Results 131 to 140 of about 998 (161)
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THE LIVER IN PORPHYRIA CUTANEA TARDA
Annals of Internal Medicine, 1960Excerpt The porphyrias belong to the group of diseases that have been called inborn errors of metabolism.
J, WALDENSTROM, B, HAEGER
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The inheritance of porphyria cutanea tarda
International Journal of Biochemistry, 1980Abstract The porphyrin excretion of 203 blood relatives of 46 PCT patients was analyzed. 48 relatives (23.64%) showed abnormalities of porphyrin pattern and 19 of them suffered overt PCT. On the contrary, in some families no one relative showed any clinical or biochemical abnormality. These data confirm the existence of two forms of PCT: the sporadic
R, Enríquez de Salamanca +5 more
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OBSERVATIONS ON PORPHYRIA CUTANEA TARDA
Archives of Dermatology, 1954PORPHYRIA is a relatively rare, inherited fault of pyrrole metabolism which produces a wide variety of clinical symptoms from time to time or remains latent for years or for life. It is characterized by the excretion of abnormal kinds and amounts of porphyrins, chiefly uroporphyrin and its precursors.
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Porphyria Cutanea Tarda and Scleroderma
JCR: Journal of Clinical Rheumatology, 2004Mukta, Panda +2 more
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Increased mortality in patients with porphyria cutanea tarda—A nationwide cohort study
Journal of the American Academy of Dermatology, 2020Anne Lindegaard Christiansen +2 more
exaly
Increased frequency of the haemochromatosis Cys282Tyr mutation in sporadic porphyria cutanea tarda
Lancet, The, 1997A G Roberts +2 more
exaly