Results 201 to 210 of about 6,433 (235)
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FAMILIAL PORPHYRIA CUTANEA TARDA *
Australasian Journal of Dermatology, 1985SUMMARYThe results of erythrocyte uroporphyrinogen decarboxylase estimations of members of the family of a child with porphyria cutanea tarda are reported.
M, Rogers, V, Poulos
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Archives of Dermatology, 1958
Introduction Porphyria is thought to be an "inborn error of metabolism" (Garrod, 1923), i. e., of pyrrole metabolism. Quite a number of classifications of porphyria have been described, but among them the best known are those of Waldenstrom (1937) and of Schmid, Schwartz, and Watson (1953, 1954). In order to avoid any confusion the classifications of
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Introduction Porphyria is thought to be an "inborn error of metabolism" (Garrod, 1923), i. e., of pyrrole metabolism. Quite a number of classifications of porphyria have been described, but among them the best known are those of Waldenstrom (1937) and of Schmid, Schwartz, and Watson (1953, 1954). In order to avoid any confusion the classifications of
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International Journal of Dermatology, 1965
High serum iron values with marked transferrin saturation were noted in four of 15 patients with porphyria cutanea tarda (PCT). Four others had serum iron and saturation levels near the upper limits of normal. In addition, the presence of hepatic dysfunction and the increased incidence of diabetes in this disease were confirmed. However, a relationship
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High serum iron values with marked transferrin saturation were noted in four of 15 patients with porphyria cutanea tarda (PCT). Four others had serum iron and saturation levels near the upper limits of normal. In addition, the presence of hepatic dysfunction and the increased incidence of diabetes in this disease were confirmed. However, a relationship
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Archiv f�r Klinische und Experimentelle Dermatologie, 1959
Porphyria cutanea tarda (PCT) is one of the inborn porphyrinopathies. It is characterized by abnormal porphyrin synthesis and excretion, cutaneous photodynamic activity, fragility of the skin, and, usually, evidence of liver disease. Schmid, Schwartz, and Watson 1 termed porphyria cutanea tarda and acute intermittent porphyria as hepatic porphyrias, a ...
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Porphyria cutanea tarda (PCT) is one of the inborn porphyrinopathies. It is characterized by abnormal porphyrin synthesis and excretion, cutaneous photodynamic activity, fragility of the skin, and, usually, evidence of liver disease. Schmid, Schwartz, and Watson 1 termed porphyria cutanea tarda and acute intermittent porphyria as hepatic porphyrias, a ...
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2013
The most common initial symptoms of porphyria cutanea tarda are cutaneous fragility and blistering of the hands, forearms, and, sometimes, the face. erosions may cause epidermal loss and infections. Healing is slow and painful, causing atrophic scars.
Robert A. Norman, Edward M. Young
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The most common initial symptoms of porphyria cutanea tarda are cutaneous fragility and blistering of the hands, forearms, and, sometimes, the face. erosions may cause epidermal loss and infections. Healing is slow and painful, causing atrophic scars.
Robert A. Norman, Edward M. Young
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Erythropoietin for the Treatment of Porphyria Cutanea Tarda in a Patient on Long-Term Hemodialysis
New England Journal of Medicine, 1990Karl E Anderson
exaly
Mutations of the Hereditary Hemochromatosis Candidate GeneHLA-Hin Porphyria Cutanea Tarda
New England Journal of Medicine, 1997Hans Clevers
exaly