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Last Updated: 03/06/2025

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Found 8963 publications

A case of type 2A juvenile hereditary hemochromatosis

A case of type 2A juvenile hereditary hemochromatosis

Journal: Zhonghua xin xue guan bing za zhi
Published: January 14, 2025

Arthropathy as the first manifestation of undiagnosed hemochromatosis: a case report on an unusual course

Arthropathy as the first manifestation of undiagnosed hemochromatosis: a case report on an unusual course

Journal: Deutsche medizinische Wochenschrift (1946)
Published: January 14, 2025

Iron Overload in Histidine-to-Aspartic Acid Substitution at 63 (H63D) Gene Heterozygous Hereditary Hemochromatosis With Erythrocytosis: A Case Report.

Iron Overload in Histidine-to-Aspartic Acid Substitution at 63 (H63D) Gene Heterozygous Hereditary Hemochromatosis With Erythrocytosis: A Case Report.

Journal: Cureus
Published: December 24, 2024

Hepcidin as a therapeutic target in iron overload.

Hepcidin as a therapeutic target in iron overload.

Journal: Expert opinion on therapeutic targets
Published: December 16, 2024

Mapping a Decade of Research: Bibliometric Analysis of Iron Overload in Chronic Kidney Disease.

Mapping a Decade of Research: Bibliometric Analysis of Iron Overload in Chronic Kidney Disease.

Journal: Cureus
Published: December 15, 2024

Dofetilide unmasks long QT in a patient presenting with atrial fibrillation-induced cardiomyopathy.

Dofetilide unmasks long QT in a patient presenting with atrial fibrillation-induced cardiomyopathy.

Journal: HeartRhythm case reports
Published: December 12, 2024

Mortality and risk of diabetes, liver disease, and heart disease in individuals with haemochromatosis HFE C282Y homozygosity and normal concentrations of iron, transferrin saturation, or ferritin: prospective cohort study.

Mortality and risk of diabetes, liver disease, and heart disease in individuals with haemochromatosis HFE C282Y homozygosity and normal concentrations of iron, transferrin saturation, or ferritin: prospective cohort study.

Journal: BMJ (Clinical research ed.)
Published: December 09, 2024

Non-expressing homozygous C282Y carriers and haemochromatosis.

Non-expressing homozygous C282Y carriers and haemochromatosis.

Journal: BMJ (Clinical research ed.)
Published: December 09, 2024

Porphyria cutanea tarda: a unique iron-related disorder.

Porphyria cutanea tarda: a unique iron-related disorder.

Journal: Hematology. American Society of Hematology. Education Program
Published: December 07, 2024

Diagnosis and management of hereditary hemochromatosis: lifestyle modification, phlebotomy, and blood donation.

Diagnosis and management of hereditary hemochromatosis: lifestyle modification, phlebotomy, and blood donation.

Journal: Hematology. American Society of Hematology. Education Program
Published: December 07, 2024

Analysis of clinical, gene mutation characteristics, and treatment prognosis of type 2A hereditary hemochromatosis in the Chinese population

Analysis of clinical, gene mutation characteristics, and treatment prognosis of type 2A hereditary hemochromatosis in the Chinese population

Journal: Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology
Published: December 03, 2024

A case report of mild hereditary hemochromatosis caused by HAMP gene mutation

A case report of mild hereditary hemochromatosis caused by HAMP gene mutation

Journal: Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology
Published: November 28, 2024
Showing 1-12 of 8,963

Last Updated: 03/06/2025