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25. Intrinsic polymorphonuclear chemotactic defect in a boy with chronic granulomatous disease. de la Cruz R; Jain M; Hsu K; Lim DT Allergol Immunopathol (Madr); 1983; 11(6):457-64. PubMed ID: 6670661 [TBL] [Abstract][Full Text] [Related]
26. [Myeloperoxidase deficiency in polymorphonuclear cells of children with recurrent infections]. Vázquez-Escobosa C; Puebla-Pérez AM; Gómez-Estrada H Bol Med Hosp Infant Mex; 1984 Nov; 41(11):614-6. PubMed ID: 6097283 [No Abstract] [Full Text] [Related]
27. Clinical syndrome of chemotaxis defect, infections, and hyperimmunoglobulinemia E. A case report. Wyre HW; Johnson WT Arch Dermatol; 1978 Jan; 114(1):74-7. PubMed ID: 619787 [TBL] [Abstract][Full Text] [Related]
28. Further evaluation of luminol-enhanced luminescence in the diagnosis of disorders of leukocyte oxidative metabolism: role of myeloperoxidase. Cohen MS; Shirley PS; DeChatelet LR Clin Chem; 1983 Mar; 29(3):513-5. PubMed ID: 6297833 [TBL] [Abstract][Full Text] [Related]
29. Leukocyte functions. van der Valk P; Herman CJ Lab Invest; 1987 Feb; 56(2):127-37. PubMed ID: 3543488 [TBL] [Abstract][Full Text] [Related]
31. [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]
32. Myeloperoxidase deficiency. Increased sensitivity for immunocytochemical compared to cytochemical detection of enzyme. Ross DW; Kaplow LS Arch Pathol Lab Med; 1985 Nov; 109(11):1005-6. PubMed ID: 2996459 [TBL] [Abstract][Full Text] [Related]
33. Quantitative slot-blot chemiluminescence assay for determination of myeloperoxidase from human granulocytes. Dahlgren C; Follin P; Lundqvist H; Sjölin C Anal Biochem; 1993 Oct; 214(1):284-8. PubMed ID: 8250236 [TBL] [Abstract][Full Text] [Related]
34. Function of granulocytes with deficient myeloperoxidase-mediated iodination in a patient with generalized pustular psoriasis. Stendahl O; Lindgren S Scand J Haematol; 1976 Feb; 16(2):144-53. PubMed ID: 176720 [TBL] [Abstract][Full Text] [Related]
35. Pattern of inheritance in hereditary myeloperoxidase deficiency associated with the R569W missense mutation. Nauseef WM; Cogley M; Bock S; Petrides PE J Leukoc Biol; 1998 Feb; 63(2):264-9. PubMed ID: 9468285 [TBL] [Abstract][Full Text] [Related]
36. Prevalence of inherited myeloperoxidase deficiency in Japan. Nunoi H; Kohi F; Kajiwara H; Suzuki K Microbiol Immunol; 2003; 47(7):527-31. PubMed ID: 12953846 [TBL] [Abstract][Full Text] [Related]
38. A case of total peripheral aneosinophilia associated with complete deficiency of myeloperoxidase. Muller-Hagedorn S; Forges T; Kutter D; Conrad R Acta Clin Belg; 1996; 51(4):275-8. PubMed ID: 8858895 [TBL] [Abstract][Full Text] [Related]