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Results 1 to 25 of 497

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Hémochromatoses héréditaires : les molécules en jeu et leur implication dans la régulation de l'homéostasie du ferCOPPIN, Hélène; ROTH, Marie-Paule.Hépato-gastro (Montrouge). 2005, Vol 12, Num 4, pp 281-288, issn 1253-7020, 8 p.Conference Paper

Relative permittivity measurements of trifluoromethyl methyl ether and pentafluoroethyl methyl etherELTRINGHAM, Wayne; CATCHPOLE, Owen J.Journal of chemical and engineering data (Print). 2007, Vol 52, Num 3, pp 1095-1099, issn 0021-9568, 5 p.Article

Critical properties of 1,2,2,2-tetrafluoroethyl trifluoromethyl ether (HFE-227me) + trifluoromethoxymethane (HFE-143m) and + methyl pentafluoroethyl ether (HFE-245mc)YASUMOTO, Masahiko; UCHIDA, Yuko; OCHI, Kenji et al.Journal of chemical and engineering data (Print). 2007, Vol 52, Num 5, pp 1726-1728, issn 0021-9568, 3 p.Article

Les hémochromatoses héréditaires = Hereditary hemochromatosisBOUIZEGARENE, P; COULHON, M.-P; DEYBACH, J.-C et al.Immuno analyse & biologie spécialisée. 2006, Vol 21, Num 2, pp 65-78, issn 0923-2532, 14 p.Article

Hemojuvelin : a supposed role in iron metabolism one year after its discoveryCELEC, Peter.Journal of molecular medicine (Berlin. Print). 2005, Vol 83, Num 7, pp 521-525, issn 0946-2716, 5 p.Article

Hemojuvelin (HJV)-associated hemochromatosis: analysis of HJV and HFE mutations and iron overload in three familiesWALLACE, Daniel F; DIXON, Jeannette L; RAMM, Grant A et al.Haematologica (Roma). 2005, Vol 90, Num 2, pp 254-255, issn 0390-6078, 2 p.Article

Increased hepcidin expression and hypoferraemia associated with an acute phase response are not affected by inactivation of HFEFRAZER, David M; WILKINS, Sarah J; MILLARD, Kirstin N et al.British journal of haematology. 2004, Vol 126, Num 3, pp 434-436, issn 0007-1048, 3 p.Article

Maniement des marqueurs génétiques autres que C282Y au cours des surcharges en fer = Practical use of genetic markers other than C282Y in iron overload disordersBRISSOT, Pierre.Gastroentérologie clinique et biologique. 2002, Vol 26, Num 11, pp 991-993, issn 0399-8320, 3 p.Article

Le dépistage de l'hémochromatose génétique = Genetic hemochromatosis screeningMOIRAND, R; JOUANOLLE, A.-M; BRISSOT, P et al.Hépato-gastro (Montrouge). 1999, Vol 6, Num 5, pp 351-356, issn 1253-7020Article

Fetal iron levels are regulated by maternal and fetal Hfe genotype and dietary ironBALESARIA, Sara; HANIF, Rumeza; SALAMA, Mohamed F et al.Haematologica (Roma). 2012, Vol 97, Num 5, pp 661-669, issn 0390-6078, 9 p.Article

Significance of H63D homozygosity in a Basque population with hemochroniatosisCASTIELLA, Agustin; ZAPTA, Eva; DE JUAN, Maria Dolores et al.Journal of gastroenterology and hepatology. 2010, Vol 25, Num 7, pp 1295-1298, issn 0815-9319, 4 p.Article

Les hémochromatoses héréditaires : partie II. L'hémochromatose héréditaire liée au HFE (HFE1) = Hereditary hemochromatosis: part II - HFE hemochromatosisBOUIZEGARENE, P; COULHON, M.-P; DEYBACH, J.-C et al.Immuno analyse & biologie spécialisée. 2006, Vol 21, Num 3, pp 128-137, issn 0923-2532, 10 p.Article

Atmospheric chemistry of HFE-7300 and HFE-7500: Temperature dependent kinetics, atmospheric lifetimes, infrared spectra and global warming potentialsRODRIGUEZ, Ana; RODRIGUEZ, Diana; MORALEDA, Araceli et al.Atmospheric environment (1994). 2014, Vol 96, pp 145-153, issn 1352-2310, 9 p.Article

Blunted hepcidin response to inflammation in the absence of Hfe and transferrin receptor 2WALLACE, Daniel F; MCDONALD, Cameron J; OSTINI, Lesa et al.Blood. 2011, Vol 117, Num 10, pp 2960-2966, issn 0006-4971, 7 p.Article

RADIO AND INFRARED STUDIES OF THE 100 MICROMETER SOURCES HFE2 AND FJM3.SIMON M; JOYCE RR; RIGHINI COHEN G et al.1977; ASTROPHYS. J.; U.S.A.; DA. 1977; VOL. 212; NO 1 PART. 1; PP. 84-93; BIBL. 17 REF.Article

Homozygous deletion of HFE produces a phenotype similar to the HFE p.C282Y/p.C282Y genotypeLE GAC, Gérald; GOURLAOUEN, Isabelle; RONSIN, Christophe et al.Blood. 2008, Vol 112, Num 13, pp 5238-5240, issn 0006-4971, 3 p.Article

New aspects of copper and iron metabolism in the myelodysplastic syndromesVARKONYI, Judit; SZABO, Terézia; SEBESTYEN, Piroska et al.Chemotherapy (Basel). 2006, Vol 52, Num 2, pp 66-68, issn 0009-3157, 3 p.Article

A previously undescribed frameshift deletion mutation of HFE (c.de1277; G93fs) associated with hemochromatosis and iron overload in a C282Y heterozygoteBARTON, J. C; WEST, C; LEE, P. L et al.Clinical genetics. 2004, Vol 66, Num 3, pp 214-216, issn 0009-9163, 3 p.Article

Screening selected blood donors with biochemical iron overload for hemochromatosis: a regional experienceDE GOBBI, Marco; D'ANTICO, Sergio; CASTAGNO, Franco et al.Haematologica (Roma). 2004, Vol 89, Num 10, pp 1161-1167, issn 0390-6078, 7 p.Article

Analysis of HFE and TFR2 mutations in selected blood donors with biochemical parameters of iron overloadDE GOBBI, Marco; DARAIO, Filomena; OBERKANINS, Christian et al.Haematologica (Roma). 2003, Vol 88, Num 4, pp 396-401, issn 0390-6078, 6 p.Article

Genetic testing for HFE hemochromatosis in Australia: The value of testing relatives of simple heterozygotesCAVANAUGH, Juleen A; WILSON, Susan R; BASSETT, Mark L et al.Journal of gastroenterology and hepatology. 2002, Vol 17, Num 7, pp 800-803, issn 0815-9319Article

Persons with screening-detected haemochromatosis: as healthy as the general population?ASBERG, A; HVEEM, K; KRÜGER, O et al.Scandinavian journal of gastroenterology. 2002, Vol 37, Num 6, pp 719-724, issn 0036-5521Article

Hereditary haemochromatosis : diagnosis and management in the gene eraOLYNYK, J. K.Liver (Copenhagen). 1999, Vol 19, Num 2, pp 73-80, issn 0106-9543Article

The haemochromatosis gene : A global perspective and implications for the Asia-Pacific regionMORTIMORE, M; MERRYWEATHER-CLARKE, A. T; ROBSON, K. J et al.Journal of gastroenterology and hepatology. 1999, Vol 14, Num 9, pp 838-843, issn 0815-9319Article

Genotyping of the hemochromatosis HFE p.H63D and p.C282Y mutations by high-resolution melting with the Rotor-Gene 6000® instrumentJUNIOR LIMA SANTOS, Paulo Caleb; GADI SOARES, Renata Alonso; EDUARDO KRIEGER, Jose et al.Clinical chemistry and laboratory medicine. 2011, Vol 49, Num 10, pp 1633-1636, issn 1434-6621, 4 p.Article

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