175 related articles for article (PubMed ID: 19233912)
1. Familial and sporadic porphyria cutanea tarda: characterization and diagnostic strategies.
Aarsand AK; Boman H; Sandberg S
Clin Chem; 2009 Apr; 55(4):795-803. PubMed ID: 19233912
[TBL] [Abstract][Full Text] [Related]
2. Porphyria cutanea tarda and hepatoerythropoietic porphyria: Identification of 19 novel uroporphyrinogen III decarboxylase mutations.
Weiss Y; Chen B; Yasuda M; Nazarenko I; Anderson KE; Desnick RJ
Mol Genet Metab; 2019 Nov; 128(3):363-366. PubMed ID: 30514647
[TBL] [Abstract][Full Text] [Related]
3. Precipitating/aggravating factors of porphyria cutanea tarda in Spanish patients.
Cruz-Rojo J; Fontanellas A; Morán-Jiménez MJ; Navarro-Ordóñez S; García-Bravo M; Méndez M; Muñoz-Rivero MC; de Salamanca RE
Cell Mol Biol (Noisy-le-grand); 2002 Dec; 48(8):845-52. PubMed ID: 12699242
[TBL] [Abstract][Full Text] [Related]
4. Comprehensive cytochrome P450 CYP1A2 gene analysis in French caucasian patients with familial and sporadic porphyria cutanea tarda.
Tchernitchko D; Robréau AM; Lefebvre T; Lamoril J; Deybach JC; Puy H
Br J Dermatol; 2012 Feb; 166(2):425-9. PubMed ID: 21929532
[TBL] [Abstract][Full Text] [Related]
5. Hemochromatosis (HFE) and transferrin receptor-1 (TFRC1) genes in sporadic porphyria cutanea tarda (sPCT).
Lamoril J; Andant C; Gouya L; Malonova E; Grandchamp B; Martásek P; Deybac JC; Puy H
Cell Mol Biol (Noisy-le-grand); 2002 Feb; 48(1):33-41. PubMed ID: 11929045
[TBL] [Abstract][Full Text] [Related]
6. Molecular heterogeneity of familial porphyria cutanea tarda in Spain: characterization of 10 novel mutations in the UROD gene.
Méndez M; Poblete-Gutiérrez P; García-Bravo M; Wiederholt T; Morán-Jiménez MJ; Merk HF; Garrido-Astray MC; Frank J; Fontanellas A; Enríquez de Salamanca R
Br J Dermatol; 2007 Sep; 157(3):501-7. PubMed ID: 17627795
[TBL] [Abstract][Full Text] [Related]
7. Porphyria cutanea tarda, hepatitis C, uroporphyrinogen decarboxylase and mutations of HFE gene. A case-control study.
Cribier B; Chiaverini C; Dali-Youcef N; Schmitt M; Grima M; Hirth C; Lacour JP; Chosidow O
Dermatology; 2009; 218(1):15-21. PubMed ID: 19001803
[TBL] [Abstract][Full Text] [Related]
8. Uroporphyrinogen decarboxylase gene mutations in Danish patients with porphyria cutanea tarda.
Christiansen L; Bygum A; Jensen A; Brandrup F; Thomsen K; Horder M; Petersen NE
Scand J Clin Lab Invest; 2000 Nov; 60(7):611-5. PubMed ID: 11202053
[TBL] [Abstract][Full Text] [Related]
9. Familial porphyria cutanea tarda in Spain: characterization of eight novel mutations in the UROD gene and haplotype analysis of the common p.G281E mutation.
Gómez-Abecia S; Morán-Jiménez MJ; Ruiz-Casares E; Henriques-Gil N; García-Pastor I; Garrido-Astray MC; Enríquez de Salamanca R; Méndez M
Gene; 2013 Jun; 522(1):89-95. PubMed ID: 23545314
[TBL] [Abstract][Full Text] [Related]
10. Porphyria cutanea tarda.
Elder GH
Semin Liver Dis; 1998; 18(1):67-75. PubMed ID: 9516680
[TBL] [Abstract][Full Text] [Related]
11. Porphyria cutanea tarda--when skin meets liver.
Frank J; Poblete-Gutiérrez P
Best Pract Res Clin Gastroenterol; 2010 Oct; 24(5):735-45. PubMed ID: 20955974
[TBL] [Abstract][Full Text] [Related]
12. Uroporphyrinogen decarboxylase: complete human gene sequence and molecular study of three families with hepatoerythropoietic porphyria.
Moran-Jimenez MJ; Ged C; Romana M; Enriquez De Salamanca R; Taïeb A; Topi G; D'Alessandro L; de Verneuil H
Am J Hum Genet; 1996 Apr; 58(4):712-21. PubMed ID: 8644733
[TBL] [Abstract][Full Text] [Related]
13. Screening for mutations in the uroporphyrinogen decarboxylase gene using denaturing gradient gel electrophoresis. Identification and characterization of six novel mutations associated with familial PCT.
Christiansen L; Ged C; Hombrados I; Brons-Poulsen J; Fontanellas A; de Verneuil H; Hørder M; Petersen NE
Hum Mutat; 1999; 14(3):222-32. PubMed ID: 10477430
[TBL] [Abstract][Full Text] [Related]
14. Erythrocyte uroporphyrinogen decarboxylase activity: diagnostic value and relationship with clinical features in hereditary porphyria cutanea tarda.
Camagna A; Del Duca P; Petrinelli P; Borelli LG; Ciancio L; Cipollone L; Misasi G; Manfredi MR; Dionisi S; de Martinis C
Am J Med Sci; 1998 Jan; 315(1):59-62. PubMed ID: 9427577
[TBL] [Abstract][Full Text] [Related]
15. Molecular analysis of the UROD gene in 17 Argentinean patients with familial porphyria cutanea tarda: characterization of four novel mutations.
Méndez M; Rossetti MV; Gómez-Abecia S; Morán-Jiménez MJ; Parera V; Batlle A; Enríquez de Salamanca R
Mol Genet Metab; 2012 Apr; 105(4):629-33. PubMed ID: 22382040
[TBL] [Abstract][Full Text] [Related]
16. Five new mutations in the uroporphyrinogen decarboxylase gene identified in families with cutaneous porphyria.
McManus JF; Begley CG; Sassa S; Ratnaike S
Blood; 1996 Nov; 88(9):3589-600. PubMed ID: 8896428
[TBL] [Abstract][Full Text] [Related]
17. Co-inheritance of mutations in the uroporphyrinogen decarboxylase and hemochromatosis genes accelerates the onset of porphyria cutanea tarda.
Brady JJ; Jackson HA; Roberts AG; Morgan RR; Whatley SD; Rowlands GL; Darby C; Shudell E; Watson R; Paiker J; Worwood MW; Elder GH
J Invest Dermatol; 2000 Nov; 115(5):868-74. PubMed ID: 11069625
[TBL] [Abstract][Full Text] [Related]
18. Enrichment of HFE mutations in Swedish patients with familial and sporadic form of porphyria cutanea tarda.
Harper P; Floderus Y; Holmström P; Eggertsen G; Gåfvels M
J Intern Med; 2004 Jun; 255(6):684-8. PubMed ID: 15147533
[No Abstract] [Full Text] [Related]
19. Case Report: Treatment of porphyria cutanea tarda with low dose hydroxychloroquine.
Awad A; Nirenberg A; Sinclair R
F1000Res; 2022; 11():945. PubMed ID: 37360939
[No Abstract] [Full Text] [Related]
20. The molecular basis of porphyria cutanea tarda in Chile: identification and functional characterization of mutations in the uroporphyrinogen decarboxylase gene.
Poblete-Gutiérrez P; Mendez M; Wiederholt T; Merk HF; Fontanellas A; Wolff C; Frank J
Exp Dermatol; 2004 Jun; 13(6):372-9. PubMed ID: 15186324
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]