Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 304 Records) |
| Query Trace: Hereditary hemochromatosis[original query] |
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| 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 |
| Genotypic and phenotypic spectra of hemojuvelin mutations in primary hemochromatosis patients: a systematic review. Orphanet journal of rare diseases 2019 7 14 (1): 171. Kong Xiaomu, Xie Lingding, Zhu Haiqing, Song Lulu, Xing Xiaoyan, Yang Wenying, Chen Xiaopi |
| Polycythemia in Patients With Hereditary Hemochromatosis: Real or Myth? Journal of clinical medicine research 2019 5 11 (6): 422-427. Asif Samia, Begemann Madeline, Raza Shahz |
| Diagnostic difficulties of primary hemochromatosis in a patient with posthemorrhagic anemia. Terapevticheskii arkhiv 2019 5 91 (4): 118-121. Podzolkov V I, Pokrovskaya A E, Vargina T S, Oganesyan K |
| Bivariate mixture models for the joint distribution of repeated serum ferritin and transferrin saturation measured 12 years apart in a cohort of healthy middle-aged Australians. PloS one 2019 3 14 (3): e0214196. McLaren Christine E, Chen Wen-Pin, Bertalli Nadine A, Delatycki Martin B, Giles Graham G, English Dallas R, Hopper John L, Allen Katrina J, Gurrin Lyle |
| Impact of natural neuromedin-B receptor variants on iron metabolism. American journal of hematology 2019 11 95 (2): 167-177. Rametta Raffaela, Dongiovanni Paola, Baselli Guido A, Pelusi Serena, Meroni Marica, Fracanzani Anna L, Busti Fabiana, Castagna Annalisa, Scarlini Stefania, Corradini Elena, Pietrangelo Antonello, Girelli Domenico, Fargion Silvia, Valenti Lu |
| Evaluation of a screening program for iron overload and HFE mutations in 50,493 blood donors. Annals of hematology 2020 8 99 (10): 2295-2301. Eckerström Carl, Frändberg Sofia, Lyxe Lena, Pardi Cecilia, Konar J |
| Plasma Lipidome, PNPLA3 polymorphism and hepatic steatosis in hereditary hemochromatosis. BMC gastroenterology 2020 Jul 20 (1): 230. Seeßle Jessica, Gan-Schreier Hongying, Kirchner Marietta, Stremmel Wolfgang, Chamulitrat Walee, Merle U |
| Clinical Penetrance of Hereditary Hemochromatosis-Related End-Organ Damage of C282Y Homozygosity, A Newfoundland Experience. Clinical and translational gastroenterology 2020 12 11 (11): e00258. Lim Dennis R, Vidyasankar Gokul, Phua Chai, Borgaonkar Ma |
| Association of Hemochromatosis HFE p.C282Y Homozygosity With Hepatic Malignancy. JAMA 2020 11 324 (20): 2048-2057. Atkins Janice L, Pilling Luke C, Masoli Jane A H, Kuo Chia-Ling, Shearman Jeremy D, Adams Paul C, Melzer Dav |
| Significance of Hereditary Hemochromatosis Gene (HFE) Mutations in Chronic Hepatitis C and Hepatocellular Carcinoma Patients in Egypt: A Pilot Study. Asian Pacific journal of cancer prevention : APJCP 2021 9 22 (9): 2837-2845. Dawood Reham M, Abd El Meguid Mai, Elrobe Walied, Salum Ghada M, Zayed Naglaa, Mousa Sherief, Medhat Em |
| Multiplex Allele-Specific PCR for Simultaneous Detection of H63D and C282Y HFE Mutations in Hereditary Hemochromatosis. The journal of applied laboratory medicine 2021 2 3 (1): 10-17. Arts Heleen H, Eng Barry, Waye John |
| HIF1A: A Putative Modifier of Hemochromatosis. International journal of molecular sciences 2021 1 22 (3): . Pelucchi Sara, Ravasi Giulia, Arosio Cristina, Mauri Mario, Piazza Rocco, Mariani Raffaella, Piperno Alber |
| HFE Genotype and Endurance Performance in Competitive Male Athletes. Medicine and science in sports and exercise 2021 1 53 (7): 1385-1390. Thakkar Drishti, Sicova Marc, Guest Nanci S, Garcia-Bailo Bibiana, El-Sohemy Ahm |
| Correlation of genotype and phenotype in 32 patients with hereditary hemochromatosis in China. Orphanet journal of rare diseases 2021 09 16 (1): 398. Wu Liyan, Zhang Wei, Li Yanmeng, Zhou Donghu, Zhang Bei, Xu Anjian, Wu Zhen, Wu Lina, Li Shuxiang, Wang Xiaoming, Zhao Xinyan, Wang Qianyi, Li Min, Wang Yu, You Hong, Huang Jian, Ou Xiaojuan, Jia Jido |
| Evidence That HFE H63D Variant Is a Potential Disease Modifier in Cluster Headache. Journal of molecular neuroscience : MN 2021 Sep . Papasavva Maria, Vikelis Michail, Katsarou Martha-Spyridoula, Siokas Vasileios, Dermitzakis Emmanouil, Papademetriou Christoforos, Karakostis Konstantinos, Lazopoulos George, Dardiotis Efthimios, Drakoulis Nikola |
| Association of Genetic Variant Linked to Hemochromatosis With Brain Magnetic Resonance Imaging Measures of Iron and Movement Disorders. JAMA neurology 2022 8 79 (9): 919-928. Loughnan Robert, Ahern Jonathan, Tompkins Cherisse, Palmer Clare E, Iversen John, Thompson Wesley K, Andreassen Ole, Jernigan Terry, Sugrue Leo, Dale Anders, Boyle Mary E T, Fan Chun Chi |
| Risk of Hepatocellular Carcinoma in Patients with Various HFE Genotypes. Digestive diseases and sciences 2022 7 68 (1): 312-322. Natarajan Yamini, Patel Parth, Chu Jinna, Yu Xian, Hernaez Ruben, El-Serag Hashem, Kanwal Fasi |
| 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 |
| Identification of novel non-HFE mutations in Chinese patients with hereditary hemochromatosis. Orphanet journal of rare diseases 2022 6 17 (1): 216. Zhang Wei, Li Yanmeng, Xu Anjian, Ouyang Qin, Wu Liyan, Zhou Donghu, Wu Lina, Zhang Bei, Zhao Xinyan, Wang Yu, Wang Xiaoming, Duan Weijia, Wang Qianyi, You Hong, Huang Jian, Ou Xiaojuan, Jia Jidong, |
| Hereditary Hemochromatosis Variant Associations with Incident Nonliver Malignancies: 11-Year Follow-up in UK Biobank. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2022 Jun . Atkins Janice L, Pilling Luke C, Torti Suzy V, Torti Frank M, Kuchel George A, Melzer Dav |
| Genetic modifiers of penetrance to liver endpoints in HFE hemochromatosis: Associations in a large community cohort. Hepatology (Baltimore, Md.) 2022 May . Pilling Luke C, Atkins Janice L, Melzer Dav |
| C282Y/H63D Compound Heterozygosity Is a Low Penetrance Genotype for Iron Overload-related Disease. Journal of the Canadian Association of Gastroenterology 2022 10 5 (5): 240-247. Hasan S M Mahmudul, Farrell James, Borgaonkar Ma |
| Hemochromatosis risk genotype is not associated with colorectal cancer or age at its diagnosis. HGG advances 2022 1 1 (1): 100010. Jarvik Gail P, Wang Xiaoliang, Fontanillas Pierre, Kim Esther, Chanprasert Sirisak, Gordon Adam S, Bastarache Lisa, Kowdley Kris V, Harrison Tabitha, Rosenthal Elisabeth A, Stanaway Ian B, Bézieau Stéphane, Weinstein Stephanie J, Newcomb Polly A, Casey Graham, Platz Elizabeth A, Visvanathan Kala, Le Marchand Loic, Ulrich Cornelia M, Hardikar Sheetal, Li Christopher I, van Duijnhoven Franzel J B, Gsur Andrea, Campbell Peter T, Moreno Victor, Vodi?ka Pavel, Brenner Hermann, Chang-Claude Jenny, Hoffmeister Michael, Slattery Martha L, Gunter Marc J, Aglago Elom K, Castellví-Bel Sergi, Kweon Sun-Seog, Chan Andrew T, Li Li, Zheng Wei, Bishop D Timothy, Giles Graham G, Rennert Gad, Offit Kenneth, Keku Temitope O, Woods Michael O, Hampe Jochen, Van Guelpen Bethan, Gallinger Steven J, de la Chapelle Albert, Hampel Heather, Berndt Sonja I, Tangen Catherine M, Lindblom Annika, Wolk Alicja, Burnett-Hartman Andrea, Wu Anna H, White Emily, , Gruber Stephen B, Jenkins Mark A, Mountain Joanna, Peters Ulrike, Crosslin David |
| Hereditary hemochromatosis beyond hyperferritinemia: Clinical and laboratory investigation of the patient's profile submitted to phlebotomy in two reference centers in southern Brazil. Genetics and molecular biology 2023 5 46 (2): e20220230. Nathalia Kersting, Juliana Cristine Fontana, Fabiane Pohlmann de Athayde, Fernanda Marcante Carlotto, Bruna Accorsi Machado, Cristiane da Silva Rodrigues de Araújo, Leo Sekine, Tor Gunnar Hugo Onsten, Sandra Leistner-Seg |
| Associations between metabolic hyperferritinaemia, fibrosis-promoting alleles and clinical outcomes in steatotic liver disease. Liver international : official journal of the International Association for the Study of the Liver 2023 11 . Deepika Suresh, Ashley Li, Matthew J Miller, Karn Wijarnpreecha, Vincent L Ch |
| Fatigue Assessment in Patients with Hereditary Hemochromatosis: First Use of the Popular Diagnostic Tools. Journal of clinical medicine 2024 9 13 (18): . Micha? ?wi?tczak, Alicja Raczak, Agata ?wi?tczak, Krzysztof M?odzi?ski, Katarzyna Sikorska, Anna Ja?wi?ska, Damian Kaufmann, Ludmi?a Dani?owicz-Szymanowi |
| Genetic Correlation of HBB, HFE and HAMP Genes to Endocrinal Complications in Egyptian Beta Thalassemia Major Patients. Biochemical genetics 2024 7 . Mona F Sokkar, Mona Hamdy, Mohamed B Taher, Heba El-Sayed, Eman Abdelmotaleb Bayomi, Khalda S Amr, Ghada Y El-Kam |
| [Analysis of clinical, gene mutation characteristics, and treatment prognosis of type 2A hereditary hemochromatosis in the Chinese population]. Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology 2024 12 32 (11): 1013-1018. W Zhang, Y M Li, A J Xu, X M Wang, Y Wang, W J Duan, X Y Zhao, H X Xu, J P Jiang, W Jiang, J Huang, X J |
| Re-evaluating the utility of iron indices in hereditary hemochromatosis genotyping: A retrospective study. Clinical biochemistry 2024 12 110860. Amy Lou, Manal O Elnenaei, Julie Zhu, Kevork Peltekian, Eric Liu, Jennifer A Jamieson, Hammam Said, Bassam A Nass |
- Page last reviewed:Feb 1, 2024
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