391 related articles for article (PubMed ID: 7303763)
1. [Porphyrin diseases with particular emphasis on hereditary].
Knapp A
Z Gesamte Inn Med; 1981 Jun; 36(11):377-81. PubMed ID: 7303763
[TBL] [Abstract][Full Text] [Related]
2. Familial porphyria cutanea tarda: the pattern of porphyrins formed from porphobilinogen by hemolysates.
Alleman MA; Wilson JH; van den Berg JW; Edixhoven-Bosdijk A; van Gastel-Quist LM
Clin Chem; 1982 May; 28(5):1144-7. PubMed ID: 7074894
[TBL] [Abstract][Full Text] [Related]
3. [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]
4. 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]
5. [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]
6. [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]
7. Why is the patient with acute intermittent porphyria not light sensitive?
Wetterberg L; Thunell S; Zetterlund P
Acta Derm Venereol Suppl (Stockh); 1982; 100():73-4. PubMed ID: 6962637
[TBL] [Abstract][Full Text] [Related]
8. Faecal porphyrin excretion in various types of porphyria. Thin layer chromatographic study.
Perrot H; Boucherat M; Thivolet J
Arch Dermatol Res; 1978; 263(1):67-73. PubMed ID: 757459
[TBL] [Abstract][Full Text] [Related]
9. [Porphyria cutanea tarda--a multifactorial hereditary disease? A working hypothesis].
Simon N; Hunyadi J; Szörényi A; Dobozy A
Hautarzt; 1978 Jul; 29(7):378-82. PubMed ID: 681174
[TBL] [Abstract][Full Text] [Related]
10. [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]
11. [Porphyrin metabolic disorders in porphyria cutanea tarda].
Krivosheev BN
Vestn Dermatol Venerol; 1989; (8):67-71. PubMed ID: 2816038
[TBL] [Abstract][Full Text] [Related]
12. [Porphyria variegata].
Meinhof W; Kraus F; Reiffers-Mettelock J; Verspohl F; Doss M
Hautarzt; 1980 Nov; 31(11):595-601. PubMed ID: 7451141
[TBL] [Abstract][Full Text] [Related]
13. A plasma porphyrin fluorescence marker for variegate porphyria.
Poh-Fitzpatrick MB
Arch Dermatol; 1980 May; 116(5):543-7. PubMed ID: 7377785
[TBL] [Abstract][Full Text] [Related]
14. [Latent porphyria cutanea tarda].
Krivosheev BN
Vestn Dermatol Venerol; 1989; (4):64-8. PubMed ID: 2763712
[TBL] [Abstract][Full Text] [Related]
15. Heterozygosity for HLA-linked hemochromatosis as a likely cause of the hepatic siderosis associated with sporadic porphyria cutanea tarda.
Kushner JP; Edwards CQ; Dadone MM; Skolnick MH
Gastroenterology; 1985 May; 88(5 Pt 1):1232-8. PubMed ID: 3979748
[TBL] [Abstract][Full Text] [Related]
16. Hepatoerythropoietic porphyria: a variant of childhood-onset porphyria cutanea tarda. Porphyrin profiles and enzymatic studies of two cases in a family.
Lim HW; Poh-Fitzpatrick MB
J Am Acad Dermatol; 1984 Dec; 11(6):1103-11. PubMed ID: 6512055
[TBL] [Abstract][Full Text] [Related]
17. Porphyria: genetic and acquired.
Cripps DJ
IARC Sci Publ; 1986; (77):549-66. PubMed ID: 3298037
[TBL] [Abstract][Full Text] [Related]
18. [Does paraneoplastic porphyria cutanea tarda exist?].
Köstler E
Dtsch Z Verdau Stoffwechselkr; 1988; 48(1):35-40. PubMed ID: 3371236
[TBL] [Abstract][Full Text] [Related]
19. Porphyria cutanea tarda. Diagnosis, management, and differentiation from other hepatic porphyrias.
Grossman ME; Poh-Fitzpatrick MB
Dermatol Clin; 1986 Apr; 4(2):297-309. PubMed ID: 3955900
[TBL] [Abstract][Full Text] [Related]
20. [Hereditary porphyria cutanea in children. Enzymatic studies (author's transl)].
Doutre MS; Beylot C; Bioulac P; Nordmann Y
Ann Dermatol Venereol; 1981; 108(10):751-7. PubMed ID: 7305216
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
