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Journal Abstract Search

116 related items for PubMed ID: 2986235

  • 1. [Hereditary myeloperoxidase deficiency syndrome: clinical and hematologic features of 10 cases].
    Lanza F, Musto P, Franzè D.
    Recenti Prog Med; 1985 Feb; 76(2):71-8. PubMed ID: 2986235
    [No Abstract] [Full Text] [Related]

  • 2. Characterization of hereditary partial myeloperoxidase deficiency.
    Bos AJ, Weening RS, Hamers MN, Wever R, Behrendt H, Roos D.
    J Lab Clin Med; 1982 Apr; 99(4):589-600. PubMed ID: 6278039
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  • 3. 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 Apr; 26(1):35-8. PubMed ID: 6324072
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  • 5. [Morphological, ultrastructural, cytochemical and functional analysis of neutrophils deficient in myeloperoxidase].
    Lanza F, Spisani S, Fietta A, Traniello S.
    Boll Soc Ital Biol Sper; 1985 Mar 30; 61(3):453-9. PubMed ID: 2992545
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  • 8. [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 Mar 30; 70(1):12-8. PubMed ID: 2989125
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  • 10. 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 Mar 30; 9(3):455-66. PubMed ID: 6326898
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  • 11. [Arakawa-Higashi syndrome].
    Higashi O.
    Nihon Rinsho; 1977 Mar 30; 35 Suppl 1():922-3. PubMed ID: 206748
    [No Abstract] [Full Text] [Related]

  • 12. Primary myeloperoxidase deficiency associated with impaired neutrophil margination and chemotaxis.
    Robertson CF, Thong YH, Hodge GL, Cheney K.
    Acta Paediatr Scand; 1979 Nov 30; 68(6):915-9. PubMed ID: 231890
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  • 13. Hereditary myeloperoxidase deficiency: study of 12 cases.
    Larrocha C, Fernández de Castro M, Fontan G, Viloria A, Fernández-Chacón JL, Jiménez C.
    Scand J Haematol; 1982 Nov 30; 29(5):389-97. PubMed ID: 6296995
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  • 14. Depressed neutrophil-mediated tumor cell cytotoxicity in subjects affected by hereditary myeloperoxidase deficiency and secondary neoplasia.
    Lanza F, Giuliani AL, Amelotti F, Spisani S, Traniello S, Castoldi G.
    Haematologica; 1988 Nov 30; 73(5):355-8. PubMed ID: 2848754
    [No Abstract] [Full Text] [Related]

  • 15. [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
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  • 17. [Coexistence of 2 distinct populations of neutrophil granulocytes, one totally, the other partially deficient in myeloperoxidase].
    Kutter D, Niedner A, Lieners C.
    Bull Soc Sci Med Grand Duche Luxemb; 1994 Apr 14; 131(2):31-4. PubMed ID: 7820907
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  • 19. Impaired neutrophil function and myeloperoxidase deficiency in myeloid metaplasia.
    El-Maallem H, Fletcher J.
    Br J Haematol; 1977 Nov 14; 37(3):323-9. PubMed ID: 203312
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  • 20. [Familial deficiency of B lymphocytes and myeloperoxidase in neutrophils coexistent with skin changes in a female patient].
    Starzycki Z, Lisiewicz J, Moszczyński P.
    Przegl Dermatol; 1985 Nov 14; 72(5):430-4. PubMed ID: 3012654
    [No Abstract] [Full Text] [Related]

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