These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

175 related items for PubMed ID: 4096525

  • 1. Hereditary uroporphyrinogen-decarboxylase deficiency predisposing porphyria cutanea tarda (chronic hepatic porphyria) in females after oral contraceptive medication.
    Sixel-Dietrich F, Doss M.
    Arch Dermatol Res; 1985; 278(1):13-6. PubMed ID: 4096525
    [Abstract] [Full Text] [Related]

  • 2. Development of chronic hepatic porphyria (porphyria cutanea tarda) with inherited uroporphyrinogen decarboxylase deficiency under exposure to dioxin.
    Doss M, Sauer H, von Tiepermann R, Colombi AM.
    Int J Biochem; 1984; 16(4):369-73. PubMed ID: 6714509
    [Abstract] [Full Text] [Related]

  • 3. [Hereditary uroporphyrinogen decarboxylase deficiency in porphyria cutanea tarda caused by hormonal contraceptives].
    Doss M.
    Dtsch Med Wochenschr; 1983 Dec 02; 108(48):1857-8. PubMed ID: 6641540
    [No Abstract] [Full Text] [Related]

  • 4. [Chronic hepatic porphyria with uroporphyrinogen decarboxylase defect in four generations (author's transl)].
    Lehr PA, Doss M.
    Dtsch Med Wochenschr; 1981 Feb 20; 106(8):241-5. PubMed ID: 7472211
    [Abstract] [Full Text] [Related]

  • 5. Uroporphyrinogen decarboxylase deficiency in experimental chronic hepatic porphyria.
    von Tiepermann R, Koss G, Doss M.
    Hoppe Seylers Z Physiol Chem; 1980 Aug 20; 361(8):1217-22. PubMed ID: 7409755
    [Abstract] [Full Text] [Related]

  • 6. [Porphyria cutanea tarda (chronic hepatic porphyria): new aspects on pathogenesis, diagnosis and therapy with a review of the workshop, "Cutaneous porphyrias" at the 17th World Congress of Dermatology in Berlin 1987].
    Doss MO.
    Z Hautkr; 1988 Apr 15; 63(4):282-9. PubMed ID: 3291437
    [Abstract] [Full Text] [Related]

  • 7. Porphyria cutanea tarda, or the uroporphyrinogen decarboxylase deficiency diseases.
    Sweeney GD.
    Clin Biochem; 1986 Feb 15; 19(1):3-15. PubMed ID: 3513989
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. 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 15; 58(6):477-84. PubMed ID: 7428280
    [Abstract] [Full Text] [Related]

  • 12. 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 15; 110(5):613-7. PubMed ID: 6722030
    [Abstract] [Full Text] [Related]

  • 13. 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 15; 36(3):613-22. PubMed ID: 6375356
    [Abstract] [Full Text] [Related]

  • 14. Decreased activity of hepatic uroporphyrinogen decarboxylase in sporadic porphyria cutanea tarda.
    Elder GH, Lee GB, Tovey JA.
    N Engl J Med; 1978 Aug 10; 299(6):274-8. PubMed ID: 661926
    [Abstract] [Full Text] [Related]

  • 15. 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 10; 42(6):847-53. PubMed ID: 3369447
    [Abstract] [Full Text] [Related]

  • 16. Dual porphyria in double heterozygotes with porphobilinogen deaminase and uroporphyrinogen decarboxylase deficiencies.
    Doss MO.
    Clin Genet; 1989 Feb 10; 35(2):146-51. PubMed ID: 2721023
    [Abstract] [Full Text] [Related]

  • 17. Genetics and pathogenesis of human uroporphyrinogen decarboxylase defects.
    Elder GH, Roberts AG, de Salamanca RE.
    Clin Biochem; 1989 Jun 10; 22(3):163-8. PubMed ID: 2786774
    [Abstract] [Full Text] [Related]

  • 18. [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 10; 41(8):617-27. PubMed ID: 3575073
    [Abstract] [Full Text] [Related]

  • 19. A potential biochemical explanation for the genesis of porphyria cutanea tarda. Studies on the inherent biochemical defect in highly purified human erythrocyte uroporphyrinogen decarboxylase and its amplification by iron.
    Mukerji SK, Pimstone NR, Tan KT.
    FEBS Lett; 1985 Sep 23; 189(2):217-20. PubMed ID: 4043380
    [Abstract] [Full Text] [Related]

  • 20. [Coexistence of hereditary coproporphyria and porphyria cutanea tarda: a new form of dual porphyria].
    Doss MO, Gross U, Puy H, Doss M, Kühnel A, Jacob K, Deybach JC, Nordmann Y.
    Med Klin (Munich); 2002 Jan 15; 97(1):1-5. PubMed ID: 11831056
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 9.