Vidaud D - Search Results

1

Familial aggregation of malignant melanoma/dysplastic naevi and tumours of the nervous system: an original syndrome of tumour proneness.

Bahuau M, Vidaud D, Kujas M, Palangié A, Assouline B, Chaignaud-Lebreton M, Prieur M, Vidaud M, Harpey JP, Lafourcade J, Caille B. Bahuau M, et al. Among authors: vidaud m, vidaud d. Ann Genet. 1997;40(2):78-91. Ann Genet. 1997. PMID: 9259954

2

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.

3

Mutations in the catalytic domain of human coagulation factor IX: rapid characterization by direct genomic sequencing of DNA fragments displaying an altered melting behavior.

Attree O, Vidaud D, Vidaud M, Amselem S, Lavergne JM, Goossens M. Attree O, et al. Among authors: vidaud m, vidaud d. Genomics. 1989 Apr;4(3):266-72. doi: 10.1016/0888-7543(89)90330-3. Genomics. 1989. PMID: 2714791

4

Haemophilia B due to a de novo insertion of a human-specific Alu subfamily member within the coding region of the factor IX gene.

Vidaud D, Vidaud M, Bahnak BR, Siguret V, Gispert Sanchez S, Laurian Y, Meyer D, Goossens M, Lavergne JM. Vidaud D, et al. Among authors: vidaud m. Eur J Hum Genet. 1993;1(1):30-6. doi: 10.1159/000472385. Eur J Hum Genet. 1993. PMID: 8069649

5

Quantification of apolipoprotein A-I and B messenger RNA in heavy drinkers according to liver disease.

Mathurin P, Vidaud D, Vidaud M, Bedossa P, Paradis V, Ratziu V, Chaput JC, Poynard T. Mathurin P, et al. Among authors: vidaud m, vidaud d. Hepatology. 1996 Jan;23(1):44-51. doi: 10.1002/hep.510230107. Hepatology. 1996. PMID: 8550047

6

Misdiagnosis revealed by genetic linkage analysis in a family with Wilson disease.

Vidaud D, Assouline B, Lecoz P, Cadranel JF, Chappuis P. Vidaud D, et al. Neurology. 1996 May;46(5):1485-6. doi: 10.1212/wnl.46.5.1485. Neurology. 1996. PMID: 8628510 No abstract available.

7

Echinococcus multilocularis: microsatellite polymorphism in U1 snRNA genes.

Bretagne S, Assouline B, Vidaud D, Houin R, Vidaud M. Bretagne S, et al. Among authors: vidaud m, vidaud d. Exp Parasitol. 1996 Apr;82(3):324-8. doi: 10.1006/expr.1996.0040. Exp Parasitol. 1996. PMID: 8631384 No abstract available.

8

Role of liver extracellular matrix in transcriptional and post-transcriptional regulation of apolipoprotein A-I by hepatocytes.

Paradis V, Laurent A, Mathurin P, Poynard T, Vidaud D, Vidaud M, Bedossa P. Paradis V, et al. Among authors: vidaud m, vidaud d. Cell Mol Biol (Noisy-le-grand). 1996 Jun;42(4):525-34. Cell Mol Biol (Noisy-le-grand). 1996. PMID: 8828908

9

Exclusion of allelism of Noonan syndrome and neurofibromatosis-type 1 in a large family with Noonan syndrome-neurofibromatosis association.

Bahuau M, Flintoff W, Assouline B, Lyonnet S, Le Merrer M, Prieur M, Guilloud-Bataille M, Feingold N, Munnich A, Vidaud M, Vidaud D. Bahuau M, et al. Among authors: vidaud m, vidaud d. Am J Med Genet. 1996 Dec 18;66(3):347-55. doi: 10.1002/(SICI)1096-8628(19961218)66:3<347::AID-AJMG20>3.0.CO;2-L. Am J Med Genet. 1996. PMID: 8985499

10

Novel recurrent nonsense mutation causing neurofibromatosis type 1 (NF1) in a family segregating both NF1 and Noonan syndrome.

Bahuau M, Houdayer C, Assouline B, Blanchet-Bardon C, Le Merrer M, Lyonnet S, Giraud S, Récan D, Lakhdar H, Vidaud M, Vidaud D. Bahuau M, et al. Among authors: vidaud m, vidaud d. Am J Med Genet. 1998 Jan 23;75(3):265-72. Am J Med Genet. 1998. PMID: 9475595

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