141 related articles for article (PubMed ID: 9017795)
1. Porphyria cutanea tarda and chronic lymphoid leukemia.
Remenyik E; Ujj G; Kiss A; Kószó F; Horkay I
Photodermatol Photoimmunol Photomed; 1996 Aug; 12(4):180-2. PubMed ID: 9017795
[TBL] [Abstract][Full Text] [Related]
2. A mutation (G281E) of the human uroporphyrinogen decarboxylase gene causes both hepatoerythropoietic porphyria and overt familial porphyria cutanea tarda: biochemical and genetic studies on Spanish patients.
Roberts AG; Elder GH; De Salamanca RE; Herrero C; Lecha M; Mascaro JM
J Invest Dermatol; 1995 Apr; 104(4):500-2. PubMed ID: 7706766
[TBL] [Abstract][Full Text] [Related]
3. [Pathogenesis of porphyria cutanea tarda].
Kószó F; Simon M
Orv Hetil; 2000 Apr; 141(14):709-13. PubMed ID: 10803012
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Familial and sporadic porphyria cutanea tarda: clinical and biochemical features and risk factors in 152 patients.
Muñoz-Santos C; Guilabert A; Moreno N; To-Figueras J; Badenas C; Darwich E; Herrero C
Medicine (Baltimore); 2010 Mar; 89(2):69-74. PubMed ID: 20517178
[TBL] [Abstract][Full Text] [Related]
6. Porphyria cutanea tarda.
Elder GH
Semin Liver Dis; 1998; 18(1):67-75. PubMed ID: 9516680
[TBL] [Abstract][Full Text] [Related]
7. Identification of two types of porphyria cutanea tarda by measurement of erythrocyte uroporphyrinogen decarboxylase.
Elder GH; Sheppard DM; De Salamanca RE; Olmos A
Clin Sci (Lond); 1980 Jun; 58(6):477-84. PubMed ID: 7428280
[TBL] [Abstract][Full Text] [Related]
8. Seven novel point mutations in the uroporphyrinogen decarboxylase (UROD) gene in patients with familial porphyria cutanea tarda (f-PCT).
Cappellini MD; Martinez di Montemuros F; Tavazzi D; Fargion S; Pizzuti A; Comino A; Cainelli T; Fiorelli G
Hum Mutat; 2001 Apr; 17(4):350. PubMed ID: 11295834
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Hepatoerythropoietic porphyria precipitated by viral hepatitis.
Hift RJ; Meissner PN; Todd G
Gut; 1993 Nov; 34(11):1632-4. PubMed ID: 7902313
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Porphyria cutanea tarda.
Fritsch C; Lang K; von Schmiedeberg S; Bolsen K; Merk H; Lehmann P; Ruzicka T
Skin Pharmacol Appl Skin Physiol; 1998; 11(6):321-35. PubMed ID: 10343203
[TBL] [Abstract][Full Text] [Related]
13. Complex pattern of alternative splicing in the normal uroporphyrinogen decarboxylase gene: implications for diagnosis of familial porphyria cutanea tarda.
McManus JF; Begley CG; Ratnaike S
Clin Chem; 1994 Oct; 40(10):1884-9. PubMed ID: 7923766
[TBL] [Abstract][Full Text] [Related]
14. Familial and sporadic porphyria cutanea tarda: clinical, biochemical and genetic features with emphasis on iron status.
Bygum A; Christiansen L; Petersen NE; Hørder M; Thomsen K; Brandrup F
Acta Derm Venereol; 2003; 83(2):115-20. PubMed ID: 12735639
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Hepatoerythropoietic porphyria and familial porphyria cutanea tarda in Spanish patients: G281E mutation in the uroporphyrinogen decarboxylase gene.
Darwich E; To-Figueras J; Badenas C; Herrero C
Arch Dermatol; 2010 Nov; 146(11):1313-4. PubMed ID: 21079081
[No Abstract] [Full Text] [Related]
17. Hepatitis C and porphyria cutanea tarda.
English JC; Peake MF; Becker LE
Cutis; 1996 Jun; 57(6):404-8. PubMed ID: 8804842
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Familial porphyria cutanea tarda with normal erythrocytic urodecarboxylase: an exception to the rule?
D'Alessandro Gandolfo L; Griso D; Macri A; Biolcati G; Topi GC
Dermatologica; 1989; 178(4):206-8. PubMed ID: 2767288
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
