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PUBMED FOR HANDHELDS

Journal Abstract Search


104 related items for PubMed ID: 2989126

  • 1. Automated differential white cell count (flow cytometry) in a case of eosinophilic total myeloperoxidase (MPO) deficiency.
    Pasini L, Briani G, Boccato P, Lippi U.
    Haematologica; 1985; 70(1):83-5. PubMed ID: 2989126
    [No Abstract] [Full Text] [Related]

  • 2. [Myeloperoxidase deficiency: prevalence in Brescia Province and a study of microbicidal activity in granulocytes].
    Airo' R, Milanesi B, Ferrari CM, Scotuzzi M, Tafuri C.
    Haematologica; 1985; 70(1):12-8. PubMed ID: 2989125
    [No Abstract] [Full Text] [Related]

  • 3. Detection of eosinophilic total myeloperoxidase deficiency (EPOd) by flow cytometry.
    Briani G, Bizzaro N, Cappelletti P, Doretto P.
    Haematologica; 1987; 72(5):471-2. PubMed ID: 2826316
    [No Abstract] [Full Text] [Related]

  • 4. Catalytic activity of neutrophil and eosinophil peroxidase. Cytochemical and biochemical study in total hereditary myeloperoxidase deficiency.
    Lippi U, Cappelletti P, Schinella M.
    Nouv Rev Fr Hematol (1978); 1984; 26(1):35-8. PubMed ID: 6324072
    [Abstract] [Full Text] [Related]

  • 5. [Proceedings: Isolated defect of eosinophilic peroxidase. Light-and electron microscopy findings in a new enzymopathy].
    Schaefer HE, Hellriegel KP, Fischer R.
    Verh Dtsch Ges Pathol; 1974; 58():574. PubMed ID: 4460582
    [No Abstract] [Full Text] [Related]

  • 6. [Peroxidase activity of neutrophil granules in two cases of congenital myeloperoxidase deficiency].
    Breton-Gorius J, Coquin Y, Guichard J.
    C R Acad Hebd Seances Acad Sci D; 1975 Apr 14; 280(14):1753-6. PubMed ID: 238749
    [Abstract] [Full Text] [Related]

  • 7. New approaches to the detection of myeloperoxidase deficiency.
    Dri P, Cramer R, Soranzo MR, Comin A, Miotti V, Patriarca P.
    Blood; 1982 Aug 14; 60(2):323-7. PubMed ID: 6284284
    [Abstract] [Full Text] [Related]

  • 8. [Peroxidase deficiency in eosinophils: an optical and electron microscopy cytologic study apropos of a case].
    Lejeune F, Dournovo M, Turpin F, Saula H, Lortholary P.
    Nouv Rev Fr Hematol (1978); 1988 Aug 14; 30(3):177-82. PubMed ID: 3419898
    [Abstract] [Full Text] [Related]

  • 9. Hereditary myeloperoxidase deficiency: a rare condition? Diagnostic possibilities of a differential white cell autoanalyzer (Hemalog-D).
    Cappelletti P, Lippi U.
    Haematologica; 1983 Aug 14; 68(6):736-41. PubMed ID: 6321302
    [No Abstract] [Full Text] [Related]

  • 10. Eosinophilic peroxidase deficiency: Identification of a point mutation (D648N) and prediction of structural changes.
    Nakagawa T, Ikemoto T, Takeuchi T, Tanaka K, Tanigawa N, Yamamoto D, Shimizu A.
    Hum Mutat; 2001 Mar 14; 17(3):235-6. PubMed ID: 11241847
    [Abstract] [Full Text] [Related]

  • 11. Clinical manifestation of myeloperoxidase deficiency.
    Lanza F.
    J Mol Med (Berl); 1998 Sep 14; 76(10):676-81. PubMed ID: 9766845
    [Abstract] [Full Text] [Related]

  • 12. Partial deficiency of eosinophil peroxidase.
    Hoffmann JJ, Tielens AG.
    Blut; 1987 Mar 14; 54(3):165-9. PubMed ID: 3814833
    [Abstract] [Full Text] [Related]

  • 13. [Hereditary myeloperoxidase deficiency. Clinical, biological and genetic study].
    Cech P, Stalder H, Boreux G, Papathanassiou A, Widmann JJ, Roth P, Rohner A, Miescher PA.
    Schweiz Med Wochenschr; 1977 Oct 15; 107(41):1458. PubMed ID: 199939
    [Abstract] [Full Text] [Related]

  • 14. The incidence of peroxidase and phospholipid deficiency in eosinophilic granulocytes among various Jewish groups in Israel.
    Joshua H, Spitzer A, Presentey B.
    Am J Hum Genet; 1970 Sep 15; 22(5):574-8. PubMed ID: 5516238
    [No Abstract] [Full Text] [Related]

  • 15. [Detection of eosinophil granulocyte myeloperoxidase deficiency].
    Kutter D, Verstraeten L.
    Ann Biol Clin (Paris); 1998 Sep 15; 56(2):205-8. PubMed ID: 9754248
    [No Abstract] [Full Text] [Related]

  • 16. [Automated hemogram and myeloperoxidase deficiency. Analysis of 33 cases].
    Verdot JJ, Bayle J, Juhan I, Aillaud MF, Guitard AM, Muratore R.
    Sem Hop; 1998 Sep 15; 57(9-10):450-7. PubMed ID: 6261386
    [Abstract] [Full Text] [Related]

  • 17. Deficiency of eosinophil peroxidase detected by automated cytochemistry.
    Valdés MD, Calero MA.
    Acta Haematol; 1987 Sep 15; 78(4):265. PubMed ID: 3122494
    [No Abstract] [Full Text] [Related]

  • 18. Acquired neutrophil myeloperoxidase deficiency: an indicator of subclinical activation of blood coagulation?
    d'Onofrio G, Mancini R, Vallone R, Alfano G, Candido A, Palla M, Mango G.
    Blood Cells; 1983 Sep 15; 9(3):455-66. PubMed ID: 6326898
    [Abstract] [Full Text] [Related]

  • 19. [Acquired and hereditary defective forms of granulocytic peroxidase].
    Schaefer HE, Weller P, Lansch D.
    Acta Histochem Suppl; 1983 Sep 15; 28():219-34. PubMed ID: 6412299
    [No Abstract] [Full Text] [Related]

  • 20. Myeloperoxidase deficiency. Immunologic study of a genetic leukocyte defect.
    Salmon SE, Cline MJ, Schultz J, Lehrer RI.
    N Engl J Med; 1970 Jan 29; 282(5):250-3. PubMed ID: 4983030
    [No Abstract] [Full Text] [Related]


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