eur J Hum Genet. 2008 Dec;16(12):1459-66. doi: 10.1038/ejhg.2008.134. Epub 2008 Jul 23. Eur J Hum Genet. 2008. PMID: 18648396

10

SPRED1 germline mutations caused a neurofibromatosis type 1 overlapping phenotype.

Pasmant E, Sabbagh A, Hanna N, Masliah-Planchon J, Jolly E, Goussard P, Ballerini P, Cartault F, Barbarot S, Landman-Parker J, Soufir N, Parfait B, Vidaud M, Wolkenstein P, Vidaud D, France RN. Pasmant E, et al. Among authors: vidaud m, vidaud d. J Med Genet. 2009 Jul;46(7):425-30. doi: 10.1136/jmg.2008.065243. Epub 2009 Apr 14. J Med Genet. 2009. PMID: 19366998 Free article.

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