Nihoul-Fékété C - Search Results

1

Germline mutations of the RET ligand GDNF are not sufficient to cause Hirschsprung disease.

Salomon R, Attié T, Pelet A, Bidaud C, Eng C, Amiel J, Sarnacki S, Goulet O, Ricour C, Nihoul-Fékété C, Munnich A, Lyonnet S. Salomon R, et al. Nat Genet. 1996 Nov;14(3):345-7. doi: 10.1038/ng1196-345. Nat Genet. 1996. PMID: 8896569

2

Heterozygous endothelin receptor B (EDNRB) mutations in isolated Hirschsprung disease.

Amiel J, Attié T, Jan D, Pelet A, Edery P, Bidaud C, Lacombe D, Tam P, Simeoni J, Flori E, Nihoul-Fékété C, Munnich A, Lyonnet S. Amiel J, et al. Hum Mol Genet. 1996 Mar;5(3):355-7. doi: 10.1093/hmg/5.3.355. Hum Mol Genet. 1996. PMID: 8852660

3

[Genetics of Hirschsprung disease].

Attié T, Amiel J, Jan D, Edery P, Pelet A, Salomon R, Munnich A, Lyonnet S, Nihoul-Fékété C. Attié T, et al. Ann Chir. 1996;50(7):538-41. Ann Chir. 1996. PMID: 9035423 French.

4

[Genetics of Hirschsprung disease].

Attié T, Salomon R, Amiel J, Edery P, Pelet A, Nihoul-Fékété C, Munnich A, Lyonnet S. Attié T, et al. C R Seances Soc Biol Fil. 1996;190(5-6):549-56. C R Seances Soc Biol Fil. 1996. PMID: 9074720 Review. French.

5

Endothelin-3 gene mutations in isolated and syndromic Hirschsprung disease.

Bidaud C, Salomon R, Van Camp G, Pelet A, Attié T, Eng C, Bonduelle M, Amiel J, Nihoul-Fékété C, Willems PJ, Munnich A, Lyonnet S. Bidaud C, et al. Eur J Hum Genet. 1997 Jul-Aug;5(4):247-51. Eur J Hum Genet. 1997. PMID: 9359047

6

[Mutations of the endothelin-3 gene in isolated and syndromic forms of Hirschsprung disease].

Bidaud C, Salomon R, Edery P, Van Camp G, Pelet A, Bonduelle M, Nihoul-Fékété C, Willems PJ, Munnich A, Lyonnet S. Bidaud C, et al. Gastroenterol Clin Biol. 1997;21(8-9):548-54. Gastroenterol Clin Biol. 1997. PMID: 9587491 Free article. French.

7

[Molecular genetics of Hirschsprung disease: a model of multigenic neurocristopathy].

Amiel J, Salomon R, Attié-Bitach T, Touraine R, Steffann J, Pelet A, Nihoul-Fékété C, Vekemans M, Munnich A, Lyonnet S. Amiel J, et al. J Soc Biol. 2000;194(3-4):125-8. J Soc Biol. 2000. PMID: 11324313 Review. French.

8

Diversity of RET proto-oncogene mutations in familial and sporadic Hirschsprung disease.

Attié T, Pelet A, Edery P, Eng C, Mulligan LM, Amiel J, Boutrand L, Beldjord C, Nihoul-Fékété C, Munnich A, et al. Attié T, et al. Hum Mol Genet. 1995 Aug;4(8):1381-6. doi: 10.1093/hmg/4.8.1381. Hum Mol Genet. 1995. PMID: 7581377

9

[Identification of mutation of RET proto-oncogene in Hirschsprung disease].

Attié T, Edery P, Lyonnet S, Nihoul-Fékété C, Munnich A. Attié T, et al. C R Seances Soc Biol Fil. 1994;188(5-6):499-504. C R Seances Soc Biol Fil. 1994. PMID: 7780793 Review. French.

10

[Mutations of RET proto-oncogene in Hirschsprung disease].

Lyonnet S, Edery P, Mulligan LM, Pelet A, Dow E, Abel L, Holder S, Nihoul-Fékéte C, Ponder BA, Munnich A. Lyonnet S, et al. C R Acad Sci III. 1994 Apr;317(4):358-62. C R Acad Sci III. 1994. PMID: 8000915 French.

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