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411 related items for PubMed ID: 32925401
1. Association of HFE Gene Mutations With Serum Ferritin Level and Heart and Liver Iron Overload in Patients With Transfusion-dependent Beta-Thalassemia. Zekavat OR, Zareian Jahromi M, Haghpanah S, Kargar Jahromi Z, Cohan N. J Pediatr Hematol Oncol; 2021 Jan; 43(1):e26-e28. PubMed ID: 32925401 [Abstract] [Full Text] [Related]
2. Investigation of correlation between H63D and C282Y mutations in HFE gene and serum Ferritin level in beta-thalassemia major patients. Rahmani R, Naseri P, Safaroghli-Azar A, Tarighi S, Hosseini T, Hojjati MT. Transfus Clin Biol; 2019 Nov; 26(4):249-252. PubMed ID: 31679808 [Abstract] [Full Text] [Related]
3. Association of frequency of hereditary hemochromatosis (HFE) gene mutations (H63D and C282Y) with iron overload in beta-thalassemia major patients in Pakistan. Sharif Y, Irshad S, Tariq A, Rasheed S, Tariq MH. Saudi Med J; 2019 Sep; 40(9):887-892. PubMed ID: 31522215 [Abstract] [Full Text] [Related]
4. The influence of hemochromatosis mutations on iron overload of thalassemia major. Longo F, Zecchina G, Sbaiz L, Fischer R, Piga A, Camaschella C. Haematologica; 1999 Sep; 84(9):799-803. PubMed ID: 10477452 [Abstract] [Full Text] [Related]
5. Evaluation of Iron Overload Between Age Groups Using Magnetic Resonance Imaging and Its Correlation with Iron Profile in Transfusion-dependent Thalassemia. Wahidiyat PA, Iskandar SD, Sekarsari D. Acta Med Indones; 2018 Jul; 50(3):230-236. PubMed ID: 30333273 [Abstract] [Full Text] [Related]
6. Evaluation of cardiac and hepatic iron overload in thalassemia major patients with T2* magnetic resonance imaging. Wahidiyat PA, Liauw F, Sekarsari D, Putriasih SA, Berdoukas V, Pennell DJ. Hematology; 2017 Sep; 22(8):501-507. PubMed ID: 28218005 [Abstract] [Full Text] [Related]
7. Effect of Hereditary Hemochromatosis Gene H63D and C282Y Mutations on Iron Overload in Sickle Cell Disease Patients. Terzi YK, Bulakbaşı Balcı T, Boğa C, Koç Z, Yılmaz Çelik Z, Özdoğu H, Karakuş S, Şahin Fİ. Turk J Haematol; 2016 Dec 01; 33(4):320-325. PubMed ID: 27095682 [Abstract] [Full Text] [Related]
8. The effect of HFE polymorphisms on cardiac iron overload in patients with beta-thalassemia major. Turedi A, Oymak Y, Meşe T, Yaman Y, Bayraktaroglu S, Alpman A, Ozkinay F, Aydınok Y, Vergin C. Pediatr Hematol Oncol; 2013 Nov 01; 30(8):755-60. PubMed ID: 24087894 [Abstract] [Full Text] [Related]
9. H63D mutation in the HFE gene increases iron overload in beta-thalassemia carriers. Melis MA, Cau M, Deidda F, Barella S, Cao A, Galanello R. Haematologica; 2002 Mar 01; 87(3):242-5. PubMed ID: 11869934 [Abstract] [Full Text] [Related]
10. [HFE gene mutations in Tunisian major beta-Thalassemia and iron overload]. Mellouli F, El Borgi W, Kaabi H, Ben Hassen E, Sassi R, Hmida H, Cherif G, Maamar M, Zouari B, Boukef K, Bejaoui M, Hmida S. Transfus Clin Biol; 2006 Dec 01; 13(6):353-7. PubMed ID: 17303462 [Abstract] [Full Text] [Related]
11. HFE mutation H63D predicts risk of iron over load in thalassemia intermedia irrespective of blood transfusions. Sharma V, Panigrahi I, Dutta P, Tyagi S, Choudhry VP, Saxena R. Indian J Pathol Microbiol; 2007 Jan 01; 50(1):82-5. PubMed ID: 17474269 [Abstract] [Full Text] [Related]
12. Comparison of Tissue Elastography With Magnetic Resonance Imaging T2* and Serum Ferritin Quantification in Detecting Liver Iron Overload in Patients With Thalassemia Major. Pipaliya N, Solanke D, Parikh P, Ingle M, Sharma R, Sharma S, Sawant P. Clin Gastroenterol Hepatol; 2017 Feb 01; 15(2):292-298.e1. PubMed ID: 27650324 [Abstract] [Full Text] [Related]
13. Frequency of Hereditary Hemochromatosis Gene (HFE) Variants in Sri Lankan Transfusion-Dependent Beta-Thalassemia Patients and Their Association With the Serum Ferritin Level. Padeniya P, Goonasekara H, Abeysekera G, Jayasekara R, Dissanayake V. Front Pediatr; 2022 Feb 01; 10():890989. PubMed ID: 35903164 [Abstract] [Full Text] [Related]
14. Assessment of iron overload in a cohort of Sri Lankan patients with transfusion dependent beta thalassaemia and its correlation with pathogenic variants in HBB, HFE, SLC40A1, and TFR2 genes. Dissanayake R, Samarasinghe N, Waidyanatha S, Pathirana S, Neththikumara N, Dissanayake VHW, Wetthasinghe K, Gooneratne L, Wickramasinghe P. BMC Pediatr; 2022 Jun 15; 22(1):344. PubMed ID: 35705926 [Abstract] [Full Text] [Related]
15. [Study on HFE gene mutations in patients with myelodysplastic syndromes and aplastic anemia]. Nie L, Ai XF, Zheng YZ, Li QH, Yang L, Xiao ZJ. Zhonghua Xue Ye Xue Za Zhi; 2009 Apr 15; 30(4):223-8. PubMed ID: 19731820 [Abstract] [Full Text] [Related]
16. Association of HFE mutations (C282Y and H63D) with iron overload in blood donors from Mexico City. Baptista-González HA, Rosenfeld-Mann F, Trueba-Gómez R, Bermejo-Martínez L, Méndez-Sánchez N. Ann Hepatol; 2007 Apr 15; 6(1):55-60. PubMed ID: 17297430 [Abstract] [Full Text] [Related]
17. Mild iron overload in patients carrying the HFE S65C gene mutation: a retrospective study in patients with suspected iron overload and healthy controls. Holmström P, Marmur J, Eggertsen G, Gåfvels M, Stål P. Gut; 2002 Nov 15; 51(5):723-30. PubMed ID: 12377814 [Abstract] [Full Text] [Related]
18. Transient elevation of serum ferritin in a Sri Lankan with homozygosity for H63D mutation in the HFE gene: a case report. Wickramasinghe W, Karunathilaka C, Jayasinghe S, Gooneratne L. J Med Case Rep; 2020 Jul 09; 14(1):93. PubMed ID: 32641120 [Abstract] [Full Text] [Related]
19. Effect of the Hemochromatosis Mutations on Iron Overload among the Indian β Thalassemia Carriers. Nadkarni AH, Singh AA, Colaco S, Hariharan P, Colah RB, Ghosh K. J Clin Lab Anal; 2017 May 09; 31(3):. PubMed ID: 27561698 [Abstract] [Full Text] [Related]
20. Hemochromatosis and iron-overload screening in a racially diverse population. Adams PC, Reboussin DM, Barton JC, McLaren CE, Eckfeldt JH, McLaren GD, Dawkins FW, Acton RT, Harris EL, Gordeuk VR, Leiendecker-Foster C, Speechley M, Snively BM, Holup JL, Thomson E, Sholinsky P, Hemochromatosis and Iron Overload Screening (HEIRS) Study Research Investigators. N Engl J Med; 2005 Apr 28; 352(17):1769-78. PubMed ID: 15858186 [Abstract] [Full Text] [Related] Page: [Next] [New Search]