Page last updated: 2024-10-20

porphobilinogen and Hemochromatosis

porphobilinogen has been researched along with Hemochromatosis in 2 studies

Hemochromatosis: A disorder of iron metabolism characterized by a triad of HEMOSIDEROSIS; LIVER CIRRHOSIS; and DIABETES MELLITUS. It is caused by massive iron deposits in parenchymal cells that may develop after a prolonged increase of iron absorption. (Jablonski's Dictionary of Syndromes & Eponymic Diseases, 2d ed)

Research Excerpts

ExcerptRelevanceReference
"This review focuses on hepatic porphyrias, which include acute intermittent porphyria (AIP), variegate porphyria (VP), hereditary coproporphyria (HCP), aminolevulinic acid dehydratase deficiency porphyria (ADP), and porphyria cutanea tarda (PCT)."2.53Hepatic porphyria: A narrative review. ( Arora, S; Kodali, S; Singal, AK; Young, S, 2016)

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's2 (100.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Olcay, L1
Hazirolan, T1
Yildirmak, Y1
Erdemli, E1
Terzi, YK1
Arda, K1
Oztürkmen, S1
Akyay, A1
Kaymak-Cihan, M1
Biçakçi, Z1
Bal, C1
Arora, S1
Young, S1
Kodali, S1
Singal, AK1

Reviews

1 review available for porphobilinogen and Hemochromatosis

ArticleYear
Hepatic porphyria: A narrative review.
    Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology, 2016, Volume: 35, Issue:6

    Topics: Acute Disease; Alcoholism; Biomarkers; Glucose; Hemin; Hemochromatosis; Hepatitis C; HIV Infections;

2016

Trials

1 trial available for porphobilinogen and Hemochromatosis

ArticleYear
Biochemical, radiologic, ultrastructural, and genetic evaluation of iron overload in acute leukemia and iron-chelation therapy.
    Journal of pediatric hematology/oncology, 2014, Volume: 36, Issue:4

    Topics: Adolescent; Aminolevulinic Acid; Bone Marrow; Bone Marrow Cells; Child; Female; Ferritins; Hemochrom

2014