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Annals of the New York Academy of Sciences

© The New York Academy of Sciences

Cover image for Vol. 1246 The Year in Human and Medical Genetics: Inborn Errors of Immunity II

December 2011

Volume 1246 The Year in Human and Medical Genetics: Inborn Errors of Immunity II

Pages 1–141

  1. Original Articles

    1. Top of page
    2. Original Articles
    3. Corrigendum
    1. You have free access to this content
      The establishment of early B cell tolerance in humans: lessons from primary immunodeficiency diseases (pages 1–10)

      Eric Meffre

      Article first published online: 3 JAN 2012 | DOI: 10.1111/j.1749-6632.2011.06347.x

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      Checkpoints of B cell differentiation: visualizing Ig-centric processes (pages 11–25)

      Magdalena A. Berkowska, Mirjam van der Burg, Jacques J.M. van Dongen and Menno C. van Zelm

      Article first published online: 3 JAN 2012 | DOI: 10.1111/j.1749-6632.2011.06278.x

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      DOCK8 deficiency (pages 26–33)

      Helen C. Su, Huie Jing and Qian Zhang

      Article first published online: 3 JAN 2012 | DOI: 10.1111/j.1749-6632.2011.06295.x

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      Molecular mechanisms of the immunological abnormalities in hyper-IgE syndrome (pages 34–40)

      Yoshiyuki Minegishi and Masako Saito

      Article first published online: 3 JAN 2012 | DOI: 10.1111/j.1749-6632.2011.06280.x

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      Perspectives on common variable immune deficiency (pages 41–49)

      Joon H. Park, Elena S. Resnick and Charlotte Cunningham-Rundles

      Article first published online: 3 JAN 2012 | DOI: 10.1111/j.1749-6632.2011.06338.x

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      DNA repair: the link between primary immunodeficiency and cancer (pages 50–63)

      Noel FCC de Miranda, Andrea Björkman and Qiang Pan-Hammarström

      Article first published online: 3 JAN 2012 | DOI: 10.1111/j.1749-6632.2011.06322.x

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      Inherited defects causing hemophagocytic lymphohistiocytic syndrome (pages 64–76)

      Geneviève de Saint Basile, Gaël Ménasché and Sylvain Latour

      Article first published online: 3 JAN 2012 | DOI: 10.1111/j.1749-6632.2011.06307.x

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      Autoimmune polyendocrinopathy candidiasis ectodermal dystrophy: known and novel aspects of the syndrome (pages 77–91)

      Kai Kisand and Pärt Peterson

      Article first published online: 3 JAN 2012 | DOI: 10.1111/j.1749-6632.2011.06308.x

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      Genetic lessons learned from X-linked Mendelian susceptibility to mycobacterial diseases (pages 92–101)

      Jacinta Bustamante, Capucine Picard, Stéphanie Boisson-Dupuis, Laurent Abel and Jean-Laurent Casanova

      Article first published online: 3 JAN 2012 | DOI: 10.1111/j.1749-6632.2011.06273.x

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      IL-10 and IL-10 receptor defects in humans (pages 102–107)

      Erik-Oliver Glocker, Daniel Kotlarz, Christoph Klein, Neil Shah and Bodo Grimbacher

      Article first published online: 3 JAN 2012 | DOI: 10.1111/j.1749-6632.2011.06339.x

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      The case for newborn screening for severe combined immunodeficiency and related disorders (pages 108–117)

      Jennifer M. Puck

      Article first published online: 3 JAN 2012 | DOI: 10.1111/j.1749-6632.2011.06346.x

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      Newborn screening for primary immunodeficiencies: beyond SCID and XLA (pages 118–130)

      Stephan Borte, Ning Wang, Sólveig Óskarsdóttir, Ulrika von Döbeln and Lennart Hammarström

      Article first published online: 3 JAN 2012 | DOI: 10.1111/j.1749-6632.2011.06350.x

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      Homologous recombination-based gene therapy for the primary immunodeficiencies (pages 131–140)

      Matthew Porteus

      Article first published online: 3 JAN 2012 | DOI: 10.1111/j.1749-6632.2011.06314.x

  2. Corrigendum

    1. Top of page
    2. Original Articles
    3. Corrigendum
    1. You have free access to this content
      Corrigendum for Ann. N.Y. Acad. Sci. 1238: 106–121 (page 141)

      Article first published online: 3 JAN 2012 | DOI: 10.1111/j.1749-6632.2011.06406.x

      This article corrects:

      Familial hemophagocytic lymphohistiocytosis and X-linked lymphoproliferative disease

      Vol. 1238, Issue 1, 106–121, Article first published online: 30 NOV 2011

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