Human Genome Epidemiology Literature Finder
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Records 1 - 22 (of 22 Records) |
| Query Trace: Syndrome and HFE[original query] |
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| [Dysmetabolic hepatosiderosis, characteristics in 51 patients]. Presse médicale (Paris, France : 1983) 2003 Mar 32 (9): 400-5. Vénat L, Loustaud-Ratti V, Liozon E, Soria P, Nadalon S, Gissot V, Labrousse F, Vidal |
| High incidence of hemochromatosis gene mutations in the myelodysplastic syndrome: the Budapest Study on 50 patients. Acta haematologica 2003 109 (2): 64-7. Várkonyi Judit, Tarkovács Gábor, Karádi István, Andrikovics Hajnalka, Varga Ferenc, Varga Fatime, Demeter Judit, Tordai Atti |
| Absence of hemochromatosis associated Cys282Tyr HFE gene mutation and low frequency of hemochromatosis phenotype in nonalcoholic chronic liver disease patients in India. Journal of gastroenterology and hepatology 2004 Jan 19 (1): 86-90. Thakur V, Guptan R C, Hashmi A Z, Sakhuja P, Malhotra V, Sarin S |
| The significance of the hemochromatosis genetic variants in multiple myeloma in comparison to that of myelodysplastic syndrome. Annals of hematology 2006 Dec 85 (12): 869-71. Várkonyi Judit, Demeter Judit, Tordai Attila, Andrikovics Hajnal |
| HFE gene mutations in patients with altered iron metabolism in Argentina. Cellular and molecular biology (Noisy-le-Grand, France) 2009 55 (2): 31-5. Rossetti M V, Méndez M, Afonso S, Gerez E, Batlle A, Muñoz A, Parera |
| Mutations in HFE causing hemochromatosis are associated with primary hypertriglyceridemia. The Journal of clinical endocrinology and metabolism 2009 Nov 94 (11): 4391-7. Solanas-Barca María, Mateo-Gallego Rocío, Calmarza Pilar, Jarauta Estíbaliz, Bea Ana M, Cenarro Ana, Civeira Fernan |
| HFE genotype and iron metabolism in Chinese patients with myelodysplastic syndromes and aplastic anemia. Annals of hematology 2010 Dec 89 (12): 1249-53. Nie Ling, Li Lin, Yang Lin, Zhang Yue, Xiao Zhiji |
| [HFE gene polymorphism in the population of Northern Asia]. Vestnik Rossi?sko? akademii meditsinskikh nauk / Rossi?skaia akademiia meditsinskikh nauk 2011 (9): 44-8. Mikha?lova S V, Romashchenko A G, Babenko V N, Gubina M A, Soboleva D E, Kobzev V F, Voevoda M |
| Dilution of candidates: the case of iron-related genes in restless legs syndrome. European journal of human genetics : EJHG 2012 Aug . Oexle K, Schormair B, Ried JS, Czamara D, Heim K, Frauscher B, Högl B, Trenkwalder C, Martin Fiedler G, Thiery J, Lichtner P, Prokisch H, Specht M, Müller-Myhsok B, Döring A, Gieger C, Peters A, Wichmann HE, Meitinger T, Winkelmann J |
| Liver steatosis correlates with iron overload but not with HFE gene mutations in chronic hepatitis C. Hepatobiliary & pancreatic diseases international : HBPD INT 2013 Aug 12 (4): 377-84. Sikorska Katarzyna, Stalke Piotr, Romanowski Tomasz, Rzepko Robert, Bielawski Krzysztof Pio |
| Polymorphisms of interleukin-1 Beta and interleukin-17Alpha genes are associated with restless legs syndrome. Biological research for nursing 2014 Apr 16 (2): 143-51. Hennessy Mary Dawn, Zak Rochelle S, Gay Caryl L, Pullinger Clive R, Lee Kathryn A, Aouizerat Bradley |
| Serum ferritin, insulin resistance, and metabolic syndrome: clinical and laboratory associations in 769 non-hispanic whites without diabetes mellitus in the HEIRS study. Metabolic syndrome and related disorders 2015 Mar 13 (2): 57-63. Acton Ronald T, Barton J Clayborn, Barton James |
| Birth Characteristics and Childhood Leukemia Risk: Correlations With Genetic Markers. Journal of pediatric hematology/oncology 2015 Jul 37 (5): e301-7. Kennedy Amy E, Kamdar Kala Y, Lupo Philip J, Okcu Mehmet F, Scheurer Michael E, Dorak Mehmet |
| Decision tree analysis of genetic risk for clinically heterogeneous Alzheimer's disease. BMC neurology 2015 15 (1): 47. Yokoyama Jennifer S, Bonham Luke W, Sears Renee L, Klein Eric, Karydas Anna, Kramer Joel H, Miller Bruce L, Coppola Giovan |
| Common founder effects of hereditary hemochromatosis, Wilson´s disease, the long QT syndrome and autosomal recessive deafness caused by two novel mutations in the WHRN and TMC1 genes. Hereditas 2017 12 154 16. Olsson K Sigvard, Wålinder Olof, Jansson Ulf, Wilbe Maria, Bondeson Marie-Louise, Stattin Eva-Lena, Raha-Chowdhury Ruma, Williams Rog |
| Insulin Resistance and Metabolic Syndrome: Clinical and Laboratory Associations in African Americans Without Diabetes in the Hemochromatosis and Iron Overload Screening Study. Metabolic syndrome and related disorders 2018 6 16 (6): 267-273. Barton James C, Barton Jackson Clayborn, Acton Ronald |
| Genetic factors influencing hemoglobin levels in 15,567 blood donors: results from the Danish Blood Donor Study. Transfusion 2019 01 59 (1): 226-231. Sørensen Erik, Rigas Andreas S, Didriksen Maria, Burgdorf Kristoffer S, Thørner Lise W, Pedersen Ole B, Hjalgrim Henrik, Petersen Mikkel S, Erikstrup Christian, Ullum Henr |
| Mutations in the HFE gene can be associated with increased lung disease severity in cystic fibrosis. Gene 2019 Jan 683 12-17. Smith Daniel J, Klein Kerenaftali, Hartel Gunter, Wainwright Claire E, Bell Scott C, Anderson Gregory J, Reid David |
| Hepcidin is a useful biomarker to evaluate hyperferritinemia associated with metabolic syndrome. Anais da Academia Brasileira de Ciencias 2019 5 91 (2): e20180286. Rauber Mariana R, Pilger Diogo A, Cecconello Daiane K, Falcetta Frederico S, Marcondes Natália A, Faulhaber Gustavo A |
| Genetic Predictors for Sinusoidal Obstruction Syndrome-A Systematic Review. Journal of personalized medicine 2021 4 11 (5): . Waespe Nicolas, Strebel Sven, Jurkovic Mlakar Simona, Krajinovic Maja, Kuehni Claudia Elisabeth, Nava Tiago, Ansari Ma |
| Analysis of Genes Involved in Oxidative Stress and Iron Metabolism in Heart Failure: A Step Forward in Risk Stratification. Cureus 2024 6 16 (5): e60707. Pedro X Silva, Laura Aguiar, Marcos Gaspar, Paula Faustino, Luiz M Falcão, Mário Barbosa, Manuel Bicho, Ângela Inác |
| Blood donor biobank as a resource in personalised biomedical genetic research. European journal of human genetics : EJHG 2024 1 . Jonna Clancy, Jarmo Ritari, Eevaleena Vaittinen, Mikko Arvas, Silja Tammi, , Satu Koskela, Jukka Partan |
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