Human Genome Epidemiology Literature Finder
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Records 1 - 25 (of 25 Records) |
| Query Trace: Liver Diseases and HFE[original query] |
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| C282Y and H63D mutations in the HFE gene have no effect on iron overload disorders in Japan. Internal medicine (Tokyo, Japan) 2001 Sep 40 (9): 852-6. Shiono Y, Ikeda R, Hayashi H, Wakusawa S, Sanae F, Takikawa T, Imaizumi Y, Yano M, Yoshioka K, Kawanaka M, Yamada |
| Distribution of HFE C282Y and H63D mutations in the Balearic Islands (NE Spain). Clinical genetics 2002 Jan 61 (1): 43-8. Guix P, Picornell A, Parera M, Galmes A, Obrador A, Ramon M M, Castro J |
| Iron and HFE or TfR1 mutations as comorbid factors for development and progression of chronic hepatitis C. Journal of hepatology 2002 Dec 37 (6): 848-54. Bonkovsky Herbert L, Troy Nicole, McNeal Kristina, Banner Barbara F, Sharma Ashish, Obando Jorge, Mehta Savant, Koff Raymond S, Liu Qin, Hsieh Chung-Che |
| Liver iron deposits in hepatitis B patients: association with severity of liver disease but not with hemochromatosis gene mutations. Journal of gastroenterology and hepatology 2004 Sep 19 (9): 1036-41. Martinelli Ana L C, Filho Antonio B Araujo, Franco Rendrik F, Tavella Marli H, Ramalho Leandra N Z, Zucoloto Sergio, Rodrigues Sandra S, Zago Marcos |
| Correlation between iron status and genetic hemochromatosis (codon C282Y) in a large German population. The Israel Medical Association journal : IMAJ 2004 Jan 6 (1): 30-3. Wrede Christian E, Hutzler Stefanie, Bollheimer L Cornelius, Buettner Roland, Hellerbrand Claus, Schöelmerich Jürgen, Palitzsch Klaus-Diet |
| HFE gene mutations in Polish patients with disturbances of iron metabolism: an initial assessment. International journal of molecular medicine 2005 Dec 16 (6): 1151-6. Sikorska Katarzyna, Bielawski Krzysztof Piotr, Stalke Piotr, Lakomy Elzbieta Anna, Michalska Zofia, Witczak-Malinowska Krystyna, Romanowski Toma |
| An open population screening study for HFE gene major mutations proves the low prevalence of C282Y mutation in Central Italy. Alimentary pharmacology & therapeutics 2007 Aug 26 (4): 577-86. Floreani A, Rosa Rizzotto E, Basso D, Navaglia F, Zaninotto M, Petridis I, DI Andrea O, Testa R, Marra M, Baldo V, Chiaramonte |
| HFE gene mutation, chronic liver disease, and iron overload In Turkey. Digestive diseases and sciences 2007 Nov 52 (11): 3298-302. Yönal Oya, Hatirnaz Ozden, Akyüz Filiz, Ozbek Ugur, Demir Kadir, Kaymakoglu Sabahattin, Okten Atilla, Mungan Zeyn |
| Could iron deposits in hepatocytes serve as a prognostic marker of HFE gene mutations? Hepato-gastroenterology 0 55 (84): 1024-8. Sikorska Katarzyna, Stalke Piotr, Jaskiewicz Kazimierz, Romanowski Tomasz, Bielawski Krzysztof Pio |
| Mutant HFE genotype leads to significant iron overload in patients with liver diseases from western Romania. Journal of applied genetics 2009 50 (2): 173-6. Neghina A-M, Anghel A, Sporea I, Popescu A, Neghina R, Collins A, Thorstensen |
| Iron overload and HFE gene mutations in Polish patients with liver cirrhosis. Hepatobiliary & pancreatic diseases international : HBPD INT 2011 Jun 10 (3): 270-5. Sikorska Katarzyna, Romanowski Tomasz, Stalke Piotr, I?ycka-?wieszewska Ewa, Bielawski Krzysztof Pio |
| Probability of C282Y homozygosity decreases as liver transaminase activities increase in participants with hyperferritinemia in the hemochromatosis and iron overload screening study. Hepatology (Baltimore, Md.) 2012 Jun 55 (6): 1722-6. Adams Paul C, Speechley Mark, Barton James C, McLaren Christine E, McLaren Gordon D, Eckfeldt John |
| Lower serum hepcidin and greater parenchymal iron in nonalcoholic fatty liver disease patients with C282Y HFE mutations. Hepatology (Baltimore, Md.) 2012 Nov 56 (5): 1730-40. Nelson James E, Brunt Elizabeth M, Kowdley Kris V, |
| Iron overload and HFE gene mutations in Czech patients with chronic liver diseases. Disease markers 2012 32 (1): 65-72. Dostalikova-Cimburova Marketa, Kratka Karolina, Stransky Jaroslav, Putova Ivana, Cieslarova Blanka, Horak Ji |
| Hereditary hemochromatosis: missed diagnosis or misdiagnosis? The American journal of medicine 2013 Sep . Cherfane CE, Hollenbeck RD, Go J, Brown KE |
| Association between inherited monogenic liver disorders and chronic hepatitis C. World journal of hepatology 2014 Feb 6 (2): 92-7. Piekuse Linda, Kreile Madara, Zarina Agnese, Steinberga Zane, Sondore Valentina, Keiss Jazeps, Lace Baiba, Krumina Astri |
| HFE genotyping in patients with elevated serum iron indices and liver diseases. BioMed research international 2015 2015 164671. Evangelista Andreia Silva, Nakhle Maria Cristina, de Araújo Thiago Ferreira, Abrantes-Lemos Clarice Pires, Deguti Marta Mitiko, Carrilho Flair José, Cançado Eduardo Luiz Rach |
| Exome sequencing in HFE C282Y homozygous men with extreme phenotypes identifies a GNPAT variant associated with severe iron overload. Hepatology (Baltimore, Md.) 2015 Aug 62 (2): 429-39. McLaren Christine E, Emond Mary J, Subramaniam V Nathan, Phatak Pradyumna D, Barton James C, Adams Paul C, Goh Justin B, McDonald Cameron J, Powell Lawrie W, Gurrin Lyle C, Allen Katrina J, Nickerson Deborah A, Louie Tin, Ramm Grant A, Anderson Gregory J, McLaren Gordon |
| Association between the HFE C282Y, H63D Polymorphisms and the Risks of Non-Alcoholic Fatty Liver Disease, Liver Cirrhosis and Hepatocellular Carcinoma: An Updated Systematic Review and Meta-Analysis of 5,758 Cases and 14,741 Controls. PloS one 0 11 (9): e0163423. Ye Qing, Qian Bao-Xin, Yin Wei-Li, Wang Feng-Mei, Han T |
| Association of HFE gene C282Y and H63D mutations with liver cirrhosis in the Lithuanian population. Medicina (Kaunas, Lithuania) 2016 52 (5): 269-275. Juz?nas Simonas, Kup?inskas Juozas, Valantien? Irena, Šumskien? Jolanta, Petrenkien? Vitalija, Kondrackien? J?rate, Ku?inskas Laimutis, Kiudelis Gediminas, Skiecevi?ien? Jurgita, Kup?inskas Lim |
| MRI-Based Iron Phenotyping and Patient Selection for Next-Generation Sequencing of Non-Homeostatic Iron Regulator Hemochromatosis Genes. Hepatology (Baltimore, Md.) 2021 5 74 (5): 2424-2435. Viveiros André, Schaefer Benedikt, Panzer Marlene, Henninger Benjamin, Plaikner Michaela, Kremser Christian, Franke André, Franzenburg Sören, Hoeppner Marc P, Stauder Reinhard, Janecke Andreas, Tilg Herbert, Zoller Hei |
| 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 |
| 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 |
| Molecular Screening via Sanger Sequencing of the Genetic Variants in Non-Alcoholic Fatty Liver Disease Subjects in the Saudi Population: A Hospital-Based Study. Metabolites 2022 12 12 (12): . Alsaif Faisal, Al-Hamoudi Waleed, Alotaiby Maram, Alsadoon Amani, Almayouf Mohammed, Almadany Hadeel, Abuhaimed Jawahir, Ghufran Noman, Merajuddin Ahmed, Ali Khan Imr |
| 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 |
- Page last reviewed:Feb 1, 2024
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