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Porphyria cutanea tarda [PDF]

open access: yesMMW - Fortschritte der Medizin, 2012
openaire   +1 more source

Paraneoplastic porphyria cutanea tarda associated with cholangiocarcinoma: Case report

open access: yesThe Turkish Journal of Gastroenterology, 2007
Mehmet SÖKMEN   +9 more
doaj  

Updates to gene-disease classifications and inheritance patterns for porphyrias. [PDF]

open access: yesMol Genet Metab
Reeves EB   +8 more
europepmc   +1 more source

From photosensitivity to autoimmunity: the role of AI metabolomics in PCT-celiac disease overlap. [PDF]

open access: yesAnn Med Surg (Lond)
Ozukum ST   +4 more
europepmc   +1 more source
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Porphyria Cutanea Tarda

Seminars in Liver Disease, 1998
Porphyria cutanea tarda (PCT) is a skin disease that results from decreased activity of uroporphyrinogen decarboxylase (UROD). About 80% of patients have the sporadic (type I) form in which UROD deficiency is restricted to the liver. Others have familial (type II) PCT in which mutations in the UROD gene are inherited in an autosomal dominant pattern ...
C, Fritsch   +2 more
  +7 more sources

HLA and porphyria cutanea tarda

Archives of Dermatological Research, 1980
R Enriquez De Salamanca
exaly   +3 more sources

Porphyria cutanea tarda

Australasian Journal of Dermatology, 2000
SUMMARYPorphyria cutanea tarda (PCT) is a metabolic disorder of haem biosynthesis caused by decreased activity of uroporphyrinogen decarboxylase. Porphyria cutanea tarda is manifest by fragility, erosions, bullae, milia and scars on sun‐exposed skin.
N R, Bleasel, G A, Varigos
openaire   +5 more sources

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