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Brain transcriptome perturbations in the Hfe―/― mouse model of genetic iron loadingJOHNSTONE, Daniel; GRAHAM, Ross M; TRINDER, Debbie et al.Brain research. 2012, Vol 1448, pp 144-152, issn 0006-8993, 9 p.Article

Du gène à la maladie : les anomalies des transporteurs du cuivre = From gene to disease : Copper-transporting P ATPases alterationGARCIA HEJL, C; VDGNAUD, C; GARCIA, C et al.Pathologie et biologie. 2009, Vol 57, Num 3, pp 272-279, issn 0369-8114, 8 p.Article

Hemochromatosis Gene Polymorphisms, Mitochondrial Haplogroups, and Peripheral Lipoatrophy during Antiretroviral Therapy. CommentaryLICHTENSTEIN, Kenneth A; HULGAN, Todd; KALLIANPUR, Asha R et al.The Journal of infectious diseases. 2008, Vol 197, Num 6, issn 0022-1899, 784-786, 858-866 [12 p.]Article

Transferrin receptor 2 mediates uptake of transferrin-bound and non-transferrin-bound ironGRAHAM, Ross M; REUTENS, Gail M; HERBISON, Carly E et al.Journal of hepatology. 2008, Vol 48, Num 2, pp 327-334, issn 0168-8278, 8 p.Article

Analysis of the T1288R mutation of the wilson disease ATP7B gene in four generations of a family : Possible genotype-phenotype correlation with hepatic onsetLEGGIO, Lorenzo; MALANDRINO, Noemi; LOUDIANOS, Georgios et al.Digestive diseases and sciences. 2007, Vol 52, Num 10, pp 2570-2575, issn 0163-2116, 6 p.Article

Flatiron mice and ferroportin diseaseJOHNSON, Erin E; WESSLING-RESNICK, Marianne.Nutrition reviews. 2007, Vol 65, Num 7, pp 341-345, issn 0029-6643, 5 p.Article

Novel mutations of the ATP7B gene among 109 Hungarian patients with Wilson's diseaseFOLHOFFER, Aniko; FERENCI, Peter; ABONYI, Margit et al.European journal of gastroenterology & hepatology. 2007, Vol 19, Num 2, pp 105-111, issn 0954-691X, 7 p.Article

Optimal management strategies for chronic iron overloadBARTON, James C.Drugs (Basel). 2007, Vol 67, Num 5, pp 685-700, issn 0012-6667, 16 p.Article

Manifestations rhumatologiques de l'hémochromatose génétique : Hémochromatose = Rheumatic manifestations of genetic hemochromatosisGUGGENBUHL, Pascal; ALBERT, Jean-David; CHALES, Gérard et al.La Presse médicale (1983). 2007, Vol 36, Num 9, pp 1313-1318, issn 0755-4982, 6 p., CAH2Article

Iron-Mediated Regulation of Liver Hepcidin Expression in Rats and Mice Is Abolished by AlcoholDEE HARRISON-FINDIK, Duygu; KLEIN, Elizabeth; CRIST, Callie et al.Hepatology (Baltimore, Md.). 2007, Vol 46, Num 6, pp 1979-1985, issn 0270-9139, 7 p.Article

A new strain of rat for functional analysis of PINAAHMED, Samreen; JIE DENG; BORJIGIN, Jimo et al.Molecular brain research. 2005, Vol 137, Num 1-2, pp 63-69, issn 0169-328X, 7 p.Article

Hereditary hemochromatosis is reflected in the iron isotope composition of bloodKRAYENBUEHL, Pierre-Alexandre; WALCZYK, Thomas; SCHOENBERG, Ronny et al.Blood. 2005, Vol 105, Num 10, pp 3812-3816, issn 0006-4971, 5 p.Article

Effects of betaine in a murine model of mild cystathionine-β-synthase deficiencySCHWAHN, Bernd C; WENDEL, Udo; LUSSIER-CACAN, Suzanne et al.Metabolism, clinical and experimental. 2004, Vol 53, Num 5, pp 594-599, issn 0026-0495, 6 p.Article

Faut-il promouvoir le dépistage systématique de l'hémochromatose génétique en France ? Discussion = Should we support large-scale screening for genetic haemochromatosis in France ? DiscussionDEUGNIER, Yves; LE GALL, Jean-Yves; BOUREL, Michel et al.Bulletin de l'Académie nationale de médecine. 2004, Vol 188, Num 2, pp 265-273, issn 0001-4079, 9 p.Article

Maladie de Wilson : Etude de 6 formes neurologiques observées au CHU de Conakry = Wilson's disease: Study of 6 neurological forms observed at the University Hospital in Conakry, GuineaCISSE, A; MOREL, Y; SYLLA, A et al.Médecine tropicale. 2004, Vol 64, Num 1, pp 53-57, issn 0025-682X, 5 p.Article

About the cover illustrationHAMMERSCHMIDT, Dale E.The Journal of laboratory and clinical medicine. 2003, Vol 141, Num 6, issn 0022-2143, p. 423Article

Longevity and carrying the C282Y mutation for haemochromatosis on the HFE gene: case control study of 492 French centenariansCOPPIN, Hélène; BENSAID, M; FRUCHON, S et al.BMJ. British medical journal (International ed.). 2003, Vol 327, Num 7407, pp 132-133, issn 0959-8146, 2 p.Article

A novel mutation in ferroportin 1 is associated with haemochromatosis in a Solomon Islands patientARDEN, K. E; WALLACE, D. F; DIXON, J. L et al.Gut. 2003, Vol 52, Num 8, pp 1215-1217, issn 0017-5749, 3 p.Article

Ankle and hindfoot arthropathy in hereditary hemochromatosisSCHMID, Holger; STRUPPLER, Christiane; BRAUN, Gerald S et al.Journal of rheumatology. 2003, Vol 30, Num 1, pp 196-199, issn 0315-162X, 4 p.Article

Duodenal mucosal reductase in wild-type and HFE knockout mice on iron adequate, iron deficient, and iron rich feedingSIMPSON, R. J; DEBNAM, E; BEAUMONT, N et al.Gut. 2003, Vol 52, Num 4, pp 510-513, issn 0017-5749, 4 p.Article

Duodenal nonheme iron content correlates with iron stores in mice, but the relationship is altered by Hfe gene knock-outSIMPSON, Robert J; DEBNAM, Edward S; LAFTAH, Abas H et al.Blood. 2003, Vol 101, Num 8, pp 3316-3318, issn 0006-4971, 3 p.Article

Evidence that the Cys282Tyr mutation of the HFE gene originated from a population in Southern Scandinavia and spread with the VikingsMILMAN, N; PEDERSEN, P.Clinical genetics. 2003, Vol 64, Num 1, pp 36-47, issn 0009-9163, 12 p.Article

Expression of hepcidin in hereditary hemochromatosis: evidence for a regulation in response to the serum transferrin saturation and to non-transferrin-bound ironGEHRKE, Sven G; KULAKSIZ, Hasan; HERRMANN, Thomas et al.Blood. 2003, Vol 102, Num 1, pp 371-376, issn 0006-4971, 6 p.Article

Use of denaturing HPLC and a heteroduplex generator to detect the HFE C282Y mutation associated with genetic hemochromatosisFRUCHON, Séverine; BENSAID, Mounia; BOROT, Nicolas et al.Clinical chemistry (Baltimore, Md.). 2003, Vol 49, Num 5, pp 822-824, issn 0009-9147, 3 p.Article

Where are all the iron men and women?LUFT, C.Journal of molecular medicine (Berlin. Print). 2003, Vol 81, Num 12, pp 747-749, issn 0946-2716, 3 p.Article

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