Human Genome Epidemiology Literature Finder
Records 1 - 23 (of 23 Records) |
Query Trace: beta-Thalassemia and HFE[original query] |
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H63D mutation in the HFE gene increases iron overload in beta-thalassemia carriers. Haematologica 2002 Mar 87 (3): 242-5. Melis Maria Antonietta, Cau Milena, Deidda Federica, Barella Susanna, Cao Antonio, Galanello Ren |
Prevalence of C282Y and H63D mutations in the haemochromatosis (HFE) gene in Tunisian population. Annales de génétique 0 47 (4): 325-30. Sassi R, Hmida Slama, Kaabi H, Hajjej A, Abid A, Abdelkefi S, Yacoub S, Maamar M, Mojaat N, Ben Hamed L, Bellali H, Dridi A, Jridi A, Midouni B, Boukef M |
Spectrum and haplotypes of the HFE hemochromatosis gene in Iran: H63D in beta-thalassemia major and the first E277K homozygous. The hematology journal : the official journal of the European Haematology Association / EHA 2004 5 (6): 524-7. Karimi Mehran, Yavarian Majid, Delbini Paola, Harteveld Cornelis L, Farjadian Shirin, Fiorelli Gemino, Giordano Piero |
The role of HFE mutations on iron metabolism in beta-thalassemia carriers. Journal of human genetics 2004 49 (12): 651-5. Martins Rute, Picanço Isabel, Fonseca Aidil, Ferreira Lídia, Rodrigues Odete, Coelho Marília, Seixas Teresa, Miranda Armandina, Nunes Baltazar, Costa Luciana, Romão Luísa, Faustino Pau |
Prevalence of the H63D mutation of the HFE in north India: its presence does not cause iron overload in beta thalassemia trait. European journal of haematology 2005 Apr 74 (4): 333-6. Garewal Gurjeewan, Das Reena, Ahluwalia Jasmina, Marwaha R |
HFE gene mutations in Brazilian thalassemic patients. Brazilian journal of medical and biological research = Revista brasileira de pesquisas médicas e biológicas / Sociedade Brasileira de Biofísica ... [et al.] 2006 Dec 39 (12): 1575-80. Oliveira T M, Souza F P, Jardim A C G, Cordeiro J A, Pinho J R R, Sitnik R, Estevão I F, Bonini-Domingos C R, Rahal |
H63D mutation of the hemochromatosis gene and serum ferritin levels in Thai thalassemia carriers. Acta haematologica 2007 118 (2): 99-105. Yamsri Supawadee, Sanchaisuriya Kanokwan, Fucharoen Supan, Fucharoen Goonnapa, Jetsrisuparb Arunee, Wiangnon Surapon, Changtrakul Yossombat, Sanchaisuriya Patta |
HFE mutation H63D predicts risk of iron over load in thalassemia intermedia irrespective of blood transfusions. Indian journal of pathology & microbiology 2007 Jan 50 (1): 82-5. Sharma Vineeta, Panigrahi Inusha, Dutta Pankhi, Tyagi Seema, Choudhry Ved Prakash, Saxena Re |
[HFE gene mutations in Tunisian major beta-Thalassemia and iron overload]. Transfusion clinique et biologique : journal de la Société française de transfusion sanguine 2006 Dec 13 (6): 353-7. 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 |
Beta-globin mutations are associated with parenchymal siderosis and fibrosis in patients with non-alcoholic fatty liver disease. Journal of hepatology 2010 Nov 53 (5): 927-33. Valenti Luca, Canavesi Elena, Galmozzi Enrico, Dongiovanni Paola, Rametta Raffaela, Maggioni Paolo, Maggioni Marco, Fracanzani Anna Ludovica, Fargion Silv |
Frequencies of C282Y and H63D alleles in the HFE gene among various Jewish ethnic groups in Israel: a change of concept required. Genetics in medicine : official journal of the American College of Medical Genetics 2010 Feb 12 (2): 122-5. Reish Orit, Shefer-Kaufmann Niva, Shimshoni Daphne Chapman, Renbaum Paul, Orr-Urtreger Avi, Steiner Hillel, Rapoport Micha, Levy-Lahad Ephrat, Altarescu Gheo |
Serum ferritin and transferrin saturation levels in ß° and ß(+) thalassemia patients. Genetics and molecular research : GMR 2011 10 (2): 632-9. Estevão I F, Peitl Junior P, Bonini-Domingos C |
The A736V TMPRSS6 polymorphism influences hepatic iron overload in nonalcoholic fatty liver disease. PloS one 2012 7 (11): e48804. Valenti Luca, Rametta Raffaela, Dongiovanni Paola, Motta Benedetta M, Canavesi Elena, Pelusi Serena, Pulixi Edoardo A, Fracanzani Anna L, Fargion Silv |
The effect of HFE polymorphisms on cardiac iron overload in patients with beta-thalassemia major. Pediatric hematology and oncology 2013 Nov 30 (8): 755-60. Turedi Aysen, Oymak Yesim, Me?e Timur, Yaman Yöntem, Bayraktaroglu Selen, Alpman Asude, Ozkinay Ferda, Ayd?nok Ye?im, Vergin Can |
Survey of Hfe Gene C282Y Mutation in Turkish Beta-Thalassemia Patients and Healthy Population: A Preliminary Study. Turkish journal of haematology : official journal of Turkish Society of Haematology 2014 Sep 31 (3): 272-275. Unal Selma, Balta Günay, Gümrük Fatma, Xu Hong-G |
Frequency of Hereditary Hemochromatosis (HFE) Gene Mutations in Egyptian Beta Thalassemia Patients and its Relation to Iron Overload. Open access Macedonian journal of medical sciences 2016 Jun 4 (2): 226-31. Enein Azza Aboul, El Dessouky Nermine A, Mohamed Khalda S, Botros Shahira K A, Abd El Gawad Mona F, Hamdy Mona, Dyaa Neh |
The Effects of HFE Polymorphisms on Biochemical Parameters of Iron Status in Arab Beta-Thalassemia Patients. Indian journal of hematology & blood transfusion : an official journal of Indian Society of Hematology and Blood Transfusion 2017 Dec 33 (4): 545-551. AlFadhli Suad, Salem Matra, Shome D K, Mahdi Najat, Nizam Rashee |
The Correlation of Cardiac and Hepatic Hemosiderosis as Measured by T2*MRI Technique with Ferritin Levels and Hemochromatosis Gene Mutations in Iranian Patients with Beta Thalassemia Major. Oman medical journal 2018 2 33 (1): 48-54. Soltanpour Mohammad Soleiman, Davari Kamb |
Association of frequency of hereditary hemochromatosis (HFE) gene mutations (H63D and C282Y) with iron overload in beta-thalassemia major patients in Pakistan. Saudi medical journal 2019 Sep 40 (9): 887-892. Sharif Yasir, Irshad Saba, Tariq Anam, Rasheed Sana, Tariq Muhammad |
Hepcidin and HFE Polymorphisms and Ferritin Level in ?-Thalassemia Major. International journal of hematology-oncology and stem cell research 2019 6 13 (1): 42-48. Fekri Kiavash, Asle Rasouli Negar, Tavallai Zavareh Seyyed Abdolhossein, Jalil Milad, Moradi Fahimeh, Hosseinpour Maryam, Teimori Hosse |
Investigation of correlation between H63D and C282Y mutations in HFE gene and serum Ferritin level in beta-thalassemia major patients. Transfusion clinique et biologique : journal de la Societe francaise de transfusion sanguine 2019 May . Rahmani Romina, Naseri Parisa, Safaroghli-Azar Ava, Tarighi Shahriar, Hosseini Tahereh, Hojjati Mohammad Tah |
Determination of mutations in iron regulating genes of beta thalassemia major patients of Khyber Pakhtunkhwa, Pakistan. Molecular genetics & genomic medicine 2020 6 8 (9): e1310. Shah Maryam, Danish Lubna, Khan Najeeb U, Zaman Fakhar, Ismail Muhammad, Hussain Mehfooz, Pervaiz Ruqiya, Iqbal Aq |
Frequency of Hereditary Hemochromatosis Gene (HFE) Variants in Sri Lankan Transfusion-Dependent Beta-Thalassemia Patients and Their Association With the Serum Ferritin Level. Frontiers in pediatrics 2022 7 10 890989. Padeniya Padmapani, Goonasekara Hemali, Abeysekera Gayan, Jayasekara Rohan, Dissanayake Vaji |
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- Page last updated:Apr 16, 2024
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