Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Aasne Karine, Aarsand"'
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-12 (2022)
Abstract Background Porphyria cutanea tarda (PCT) is a skin disorder caused by a defect in the liver enzyme uroporphyrinogen decarboxylase and is associated with hepatitis C virus infection, high alcohol intake, smoking and iron overload. Data on the
Externí odkaz:
https://doaj.org/article/f841f9595f4a4eb48125b539862946b1
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-11 (2020)
Abstract Background Acute hepatic porphyria (AHP) consists of three rare metabolic disorders. We investigated the risk of long-term sick leave, disability pension, and premature death in individuals with AHP compared to the general population. Method
Externí odkaz:
https://doaj.org/article/3144a9fc6f6f4e39b7f5f4145810c6c9
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-2 (2022)
Externí odkaz:
https://doaj.org/article/e95246096e1b47ccbf616666ae2788db
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 14, Iss 1, Pp 1-10 (2019)
Abstract Background Porphyria cutanea tarda (PCT) is a skin disorder originating from a deficit of the liver enzyme uroporphyrinogen decarboxylase. PCT may be a risk factor for hepatocellular carcinoma (HCC) and other cancers, but the evidence is unc
Externí odkaz:
https://doaj.org/article/298742d122e14f80b25a2933ddf72abc
Background: Porphyria cutanea tarda (PCT) is a skin disorder caused by a defect in the liver enzyme uroporphyrinogen decarboxylase and is associated with hepatitis C virus infection, high alcohol intake, smoking and iron overload. Data on the long-te
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa19fea142507164de3fac1b68835d34
https://doi.org/10.21203/rs.3.rs-929947/v1
https://doi.org/10.21203/rs.3.rs-929947/v1
Autor:
Mira, Mykletun, Aasne Karine, Aarsand, Egil, Støle, Jørild Haugen, Villanger, Mette Christophersen, Tollånes, Carl, Baravelli, Sverre, Sandberg
Publikováno v:
Tidsskrift for den Norske laegeforening : tidsskrift for praktisk medicin, ny raekke. 134(8)
Porphyria is an umbrella term for a group of largely hereditary diseases that are due to defective haem synthesis. The diseases have a varied and partly overlapping range of symptoms and presentations. The commonest forms of porphyria are porphyria c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6b85991e98efe855e1888c4214d89a0a
https://pubmed.ncbi.nlm.nih.gov/24780981
https://pubmed.ncbi.nlm.nih.gov/24780981