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Albert Iron

Research Profile

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France

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Isabelle Sermet-Gaudelus; Emmanuelle Girodon; Dorota Sands; Nathalie Stremmler; Vera Vavrova; Eric Deneuville; Philippe Reix; Stéphanie Bui; Frédéric Huet; Muriel Lebourgeois; Anne Munck; Albert Iron; Veronika Skalicka; Thierry Bienvenu; Delphine Roussel; Gérard Lenoir; Gabriel Bellon; Jacques Sarles; Milan Macek Jr.; Michel Roussey; Isabelle Fajac; Aleksander Edelman
Clinical phenotype and genotype of children with borderline sweat test and abnormal nasal epithelial chloride transport.
Annick Andrieux; Jérôme Harambat; Stéphanie Bui; Fabienne Nacka; Albert Iron; Brigitte Llanas; Michael Fayon
Renal impairment in children with cystic fibrosis.
Ayman El-Seedy; Tony Dudognon; Frédéric Bilan; Marie-Claude Pasquet; Marie-Pierre Reboul; Albert Iron; Alain Kitzis; Véronique Ladeveze
Influence of the duplication of CFTR exon 9 and its flanking sequences on diagnosis of cystic fibrosis mutations.

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All Publications

2010: Isabelle Sermet-Gaudelus; Emmanuelle Girodon; Dorota Sands; Nathalie Stremmler; Vera Vavrova; Eric Deneuville; Philippe Reix; Stéphanie Bui; Frédéric Huet; Muriel Lebourgeois; Anne Munck; Albert Iron; Veronika Skalicka; Thierry Bienvenu; Delphine Roussel; Gérard Lenoir; Gabriel Bellon; Jacques Sarles; Milan Macek Jr.; Michel Roussey; Isabelle Fajac; Aleksander Edelman
Clinical phenotype and genotype of children with borderline sweat test and abnormal nasal epithelial chloride transport.
American journal of respiratory and critical care medicine 2010;182(7):929-36.
2010: Annick Andrieux; Jérôme Harambat; Stéphanie Bui; Fabienne Nacka; Albert Iron; Brigitte Llanas; Michael Fayon
Renal impairment in children with cystic fibrosis.
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society 2010;9(4):263-8.
2009: Ayman El-Seedy; Tony Dudognon; Frédéric Bilan; Marie-Claude Pasquet; Marie-Pierre Reboul; Albert Iron; Alain Kitzis; Véronique Ladeveze
Influence of the duplication of CFTR exon 9 and its flanking sequences on diagnosis of cystic fibrosis mutations.
The Journal of molecular diagnostics : JMD 2009;11(5):488-93.
2008: Phillis Lakeman; Johan J P Gille; Jeannette E Dankert-Roelse; Harry G M Heijerman; Anne Munck; Albert Iron; Hartmut Grasemann; Antje Schuster; Martina C Cornel; Leo P ten Kate
CFTR mutations in Turkish and North African cystic fibrosis patients in Europe: implications for screening.
Genetic testing 2008;12(1):25-35.
2006: Virginie Rondeau; Albert Iron; Luc Letenneur; Daniel Commenges; F Duchêne; Benoît Arveiler; Jean-François Dartigues
Analysis of the effect of aluminum in drinking water and transferrin C2 allele on Alzheimer's disease.
European journal of neurology : the official journal of the European Federation of Neurological Societies 2006;13(9):1022-5.
2006: Marie-Pierre Reboul; O Tandonnet; Nicolas Biteau; C Belet-de Putter; Laurent Rebouissoux; Kamran Moradkhani; P Y Vu; Robert Saura; Benoît Arveiler; Didier Lacombe; Laurence Taine; Albert Iron
Mosaic maternal uniparental isodisomy for chromosome 7q21-qter.
Clinical genetics 2006;70(3):207-13.
2005: Marie-Pierre Reboul; Laurent Higueret; Nicolas Biteau; Albert Iron
Rapid and accurate detection of the CFTR gene mutation 1811+1.6 kbA>G by real-time fluorescence resonance energy transfer PCR.
Molecular and cellular probes 2005;19(5):358-62.
2003: Delphine Feldmann; Rémy Couderc; Marie-Pierre Audrezet; Claude Ferec; Thierry Bienvenu; Marie Desgeorges; Mireille Claustres; herve mittre; Martine Blayau; Dominique Bozon; Marie-Claire Malinge; Nicole Monnier; Jean-Paul Bonnefont; Albert Iron; Eric Bieth; Viviane Dumur; Christine Clavel; Cécile Cazeneuve; Emmanuelle Girodon
CFTR genotypes in patients with normal or borderline sweat chloride levels.
Human mutation 2003;22(4):340.
2003: Marie-Pierre Reboul; David Laharie; Michel Amouretti; Didier Lacombe; Albert Iron
Isolated idiopathic chronic pancreatitis associated with a compound heterozygosity for two mutations of the CFTR gene.
Gastroentérologie clinique et biologique 2003;27(8-9):821-4.
2002: Marie-Pierre Reboul; Eric Bieth; M Fayon; Nicolas Biteau; R Barbier; C Dromer; Marie Desgeorges; Mireille Claustres; F Bremont; Didier Lacombe; Albert Iron
Splice mutation 1811+1.6kbA>G causes severe cystic fibrosis with pancreatic insufficiency: report of 11 compound heterozygous and two homozygous patients.
Journal of medical genetics 2002;39(11):e73.
2001: S Federici; Albert Iron; Marie-Pierre Reboul; Marie Desgeorges; Mireille Claustres; F Bremont; Eric Bieth
[CFTR gene analyis in 207 patients with cystic fibrosis in southwest France: high frequency of N1303K and 1811+1.6bA>G mutations].
Archives de pédiatrie : organe officiel de la Sociéte française de pédiatrie 2001;8(2):150-7.
2000: M Bonarek; Pascale Barberger-Gateau; Luc Letenneur; Valérie Deschamps; Albert Iron; Bénédicte Dubroca; Jean-François Dartigues
Relationships between cholesterol, apolipoprotein E polymorphism and dementia: a cross-sectional analysis from the PAQUID study.
Neuroepidemiology 2000;19(3):141-8.
2000: Mireille Claustres; Caroline Guittard; Dominique Bozon; F Chevalier; C Verlingue; Claude Ferec; Emmanuelle Girodon; Cécile Cazeneuve; Thierry Bienvenu; Guy Lalau; Viviane Dumur; Delphine Feldmann; Eric Bieth; Martine Blayau; Christine Clavel; I Creveaux; Marie-Claire Malinge; Nicole Monnier; P Malzac; herve mittre; J C Chomel; Jean-Paul Bonnefont; Albert Iron; M Chery; M D Georges
Spectrum of CFTR mutations in cystic fibrosis and in congenital absence of the vas deferens in France.
Human mutation 2000;16(2):143-56.
1999: AN Abdallah; P Cucchi-Mouillot; Nicolas Biteau; André Cassaigne; D Haras; Albert Iron
Analysis of the polymorphism of the tumour necrosis factor (TNF) gene and promoter and of circulating TNF-alpha levels in heart-transplant patients suffering or not suffering from severe rejection.
European journal of immunogenetics : official journal of the British Society for Histocompatibility and Immunogenetics 1999;26(4):249-55.
1997: P Richard; I Beucler; M Pascual De Zulueta; Nicolas Biteau; J L De Gennes; Albert Iron
Compound heterozygote for both rare apolipoprotein E1 (Gly127-->Asp, Arg158-->Cys) and E3(Cys112-->Arg, Arg251-->Gly) alleles in a multigeneration pedigree with hyperlipoproteinaemia.
Clinical science (London, England : 1979) 1997;93(1):89-95.
1997: AN Abdallah; M A Billes; Y Attia; C Doutremepuich; André Cassaigne; Albert Iron
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 biopsy.
European heart journal 1997;18(6):1024-9.
1997: C Coutelle; PJ Ward; B Fleury; P Quattrocchi; H Chambrin; Albert Iron; P Couzigou; André Cassaigne
Laryngeal and oropharyngeal cancer, and alcohol dehydrogenase 3 and glutathione S-transferase M1 polymorphisms.
Human genetics 1997;99(3):319-25.
1997: AN Abdallah; Jean-Michel Boiron; Y Attia; André Cassaigne; J Reiffers; Albert Iron
Plasma cytokines in graft vs host disease and complications following bone marrow transplantation.
Hematology and cell therapy 1997;39(1):27-32.
1996: Valérie de Précigout; D Higueret; N Larroumet; Christian Combe; Albert Iron; V Blanchetier; Luc Potaux; Michel Aparicio
Improvement in lipid profiles and triglyceride removal in patients on polyamide membrane hemodialysis.
Blood purification 1996;14(2):170-6.
1995: G Perro; B Bourdarias; M Cutillas; D Higueret; R Sanchez; Albert Iron
Assessment of vitamin and trace element supplementation in severely burned patients undergoing long-term parenteral and enteral nutrition.
Clinical nutrition (Edinburgh, Scotland) 1995;14(5):289-93.
1995: F Dandré; André Cassaigne; Albert Iron
The frequency of the mitochondrial aldehyde dehydrogenase I2 (atypical) allele in Caucasian, Oriental and African black populations determined by the restriction profile of PCR-amplified DNA.
Molecular and cellular probes 1995;9(3):189-93.
1995: P Richard; M P de Zulueta; I Beucler; J L De Gennes; André Cassaigne; Albert Iron
Identification of a new apolipoprotein E variant (E2 Arg142-->Leu) in type III hyperlipidemia.
Atherosclerosis 1995;112(1):19-28.
1995: Albert Iron; P Richard; M P de Zulueta; G Thomas; M Thomas
Genotyping of a patient homozygous for a rare apolipoprotein E1 [Gly127-->Asp; Arg158-->Cys] (Weisgraber allele).
Journal of inherited metabolic disease 1995;18(6):723-6.
1994: Albert Iron; P Richard; M Pascual De Zulueta; F Dumas; André Cassaigne; Patrice Couzigou
Genetic polymorphism of apolipoprotein E in Caucasian alcoholic cirrhotics.
Alcohol and alcoholism (Oxford, Oxfordshire) 1994;29(6):715-8.
1994: P Richard; M P de Zulueta; F Weill; André Cassaigne; Albert Iron
Application of PCR site-directed mutagenesis for a rapid and accurate detection of mutation 3500 (Arg-->Gln) of human apolipoprotein B-100.
Molecular and cellular probes 1994;8(3):257-60.
1994: Albert Iron; P Richard; I Beucler; G Thomas; M Pascual de Zulueta; G Bereziat; André Cassaigne; J L de Gennes
[Pathology of the human apolipoprotein E gene].
Bulletin de l'Académie nationale de médecine 1994;178(3):415-26.
1994: Patrice Couzigou; C Coutelle; B Fleury; Albert Iron
Alcohol and aldehyde dehydrogenase genotypes, alcoholism and alcohol related disease.
Alcohol and alcoholism (Oxford, Oxfordshire). Supplement 1994;2():21-7.
1994: P Richard; G Thomas; M P de Zulueta; J L De Gennes; M Thomas; André Cassaigne; G Béréziat; Albert Iron
Common and rare genotypes of human apolipoprotein E determined by specific restriction profiles of polymerase chain reaction-amplified DNA.
Clinical chemistry 1994;40(1):24-9.
1992: C Coutelle; Albert Iron; D Higueret; André Cassaigne
[Optimization of a spectrophotometry assay of total and oxidized blood glutathione: comparison with a fluorimetric method].
Annales de biologie clinique 1992;50(2):71-6.
1992: Albert Iron; A Groppi; B Fleury; J Begueret; André Cassaigne; Patrice Couzigou
Polymorphism of class I alcohol dehydrogenase in French, Vietnamese and Niger populations: genotyping by PCR amplification and RFLP analysis on dried blood spots.
Annales de génétique 1992;35(3):152-6.
1991: A Groppi; C Coutelle; B Fleury; Albert Iron; J Begueret; Patrice Couzigou
Glutathione S-transferase class mu in French alcoholic cirrhotic patients.
Human genetics 1991;87(5):628-30.
1991: Patrice Couzigou; B Fleury; A Groppi; Albert Iron; C Coutelle; André Cassaigne; Joël Bégueret
Role of alcohol dehydrogenase polymorphism in ethanol metabolism and alcohol-related diseases.
Advances in experimental medicine and biology 1991;284():263-70.
1990: A Groppi; J Begueret; Albert Iron
Improved methods for genotype determination of human alcohol dehydrogenase (ADH) at ADH 2 and ADH 3 loci by using polymerase chain reaction-directed mutagenesis.
Clinical chemistry 1990;36(10):1765-8.
1990: Patrice Couzigou; B Fleury; A Groppi; André Cassaigne; J Begueret; Albert Iron
Genotyping study of alcohol dehydrogenase class I polymorphism in French patients with alcoholic cirrhosis. The French Group for Research on Alcohol and Liver.
Alcohol and alcoholism (Oxford, Oxfordshire) 1990;25(6):623-6.
1989: Albert Iron; J J Peroua; R Delpech; André Cassaigne
[Identification by electrophoretic immunofixation of an immunoglobulin D myeloma with serum and urine free light chains].
Presse médicale (Paris, France : 1983) 1989;18(7):358-9.
1988: B Fleury; Bertrand Nalpas; Patrice Couzigou; Albert Iron; Raoul Poupon
[Alcohol dehydrogenase and aldehyde dehydrogenase isoenzymes: role in metabolism and hepatic toxicity of alcohol].
Gastroentérologie clinique et biologique 1988;12(12):912-20.