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209 related items for PubMed ID: 16055358
1. Unique genetic profile of hereditary hemochromatosis in Russians: high frequency of C282Y mutation in population, but not in patients. Potekhina ES, Lavrov AV, Samokhodskaya LM, Efimenko AY, Balatskiy AV, Baev AA, Litvinova MM, Nikitina LA, Shipulin GA, Bochkov NP, Tkachuk VA, Bochkov VN. Blood Cells Mol Dis; 2005; 35(2):182-8. PubMed ID: 16055358 [Abstract] [Full Text] [Related]
3. Distribution of the C282Y and H63D polymorphisms in hereditary hemochromatosis patients from the French Basque Country. Bauduer F, Scribans C, Degioanni A, Renoux M, Dutour O. Ann Hematol; 2005 Feb; 84(2):99-102. PubMed ID: 15503019 [Abstract] [Full Text] [Related]
4. [Significance and prevalence of the C282Y gene mutation of primary hemochromatosis in the pathogenesis of pophyria cutanea tarda]. Malina L, Zd'árský E, Dandová S, Michalíková H, Cerná M, Cimburová M. Cas Lek Cesk; 2000 Nov 22; 139(23):728-30. PubMed ID: 11191743 [Abstract] [Full Text] [Related]
5. Survival after liver transplantation in patients with hepatic iron overload: the national hemochromatosis transplant registry. Kowdley KV, Brandhagen DJ, Gish RG, Bass NM, Weinstein J, Schilsky ML, Fontana RJ, McCashland T, Cotler SJ, Bacon BR, Keeffe EB, Gordon F, Polissar N, National Hemochromatosis Transplant Registry. Gastroenterology; 2005 Aug 22; 129(2):494-503. PubMed ID: 16083706 [Abstract] [Full Text] [Related]
6. Genetic screening for HFE hemochromatosis in 6,020 Danish men: penetrance of C282Y, H63D, and S65C variants. Pedersen P, Milman N. Ann Hematol; 2009 Aug 22; 88(8):775-84. PubMed ID: 19159930 [Abstract] [Full Text] [Related]
7. DMT1 genetic variability is not responsible for phenotype variability in hereditary hemochromatosis. Kelleher T, Ryan E, Barrett S, O'Keane C, Crowe J. Blood Cells Mol Dis; 2004 Aug 22; 33(1):35-9. PubMed ID: 15223008 [Abstract] [Full Text] [Related]
8. [A new method of molecular testing in the differential diagnosis of hereditary hemochromatosis]. Andrikovics H, Klein I, Kalmár L, Bors A, Jermendy G, Petri I, Kalász L, Váradi A, Tordai A. Orv Hetil; 1999 Nov 07; 140(45):2517-22. PubMed ID: 10586619 [Abstract] [Full Text] [Related]
9. High prevalence of a screening-detected, HFE-unrelated, mild idiopathic iron overload in Northern Italy. Barosi G, Salvaneschi L, Grasso M, Martinetti M, Marchetti M, Bodini U, Reggiani A, D'Agostino F, Nalli G, Degiuli A, De Silvestri A, Arbustini E. Haematologica; 2002 May 07; 87(5):472-8. PubMed ID: 12010659 [Abstract] [Full Text] [Related]
10. [Hemochromatosis. Determination of the C282Y mutation frequency in the population of the Czech Republic and sensitivity of hemochromatosis detection using Guthrie cards]. Zdárský E, Horák J, Stríteský J, Heirler F. Cas Lek Cesk; 1999 Aug 23; 138(16):497-9. PubMed ID: 10566227 [Abstract] [Full Text] [Related]
11. Clinical characteristics of hereditary hemochromatosis patients who lack the C282Y mutation. Shaheen NJ, Bacon BR, Grimm IS. Hepatology; 1998 Aug 23; 28(2):526-9. PubMed ID: 9696020 [Abstract] [Full Text] [Related]
12. Unique genetic profile of hereditary haemochromatosis in Russians: High frequency of C282Y mutation in population, but not in patients. McCune CA, Worwood M. Blood Cells Mol Dis; 2006 Aug 23; 36(2):329; author reply 330. PubMed ID: 16466945 [No Abstract] [Full Text] [Related]
13. Low frequency of HFE gene mutations in Croatian patients suspected of having hereditary hemochromatosis. Milić S, Ristić S, Starčević-Čizmarević N, Brajenović-Milić B, Crnić-Martinović M, Kapović M, Peterlin B, Štimac D. Med Sci Monit; 2011 Oct 23; 17(10):CR552-6. PubMed ID: 21959608 [Abstract] [Full Text] [Related]
14. H63D homozygotes with hyperferritinaemia: Is this genotype, the primary cause of iron overload? de Diego C, Opazo S, Murga MJ, Martínez-Castro P. Eur J Haematol; 2007 Jan 23; 78(1):66-71. PubMed ID: 17042772 [Abstract] [Full Text] [Related]
15. Hemochromatosis gene mutations, liver function tests and iron status in alcohol-dependent patients admitted for detoxification. Robinson G, Narasimhan S, Weatherall M, Beasley R. J Gastroenterol Hepatol; 2007 Jun 23; 22(6):852-4. PubMed ID: 17565641 [Abstract] [Full Text] [Related]
16. Population-based study of the relationship between mutations in the hemochromatosis (HFE) gene and arthritis. Sherrington CA, Knuiman MW, Divitini ML, Bartholomew HC, Cullen DJ, Olynyk JK. J Gastroenterol Hepatol; 2006 Mar 23; 21(3):595-8. PubMed ID: 16638105 [Abstract] [Full Text] [Related]
17. High prevalence of the Cys282Tyr HFE mutation facilitates an improved diagnostic service for hereditary haemochromatosis in South Africa. de Villiers JN, Hillerman R, de Jong G, Langenhoven E, Rossouw H, Marx MP, Kotze MJ. S Afr Med J; 1999 Mar 23; 89(3):279-82. PubMed ID: 10226674 [Abstract] [Full Text] [Related]
18. Presence of hemochromatosis-associated mutations in Hispanic patients with iron overload. Nieves-Santiago P, Cancel D, Canales D, Toro DH. P R Health Sci J; 2011 Sep 23; 30(3):135-8. PubMed ID: 21932715 [Abstract] [Full Text] [Related]
19. The CD8+ T-lymphocyte profile as a modifier of iron overload in HFE hemochromatosis: an update of clinical and immunological data from 70 C282Y homozygous subjects. Cruz E, Melo G, Lacerda R, Almeida S, Porto G. Blood Cells Mol Dis; 2006 Sep 23; 37(1):33-9. PubMed ID: 16762569 [Abstract] [Full Text] [Related]
20. HFE genotypes and dietary heme iron: no evidence of strong gene-nutrient interaction on serum ferritin concentrations in middle-aged women. van der A DL, Peeters PH, Grobbee DE, Roest M, Voorbij HA, van der Schouw YT. Nutr Metab Cardiovasc Dis; 2006 Jan 23; 16(1):60-8. PubMed ID: 16399493 [Abstract] [Full Text] [Related] Page: [Next] [New Search]