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Journal Abstract Search

696 related items for PubMed ID: 8998263

  • 1. [Molecular genetics of X-linked primary immunodeficiencies: advances in diagnosis and prevention].
    Carbonara A, Brusco A, Carbonara C.
    Ann Ital Med Int; 1996; 11(3):180-6. PubMed ID: 8998263
    [Abstract] [Full Text] [Related]

  • 2. Molecular genetic analysis of X-linked immunodeficiencies.
    Conley ME.
    Year Immunol; 1993; 7():162-7. PubMed ID: 8372504
    [No Abstract] [Full Text] [Related]

  • 3. The primary immunodeficiencies.
    Rosen FS, Cooper MD, Wedgwood RJ.
    N Engl J Med; 1995 Aug 17; 333(7):431-40. PubMed ID: 7616993
    [No Abstract] [Full Text] [Related]

  • 4. CD40 ligand (CD40L) expression and B cell function in agammaglobulinemia with normal or elevated levels of IgM (HIM). Comparison of X-linked, autosomal recessive, and non-X-linked forms of the disease, and obligate carriers.
    Callard RE, Smith SH, Herbert J, Morgan G, Padayachee M, Lederman S, Chess L, Kroczek RA, Fanslow WC, Armitage RJ.
    J Immunol; 1994 Oct 01; 153(7):3295-306. PubMed ID: 7916370
    [Abstract] [Full Text] [Related]

  • 5. The molecular basis of X-linked agammaglobulinemia, hyper-IgM syndrome, and severe combined immunodeficiency in humans.
    Aruffo A, Hollenbaugh D, Wu LH, Ochs HD.
    Curr Opin Hematol; 1994 Jan 01; 1(1):12-8. PubMed ID: 9371254
    [Abstract] [Full Text] [Related]

  • 6. CD40 ligand mutations in x-linked immunodeficiency with hyper-IgM.
    DiSanto JP, Bonnefoy JY, Gauchat JF, Fischer A, de Saint Basile G.
    Nature; 1993 Feb 11; 361(6412):541-3. PubMed ID: 8094231
    [Abstract] [Full Text] [Related]

  • 7. Carrier detection in X-linked immunodeficiencies. II: An X inactivation assay based on differential methylation of a line-1 repeat at the DXS255 locus.
    Hinds H, Craig IW, Chen ZY, Kraakman ME, Schuurman RK, Hendriks RW.
    Immunodeficiency; 1993 Feb 11; 4(1-4):213-5. PubMed ID: 8167703
    [Abstract] [Full Text] [Related]

  • 8. Prenatal diagnosis and genetic analysis of X-linked immunodeficiency disorders.
    Puck JM.
    Pediatr Res; 1993 Jan 11; 33(1 Suppl):S29-33; discussion S33-4. PubMed ID: 8433872
    [Abstract] [Full Text] [Related]

  • 9. Carrier detection in X-linked immunodeficiencies. I: A PCR-based X chromosome inactivation assay at the MAOA locus.
    Hendriks RW, Chen ZY, Hinds H, Schuurman RK, Craig IW.
    Immunodeficiency; 1993 Jan 11; 4(1-4):209-11. PubMed ID: 8167702
    [Abstract] [Full Text] [Related]

  • 10. Molecular approaches to analysis of X-linked immunodeficiencies.
    Conley ME.
    Annu Rev Immunol; 1992 Jan 11; 10():215-38. PubMed ID: 1590986
    [Abstract] [Full Text] [Related]

  • 11. The X-linked hyper-IgM syndrome: clinical and immunologic features of 79 patients.
    Winkelstein JA, Marino MC, Ochs H, Fuleihan R, Scholl PR, Geha R, Stiehm ER, Conley ME.
    Medicine (Baltimore); 2003 Nov 11; 82(6):373-84. PubMed ID: 14663287
    [Abstract] [Full Text] [Related]

  • 12. Nonrandom X chromosome inactivation in natural killer cells from obligate carriers of X-linked severe combined immunodeficiency.
    Wengler GS, Allen RC, Parolini O, Smith H, Conley ME.
    J Immunol; 1993 Jan 15; 150(2):700-4. PubMed ID: 8093460
    [Abstract] [Full Text] [Related]

  • 13. Hyper immunoglobulin M syndrome due to CD40 deficiency: clinical, molecular, and immunological features.
    Lougaris V, Badolato R, Ferrari S, Plebani A.
    Immunol Rev; 2005 Feb 15; 203():48-66. PubMed ID: 15661021
    [Abstract] [Full Text] [Related]

  • 14. Missense mutation in exon 7 of the common gamma chain gene causes a moderate form of X-linked combined immunodeficiency.
    Schmalstieg FC, Leonard WJ, Noguchi M, Berg M, Rudloff HE, Denney RM, Dave SK, Brooks EG, Goldman AS.
    J Clin Invest; 1995 Mar 15; 95(3):1169-73. PubMed ID: 7883965
    [Abstract] [Full Text] [Related]

  • 15. Hyper-immunoglobulin M syndrome caused by a mutation in the promotor for CD40L.
    Van Hoeyveld E, Zhang PX, De Boeck K, Fuleihan R, Bossuyt X.
    Immunology; 2007 Apr 15; 120(4):497-501. PubMed ID: 17244160
    [Abstract] [Full Text] [Related]

  • 16. X-linked immunodeficiencies.
    Conley ME.
    Curr Opin Genet Dev; 1994 Jun 15; 4(3):401-6. PubMed ID: 7919918
    [Abstract] [Full Text] [Related]

  • 17. X-linked immunodeficiencies.
    Ochs HD, Notarangelo LD.
    Curr Allergy Asthma Rep; 2004 Sep 15; 4(5):339-48. PubMed ID: 15283872
    [Abstract] [Full Text] [Related]

  • 18. Genetic study of a new X-linked recessive immunodeficiency syndrome.
    de Saint-Basile G, Le Deist F, Caniglia M, Lebranchu Y, Griscelli C, Fischer A.
    J Clin Invest; 1992 Mar 15; 89(3):861-6. PubMed ID: 1347296
    [Abstract] [Full Text] [Related]

  • 19. X-linked SCID and other defects of cytokine pathways.
    Uribe L, Weinberg KI.
    Semin Hematol; 1998 Oct 15; 35(4):299-309. PubMed ID: 9801259
    [Abstract] [Full Text] [Related]

  • 20. Defective expression of T-cell CD40 ligand causes X-linked immunodeficiency with hyper-IgM.
    Korthäuer U, Graf D, Mages HW, Brière F, Padayachee M, Malcolm S, Ugazio AG, Notarangelo LD, Levinsky RJ, Kroczek RA.
    Nature; 1993 Feb 11; 361(6412):539-41. PubMed ID: 7679206
    [Abstract] [Full Text] [Related]

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