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.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

128 related articles for article (PubMed ID: 285036)

  • 21. Red blood cell porphobilinogen deaminase in the evaluation of acute intermittent porphyria.
    Pierach CA; Weimer MK; Cardinal RA; Bossenmaier IC; Bloomer JR
    JAMA; 1987 Jan; 257(1):60-1. PubMed ID: 3783903
    [TBL] [Abstract][Full Text] [Related]  

  • 22. [Evaluation of the diagnostic usefulness of determining porphobilinogen deaminase activity in the erythrocytes in patients with acute intermittent porphyria and in carriers of the gene of this type of porphyria].
    Gregor A; Kocyłowski M; Kostrzewska E
    Przegl Lek; 1986; 43(11):703-5. PubMed ID: 3575772
    [No Abstract]   [Full Text] [Related]  

  • 23. [Acute intermittent porphyria. Familial study: detection of latent cases by the determination of erythrocyte uroporphyrinogen-1-synthetase activity].
    Guijarro Merino R; Villar Ortiz J; Lapetra Peralta J; Melero Bellido M; García Donas MA; Carneado de la Fuente J
    Med Clin (Barc); 1986 Mar; 86(8):323-7. PubMed ID: 3713356
    [No Abstract]   [Full Text] [Related]  

  • 24. Molecular analysis of acute intermittent porphyria in a Finnish family with normal erythrocyte porphobilinogen deaminase.
    Grandchamp B; Picat C; Kauppinen R; Mignotte V; Peltonen L; Mustajoki P; Roméo PH; Goossens M; Nordmann Y
    Eur J Clin Invest; 1989 Oct; 19(5):415-8. PubMed ID: 2511016
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Heme biosynthesis in sideroblastic anemia.
    Pasanen AV; Salmi M; Vuopio P; Tenhunen R
    Int J Biochem; 1980; 12(5-6):969-74. PubMed ID: 7450158
    [No Abstract]   [Full Text] [Related]  

  • 26. Diagnostic strategies for autosomal dominant acute porphyrias: retrospective analysis of 467 unrelated patients referred for mutational analysis of the HMBS, CPOX, or PPOX gene.
    Whatley SD; Mason NG; Woolf JR; Newcombe RG; Elder GH; Badminton MN
    Clin Chem; 2009 Jul; 55(7):1406-14. PubMed ID: 19460837
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Increased activity of porphobilinogen deaminase in erythrocytes during attacks of acute intermittent porphyria.
    Kostrzewska E; Gregor A
    Ann Clin Res; 1986; 18(4):195-8. PubMed ID: 3789651
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Haplotyping of the human porphobilinogen deaminase gene in acute intermittent porphyria by polymerase chain reaction.
    Lee JS; Lindsten J; Anvret M
    Hum Genet; 1990 Feb; 84(3):241-3. PubMed ID: 2303246
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The measurement of erythrocyte uroporphyrinogen 1 synthase in the diagnosis of latent and acute intermittent porphyria.
    Brocklehurst D; Wider de Xifra EA; Batlle A
    Int J Biochem; 1980; 12(5-6):791-3. PubMed ID: 7450134
    [No Abstract]   [Full Text] [Related]  

  • 30. The treatment of acute intermittent porphyria with laevulose.
    Brodie MJ; Moore MR; Thompson GG; Goldberg A
    Clin Sci Mol Med; 1977 Oct; 53(4):365-71. PubMed ID: 913061
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Experience with the red cell uroporphyrinogen synthase (URO-S) assay in kindreds with acute intermittent porphyria (AIP).
    Kreimer-Birnbaum M; Bonkowsky HL; Bottomley SS
    Int J Biochem; 1980; 12(5-6):807-10. PubMed ID: 7450137
    [No Abstract]   [Full Text] [Related]  

  • 32. Induction of terminal enzymes for heme biosynthesis during differentiation of mouse erythroleukemia cells.
    Taketani S; Yoshinaga T; Furukawa T; Kohno H; Tokunaga R; Nishimura K; Inokuchi H
    Eur J Biochem; 1995 Jun; 230(2):760-5. PubMed ID: 7607249
    [TBL] [Abstract][Full Text] [Related]  

  • 33. An unusual case of variegate porphyria with possible homozygous inheritance.
    Coakley J; Hawkins R; Crinis N; McManus J; Blake D; Nordmann Y; Sloan L; Connelly J
    Aust N Z J Med; 1990 Aug; 20(4):587-9. PubMed ID: 2222353
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Studies in porphyria. VII. Induction of uroporphyrinogen-I synthase and expression of the gene defect of acute intermittent porphyria in mitogen-stimulated human lymphocytes.
    Sassa S; Zalar GL; Kappas A
    J Clin Invest; 1978 Feb; 61(2):499-508. PubMed ID: 621286
    [TBL] [Abstract][Full Text] [Related]  

  • 35. The activities of the enzymes of haem biosynthesis in the porphyrias and during treatment of acute intermittent porphyrias.
    Moore MR; McColl KE; Goldberg A
    Int J Biochem; 1980; 12(5-6):941-6. PubMed ID: 7450153
    [No Abstract]   [Full Text] [Related]  

  • 36. DNA polymorphism of human porphobilinogen deaminase gene in acute intermittent porphyria.
    Llewellyn DH; Elder GH; Kalsheker NA; Marsh OW; Harrison PR; Grandchamp B; Picat C; Nordmann Y; Romeo PH; Goossens M
    Lancet; 1987 Sep; 2(8561):706-8. PubMed ID: 2888941
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Erythrocyte uroporphyrinogen I synthase activity as an indicator of acute porphyria.
    Forman DT
    Ann Clin Lab Sci; 1989; 19(2):128-32. PubMed ID: 2751241
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Review: molecular pathogenesis of hepatic acute porphyrias.
    Grandchamp B; Puy H; Lamoril J; Deybach JC; Nordmann Y
    J Gastroenterol Hepatol; 1996 Nov; 11(11):1046-52. PubMed ID: 8985829
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Linkage disequilibrium between DNA polymorphisms within the porphobilinogen deaminase gene.
    Scobie GA; Urquhart AJ; Elder GH; Kalsheker NA; Llewellyn DH; Smyth J; Harrison PR
    Hum Genet; 1990 Jul; 85(2):157-9. PubMed ID: 1973402
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Normal erythrocyte uroporphyrinogen I synthase in a kindred with acute intermittent porphyria.
    Mustajoki P
    Ann Intern Med; 1981 Aug; 95(2):162-6. PubMed ID: 7258864
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.