A megváltozott vasanyagcsere genetikai hátterének vizsgálata krónikus májbetegségekben = The genetic background of the changes of iron metabolism in different chronic hepatic disorders [PDF]
50 porphyria cutanea tardás (PCT) beteg klinikai és genetikai adatainak statisztikai értékelése történt. A HCV infekció 44%-os, ez közepesen gyakorinak mondható a nemzetközi adatokhoz viszonyítva.
Debreceni, András +4 more
core
Localized Scleroderma Associated with Chronic Hepatitis C
Hepatitis C virus has been associated with various skin conditions, such as porphyria cutanea tarda and lichen planus, as an example. The objective of this paper is based on the description of a case of localized morphea, which came years after the ...
Felipe Ladeira de Oliveira +3 more
doaj +1 more source
Challenge of liver disease in systemic lupus erythematosus: Clues for diagnosis and hints for pathogenesis [PDF]
Systemic lupus erythematosus (SLE) encompass a broad spectrum of liver diseases. We propose here to classify them as follows: (1) immunological comorbilities (overlap syndromes); (2) non-immunological comorbilities associated to SLE; and (3) a putative ...
Bessone, Fernando +2 more
core +2 more sources
Practical recommendations for biochemical and genetic diagnosis of the porphyrias
Abstract The porphyrias are a group of rare inborn errors of metabolism associated with various clinical presentations and long‐term complications, making them relevant differential diagnoses to consider for many clinical specialities, especially hepatologists, gastroenterologists and dermatologists.
Aasne K. Aarsand +4 more
wiley +1 more source
Ferritin accumulation and uroporphyrin crystal formation in hepatocytes of C57BL/10 mice: A time-course study [PDF]
To establish the time-sequence relationship between ferritin accumulation and uroporphyrin crystal formation in livers of C57BL/10 mice, a biochemical, morphological and morphometrical study was performed.
Bruijn, W.C. (Wim) de +5 more
core +2 more sources
Hereditary Hemochromatosis Unmasked by Yersiniosis: Report of Three Cases
ABSTRACT Yersiniosis has a causal relationship with hereditary hemochromatosis (HH). Physicians should have a high index of suspicion for the diagnosis of HH when approaching a patient with yersiniosis in the setting of high ferritin levels and increased iron saturation. Yersiniosis serves as a precursor for the diagnosis of HH.
Karam Karam, Elias Fiani
wiley +1 more source
Distribution and quantitation of skin iron in primary haemochromatosis: correlation with total body iron stores in patients undergoing phlebotomy [PDF]
Measurement of the concentration of iron in the skin, if correlated with total body iron stores, may enable better informed decisions on when to initiate, change or stop therapy in hereditary heamochromatosis.
Barreiros, M. Alexandra +8 more
core +1 more source
Erythropoietic protoporphyrias: Pathogenesis, diagnosis and management
Abstract The erythropoietic protoporphyrias consist of three ultra‐rare genetic disorders of the erythroid heme biosynthesis, including erythropoietic protoporphyria (EPP1), X‐linked protoporphyria (XLEPP) and CLPX‐protoporphyria (EPP2), which all lead to the accumulation of protoporphyrin IX (PPIX) in erythrocytes.
Anna‐Elisabeth Minder +4 more
wiley +1 more source
Abstract Background The field of artificial intelligence is rapidly evolving. As an easily accessible platform with vast user engagement, the Chat Generative Pre‐Trained Transformer (ChatGPT) holds great promise in medicine, with the latest version, GPT‐4, capable of analyzing clinical images.
Jacob P. S. Nielsen +3 more
wiley +1 more source
Timing for treatment of HCV recurrence after liver transplantation: the earlier the better. [PDF]
HCV is the leading cause of death from liver disease and is the most common indication for a liver transplantation. Although HCV is a widespread health problem, disease management is particularly challenging in several key subpopulations, including liver
Burra, Patrizia +2 more
core +1 more source

