Hereditary Hemochromatosis — A New Look at an Old Disease

A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosis

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Hepcidin, a urinary antimicrobial peptide synthesized in the liver

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A New Mouse Liver-specific Gene, Encoding a Protein Homologous to Human Antimicrobial Peptide Hepcidin, Is Overexpressed during Iron Overload

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Hepcidin, a key regulator of iron metabolism and mediator of anemia of inflammation

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Hepcidin, a putative mediator of anemia of inflammation, is a type II acute-phase protein

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LEAP-1, a novel highly disulfide-bonded human peptide, exhibits antimicrobial activity

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Survival and Causes of Death in Cirrhotic and in Noncirrhotic Patients with Primary Hemochromatosis

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Mutations in HFE2 cause iron overload in chromosome 1q–linked juvenile hemochromatosis

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Mutant antimicrobial peptide hepcidin is associated with severe juvenile hemochromatosis

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Occurrence of Hereditary Hemochromatosis Among β- Thalassemia Intermediate and β -Thalassemia Minor Subjects In Gaza Strip - Palestine

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Diseases of Mineral Metabolism

Szeimies, R., & Dirschka, T. (2020) · Springer eBooks · doi:10.1007/978-3-662-58713-3_96-1 · Cited by 1

Iron-Regulatory Function of Hepcidin in the Channel Catfish and Western Clawed Frog

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Metabolic Diseases

Tendler, D. A. (2006) · doi:10.1002/9780470751541.ch11 · Cited by 1

Ironed Out: A Bacterial Siderophore Primer

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Chronic iron intoxication as an occupational disease

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Cirrhosis and Portal Hypertension: Pathologic Aspects

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Storage and Deposition Diseases

Gordon, D. A. (2008) · Springer eBooks · doi:10.1007/978-0-387-68566-3_68 · Cited by 1

Hemochromatosis

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Directions for clinical practice improvement in HFE gene mutation testing

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Caracterização fenotípica e genotipagem HFE em portadores de doença hepática crônica com sobrecarga de ferro

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Dietary advice in HFE-hemochromatosis

van Doorn, G. M., & Gosselink, I. M. G. (2012)

Genetic polymorphisms in bovine ferroportin are associated with beef iron content

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Estudio para el mejoramiento de la calidad analítica en la determinación de hierro sérico en laboratorios de análisis bioquímicos

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Micronutrients, Trace Elements

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Non-Neoplastic Hepatobiliary Disease

Saxena, R., Blaszyk, H., & Batts, K. P. (2006) · Humana Press eBooks · doi:10.1007/978-1-60327-173-8_37

Cambios en el transportador de hierro DMT-1 en yeyuno proximal de pacientes obesos sometidos a bypass gástrico

Mañaricúa, Z., & Fabiola, R. (2011) · Universidad de Chile

Iron Homeostasis: Hepcidin Regulation

Camaschella, C., & Silvestri, L. (2004) · Wiley eBooks · doi:10.1002/9781119951438.eibc2131

Metabolic Liver Disease

Taylor, R. M., & Corbani, T. (2009) · doi:10.1002/9781444322682.ch12

Metabolic Liver Diseases

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FAT1 expression and function in chronic liver disease and hepatocellular carcinoma

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Lack of Transferrin Receptor 1 in the Heart Causes Lethal Cardiomyopathy and Disruption of Mitophagy in Mice

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Vitamin B2 als Antioxidans : Messung von Vitamin B2 und seinen Coenzymformen in Proben von eisenüberladenen Patienten und eisenüberladenen Versuchstieren

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Porphyria Cutanea Tarda and HFE Gene Mutations in Argentina

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ESTUDO DO CONTROLO PÓS-TRANSCRICIONAL DA HEMOJUVELINA E SUA INFLUÊNCIA NA HOMEOSTASE DO FERRO

Tomé, F. (2010) · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT)

Molecular-Genetic Testing in Hepatocellular Carcinoma and Its Premalignant Conditions

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Hepatopatías metabólicas

Monteiro, E., Freire, A., Martins, A., & Barroso, E. (2008) · Elsevier eBooks · doi:10.1016/b978-84-8086-310-0.50038-5

Der Einfluss der Hämochromatose (HFE)-Gen-Varianten auf die Progression chronischer Lebererkrankungen und die Entwicklung eines hepatozellulären Karzinoms

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Um caso de hemocromatose primária

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Cuantificación de hierro hepático por espectrometría de absorción atómica con vaporización electrotérmica

Véliz, M. A., Balverdi, M. D. P., Rodríguez, R. R., Villamil, F., & Sales, A. M. (2012) · Redalyc (Universidad Autónoma del Estado de México)

Zebrafish Models of Heme Synthesis and Iron Metabolism

Fraenkel, P. G. (2011) · Humana Press eBooks · doi:10.1007/978-1-60327-485-2_31

Dietary factors influencing non-heme iron absorption

Bonsmann, S. S. G. (2007) · Repository for Publications and Research Data (ETH Zurich) · doi:10.3929/ethz-a-005332658

Enfermedades hep?ticas de origen metab?lico

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MENDELIAN GENETIC TRAITS

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Investigations of Potential Modifier Genes in Hereditary Haemochromatosis

Brew, J. (2010) · ANU Open Research (Australian National University) · doi:10.25911/5d7a265387fd8

Analysis of genes implicated in iron regulation in individuals presenting with primary iron overload in the South African population

Booley, F. (2007) · SUNScholar (Stellenbosch University)

In-vitro-Diagnostik systemischer Autoimmunkrankheiten

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Cell‐specific location of Hfe

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A presentation of stage 2 HFE haemochromatosis in a young woman with epilepsy

Mougiou, A., Lempousi, D., & Καρακάντζα, Μ. (2007) · European Journal of Internal Medicine · doi:10.1016/j.ejim.2007.10.007

Iron overload (with attention to genetic testing and diagnosis/management of HFE wild type patients)

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Efeito da tibolona na morfologia do músculo esquelético, nas enzimas hepáticas e no nível sérico de glicose em ratas castradas

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A complex clinical case linking genetic disorders and infectious disease

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Fenotipo, genotipo e historia de las enfermedades de sobrecarga de hierro

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Muerte súbita y hemocromatosis

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Hemocromatosis. nuevos aspectos clínicos y diagnósticos

Altés, A. (2008) · Gaceta Médica de Bilbao · doi:10.1016/s0304-4858(08)74633-x

Biochemische und genetische Analytik - Den Verdacht auf eine hereditäre Hämochromatose früh und nichtinvasiv bestätigen

Steiner, M. L., & von Ahsen, N. (2005) · Der Klinikarzt · doi:10.1055/s-2005-865190

Hereditary haemochromatosis in a man of Pakistani descent

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Enfermedades hepáticas de origen metabólico

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Diabète et hémochromatose

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Synchrotron X-ray microscopy and spectroscopy analysis of iron in hemochromatosis liver and intestines

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Growth in Hemochromatosis

Nagayoshi, Y. (2011) · Springer eBooks · doi:10.1007/978-1-4419-1795-9_125

Association of HFE Gene Mutations With Liver Cirrhosis Depends on Induction of Iron Homeostasis Disturbances

Sikorska, K. (2012) · Hepatitis Monthly · doi:10.5812/hepatmon.5128

Estudo de efeito da superação genética da via de sinalização do Nrf2 num modelo animal de sobrecarga de ferro espontânea (Hfe knock-out)

Pontes, C. N. R., & Caldas, G. (2013)

Letter by Ryan et al Regarding Article, “Do Hemochromatosis Mutations Protect Against Iron-Mediated Atherogenesis?”

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Session 2: Personalised nutrition Genetic variation and disease risk: new advances

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Osteoporosis in an elderly man as interplay of multiple diseases

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Hereditary Hemochromatosis and Iron Overload

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Hepatocellular Carcinoma Arising in the Non-viral, Non-alcoholic Liver

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Treatments for hereditary haemochromatosis: a network meta-analysis

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NEUROSCIENCES AND NEUROANAESTHESIA Regional cerebral metabolic rate (positron emission tomography) during inhalation of nitrous oxide 50% in humans

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Iron Excess and Cancer

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Storage Disorders in Hematology

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Hereditary hemochromatosis and alcohol: pathogenic synergism - a clinical case

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Lack of association of C282Y and H63D mutations in the hemochromatosis (HFE) gene with diabetes mellitus type 2 in a case-control study of women in Brazil

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Quando o Índice Bispectral (BIS) Pode Fornecer Valores Espúrios* When the Bispectral Index (Bis) can Give False Results*

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Einfluss von Eisenüberladung auf Fettsäureprofile in Leber, Fett und Plasma von Ratten

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Hämatologie, Onkologie und Gerinnungsstörungen

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Iron overload as a consequence of red blood cell transfusions in patients with hematological diseases

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UNIVERSIDADE FEDERAL DO RIO GRANDE DO SUL FACULDADE DE MEDICINA PROGRAMA DE PÓS-GRADUAÇÃO EM MEDICINA: CIÊNCIAS MÉDICAS USO DE HIDRATO DE CLORAL PARA SEDAÇÃO EM UNIDADE DE TRATAMENTO INTENSIVO PEDIÁTRICA: INDICAÇÕES, EFEITOS ADVERSOS E FATORES DE RISCO ASSOCIADOS

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COMPARISON OF ATHEROSCLEROTIC RISK FACTORS BETWEEN DONORS WITH ASSOCIATED ACUTE NON-HEMOLYTIC TRANSFUSION REACTIONS AND DONORS WITHOUT ASSOCIATION

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Hypersidéroses de l'enfant

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Hereditary hemochromatosis in a male patient with TFR2 (1861_1872del12) gene mutation: the second biopsy 19 years after diagnosis

Kawanaka, M., Nakamura, J., Oka, Y., Kimura, T., Goto, D., Yamato, R., Nishino, K., Suehiro, M., Kawamoto, H., Yamada, G., et al. (2011) · Kanzo · doi:10.2957/kanzo.52.745

Genetisch bedingte Hämochromatose

Stremmel, W. (2007) · Die Gastroenterologie · doi:10.1007/s11377-007-0074-9

Syndrome endocrinien de l'hémochromatose idiopathique

Sonnet, E., & Kerlan, V. (2006) · EMC - Endocrinologie - Nutrition · doi:10.1016/s1155-1941(06)40972-0

Hepcidin knockout mice as a model of iron-overload associated liver disease

Lunová, M., Vaulont, S., Haybaeck, J., Lackner, K., Adler, G., & Strnad, P. (2011) · Zeitschrift für Gastroenterologie · doi:10.1055/s-0030-1269571

of Hepatic Fat and Iron with Magnetic Resonance Imaging

Wells, S. A. (2014)

Whole genome analysis of an extended pedigree with Prader–Willi Syndrome, hereditary hemochromatosis, and dysautonomia-like symptomsPreprint

Fang, H., Wu, Y., Yoon, M. S., Jiménez-Barrón, L. T., O'Rawe, J., Highnam, G., Mittelman, D., & Lyon, G. J. (2015) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/019182

El nuevo paradigma de la hemocromatosis neonatal: hepatitis fetal aloinmunitaria The new paradigm of neonatal hemochromatosis: fetal alloimmune hepatitis

Justine, S. (2012)

Hemocromatose em tucano - Ramphastos toco - Relato de caso Hemochromatosis in toucan - Ramphastos toco - case report

Vieira, F. D. T., Hardt, I., Rangel, M. C. V., Flecher, M. C., & Rossi, J. L. (2015)

Disorders of Iron MetabolismProgress in Hematology

Domenico, I. D., Ward, D. M., Musci, G., & Kaplan, J. (2006)

Could 18F-FDG PET Be a Diagnostic Tool for Hemochromatosis?

Zanella, I., Bertagna, F., & Biasiotto, G. (2015) · Clinical Nuclear Medicine · doi:10.1097/rlu.0000000000001070

Hemokromatosia. alderdi kliniko eta diagnostiko berriak

Altés, A. (2008) · Gaceta Médica de Bilbao

Genetisch bedingte Stoffwechselerkrankungen des Gastrointestinaltrakts

Stremmel, W., Merle, U., Stölzel, U., & Manfred Otto, D. O. S. S. (2015) · Springer eBooks · doi:10.1007/978-3-642-14301-4_41

Algoritmos de laboratorio para el estudio del estado del hierro Laboratory algorithms for the study of iron status Algoritmos de laboratório para o estudo do estado do ferro

Cailliat, M. C., & Fink, N. E. (2013)

Metabolic Genetic DisordersWith Prominent Skin Findings

Mizelle, C. B., & Goldsmith, L. A. (2007) · Humana Press eBooks · doi:10.1007/978-1-59259-963-9_109

Role of iron in ethanol derived hepatic stress

Thornton, J. A. (2013)

Investigations on potential digenic HAMP (hepcidin) and HFE haemochromatosis gene mutations in the development of iron overload in Irish patients with dilated cardiomyopathy

Jereza, N. A. (2016) · UWE Research Repository (UWE Bristol)

REVISTA ARGENTINA de DERMATOLOGÍA REVISTA ARGENTINA de DERMATOLOGÍA

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Valutazione del rischio genetico

Korf, B. R. (2009) · Springer eBooks · doi:10.1007/978-88-470-1150-2_14

Metabolic Liver Disease

Sánchez, W. (2014) · doi:10.1093/med/9780199373338.003.0034

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Hes, F. J., & Breuning, M. H. (2010) · Bohn Stafleu van Loghum eBooks · doi:10.1007/978-90-313-7361-1_4

Liver Transplantation for Hematological Disorders

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Iron inhibits replication of infectious hepatitis C virus in permissive Huh7.5.1 cells

Davis, L., Mortimer, S., & Lynn, B. C. D. (2010)

Contiguous gene deletion in HFE2 region (1q21.1) and pathogenic HFE2 mutations in a Chinese hereditary hemochromatosis patient

Wang, Y., Du, Y., Liu, G., Guo, S., Yang, N., Hou, B., Jiang, X., Han, B., Chang, Y., & Nie, G. (2016) · Gene Reports · doi:10.1016/j.genrep.2016.10.010

Investigations into the role of zinc and zinc transporters in the pathogenesis of type 2 diabetes in db/db mice

Bosco, M. D. (2015) · Adelaide Research & Scholarship (AR&S) (University of Adelaide)

Metabolic and Genetic Liver Diseases: Hemochromatosis

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Regulation of transferrin receptor 2 stability and trafficking in hepatoma cells

Johnson, M. B. (2006) · doi:10.6083/m4wm1bpk

Clinical-Pathological Conference Series from the Medical University of Graz

Fabian, E., Schiller, D., Graninger, W. B., Langner, C., Frei, J., Schoellnast, H., Alibegovic, V., Stauber, R. E., Schoefl, R., & Krejs, G. J. (2016) · Wiener klinische Wochenschrift · doi:10.1007/s00508-016-1010-0

Revisiting Hereditary Hemochromatosis: Current Concepts and Progress

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Advances in pathophysiology, diagnosis and management of hereditary hemochromatosis

Zhang, Z. (2012) · Shengming kexue

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Molecular insights into the pathogenesis of hereditary haemochromatosis

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