137 related articles for article (PubMed ID: 1935224)
1. Porphyria cutanea tarda: erythrocyte uroporphyrinogen decarboxylase activity in 471 consecutive patients.
Doss MO; Frank M; Braun-Falco O
Curr Probl Dermatol; 1991; 20():97-105. PubMed ID: 1935224
[No Abstract] [Full Text] [Related]
2. Is hepatoerythropoietic porphyria a homozygous form of porphyria cutanea tarda? Inheritance of uroporphyrinogen decarboxylase deficiency in a Spanish family.
Lazaro P; de Salamanca RE; Elder GH; Villaseca ML; Chinarro S; Jaqueti G
Br J Dermatol; 1984 May; 110(5):613-7. PubMed ID: 6722030
[TBL] [Abstract][Full Text] [Related]
3. Different types of porphyria cutanea tarda.
Doss M; Sauer H; Sixel-Dietrich F; von Tiepermann R
Arch Dermatol Res; 1984; 276(3):207-8. PubMed ID: 6476891
[No Abstract] [Full Text] [Related]
4. Immunoreactive uroporphyrinogen decarboxylase in porphyria cutanea tarda.
Elder GH; Sheppard DM; Tovey JA; Urquhart AJ
Lancet; 1983 Jun; 1(8337):1301-4. PubMed ID: 6134095
[TBL] [Abstract][Full Text] [Related]
5. [Decreased erythrocyte uroporphyrinogen decarboxylase activity in porphyria cutanea tarda].
Kondo M
Nihon Hifuka Gakkai Zasshi; 1985 Aug; 95(9):995-6. PubMed ID: 4079084
[No Abstract] [Full Text] [Related]
6. Enzymatic and immunological studies of uroporphyrinogen decarboxylase in familial porphyria cutanea tarda and hepatoerythropoietic porphyria.
de Verneuil H; Beaumont C; Deybach JC; Nordmann Y; Sfar Z; Kastally R
Am J Hum Genet; 1984 May; 36(3):613-22. PubMed ID: 6375356
[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. Familial porphyria cutanea tarda.
Rogers M; Poulos V
Australas J Dermatol; 1985 Aug; 26(2):58-60. PubMed ID: 4084158
[No Abstract] [Full Text] [Related]
9. Heterogeneity of familial porphyria cutanea tarda.
Roberts AG; Elder GH; Newcombe RG; Enriquez de Salamanca R; Munoz JJ
J Med Genet; 1988 Oct; 25(10):669-76. PubMed ID: 3225822
[TBL] [Abstract][Full Text] [Related]
10. Defective human erythrocyte uroporphyrinogen decarboxylase in familial porphyria cutanea tarda: the metabolic lesion or the result of endogenous porphyrinemia?
Mukerji SK; Pimstone NR
Biochem Biophys Res Commun; 1988 Jul; 154(1):39-46. PubMed ID: 3395340
[TBL] [Abstract][Full Text] [Related]
11. Uroporphyrinogen decarboxylase deficiency in hepatoerythropoietic porphyria: further evidence for genetic heterogeneity.
Kószó F; Elder GH; Roberts A; Simon N
Br J Dermatol; 1990 Mar; 122(3):365-70. PubMed ID: 2322500
[TBL] [Abstract][Full Text] [Related]
12. Erythrocyte uroporphyrinogen decarboxylase activity in porphyria cutanea tarda: a study of 40 consecutive patients.
Held JL; Sassa S; Kappas A; Harber LC
J Invest Dermatol; 1989 Sep; 93(3):332-4. PubMed ID: 2768832
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. [The porphyria cutanea tarda group: their role among the enzyme defects of heme biosynthesis].
Adrien A; Guillet G
Sem Hop; 1984 Apr; 60(16):1148-52. PubMed ID: 6326308
[TBL] [Abstract][Full Text] [Related]
15. Genetics and pathogenesis of human uroporphyrinogen decarboxylase defects.
Elder GH; Roberts AG; de Salamanca RE
Clin Biochem; 1989 Jun; 22(3):163-8. PubMed ID: 2786774
[TBL] [Abstract][Full Text] [Related]
16. Manifestation of familial porphyria cutanea tarda after childbirth.
Malina L; Lim CK
Br J Dermatol; 1988 Feb; 118(2):243-5. PubMed ID: 3348969
[TBL] [Abstract][Full Text] [Related]
17. New form of dual porphyria: coexistent acute intermittent porphyria and porphyria cutanea tarda.
Doss MO
Eur J Clin Invest; 1989 Feb; 19(1):20-5. PubMed ID: 2499457
[TBL] [Abstract][Full Text] [Related]
18. Erythrocyte uroporphyrinogen decarboxylase activity in 80 unrelated patients with porphyria cutanea tarda.
Kószó F; Morvay M; Dobozy A; Simon N
Br J Dermatol; 1992 May; 126(5):446-9. PubMed ID: 1610684
[TBL] [Abstract][Full Text] [Related]
19. Reduced substrate affinity for human erythrocyte uroporphyrinogen decarboxylase constitutes the inherent biochemical defect in porphyria cutanea tarda.
Mukerji SK; Pimstone NR
Biochem Biophys Res Commun; 1985 Mar; 127(2):517-25. PubMed ID: 3977935
[TBL] [Abstract][Full Text] [Related]
20. [Porphyria cutanea tarda].
Perrot H
Ann Dermatol Venereol; 1987; 114(8):1023-6. PubMed ID: 3426071
[No Abstract] [Full Text] [Related]
[Next] [New Search]