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Porphyria cutanea tarda: Recent update.
Singal AK. Singal AK. Mol Genet Metab. 2019 Nov;128(3):271-281. doi: 10.1016/j.ymgme.2019.01.004. Epub 2019 Jan 18. Mol Genet Metab. 2019. PMID: 30683557 Review.
Porphyria cutanea tarda (PCT) is the most common human porphyria, due to hepatic deficiency of uroporphyrinogen decarboxylase (UROD), which is acquired in the presence of iron overload and various susceptibility factors, such as alcohol abuse, smoking,
Porphyria cutanea tarda (PCT) is the most common human porphyria, due to hepatic deficiency of uroporphyrinogen
Porphyria cutanea tarda.
Bleasel NR, Varigos GA. Bleasel NR, et al. Australas J Dermatol. 2000 Nov;41(4):197-206; quiz 207-8. doi: 10.1046/j.1440-0960.2000.00437.x. Australas J Dermatol. 2000. PMID: 11105361 Review.
Porphyria 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
Porphyria cutanea tarda (PCT) is a metabolic disorder of haem biosynthesis caused by decreased activity of uroporphyrin
Dual porphyrias revisited.
Poblete-Gutiérrez P, Badeloe S, Wiederholt T, Merk HF, Frank J. Poblete-Gutiérrez P, et al. Exp Dermatol. 2006 Sep;15(9):685-91. doi: 10.1111/j.1600-0625.2006.00464.x. Exp Dermatol. 2006. PMID: 16881965 Review.
Currently, at least eight different forms of porphyrias can be differentiated, all of them characterized by a specific enzyme deficiency that is either inherited in an autosomal-dominant fashion, autosomal recessively or, in the case of porphyria cutanea tarda
Currently, at least eight different forms of porphyrias can be differentiated, all of them characterized by a specific enzyme deficiency tha …
Porphyria cutanea tarda.
Elder GH. Elder GH. Semin Liver Dis. 1998;18(1):67-75. doi: 10.1055/s-2007-1007142. Semin Liver Dis. 1998. PMID: 9516680 Review.
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
Porphyria cutanea tarda (PCT) is a skin disease that results from decreased activity of uroporphyrinogen decarboxylase
Prevalence of hepatitis C virus infection in porphyria cutanea tarda: systematic review and meta-analysis.
Gisbert JP, García-Buey L, Pajares JM, Moreno-Otero R. Gisbert JP, et al. J Hepatol. 2003 Oct;39(4):620-7. doi: 10.1016/s0168-8278(03)00346-5. J Hepatol. 2003. PMID: 12971974 Review.
BACKGROUND/AIMS: To conduct a systematic review and meta-analysis on the prevalence of hepatitis C virus (HCV) infection in porphyria cutanea tarda (PCT). METHODS: Studies evaluating prevalence of HCV infection in patients with PCT were considered. ...HCV pre …
BACKGROUND/AIMS: To conduct a systematic review and meta-analysis on the prevalence of hepatitis C virus (HCV) infection in porphyria
Porphyria cutanea tarda--when skin meets liver.
Frank J, Poblete-Gutiérrez P. Frank J, et al. Best Pract Res Clin Gastroenterol. 2010 Oct;24(5):735-45. doi: 10.1016/j.bpg.2010.07.002. Best Pract Res Clin Gastroenterol. 2010. PMID: 20955974 Review.
Porphyria cutanea tarda (PCT) is the most frequent type of porphyria worldwide and results from a catalytic deficiency of uroporphyrinogen decarboxylase (UROD), the fifth enzyme in heme biosynthesis. At least two different types of PCT are currently di
Porphyria cutanea tarda (PCT) is the most frequent type of porphyria worldwide and results from a catalytic defi
Performing therapeutic venesection in a doctor's surgery.
Hy L, Ho HW. Hy L, et al. Aust Fam Physician. 2017 Mar;46(3):132-138. Aust Fam Physician. 2017. PMID: 28260267 Free article. Review.
BACKGROUND: Although venesection was widely applied in the past for the treatment of various ailments and diseases, in modern medical practice, it is indicated in very few conditions, namely, hereditary haemochromatosis, polycythaemia and porphyria cutanea tarda
BACKGROUND: Although venesection was widely applied in the past for the treatment of various ailments and diseases, in modern medical practi …
Hepatic porphyrias in children.
Elder GH. Elder GH. J Inherit Metab Dis. 1997 Jun;20(2):237-46. doi: 10.1023/a:1005313024076. J Inherit Metab Dis. 1997. PMID: 9211196 Review.
Clinically overt hepatic porphyria is uncommon in children. The autosomal dominant acute hepatic porphyrias, acute intermittent porphyria (AIP), variegate porphyria (VP) and hereditary coproporphyria (HCP), are rarely present before puberty. ...Two cutaneous …
Clinically overt hepatic porphyria is uncommon in children. The autosomal dominant acute hepatic porphyrias, acute intermittent po
Erythropoietic and hepatic porphyrias.
Gross U, Hoffmann GF, Doss MO. Gross U, et al. J Inherit Metab Dis. 2000 Nov;23(7):641-61. doi: 10.1023/a:1005645624262. J Inherit Metab Dis. 2000. PMID: 11117426 Review.
In contrast to the acute porphyrias, nonacute, chronic hepatic porphyrias such as porphyria cutanea tarda are porphyrin accumulation disorders leading to cutaneous symptoms associated with liver disease, especially caused by alcohol or viral hepatitis. Alcoho …
In contrast to the acute porphyrias, nonacute, chronic hepatic porphyrias such as porphyria cutanea tarda are porphyrin …
The management of porphyria cutanea tarda.
Sarkany RP. Sarkany RP. Clin Exp Dermatol. 2001 May;26(3):225-32. doi: 10.1046/j.1365-2230.2001.00825.x. Clin Exp Dermatol. 2001. PMID: 11422163 Review.
Porphyria cutanea tarda (PCT), the commonest of all porphyrias, is usually characterized by blisters and fragility of skin in light-exposed areas. It can be clinically indistinguishable from other disorders including variegate porphyria and the diagnos
Porphyria cutanea tarda (PCT), the commonest of all porphyrias, is usually characterized by blisters and fragility of s
36 results