Roussey M - Search Results

1

Impact of public health strategies on the birth prevalence of cystic fibrosis in Brittany, France.

Scotet V, Audrézet MP, Roussey M, Rault G, Blayau M, De Braekeleer M, Férec C. Scotet V, et al. Among authors: roussey m. Hum Genet. 2003 Aug;113(3):280-5. doi: 10.1007/s00439-003-0962-0. Epub 2003 May 27. Hum Genet. 2003. PMID: 12768409

2

Evidence for decline in the incidence of cystic fibrosis: a 35-year observational study in Brittany, France.

Scotet V, Duguépéroux I, Saliou P, Rault G, Roussey M, Audrézet MP, Férec C. Scotet V, et al. Among authors: roussey m. Orphanet J Rare Dis. 2012 Mar 1;7:14. doi: 10.1186/1750-1172-7-14. Orphanet J Rare Dis. 2012. PMID: 22380742 Free PMC article.

3

Cascade testing in families of carriers identified through newborn screening in Western Brittany (France).

Duguépéroux I, Audrézet MP, Parent P, Audebert-Bellanger S, Roussey M, Férec C, Scotet V. Duguépéroux I, et al. Among authors: roussey m. J Cyst Fibros. 2013 Jul;12(4):338-44. doi: 10.1016/j.jcf.2012.11.009. Epub 2012 Dec 28. J Cyst Fibros. 2013. PMID: 23273514 Free article.

4

Comprehensive CFTR gene analysis of the French cystic fibrosis screened newborn cohort: implications for diagnosis, genetic counseling, and mutation-specific therapy.

Audrézet MP, Munck A, Scotet V, Claustres M, Roussey M, Delmas D, Férec C, Desgeorges M. Audrézet MP, et al. Among authors: roussey m. Genet Med. 2015 Feb;17(2):108-16. doi: 10.1038/gim.2014.113. Epub 2014 Aug 14. Genet Med. 2015. PMID: 25122143 Free article.

5

Spatial and temporal distribution of cystic fibrosis and of its mutations in Brittany, France: a retrospective study from 1960.

Scotet V, Gillet D, Duguépéroux I, Audrézet MP, Bellis G, Garnier B, Roussey M, Rault G, Parent P, De Braekeleer M, Férec C; Réseau Mucoviscidose Bretagne et Pays de Loire. Scotet V, et al. Among authors: roussey m. Hum Genet. 2002 Sep;111(3):247-54. doi: 10.1007/s00439-002-0788-1. Epub 2002 Aug 1. Hum Genet. 2002. PMID: 12215837

6

Immunoreactive trypsin/DNA newborn screening for cystic fibrosis: should the R117H variant be included in CFTR mutation panels?

Scotet V, Audrézet MP, Roussey M, Rault G, Dirou-Prigent A, Journel H, Moisan-Petit V, Storni V, Férec C. Scotet V, et al. Among authors: roussey m. Pediatrics. 2006 Nov;118(5):e1523-9. doi: 10.1542/peds.2005-3161. Epub 2006 Oct 2. Pediatrics. 2006. PMID: 17015492

7

Neonatal screening for cystic fibrosis: result of a pilot study using both immunoreactive trypsinogen and cystic fibrosis gene mutation analyses.

Férec C, Verlingue C, Parent P, Morin JF, Codet JP, Rault G, Dagorne M, Lemoigne A, Journel H, Roussey M, et al. Férec C, et al. Among authors: roussey m. Hum Genet. 1995 Nov;96(5):542-8. doi: 10.1007/BF00197409. Hum Genet. 1995. PMID: 8530001

8

Neonatal screening for cystic fibrosis in Brittany, France: assessment of 10 years' experience and impact on prenatal diagnosis.

Scotet V, de Braekeleer M, Roussey M, Rault G, Parent P, Dagorne M, Journel H, Lemoigne A, Codet JP, Catheline M, David V, Chaventré A, Duguépéroux I, Verlingue C, Quéré I, Mercier B, Audrézet MP, Férec C. Scotet V, et al. Among authors: roussey m. Lancet. 2000 Sep 2;356(9232):789-94. doi: 10.1016/S0140-6736(00)02652-0. Lancet. 2000. PMID: 11022925

9

CFTR p.Arg117His associated with CBAVD and other CFTR-related disorders.

Thauvin-Robinet C, Munck A, Huet F, de Becdelièvre A, Jimenez C, Lalau G, Gautier E, Rollet J, Flori J, Nové-Josserand R, Soufir JC, Haloun A, Hubert D, Houssin E, Bellis G, Rault G, David A, Janny L, Chiron R, Rives N, Hairion D, Collignon P, Valeri A, Karsenty G, Rossi A, Audrézet MP, Férec C, Leclerc J, Georges Md, Claustres M, Bienvenu T, Gérard B, Boisseau P, Cabet-Bey F, Cheillan D, Feldmann D, Clavel C, Bieth E, Iron A, Simon-Bouy B, Izard V, Steffann J, Viville S, Costa C, Drouineaud V, Fauque P, Binquet C, Bonithon-Kopp C, Morris MA, Faivre L, Goossens M, Roussey M, Girodon E; collaborating working group on p.Arg117His. Thauvin-Robinet C, et al. Among authors: roussey m. J Med Genet. 2013 Apr;50(4):220-7. doi: 10.1136/jmedgenet-2012-101427. Epub 2013 Feb 1. J Med Genet. 2013. PMID: 23378603

10

Optimization of the French cystic fibrosis newborn screening programme by a centralized tracking process.

Munck A, Delmas D, Audrézet MP, Lemonnier L, Cheillan D, Roussey M. Munck A, et al. Among authors: roussey m. J Med Screen. 2018 Mar;25(1):6-12. doi: 10.1177/0969141317692611. Epub 2017 Apr 28. J Med Screen. 2018. PMID: 28454512 Free PMC article.

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