BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

189 related articles for article (PubMed ID: 730158)

  • 1. Familial and sporadic porphyria cutanea: two different diseases.
    de Verneuil H; Aitken G; Nordmann Y
    Hum Genet; 1978 Oct; 44(2):145-51. PubMed ID: 730158
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. 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]  

  • 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. 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]  

  • 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. 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]  

  • 8. 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]  

  • 9. 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]  

  • 10. Familial porphyria cutanea tarda: hybridization analysis of the uroporphyrinogen decarboxylase locus.
    Hansen JL; O'Connell P; Romana M; Romeo PH; Kushner JP
    Hum Hered; 1988; 38(5):283-6. PubMed ID: 2906904
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [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]  

  • 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. The enzymatic defects in porphyria cutanea tarda and variegate porphyria.
    Kushner JP
    Acta Derm Venereol Suppl (Stockh); 1982; 100():51-6. PubMed ID: 6962633
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. 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]  

  • 17. Decreased hepatic uroporphyrinogen decarboxylase activity in porphyria cutanea tarda.
    Felsher BF; Carpio NM; Engleking DW; Nunn AT
    N Engl J Med; 1982 Apr; 306(13):766-9. PubMed ID: 7062951
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Uroporphyrinogen decarboxylase: a splice site mutation causes the deletion of exon 6 in multiple families with porphyria cutanea tarda.
    Garey JR; Harrison LM; Franklin KF; Metcalf KM; Radisky ES; Kushner JP
    J Clin Invest; 1990 Nov; 86(5):1416-22. PubMed ID: 2243121
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Steady-state levels of uroporphyrinogen decarboxylase mRNA in lymphoblastoid cell lines from patients with familial porphyria cutanea tarda and their relatives.
    Hansen JL; Pryor MA; Kennedy JB; Kushner JP
    Am J Hum Genet; 1988 Jun; 42(6):847-53. PubMed ID: 3369447
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 10.