Vidaud D - Search Results

1

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

2

Towards a transgenic mouse model of sickle cell disease: hemoglobin SAD.

Trudel M, Saadane N, Garel MC, Bardakdjian-Michau J, Blouquit Y, Guerquin-Kern JL, Rouyer-Fessard P, Vidaud D, Pachnis A, Roméo PH, et al. Trudel M, et al. Among authors: vidaud d. EMBO J. 1991 Nov;10(11):3157-65. doi: 10.1002/j.1460-2075.1991.tb04877.x. EMBO J. 1991. PMID: 1915288 Free PMC article.

3

Novel double mutant CF allele identified in a cystic fibrosis patient with meconium ileus.

Steffann J, Vidaud D, Bousquet S, Jullien M, Ninot A, Kaplan JC, Beldjord C, Bienvenu T. Steffann J, et al. Among authors: vidaud d. Ann Genet. 1998;41(4):213-5. Ann Genet. 1998. PMID: 9881185 No abstract available.

4

Towards a mouse model for sickle cell disease: HB SAD.

Trudel M, Garel MC, Saadane N, Rouyer-Fessard P, Vidaud D, Costantini F, Beuzard Y. Trudel M, et al. Among authors: vidaud d. Nouv Rev Fr Hematol (1978). 1990;32(6):407-8. Nouv Rev Fr Hematol (1978). 1990. PMID: 2101873

5

Growth Hormone Deficiency in a Child with Neurofibromatosis-Noonan Syndrome.

Vurallı D, Gönç N, Vidaud D, Özön A, Alikaşifoğlu A, Kandemir N. Vurallı D, et al. Among authors: vidaud d. J Clin Res Pediatr Endocrinol. 2016 Mar 5;8(1):96-100. doi: 10.4274/jcrpe.2070. Epub 2015 Dec 18. J Clin Res Pediatr Endocrinol. 2016. PMID: 26758488 Free PMC article.

6

A new series of mycobacterial expression vectors for the development of live recombinant vaccines.

Baulard A, Kremer L, Supply P, Vidaud D, Bidart JM, Bellet D, Locht C. Baulard A, et al. Among authors: vidaud d. Gene. 1996 Oct 17;176(1-2):149-54. doi: 10.1016/0378-1119(96)00239-9. Gene. 1996. PMID: 8918246

7

Comment on Intragenic inversions in NF1 gene as pathogenic mechanism in neurofibromatosis type 1.

Pacot L, Chansavang A, Jacques S, Laurendeau I, Hadjadj D, Ferkal S, Wolkenstein P, Vidaud D, Pasmant E. Pacot L, et al. Among authors: vidaud d. Eur J Hum Genet. 2023 Apr;31(4):380-382. doi: 10.1038/s41431-023-01304-0. Epub 2023 Feb 3. Eur J Hum Genet. 2023. PMID: 36732663 Free PMC article. No abstract available.

8

A novel missense mutation D513G in exon 10 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene identified in a French CBAVD patient. Mutations in brief no. 175. Online.

Bienvenu T, Bousquet S, Vidaud D, Hubert D, Francoual C, Beldjord C, Kaplan JC. Bienvenu T, et al. Among authors: vidaud d. Hum Mutat. 1998;12(3):213-4. Hum Mutat. 1998. PMID: 10651488

9

Sex differences in mutational rate and mutational mechanism in the NF1 gene in neurofibromatosis type 1 patients.

Lázaro C, Gaona A, Ainsworth P, Tenconi R, Vidaud D, Kruyer H, Ars E, Volpini V, Estivill X. Lázaro C, et al. Among authors: vidaud d. Hum Genet. 1996 Dec;98(6):696-9. doi: 10.1007/s004390050287. Hum Genet. 1996. PMID: 8931703

10

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.

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