| Edition |
2nd ed. |
| Description |
1 online resource (xvii, 726 pages, 32 unnumbered pages of plates) : illustrations (some color) |
| Physical Medium |
polychrome |
| Description |
text file |
| Bibliography |
Includes bibliographical references and index. |
| Contents |
Genetically determined immunodeficiency diseases / C.I. Edvard Smith, Hans D. Ochs, and Jennifer M. Puck -- Genetic principles and technologies in the study of immune disorders / Jennifer M. Puck and Robert L. Nussbaum -- Mammalian hematopoietic development and function / Gerald J. Sprangrude -- T cell development / Rae S.M. Yeung [and others] -- Molecular mechanisms guiding B cell development / Antonius Rolink [and others] -- Signal transduction by T and B lymphocyte antigen receptors / Neetu Gupta, Anthony L. DeFranco, and Arthur Weiss -- Lymphoid organ development, cell trafficking, and lymphocute responses / Sirpa Jalkanen and Marko Salmi -- Phagocytic system / Kuender D. Yang, Paul G. Quie, and Harry R. Hill -- X-linked severe combined immunodeficiency / Jennifer M. Puck -- Autosomal recessive severe combined immunodeficiency due to defects of cytokine signaling pathways / Fabio Candotti and Luigi Notarangelo -- V(D)J recombination defects / Jean-Pierre de Villartay, Klaus Schwarz, and Anna Villa -- Immunodeficiency due to defects of purine metabolism / Rochelle Hirschhorn, Fabio Candotti -- Severe combined immunodeficiency due to mutations in the CD45 gene / Talal Chatila and Markku Heikinheimo -- Severe combined immunodeficiency due to defects in T cell receptor-associated protein kinases / Melissa E. Elder -- Human interleukin-2 receptor [alpha] deficiency / Chaim M. Roifman -- CD3 and CD8 deficiencies / José R. Regueiro and Teresa Espanol -- Molecular basis of major histocompatibility complex class II deficiency / Walter Reith, Barbara Lisowska-Grospierre, and Alain Fischer -- Peptide transporter defects in human leukocyte antigen class I deficiency / Henri de la Salle, Lionel Donato, and Daniel Hanau -- CD40, CD40 ligand, and the hyper-IgM syndrome / Raif S. Geha, Alessandro Plebani, and Luigi Notarangelo -- Autosomal hyper-IgM syndromes caused by an intrinsic B cell defect / Anne Durandy, Patrick Revy, and Alain Fischer -- X-linked agammaglobulinemia / C.I. Edvard Smith, Anne B. Satterthwaite, and Owen N. Witte -- Autosomal recessive agammaglobulinemia / Mary Ellen Conley -- Genetic approach to common variable immunodeficiency and IgA deficiency / Lennart Hammarström and C.I. Edvard Smith -- Autoimmune lymphoproliferative syndrome / Jennifer M. Puck [and others]. |
|
Autoimmune polyendocrinopathy, candidiasis and ectodermal dystrophy / Leena Peltonen-Palotie, Maria Halonen, and Jaakko Perheentupa -- Immune dysregulation, polyendocrinopathy, enteropathy; X-linked inheritance / Troy R. Torgerson [and others] -- Periodic fever syndromes / Daniel Kastner, Susannah Brydges, and Keith M. Hull -- Inherited disorders of the interleukin-12/23-interferon gamma axis / Melanie Newport [and others] -- Ataxia-telangiectasia / Martin F. Lavin and Yosef Shiloh -- Chromosomal instability syndromes other than ataxia-telangiectasia / Rolf-Dieter Wegner [and others] -- Wiskott-Aldrich syndrome / Hans D. Ochs, Fred S. Rosen. |
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X-linked lymphoproliferative disease due to defects of SH2D1A / Volker Schuster and Cox Terhorst -- DiGeorge syndrome / Deborah A. Driscoll and Kathleen E. Sullivan -- Hyper IgE recurrent infection syndromes / Bodo Grimbacher, Jennifer F. Puck, and Stevn M. Holland -- Immunodeficiency with centromere instability and facial anomalies / R. Scott Hansen, Corry Weemaes, and Cisca Wijmenga -- Immunodeficiencies with associated manifestations of skin, hair, teeth, and skeleton / Mario Abinun, Ilkka Kaitila and Jean-Laurent Casanova -- Chronic granulomatous disease / Dirk Roos, Taco W. Kuijpers, and John T. Curnutte -- Cell adhesion and leukocyte adhesion defects / Amos Etzioni and John M. Harlan. |
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Cyclic and congenital neutropenia due to defects in neutrophil elastase / David Dale and Andrew Aprikyan -- Chediak-Higashi syndrome / Richard A. Spritz -- Inherited hemophagocytic syndromes / Geneviève de Saint Basile -- Genetically determined deficiencies of the complement system / Kathleen E. Sullivan and Jerry A. Winkelstein -- Assessment of the immune system / Helen M. Chapel, Siraj Misbah, and A. David Webster -- Genetic aspects of primary immunodeficiencies / Jennifer M. Puck -- Immunodeficiency information systems / Jouni Väliaho [and others] -- Conventional therapy of primary immunodeficiency diseases / E. Richard Stiehm and Helen M. Chapel -- Bone marrow transplantation for primary immunodeficiency diseases / Rebecca H. Buckley and Alain Fischer -- Gene therapy / Fabio Candotti and Alain Fischer. |
| Local Note |
eBooks on EBSCOhost EBSCO eBook Subscription Academic Collection - North America |
| Subject |
Immunological deficiency syndromes -- Genetic aspects.
|
|
Immunological deficiency syndromes. |
|
Immunologic Deficiency Syndromes -- genetics. |
| Genre/Form |
Electronic books.
|
| Added Author |
Ochs, Hans D., 1936-
|
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Smith, C. I. Edvard, 1951-
|
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Puck, Jennifer, 1949-
|
| Other Form: |
Print version: Primary immunodeficiency diseases. 2nd ed. New York : Oxford University Press, 2007 9780195147742 (DLC) 2005027951 (OCoLC)61745545 |
|
Print version: Primary immunodeficiency diseases. 2nd ed. New York : Oxford University Press, 2007 019514774X 9780195147742 (DLC) 2005027951 (OCoLC)61745545 |
| ISBN |
9780199747962 (electronic book) |
|
0199747962 (electronic book) |
|
019514774X (alkaline paper) |
|
9780195147742 (alkaline paper) |
|
