Génétique épidémiologique et moléculaire de l'obésité humaine : Corps gras, nutrition et santé questions d'actualité = Epidemiological and molecular genetics in humanIRON, A.OCL. Oléagineux, corps gras, lipides. 2000, Vol 7, Num 1, pp 86-90, issn 1258-8210Conference Paper

MORPHOLOGIC STRUCTURE OF BILE CANALICULI AFTER BILE DUCT LIGATION IN THE RAT: A TIME-COURSE STUDYVITAL A; BIOULAC SAGE P; IRON A et al.1982; ARCH. PATHOL. LAB. MED.; ISSN 0096-8528; USA; DA. 1982; VOL. 106; NO 9; PP. 464-467; BIBL. 17 REF.Article

FREQUENCE DES DIFFERENTES PAIRES D'ACIDES AMINES ADJACENTS DANS LES PROTEINESNEUZIL E; PAUPLIN Y; IRON A et al.1979; C. R. SOC. BIOL.; FRA; DA. 1979; VOL. 173; NO 1; PP. 68-74; ABS. ENG; BIBL. 11 REF.Article

Polymorphism of class I alcohol dehydrogenase in French, Vietnamese and Niger populations : genotyping by PCR amplification and RFLP analysis on dried blood sportsIRON, A; GROPPI, A; FLEURY, B et al.Annales de génétique (Paris). 1992, Vol 35, Num 3, pp 152-156, issn 0003-3995Article

Les isoenzymes de l'alcool déshydrogénase et de l'aldéhyde déshydrogénase: rôle dans le métabolisme et la toxicité hépatique de l'alcool = Alcohol dehydrogenase and aldehyde dehydrogenase isoenzymes: role in metabolism and hepatic toxicity of alcoholFLEURY, B; NALPAS, B; COUZIGOU, P et al.Gastroentérologie clinique et biologique. 1988, Vol 12, Num 12, pp 912-920, issn 0399-8320Article

Vision screening in children by Plusoptix Vision Screener compared with gold-standard orthoptic assessmentDAHLMANN-NOOR, A. H; VROTSOU, K; KOSTAKIS, V et al.British journal of ophthalmology. 2009, Vol 93, Num 3, pp 342-345, issn 0007-1161, 4 p.Article

Evaluation of plasma levels of tumour necrosis factor alpha and interleukin-6 as rejection markers in a cohort of 142 heart-grafted patients followed by endomyocardial biopsyABDALLAH, A. N; BILLES, M. A; ATTIA, Y et al.European heart journal. 1997, Vol 18, Num 6, pp 1024-1029, issn 0195-668XArticle

Lipid-carbohydrate interactions in post-absorptive non-insulin-dependent diabetic patientsRIGALLEAU, V; DE TINGUY, E; IRON, A et al.Annals of nutrition and metabolism. 1997, Vol 41, Num 2, pp 108-117, issn 0250-6807Article

Secretion of human apolipoprotein A-II by a mutant of Saccharomyces cerevisiæPASCUAL DE ZULUETA, M; RICHARD, P; HAMON, C et al.Biotechnology letters. 1996, Vol 18, Num 3, pp 355-360, issn 0141-5492Article

Genotyping of a patient homozygous for a rare apolipoprotein E1 [Gly₁₂₇→Asp; Arg₁₅₈→Cys] (Weisgraber allele)IRON, A; RICHARD, P; PASCUAL DE ZULUETA, M et al.Journal of inherited metabolic disease. 1995, Vol 18, Num 6, pp 723-726, issn 0141-8955Article

Mosaic maternal uniparental isodisomy for chromosome 7q21-qterREBOUL, M.-P; TANDONNET, O; TAINE, L et al.Clinical genetics. 2006, Vol 70, Num 3, pp 207-213, issn 0009-9163, 7 p.Article

Improvement in lipid profiles and triglyceride removal in patients on polyamide membrane hemodialysisDE PRECIGOUT, V; HIGUERET, D; LARROUMET, N et al.Blood purification. 1996, Vol 14, Num 2, pp 170-176, issn 0253-5068Article

Assessment of vitamin and trace element supplementation in severely burned patients undergoing long-term parenteral and enteral nutritionPERRO, G; BOURDARIAS, B; CUTILLAS, M et al.Clinical nutrition (Edinburgh). 1995, Vol 14, Num 5, pp 289-293, issn 0261-5614Article

Pathologie du gène de l'apolipoprotéine E humaine. Discussion = Pathology of the human apolipoprotein E geneIRON, A; RICHARD, P; BEUCLER, I et al.Bulletin de l'Académie nationale de médecine. 1994, Vol 178, Num 3, pp 415-426, issn 0001-4079Article

Genetic polymorphism of apoliprotein E in Caucasian alcoholic cirrhotics : Genetics and alcohol-related diseaseIRON, A; RICHARD, P; PASCUAL DE ZULUETA, M et al.Alcohol and alcoholism (Oxford). 1994, Vol 29, Num 6, pp 715-718, issn 0735-0414Conference Paper

PRIMARY SEQUENCE OF THE BETA -CHAIN OF BADGER HAEMOGLOBIN.HOMBRADOS I; DUCASTAING S; IRON A et al.1976; BIOCHIM. BIOPHYS. ACTA; PAYS-BAS; DA. 1976; VOL. 427; NO 1; PP. 107-118; BIBL. 30 REF.Article

Plusoptix Vision Screener : the accuracy and repeatability of refractive measurements using a new autorefractorDAHLMANN-NOOR, A. H; COMYN, O; VIVIAN, A. J et al.British journal of ophthalmology. 2009, Vol 93, Num 3, pp 346-349, issn 0007-1161, 4 p.Article

The very low penetrance of cystic fibrosis for the R117H mutation: a reappraisal for genetic counselling and newborn screeningTHAUVIN-ROBINET, C; MUNCK, A; CLAUSTRES, M et al.Journal of medical genetics. 2009, Vol 46, Num 11, pp 752-758, issn 0022-2593, 7 p.Article

Étude du gène CFTR chez 207 patients du Sud-Ouest de la France atteints de mucoviscidose : fréquence élevée des mutations N1303K et 1811+1,6kbA>G = CFTR gene analysis in 207 patients with cystic fibrosis in southwest France : high frequency of N1303K and 1811 + 1,6 kbA > G mutationsFEDERICI, S; IRON, A; REBOUL, M. P et al.Archives de pédiatrie (Paris). 2001, Vol 8, Num 2, pp 150-157, issn 0929-693XConference Paper

Laryngeal and oropharyngeal cancer, and alcohol dehydrogenase 3 and glutathione S-transferase M1 polymorphismsCOUTELLE, C; WARD, P. J; FLEURY, B et al.Human genetics. 1997, Vol 99, Num 3, pp 319-325, issn 0340-6717Article

Identification of a new apolipoprotein E variant (E₂Arg₁₄₂→Leu) in type III hyperlipidemiaRICHARD, P; DE ZULUETA, M. P; BEUCLER, I et al.Atherosclerosis. 1995, Vol 112, Num 1, pp 19-28, issn 0021-9150Article

Glutathione S-transferase class μ in French alcoholic cirrhotic patientsGROPPI, A; COUTELLE, C; FLEURY, B et al.Human genetics. 1991, Vol 87, Num 5, pp 628-630, issn 0340-6717Article

Identification par immunofixation électrophorétique d'un myélome à immunoglobulines D avec chaînes légères libres sériques et urinaires = Electrophoretic immunofixation identification of an IgD multiple myeloma with free light chains in serum and urineIRON, A; PEROUA, J. J; DELPECH, R et al.La Presse médicale (1983). 1989, Vol 18, Num 7, pp 358-359, issn 0755-4982Article