Results 81 to 90 of about 998 (161)

Genetic hemochromatosis in italian patients with porphyria cutanea tarda : possible explanation for iron overload

open access: yes, 1996
BACKGROUND/AIMS: Mild to moderate iron overload is found in most patients with porphyria cutanea tarda. This study aimed to evaluate whether iron overload in patients with porphyria cutanea tarda is related to the presence of a coexistent genetic ...
A.L. Fracanzani   +17 more
core   +1 more source

Skin changes in chronic kidney disease

open access: yesPrzegląd Dermatologiczny, 2017
Chronic kidney disease causes skin changes which may sometimes be the first sign of kidney failure. Specific skin changes include acquired perforating dermatosis, porphyria cutanea tarda, pseudoporphyria, calcinosis and nephrogenic systemic fibrosis. The
Joanna M. Przepiórka-Kosińska   +4 more
doaj   +1 more source

Laudatio zum 100. Geburtstag von Prof. Dr. Klaus Steigleder

open access: yes
JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 23, Issue 3, Page 409-410, March 2025.
Hans F. Merk   +2 more
wiley   +1 more source

Sclerodermoid lesions in a patient with multiple transplants and porphyria cutanea tarda [PDF]

open access: yes, 2015
Patients with chronic graft versus host disease may exhibit a range of sclerotic features. Herein we present a patient with confirmed porphyria cutanea tarda who subsequently developed chronic graft versus host ...
Fox, Lindy P   +3 more
core   +1 more source

Role of Vitamin C in Skin Diseases

open access: yesFrontiers in Physiology, 2018
Vitamin C (ascorbic acid) plays an important role in maintaining skin health and can promote the differentiation of keratinocytes and decrease melanin synthesis, leading to antioxidant protection against UV-induced photodamage.
Kaiqin Wang   +5 more
doaj   +1 more source

Clinically Important Features of Porphyrin and Heme Metabolism and the Porphyrias

open access: yesMetabolites, 2014
Heme, like chlorophyll, is a primordial molecule and is one of the fundamental pigments of life. Disorders of normal heme synthesis may cause human diseases, including certain anemias (X-linked sideroblastic anemias) and porphyrias.
Siddesh Besur   +3 more
doaj   +1 more source

Pregnancy and porphyria cutanea tarda

open access: yesActa Dermato-Venereologica, 1984
A 31-year-old woman developed typical clinical and laboratory signs of PCT at the end of her second pregnancy coincident with the summer season. She had elevated liver function values without history of alcoholism, hepatitis or chemical liver damage. She had taken oral contraceptive only before her first pregnancy which was normal. Her hormone analytic
openaire   +2 more sources

A Mutation (G281E) of the Human Uroporphyrinogen Decarboxylase Gene Causes Both Hepatoerythropoietic Porphyria and Overt Familial Porphyria Cutanea Tarda: Biochemical and Genetic Studies on Spanish Patients

open access: yes, 1995
Hepatoerythropoietic porphyria is a severe cutaneous porphyria caused by deficiency of uroporphyrinogen decarboxylase and is considered to be the homozygous form of familial (type II) porphyria cutanea tarda.
Roberts, Andrew G.   +11 more
core   +1 more source

Hepatitis C virus infection and non-Hodgkin’s lymphoma: a review and case report of nine patients

open access: yesAnnals of Hepatology, 2006
The role of hepatitis C virus (HCV) is well established in the development of chronic hepatitis, cirrhosis and hepatic carcinoma, as well as in mixed type II cryoglobulinemia, membranoproliferative glomerulonephritis (MPGN) and porphyria cutanea tarda ...
Javier Lizardi-Cervera   +6 more
doaj   +1 more source

High prevalence of hepatitis C virus type 1b in Italian patients with Porphyria cutanea tarda

open access: yes, 1997
BACKGROUND: A strong association between sporadic porphyria cutanea tarda and chronic hepatitis C virus infection was recently described in Italy, France and Spain.
A.L. Fracanzani   +7 more
core  

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