185 related articles for article (PubMed ID: 3821794)
1. Hepatoerythropoietic porphyria: clinical, biochemical, and enzymatic studies in a three-generation family lineage.
Toback AC; Sassa S; Poh-Fitzpatrick MB; Schechter J; Zaider E; Harber LC; Kappas A
N Engl J Med; 1987 Mar; 316(11):645-50. PubMed ID: 3821794
[TBL] [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. Molecular analysis of uroporphyrinogen decarboxylase deficiency in a family with two cases of hepatoerythropoietic porphyria.
de Verneuil H; Grandchamp B; Romeo PH; Raich N; Beaumont C; Goossens M; Nicolas H; Nordmann Y
J Clin Invest; 1986 Feb; 77(2):431-5. PubMed ID: 3753711
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. Immunochemical study of uroporphyrinogen decarboxylase in a patient with mild hepatoerythropoietic porphyria.
Fujita H; Sassa S; Toback AC; Kappas A
J Clin Invest; 1987 May; 79(5):1533-7. PubMed ID: 3571497
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. [Early forms of porphyria cutanea tarda. Apropos of 2 cases with a study of familial enzymatic deficiency and definition of the mode of genetic transmission].
Herrero C; Muniesa AM; Lecha M; Elder GH; Mascaro JM
Ann Dermatol Venereol; 1984; 111(11):973-8. PubMed ID: 6524816
[TBL] [Abstract][Full Text] [Related]
8. [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]
9. [Uroporphyrinogen decarboxylase in erythrocytes: studies on the primary genetic enzyme defect in chronic hepatic porphyria (author's transl)].
von Tiepermann R; Doss M
J Clin Chem Clin Biochem; 1978 Sep; 16(9):513-7. PubMed ID: 712342
[TBL] [Abstract][Full Text] [Related]
10. [Chronic hepatic porphyria with uroporphyrinogen decarboxylase defect in four generations (author's transl)].
Lehr PA; Doss M
Dtsch Med Wochenschr; 1981 Feb; 106(8):241-5. PubMed ID: 7472211
[TBL] [Abstract][Full Text] [Related]
11. An inherited enzymatic defect in porphyria cutanea tarda: decreased uroporphyrinogen decarboxylase activity.
Kushner JP; Barbuto AJ; Lee GR
J Clin Invest; 1976 Nov; 58(5):1089-97. PubMed ID: 993332
[TBL] [Abstract][Full Text] [Related]
12. Decreased activity of hepatic uroporphyrinogen decarboxylase in sporadic porphyria cutanea tarda.
Elder GH; Lee GB; Tovey JA
N Engl J Med; 1978 Aug; 299(6):274-8. PubMed ID: 661926
[TBL] [Abstract][Full Text] [Related]
13. [Porphyria cutanea tarda in a 4-year-old child with uroporphyrinogen decarboxylase deficiency].
Cotton JB; Abeille A; Jeune R; Ladreyt-Ponchon JP; Grenier JL
Pediatrie; 1986 Dec; 41(8):617-27. PubMed ID: 3575073
[TBL] [Abstract][Full Text] [Related]
14. [Hepato-erythropoietic porphyria].
Boudghène-Stambouli O; Mérad-Boudia A
Ann Dermatol Venereol; 1995; 122(9):615-7. PubMed ID: 8745689
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. Red-cell uroporphyrinogen decarboxylase activity in porphyria cutanea tarda and in other forms of porphyria.
Felsher BF; Norris ME; Shih JC
N Engl J Med; 1978 Nov; 299(20):1095-8. PubMed ID: 703786
[TBL] [Abstract][Full Text] [Related]
17. Uroporphyrinogen decarboxylase structural mutant (Gly281----Glu) in a case of porphyria.
de Verneuil H; Grandchamp B; Beaumont C; Picat C; Nordmann Y
Science; 1986 Nov; 234(4777):732-4. PubMed ID: 3775362
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Hepatoerythropoietic porphyria: a new uroporphyrinogen decarboxylase defect or homozygous porphyria cutanea tarda?
Elder GH; Smith SG; Herrero C; Lecha M; Mascaro JM; Muniesa AM; Czarnecki DB; Brenan J; Poulos V; DE Salamanca RE
Lancet; 1981 Apr; 1(8226):916-9. PubMed ID: 6112327
[TBL] [Abstract][Full Text] [Related]
20. Porphyria cutanea tarda in three generations of a single family.
Benedetto AV; Kushner JP; Taylor JS
N Engl J Med; 1978 Feb; 298(7):358-62. PubMed ID: 622106
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]