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Journal Abstract Search

268 related items for PubMed ID: 4258194

  • 1. Fatal familial Leiner's disease: a deficiency of the opsonic activity of serum complement.
    Jacobs JC, Miller ME.
    Pediatrics; 1972 Feb; 49(2):225-32. PubMed ID: 4258194
    [No Abstract] [Full Text] [Related]

  • 2. Leiner's disease and deficiency of C5.
    Miller ME, Koblenzer PJ.
    J Pediatr; 1972 May; 80(5):879-80. PubMed ID: 4259692
    [No Abstract] [Full Text] [Related]

  • 3. Leiner's disease and C5 deficiency.
    Ammann AJ.
    J Pediatr; 1972 Dec; 81(6):1221-2. PubMed ID: 4404926
    [No Abstract] [Full Text] [Related]

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  • 5. Introduction: complement diseases in man.
    Miller ME.
    Birth Defects Orig Artic Ser; 1975 Dec; 11(1):299-300. PubMed ID: 1148384
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  • 6. Familial opsonization defect associated with fatal infantile dermatitis, infections, and histiocytosis.
    Scott H, Moynahan EJ, Risdon RA, Harvey BA, Soothill JF.
    Arch Dis Child; 1975 Apr; 50(4):311-7. PubMed ID: 1096830
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  • 7. A familial deficiency of the phagocytosis-enhancing activity of serum related to a dysfunction of the fifth component of complement (C5).
    Miller ME, Nilsson UR.
    N Engl J Med; 1970 Feb 12; 282(7):354-8. PubMed ID: 5411128
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  • 10. An infant with erythroderma, skin scaling, chronic emesis, and intractable diarrhea.
    Redding AR, Lew DB, Conley ME, Pivnick EK.
    Clin Pediatr (Phila); 2009 Nov 12; 48(9):978-80. PubMed ID: 18832538
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  • 19. [Pustular psoriasis in infants and Leiner-Moussous desquamative erythroderma].
    Beylot C, Bioulac P.
    Nouv Presse Med; 1973 Apr 14; 2(15):1000. PubMed ID: 4267564
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