Dusser D - Search Results

1

Unexpected inactivation of acceptor consensus splice sequence by a -3 C to T transition in intron 2 of the CFTR gene.

Bienvenu T, Hubert D, Fonknechten N, Dusser D, Kaplan JC, Beldjord C. Bienvenu T, et al. Among authors: dusser d. Hum Genet. 1994 Jul;94(1):65-8. doi: 10.1007/BF02272843. Hum Genet. 1994. PMID: 7518409

2

Genotype-phenotype relationships in a cohort of adult cystic fibrosis patients.

Hubert D, Bienvenu T, Desmazes-Dufeu N, Fajac I, Lacronique J, Matran R, Kaplan JC, Dusser DJ. Hubert D, et al. Among authors: dusser dj. Eur Respir J. 1996 Nov;9(11):2207-14. doi: 10.1183/09031936.96.09112207. Eur Respir J. 1996. PMID: 8947061 Free article.

3

A new missense mutation (G27E) in exon 2 of the CFTR gene in a mildly affected cystic fibrosis patient.

Bienvenu T, Cazeneuve C, Beldjord C, Dusser D, Kaplan JC, Hubert D. Bienvenu T, et al. Among authors: dusser d. Hum Mol Genet. 1994 Feb;3(2):365-6. doi: 10.1093/hmg/3.2.365. Hum Mol Genet. 1994. PMID: 7516232 No abstract available.

4

Identification of a novel missense mutation G239R in exon 6a of the CFTR gene.

Bienvenu T, Cazeneuve C, Fajac I, Dusser D, Hubert D, Kaplan JC, Beldjord C. Bienvenu T, et al. Among authors: dusser d. Hum Hered. 1995 Jan-Feb;45(1):53-4. doi: 10.1159/000154255. Hum Hered. 1995. PMID: 7534748 No abstract available.

5

A novel missense mutation in exon 16 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene identified in CBAVD patients.

Bienvenu T, Hubert D, Setbon E, Dusser D, Kaplan JC, Beldjord C. Bienvenu T, et al. Among authors: dusser d. Hum Mutat. 1996;7(2):182. doi: 10.1002/(SICI)1098-1004(1996)7:2<182::AID-HUMU19>3.0.CO;2-Z. Hum Mutat. 1996. PMID: 8829643 No abstract available.

6

Analysis of alternative splicing patterns in the cystic fibrosis transmembrane conductance regulator gene using mRNA derived from lymphoblastoid cells of cystic fibrosis patients.

Bienvenu T, Beldjord C, Chelly J, Fonknechten N, Hubert D, Dusser D, Kaplan JC. Bienvenu T, et al. Among authors: dusser d. Eur J Hum Genet. 1996;4(3):127-34. doi: 10.1159/000472186. Eur J Hum Genet. 1996. PMID: 8840112

7

Non-classic cystic fibrosis associated with D1152H CFTR mutation.

Burgel PR, Fajac I, Hubert D, Grenet D, Stremler N, Roussey M, Siret D, Languepin J, Mely L, Fanton A, Labbé A, Domblides P, Vic P, Dagorne M, Reynaud-Gaubert M, Counil F, Varaigne F, Bienvenu T, Bellis G, Dusser D. Burgel PR, et al. Among authors: dusser d. Clin Genet. 2010 Apr;77(4):355-64. doi: 10.1111/j.1399-0004.2009.01294.x. Epub 2009 Oct 15. Clin Genet. 2010. PMID: 19843100

8

Distal intestinal obstruction syndrome in adults with cystic fibrosis.

Dray X, Bienvenu T, Desmazes-Dufeu N, Dusser D, Marteau P, Hubert D. Dray X, et al. Among authors: dusser d. Clin Gastroenterol Hepatol. 2004 Jun;2(6):498-503. doi: 10.1016/s1542-3565(04)00169-7. Clin Gastroenterol Hepatol. 2004. PMID: 15181619

9

Diagnosis of cystic fibrosis in adults with diffuse bronchiectasis.

Hubert D, Fajac I, Bienvenu T, Desmazes-Dufeu N, Ellaffi M, Dall'ava-Santucci J, Dusser D. Hubert D, et al. Among authors: dusser d. J Cyst Fibros. 2004 Mar;3(1):15-22. doi: 10.1016/j.jcf.2003.12.004. J Cyst Fibros. 2004. PMID: 15463882 Free article.

10

Cystic fibrosis transmembrane conductance regulator channel dysfunction in non-cystic fibrosis bronchiectasis.

Bienvenu T, Sermet-Gaudelus I, Burgel PR, Hubert D, Crestani B, Bassinet L, Dusser D, Fajac I. Bienvenu T, et al. Among authors: dusser d. Am J Respir Crit Care Med. 2010 May 15;181(10):1078-84. doi: 10.1164/rccm.200909-1434OC. Epub 2010 Feb 18. Am J Respir Crit Care Med. 2010. PMID: 20167849

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