Ferec C - Search Results

1

Do pregnancies reduce iron overload in HFE hemochromatosis women? results from an observational prospective study.

Scotet V, Saliou P, Uguen M, L'Hostis C, Merour MC, Triponey C, Chanu B, Nousbaum JB, Le Gac G, Ferec C. Scotet V, et al. Among authors: ferec c. BMC Pregnancy Childbirth. 2018 Feb 17;18(1):53. doi: 10.1186/s12884-018-1684-6. BMC Pregnancy Childbirth. 2018. PMID: 29454332 Free PMC article.

2

p53 protein accumulation in oesophageal squamous cell carcinomas and precancerous lesions.

Volant A, Nousbaum JB, Giroux MA, Roué-Quintin I, Metges JP, Férec C, Gouérou H, Robaszkiewicz M. Volant A, et al. Among authors: ferec c. J Clin Pathol. 1995 Jun;48(6):531-4. doi: 10.1136/jcp.48.6.531. J Clin Pathol. 1995. PMID: 7665695 Free PMC article.

3

Molecular analysis of the TP53 gene in Barrett's adenocarcinoma.

Audrézet MP, Robaszkiewicz M, Mercier B, Nousbaum JB, Hardy E, Bail JP, Volant A, Lozac'h P, Gouérou H, Férec C. Audrézet MP, et al. Among authors: ferec c. Hum Mutat. 1996;7(2):109-13. doi: 10.1002/(SICI)1098-1004(1996)7:2<109::AID-HUMU4>3.0.CO;2-7. Hum Mutat. 1996. PMID: 8829627

4

Phenotype-genotype correlation in haemochromatosis subjects.

Mura C, Nousbaum JB, Verger P, Moalic MT, Raguenes O, Mercier AY, Ferec C. Mura C, et al. Among authors: ferec c. Hum Genet. 1997 Dec;101(3):271-6. doi: 10.1007/s004390050628. Hum Genet. 1997. PMID: 9439654

5

[The hemochromatosis gene (HFE). Molecular analysis--diagnostic applications].

Ferec C, Raguenes O, Mercier AY, Le Faou T, Chanu B, Le Poupon AM, Mercier B, Mura C. Ferec C, et al. Transfus Clin Biol. 1998 Aug;5(4):283-9. doi: 10.1016/s1246-7820(98)80407-2. Transfus Clin Biol. 1998. PMID: 9789968 French.

6

Clinical and molecular aspects of juvenile hemochromatosis in Saguenay-Lac-Saint-Jean (Quebec, canada).

Rivard SR, Mura C, Simard H, Simard R, Grimard D, Le Gac G, Raguenes O, Férec C, De Braekeleer M. Rivard SR, et al. Among authors: ferec c. Blood Cells Mol Dis. 2000 Feb;26(1):10-4. doi: 10.1006/bcmd.2000.0271. Blood Cells Mol Dis. 2000. PMID: 10772871

7

Mutation analysis in the HFE gene in patients with hereditary haemochromatosis in Saguenay-Lac-Saint-Jean (Quebec, Canada).

Rivard SR, Mura C, Simard H, Simard R, Grimard D, Le Gac G, Raguenes O, Férec C, De Braekeleer M. Rivard SR, et al. Among authors: ferec c. Br J Haematol. 2000 Mar;108(4):854-8. doi: 10.1046/j.1365-2141.2000.01954.x. Br J Haematol. 2000. PMID: 10792295 Free article.

8

Relation between HFE mutations and mild iron-overload expression.

Mura C, Le Gac G, Raguénes O, Mercier AY, Le Guen A, Férec C. Mura C, et al. Among authors: ferec c. Mol Genet Metab. 2000 Apr;69(4):295-301. doi: 10.1006/mgme.2000.2981. Mol Genet Metab. 2000. PMID: 10870847

9

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: ferec c. Mol Genet Metab. 2000 Sep-Oct;71(1-2):245-9. doi: 10.1006/mgme.2000.3041. Mol Genet Metab. 2000. PMID: 11001817 Review.

10

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: ferec c. Lancet. 2000 Sep 2;356(9232):789-94. doi: 10.1016/S0140-6736(00)02652-0. Lancet. 2000. PMID: 11022925

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