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421 related items for PubMed ID: 26799139
21. TFR2-related hereditary hemochromatosis as a frequent cause of primary iron overload in patients from Central-Southern Italy. Radio FC, Majore S, Binni F, Valiante M, Ricerca BM, De Bernardo C, Morrone A, Grammatico P. Blood Cells Mol Dis; 2014; 52(2-3):83-7. PubMed ID: 24055163 [Abstract] [Full Text] [Related]
22. HFE, SLC40A1, HAMP, HJV, TFR2, and FTL mutations detected by denaturing high-performance liquid chromatography after iron phenotyping and HFE C282Y and H63D genotyping in 785 HEIRS Study participants. Barton JC, Lafreniere SA, Leiendecker-Foster C, Li H, Acton RT, Press RD, Eckfeldt JH. Am J Hematol; 2009 Nov; 84(11):710-4. PubMed ID: 19787796 [Abstract] [Full Text] [Related]
23. Mutations of the HFE gene among Turkish hereditary hemochromatosis patients. Simsek H, Balaban YH, Yilmaz E, Sumer H, Buyukasik Y, Cengiz C, Ozcebe O, Hascelik G, Tatar G. Ann Hematol; 2005 Oct; 84(10):646-9. PubMed ID: 15871018 [Abstract] [Full Text] [Related]
24. HFE and Non-HFE Hereditary Hemochromatosis Based on Screening of 854 Individuals: 12 Years of an Iranian Experience. Zarifian Yeganeh R, Akbari Kelishomi M, Ahmadpour Jenaghard A, Salmani B, Vahidi Z, Makvand M, Azad M, Kooshki M, Bouraqi Y, Azarkeivan A, Najmabadi H, Neishabury M. Genet Test Mol Biomarkers; 2024 Jul; 28(7):289-296. PubMed ID: 38980801 [Abstract] [Full Text] [Related]
25. Analysis of HFE and TFR2 mutations in selected blood donors with biochemical parameters of iron overload. De Gobbi M, Daraio F, Oberkanins C, Moritz A, Kury F, Fiorelli G, Camaschella C. Haematologica; 2003 Apr; 88(4):396-401. PubMed ID: 12681966 [Abstract] [Full Text] [Related]
26. [Hereditary and acquired iron overload]. de Korwin JD. Nephrol Ther; 2006 Nov; 2 Suppl 5():S304-12. PubMed ID: 17373275 [Abstract] [Full Text] [Related]
27. Analysis of HFE and non-HFE gene mutations in Brazilian patients with hemochromatosis. Bittencourt PL, Marin ML, Couto CA, Cançado EL, Carrilho FJ, Goldberg AC. Clinics (Sao Paulo); 2009 Nov; 64(9):837-41. PubMed ID: 19759876 [Abstract] [Full Text] [Related]
29. Phenotypic analysis of hemochromatosis subtypes reveals variations in severity of iron overload and clinical disease. Sandhu K, Flintoff K, Chatfield MD, Dixon JL, Ramm LE, Ramm GA, Powell LW, Subramaniam VN, Wallace DF. Blood; 2018 Jul 05; 132(1):101-110. PubMed ID: 29743178 [Abstract] [Full Text] [Related]
30. Iron storage disease in Asia-Pacific populations: the importance of non-HFE mutations. McDonald CJ, Wallace DF, Crawford DH, Subramaniam VN. J Gastroenterol Hepatol; 2013 Jul 05; 28(7):1087-94. PubMed ID: 23577916 [Abstract] [Full Text] [Related]
31. [Molecular genetic diagnostics and screening of hereditary hemochromatosis]. Zlocha J, Kovács L, Pozgayová S, Kupcová V, Durínová S. Vnitr Lek; 2006 Jun 05; 52(6):602-8. PubMed ID: 16871764 [Abstract] [Full Text] [Related]
32. Screening selected blood donors with biochemical iron overload for hemochromatosis: a regional experience. De Gobbi M, D'Antico S, Castagno F, Testa D, Merlini R, Bondi A, Camaschella C. Haematologica; 2004 Oct 05; 89(10):1161-7. PubMed ID: 15477198 [Abstract] [Full Text] [Related]
33. Disruption of hemochromatosis protein and transferrin receptor 2 causes iron-induced liver injury in mice. Delima RD, Chua AC, Tirnitz-Parker JE, Gan EK, Croft KD, Graham RM, Olynyk JK, Trinder D. Hepatology; 2012 Aug 05; 56(2):585-93. PubMed ID: 22383097 [Abstract] [Full Text] [Related]
34. HJV and HFE Play Distinct Roles in Regulating Hepcidin. Wu Q, Wang H, An P, Tao Y, Deng J, Zhang Z, Shen Y, Chen C, Min J, Wang F. Antioxid Redox Signal; 2015 May 20; 22(15):1325-36. PubMed ID: 25608116 [Abstract] [Full Text] [Related]
36. Mutations in HAMP and HJV genes and their impact on expression of clinical hemochromatosis in a cohort of 100 Spanish patients homozygous for the C282Y mutation of HFE gene. Altès A, Bach V, Ruiz A, Esteve A, Felez J, Remacha AF, Sardà MP, Baiget M. Ann Hematol; 2009 Oct 20; 88(10):951-5. PubMed ID: 19214511 [Abstract] [Full Text] [Related]
37. Epidemiology and diagnostic testing for hemochromatosis and iron overload. Adams PC. Int J Lab Hematol; 2015 May 20; 37 Suppl 1():25-30. PubMed ID: 25976957 [Abstract] [Full Text] [Related]
38. Identification of novel non-HFE mutations in Chinese patients with hereditary hemochromatosis. Zhang W, Li Y, Xu A, Ouyang Q, Wu L, Zhou D, Wu L, Zhang B, Zhao X, Wang Y, Wang X, Duan W, Wang Q, You H, Huang J, Ou X, Jia J, China Registry of Genetic/Metabolic Liver Diseases (CR-GMLD) Group. Orphanet J Rare Dis; 2022 Jun 06; 17(1):216. PubMed ID: 35668470 [Abstract] [Full Text] [Related]
39. Identification of new mutations of the HFE, hepcidin, and transferrin receptor 2 genes by denaturing HPLC analysis of individuals with biochemical indications of iron overload. Biasiotto G, Belloli S, Ruggeri G, Zanella I, Gerardi G, Corrado M, Gobbi E, Albertini A, Arosio P. Clin Chem; 2003 Dec 06; 49(12):1981-8. PubMed ID: 14633868 [Abstract] [Full Text] [Related]
40. EASL clinical practice guidelines for HFE hemochromatosis. European Association For The Study Of The Livereasl@easloffice.eu. J Hepatol; 2010 Jul 06; 53(1):3-22. PubMed ID: 20471131 [Abstract] [Full Text] [Related] Page: [Previous] [Next] [New Search]