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H63D CG genotype of HFE is associated with increased risk of sporadic amyotrophic lateral sclerosis in a single population

Journal of integrative neuroscience, 2020-09, Vol.19 (3), p.495-499

2020

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Hereditary hemochromatosis caused by a C282Y/H63D mutation in the HFE gene: A case report

Heliyon, 2024-04, Vol.10 (7), p.e28046, Article e28046

2024

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Iron Metabolism in Cancer Progression

International journal of molecular sciences, 2020-03, Vol.21 (6), p.2257

2020

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Screening for Hereditary Hemochromatosis in Newly Referred Diabetes Mellitus

American journal of medicine open, 2023-12, Vol.10, p.100046, Article 100046

2023

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Effect of homeostatic iron regulator protein gene mutation on Wilson's disease clinical manifestation: original data and literature review

International journal of neuroscience, 2022-09, Vol.132 (9), p.894-900

2022

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HFE Genotype, Parenchymal Iron Accumulation, and Liver Fibrosis in Patients With Nonalcoholic Fatty Liver Disease

Gastroenterology (New York, N.Y. 1943), 2010-03, Vol.138 (3), p.905-912

2010

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Hemocromatosis y rendimiento deportivo: una revisión sistemática

Revista andaluza de medicina del deporte, 2020-10, Vol.14 (1), p.53-57

2020

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HFE mutations and risk of coronary heart disease in middle-aged women

European journal of clinical investigation, 2006-10, Vol.36 (10), p.682-690

2006

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Dysmetabolic iron overload syndrome and its relationship with HFE gene mutations and with liver steatosis

Digestive and liver disease, 2020-06, Vol.52 (6), p.683-685

2020

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Erythropoietin Concentration in Boys With p.His63Asp Polymorphism of the HFE Gene

Journal of pediatric hematology/oncology, 2022-01, Vol.44 (1), p.e68

2022

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Impaired Bone Microarchitecture in Patients with Hereditary Hemochromatosis and Skeletal Complications

Calcified tissue international, 2020-05, Vol.106 (5), p.465-475

2020

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Características radiológicas de la artropatía microcristalina asociada a hemocromatosis hereditaria con mutación homocigota C282Y

Reumatología clinica, 2020-03, Vol.16 (2), p.122-124

García García, Miriam

2020

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Hämochromatose

Zeitschrift für Rheumatologie, 2015-09, Vol.74 (7), p.609-617

2015

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Serum hepcidin levels, iron status, and HFE gene alterations during the first year of life in healthy Spanish infants

Annals of hematology, 2018-06, Vol.97 (6), p.1071-1080

2018

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Association between hereditary hemochromatosis and hepatocellular carcinoma: a comprehensive review

Hepatoma research, 2020-03, Vol.2020 (3), p.1-14

2020

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MUTATIONS H1069Q OF ATP7B GENE AND C282Y AND H63D OF HFE GENE IN PERSONS WITH HEPATOBILARY DISEASES OF UNDEFINED GENESIS

Visnyk problem biolohiï i medyt︠s︡yny, 2019-04, Vol.1 (2), p.224-229

2019

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Non- HFE mutations in haemochromatosis in China: combination of heterozygous mutations involving HJV signal peptide variants

Journal of medical genetics, 2018-10, Vol.55 (10), p.650

2018

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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, 2021-09, Vol.22 (9), p.2837-2845

2021

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Clinical and genetic predictors of cardiac dysfunction assessed by echocardiography in patients with hereditary hemochromatosis

The international journal of cardiovascular imaging, 2024-01, Vol.40 (1), p.45-53

2024

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HFE-associated hereditary hemochromatosis

Genetics in medicine, 2009-05, Vol.11 (5), p.307-313

2009

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Radiological features of crystal-induced arthropathy associated with hereditary hemochromatosis with homozygous C282Y mutation

Reumatología clinica (Barcelona), 2020-03, Vol.16 (2), p.122-124

García García, Miriam

2020

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Haemochromatosis: The bone and the joint

Best practice & research. Clinical rheumatology, 2011, Vol.25 (5), p.649-664

2011

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Association of HFE Gene Mutations With Serum Ferritin Level and Heart and Liver Iron Overload in Patients With Transfusion-dependent Beta-Thalassemia

Journal of pediatric hematology/oncology, 2021-01, Vol.43 (1), p.e26

2021

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Hereditary hemochromatosis associated with the development of liver cirrhosis

Jornal brasileiro de patologia e medicina laboratorial, 2021, Vol.57

2021

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The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22

Nature genetics, 2000-05, Vol.25 (1), p.14-15

2000

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H63D CG genotype of HFE is associated with increased risk of sporadic amyotrophic lateral sclerosis in a single population

Hereditary hemochromatosis caused by a C282Y/H63D mutation in the HFE gene: A case report

Iron Metabolism in Cancer Progression

Screening for Hereditary Hemochromatosis in Newly Referred Diabetes Mellitus

Effect of homeostatic iron regulator protein gene mutation on Wilson's disease clinical manifestation: original data and literature review

HFE Genotype, Parenchymal Iron Accumulation, and Liver Fibrosis in Patients With Nonalcoholic Fatty Liver Disease

Hemocromatosis y rendimiento deportivo: una revisión sistemática

HFE mutations and risk of coronary heart disease in middle-aged women

Dysmetabolic iron overload syndrome and its relationship with HFE gene mutations and with liver steatosis

Erythropoietin Concentration in Boys With p.His63Asp Polymorphism of the HFE Gene

Impaired Bone Microarchitecture in Patients with Hereditary Hemochromatosis and Skeletal Complications

Características radiológicas de la artropatía microcristalina asociada a hemocromatosis hereditaria con mutación homocigota C282Y

Hämochromatose

Serum hepcidin levels, iron status, and HFE gene alterations during the first year of life in healthy Spanish infants

Association between hereditary hemochromatosis and hepatocellular carcinoma: a comprehensive review

MUTATIONS H1069Q OF ATP7B GENE AND C282Y AND H63D OF HFE GENE IN PERSONS WITH HEPATOBILARY DISEASES OF UNDEFINED GENESIS

Non- HFE mutations in haemochromatosis in China: combination of heterozygous mutations involving HJV signal peptide variants

Significance of Hereditary Hemochromatosis Gene (HFE) Mutations in Chronic Hepatitis C and Hepatocellular Carcinoma Patients in Egypt: A Pilot Study

Clinical and genetic predictors of cardiac dysfunction assessed by echocardiography in patients with hereditary hemochromatosis

HFE-associated hereditary hemochromatosis

Radiological features of crystal-induced arthropathy associated with hereditary hemochromatosis with homozygous C282Y mutation

Haemochromatosis: The bone and the joint

Association of HFE Gene Mutations With Serum Ferritin Level and Heart and Liver Iron Overload in Patients With Transfusion-dependent Beta-Thalassemia

Hereditary hemochromatosis associated with the development of liver cirrhosis

The gene TFR2 is mutated in a new type of haemochromatosis mapping to 7q22

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