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1. Full Text EASL clinical practice guidelines for HFE hemochromatosis
by European Association for the Study of the Liver and European Assoc Study Liver and European Association For The Study Of The Liver and European Association for the Study of the Liver
Journal of hepatology, ISSN 0168-8278, 2010, Volume 53, Issue 1, pp. 3 - 22
Gastroenterology and Hepatology | Gastroenterology & Hepatology | Life Sciences & Biomedicine | Science & Technology | Gastroenterology. Liver. Pancreas. Abdomen | Biological and medical sciences | Metabolic diseases | Medical sciences | Other metabolic disorders | Metals (hemochromatosis...) | Hemochromatosis - therapy | Genetic Testing | Iron Overload - genetics | Hemochromatosis Protein | Membrane Proteins - genetics | Gene Frequency | Humans | Male | Histocompatibility Antigens Class I - genetics | Polymorphism, Genetic | Pregnancy | Homozygote | Female | Hemochromatosis - diagnosis | Mutation | Hemochromatosis - genetics | Practice guidelines (Medicine) | Hemochromatosis | Index Medicus
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2. Full Text Hereditary Hemochromatosis: Pathogenesis, Diagnosis, and Treatment
by Pietrangelo, Antonello
Gastroenterology (New York, N.Y. 1943), ISSN 0016-5085, 2010, Volume 139, Issue 2, pp. 393 - 408.e2
Gastroenterology and Hepatology | Hereditary Disorders | Micronutrients | Iron Metabolism | Hepcidin | HFE | Gastroenterology & Hepatology | Life Sciences & Biomedicine | Science & Technology | Hemochromatosis - therapy | Predictive Value of Tests | Genetic Predisposition to Disease | Liver - pathology | Humans | Liver - metabolism | Risk Factors | Treatment Outcome | Heredity | Hemochromatosis - metabolism | Hemochromatosis - pathology | Polymorphism, Genetic | Phenotype | Animals | Pedigree | Hemochromatosis - diagnosis | Mutation | Hemochromatosis - genetics | Iron - blood | Proteins | Transferrin | Genetic disorders | Hemochromatosis | Physiological aspects | Development and progression | Diagnosis | Index Medicus | Abridged Index Medicus
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3. Full Text Hereditary Hemochromatosis — A New Look at an Old Disease
by Pietrangelo, Antonello
The New England journal of medicine, ISSN 0028-4793, 06/2004, Volume 350, Issue 23, pp. 2383 - 2397
Biological and medical sciences | Metabolic diseases | General aspects | Medical sciences | Other metabolic disorders | Metals (hemochromatosis...) | Hemochromatosis - therapy | Iron Overload - genetics | Hemochromatosis Protein | Membrane Proteins - genetics | Humans | Histocompatibility Antigens Class I - physiology | Homeostasis | Genotype | Histocompatibility Antigens Class I - genetics | Antimicrobial Cationic Peptides - metabolism | Iron - metabolism | Phenotype | Hepcidins | Membrane Proteins - physiology | Hemochromatosis - diagnosis | Mutation | Receptors, Transferrin - genetics | Hemochromatosis - genetics | Hemochromatosis - physiopathology | Genetic disorders | Hemochromatosis | Research | Index Medicus | Abridged Index Medicus
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4. Full Text Hereditary hemochromatosis disrupts uric acid homeostasis and causes hyperuricemia via altered expression/activity of xanthine oxidase and ABCG2
by Ristic, Bojana and Sivaprakasam, Sathish and Narayanan, Monisha and Ganapathy, Vadivel
Biochemical journal, ISSN 0264-6021, 04/2020, Volume 477, Issue 8, pp. 1499 - 1513
Life Sciences & Biomedicine | Biochemistry & Molecular Biology | Science & Technology | Xanthine Oxidase - metabolism | Uric Acid - metabolism | ATP Binding Cassette Transporter, Subfamily G, Member 2 - metabolism | Humans | Liver - metabolism | Mice, Inbred C57BL | ATP Binding Cassette Transporter, Subfamily G, Member 2 - genetics | Hemochromatosis - enzymology | Homeostasis | Male | Hemochromatosis Protein - metabolism | Hyperuricemia - metabolism | Hemochromatosis - metabolism | Hyperuricemia - etiology | Mice, Knockout | Animals | Hemochromatosis - complications | Hemochromatosis - congenital | Hemochromatosis Protein - genetics | Female | Mice | Xanthine Oxidase - genetics | Hyperuricemia - enzymology | Index Medicus | Gastrointestinal, Renal & Hepatic Systems | hyperuricemia | hemochromatosis | Diabetes & Metabolic Disorders | iron | heme overload | Cell Homeostasis & Autophagy | hfe-null mouse | Molecular Bases of Health & Disease | ABCG2 | p53
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5. Full Text Reduced phenotypic expression in genetic hemochromatosis with time: Role of exposure to non-genetic modifiers
by Deugnier, Yves and Morcet, Jeff and Lainé, Fabrice and Hamdi-Roze, Houda and Bollard, Anne-Sophie and Guyader, Dominique and Moirand, Romain and Bardou-Jacquet, Edouard
Journal of hepatology, ISSN 0168-8278, 01/2019, Volume 70, Issue 1, pp. 118 - 125
Phenotype | Tobacco | Genotype | Evolution | Alcohol | HFE hemochromatosis | BMI | Gastroenterology & Hepatology | Life Sciences & Biomedicine | Science & Technology | Genetic Testing | Prospective Studies | Follow-Up Studies | Humans | Middle Aged | Child, Preschool | Infant | Male | Hemochromatosis - metabolism | Young Adult | DNA Mutational Analysis | Aged, 80 and over | Adult | Female | Retrospective Studies | Child | Hemochromatosis - genetics | Infant, Newborn | Hemochromatosis Protein - metabolism | DNA - genetics | Hemochromatosis Protein - genetics | Adolescent | Aged | Hemochromatosis - diagnosis | Mutation | Transferrin | Body weight | Liver | Ferritin | Tobacco smoking | Arthritis | Males | Risk factors | Cofactors | Genetic screening | Genetic factors | Diagnosis | Pancreas | Hemochromatosis | Diabetes mellitus | Fatigue | Homozygotes | Cirrhosis | Fibrosis | HFE protein | Diabetes | Females | Hepcidin | Smoking | Index Medicus
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6. Full Text Hemochromatosis and Iron-Overload Screening in a Racially Diverse Population
by Adams, Paul C and Reboussin, David M and Barton, James C and McLaren, Gordon D and McLaren, Christine E and Eckfeldt, John H and Dawkins, Fitzroy W and Acton, Ronald T and Harris, Emily L and Gordeuk, Victor R and Leiendecker-Foster, Catherine and Speechley, Mark and Snively, Beverly M and Holup, Joan L and Thomson, Elizabeth and Sholinsky, Phyliss and HEIRS Study Res Investigators and Hemochromatosis and Iron Overload Screening (HEIRS) Study Research Investigators
The New England journal of medicine, ISSN 0028-4793, 04/2005, Volume 352, Issue 17, pp. 1769 - 1778
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Biological and medical sciences | Metabolic diseases | General aspects | Medical sciences | Other metabolic disorders | Metals (hemochromatosis...) | United States - epidemiology | Diabetes Complications | Iron Overload - ethnology | Hemochromatosis - ethnology | Hemochromatosis Protein | Humans | Male | Iron | Iron Overload - blood | Hemochromatosis - complications | Ferritins - blood | Liver Diseases - etiology | Arthritis - etiology | Female | Hemochromatosis - genetics | Iron Overload - genetics | Membrane Proteins - genetics | Gene Frequency | Genotype | Logistic Models | Histocompatibility Antigens Class I - genetics | Transferrin - analysis | Homozygote | Heart Diseases - etiology | Phenotype | Iron Overload - epidemiology | Sex Distribution | Mutation | Iron metabolism disorders | Genetic aspects | Hemochromatosis | Diagnosis | Anemia | Older people | Hispanics | Index Medicus | Abridged Index Medicus
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