Scotet V - Search Results

1

Intake of flavonoids and risk of dementia.

Commenges D, Scotet V, Renaud S, Jacqmin-Gadda H, Barberger-Gateau P, Dartigues JF. Commenges D, et al. Among authors: scotet v. Eur J Epidemiol. 2000 Apr;16(4):357-63. doi: 10.1023/a:1007614613771. Eur J Epidemiol. 2000. PMID: 10959944

2

Endometrial vascularity and ongoing pregnancy after IVF.

Maugey-Laulom B, Commenges-Ducos M, Jullien V, Papaxanthos-Roche A, Scotet V, Commenges D. Maugey-Laulom B, et al. Among authors: scotet v. Eur J Obstet Gynecol Reprod Biol. 2002 Sep 10;104(2):137-43. doi: 10.1016/s0301-2115(02)00102-1. Eur J Obstet Gynecol Reprod Biol. 2002. PMID: 12206926

3

Hereditary hemochromatosis: effect of excessive alcohol consumption on disease expression in patients homozygous for the C282Y mutation.

Scotet V, Mérour MC, Mercier AY, Chanu B, Le Faou T, Raguénes O, Le Gac G, Mura C, Nousbaum JB, Férec C. Scotet V, et al. Am J Epidemiol. 2003 Jul 15;158(2):129-34. doi: 10.1093/aje/kwg123. Am J Epidemiol. 2003. PMID: 12851225

4

Genetic analysis of the glycoprotein 2 gene in patients with chronic pancreatitis.

Masson E, Paliwal S, Bhaskar S, Prakash S, Scotet V, Reddy DN, Le Maréchal C, Ratan Chandak G, Chen JM, Férec C. Masson E, et al. Among authors: scotet v. Pancreas. 2010 Apr;39(3):353-8. doi: 10.1097/MPA.0b013e3181bb9620. Pancreas. 2010. PMID: 20335779

5

Definition of a "functional R domain" of the cystic fibrosis transmembrane conductance regulator.

Chen JM, Scotet V, Ferec C. Chen JM, et al. Among authors: scotet v. Mol Genet Metab. 2000 Sep-Oct;71(1-2):245-9. doi: 10.1006/mgme.2000.3041. Mol Genet Metab. 2000. PMID: 11001817 Review.

6

Prevalence of CFTR mutations in hypertrypsinaemia detected through neonatal screening for cystic fibrosis.

Scotet V, De Braekeleer M, Audrézet MP, Lodé L, Verlingue C, Quéré I, Mercier B, Duguépéroux I, Codet JP, Moineau MP, Parent P, Férec C. Scotet V, et al. Clin Genet. 2001 Jan;59(1):42-7. doi: 10.1034/j.1399-0004.2001.590107.x. Clin Genet. 2001. PMID: 11168024

7

Variation of iron loading expression in C282Y homozygous haemochromatosis probands and sib pairs.

Mura C, Le Gac G, Scotet V, Raguenes O, Mercier AY, Férec C. Mura C, et al. Among authors: scotet v. J Med Genet. 2001 Sep;38(9):632-6. doi: 10.1136/jmg.38.9.632. J Med Genet. 2001. PMID: 11565552 Free PMC article. No abstract available.

8

Determination of the relative contribution of three genes-the cystic fibrosis transmembrane conductance regulator gene, the cationic trypsinogen gene, and the pancreatic secretory trypsin inhibitor gene-to the etiology of idiopathic chronic pancreatitis.

Audrézet MP, Chen JM, Le Maréchal C, Ruszniewski P, Robaszkiewicz M, Raguénès O, Quéré I, Scotet V, Férec C. Audrézet MP, et al. Among authors: scotet v. Eur J Hum Genet. 2002 Feb;10(2):100-6. doi: 10.1038/sj.ejhg.5200786. Eur J Hum Genet. 2002. PMID: 11938439

9

Relationship between genotype and phenotype for the CFTR gene W846X mutation.

Duguépéroux I, Bellis G, Férec C, Gillet D, Scotet V, De Braekeleer M; Participating centres of the French CF registry. Duguépéroux I, et al. Among authors: scotet v. J Med Genet. 2002 Jun;39(6):E32. doi: 10.1136/jmg.39.6.e32. J Med Genet. 2002. PMID: 12070264 Free PMC article. No abstract available.

10

Quantification of CFTR splice variants in adults with disseminated bronchiectasis, using the TaqMan fluorogenic detection system.

Andrieux J, Audrézet MP, Frachon I, Leroyer C, Roge C, Scotet V, Férec C. Andrieux J, et al. Among authors: scotet v. Clin Genet. 2002 Jul;62(1):60-7. doi: 10.1034/j.1399-0004.2002.620108.x. Clin Genet. 2002. PMID: 12123489

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