Primary immunodeficiency diseases :: a molecular and genetic approach /
This book will present the principles of immunology, genetics, and molecular biology as they pertain to the primary immunodeficiency diseases; the hallmark of these diseases is an increased susceptbility to infections. The major authorities in the field address both the scientific aspects and the pr...
Gespeichert in:
| Weitere Verfasser: | , , |
|---|---|
| Format: | Elektronisch E-Book |
| Sprache: | English |
| Veröffentlicht: |
New York :
Oxford University Press,
2007.
|
| Ausgabe: | 2nd ed. |
| Schlagworte: | |
| Online-Zugang: | Volltext |
| Zusammenfassung: | This book will present the principles of immunology, genetics, and molecular biology as they pertain to the primary immunodeficiency diseases; the hallmark of these diseases is an increased susceptbility to infections. The major authorities in the field address both the scientific aspects and the practical, clinical aspects of these disorders, including therapeutic strategies. The second edition features 11 new chapters as well as a significant updating of all the first edition material in this fast-developing field. The book should appeal to geneticists, pediatricians, immunologists, infectio. |
| Beschreibung: | 1 online resource (xvii, 726 pages, 32 unnumbered pages of plates) : illustrations (some color) |
| Bibliographie: | Includes bibliographical references and index. |
| ISBN: | 9780199747962 0199747962 019514774X 9780195147742 9786610564279 6610564272 1429420456 9781429420457 |
Internformat
MARC
| LEADER | 00000cam a2200000 a 4500 | ||
|---|---|---|---|
| 001 | ZDB-4-EBA-ocm76909372 | ||
| 003 | OCoLC | ||
| 005 | 20241004212047.0 | ||
| 006 | m o d | ||
| 007 | cr cnu---unuuu | ||
| 008 | 061208s2007 nyuaf ob 001 0 eng d | ||
| 010 | |z 2005027951 | ||
| 040 | |a N$T |b eng |e pn |c N$T |d YDXCP |d OCLCQ |d OCLCG |d OCLCQ |d N$T |d OCLCQ |d IDEBK |d OKC |d DKDLA |d OCLCQ |d NLGGC |d OCLCQ |d TOA |d AGLDB |d OCLCO |d PIFAG |d OCLCO |d OCLCQ |d WY@ |d OCLCO |d OCLCA |d LUE |d OCLCO |d STF |d OCLCO |d VNS |d UAB |d OCLCQ |d VTS |d OCLCQ |d REC |d OCLCQ |d M8D |d OCLCO |d OCLCA |d VLY |d OCLCO |d OCLCQ |d INARC |d OCLCL |d OCLCQ |d OCLCL | ||
| 016 | 7 | |z 101257982 |2 DNLM | |
| 019 | |a 144222136 |a 427962335 |a 482023971 |a 666967197 |a 1162007393 | ||
| 020 | |a 9780199747962 |q (electronic bk.) | ||
| 020 | |a 0199747962 |q (electronic bk.) | ||
| 020 | |a 019514774X |q (alk. paper) | ||
| 020 | |a 9780195147742 |q (alk. paper) | ||
| 020 | |a 9786610564279 | ||
| 020 | |a 6610564272 | ||
| 020 | |a 1429420456 | ||
| 020 | |a 9781429420457 | ||
| 035 | |a (OCoLC)76909372 |z (OCoLC)144222136 |z (OCoLC)427962335 |z (OCoLC)482023971 |z (OCoLC)666967197 |z (OCoLC)1162007393 | ||
| 050 | 4 | |a RC606 |b .G46 2007eb | |
| 060 | 4 | |a WD 308 |b P9523 2006 | |
| 072 | 7 | |a MED |x 044000 |2 bisacsh | |
| 072 | 7 | |a HEA |x 027000 |2 bisacsh | |
| 072 | 7 | |a HEA |x 039090 |2 bisacsh | |
| 082 | 7 | |a 616.97/9042 |2 22 | |
| 049 | |a MAIN | ||
| 245 | 0 | 0 | |a Primary immunodeficiency diseases : |b a molecular and genetic approach / |c edited by Hans D. Ochs, C.I. Edvard Smith, Jennifer M. Puck. |
| 250 | |a 2nd ed. | ||
| 260 | |a New York : |b Oxford University Press, |c 2007. | ||
| 300 | |a 1 online resource (xvii, 726 pages, 32 unnumbered pages of plates) : |b illustrations (some color) | ||
| 336 | |a text |b txt |2 rdacontent | ||
| 337 | |a computer |b c |2 rdamedia | ||
| 338 | |a online resource |b cr |2 rdacarrier | ||
| 504 | |a Includes bibliographical references and index. | ||
| 505 | 0 | |a 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]. | |
| 505 | 0 | |a 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. | |
| 505 | 0 | |a 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. | |
| 505 | 0 | |a 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. | |
| 588 | 0 | |a Print version record. | |
| 520 | |a This book will present the principles of immunology, genetics, and molecular biology as they pertain to the primary immunodeficiency diseases; the hallmark of these diseases is an increased susceptbility to infections. The major authorities in the field address both the scientific aspects and the practical, clinical aspects of these disorders, including therapeutic strategies. The second edition features 11 new chapters as well as a significant updating of all the first edition material in this fast-developing field. The book should appeal to geneticists, pediatricians, immunologists, infectio. | ||
| 546 | |a English. | ||
| 650 | 0 | |a Immunological deficiency syndromes |x Genetic aspects. | |
| 650 | 2 | |a Immunologic Deficiency Syndromes |x genetics | |
| 650 | 6 | |a Syndromes de déficit immunitaire |x Aspect génétique. | |
| 650 | 7 | |a MEDICAL |x Immunology. |2 bisacsh | |
| 650 | 7 | |a HEALTH & FITNESS |x Allergies. |2 bisacsh | |
| 650 | 7 | |a HEALTH & FITNESS |x Diseases |x Immune System. |2 bisacsh | |
| 700 | 1 | |a Ochs, Hans D., |d 1936- |1 https://id.oclc.org/worldcat/entity/E39PBJghjjChHbFhxDhwvjmPQq |0 http://id.loc.gov/authorities/names/n97803607 | |
| 700 | 1 | |a Smith, C. I. Edvard, |d 1951- |1 https://id.oclc.org/worldcat/entity/E39PCjwfvjfbHb7qcFbvT8qvVy |0 http://id.loc.gov/authorities/names/n97803608 | |
| 700 | 1 | |a Puck, Jennifer, |d 1949- |1 https://id.oclc.org/worldcat/entity/E39PCjKFgtWjd8MGYBbG6kTBHd |0 http://id.loc.gov/authorities/names/n97803609 | |
| 758 | |i has work: |a Primary immunodeficiency diseases (Text) |1 https://id.oclc.org/worldcat/entity/E39PCFRPm7dDFYYrGkc6XmXC43 |4 https://id.oclc.org/worldcat/ontology/hasWork | ||
| 776 | 0 | 8 | |i Print version: |t Primary immunodeficiency diseases. |b 2nd ed. |d New York : Oxford University Press, 2007 |z 9780195147742 |w (DLC) 2005027951 |w (OCoLC)61745545 |
| 776 | 0 | 8 | |i Print version: |t Primary immunodeficiency diseases. |b 2nd ed. |d New York : Oxford University Press, 2007 |z 019514774X |z 9780195147742 |w (DLC) 2005027951 |w (OCoLC)61745545 |
| 856 | 4 | 0 | |l FWS01 |p ZDB-4-EBA |q FWS_PDA_EBA |u https://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&AN=167565 |3 Volltext |
| 938 | |a Internet Archive |b INAR |n primaryimmunodef0000unse_h6g5 | ||
| 938 | |a EBSCOhost |b EBSC |n 167565 | ||
| 938 | |a ProQuest MyiLibrary Digital eBook Collection |b IDEB |n 56427 | ||
| 938 | |a YBP Library Services |b YANK |n 2495777 | ||
| 938 | |a YBP Library Services |b YANK |n 3288981 | ||
| 994 | |a 92 |b GEBAY | ||
| 912 | |a ZDB-4-EBA | ||
| 049 | |a DE-863 | ||
Datensatz im Suchindex
| DE-BY-FWS_katkey | ZDB-4-EBA-ocm76909372 |
|---|---|
| _version_ | 1816881643262050304 |
| adam_text | |
| any_adam_object | |
| author2 | Ochs, Hans D., 1936- Smith, C. I. Edvard, 1951- Puck, Jennifer, 1949- |
| author2_role | |
| author2_variant | h d o hd hdo c i e s cie cies j p jp |
| author_GND | http://id.loc.gov/authorities/names/n97803607 http://id.loc.gov/authorities/names/n97803608 http://id.loc.gov/authorities/names/n97803609 |
| author_facet | Ochs, Hans D., 1936- Smith, C. I. Edvard, 1951- Puck, Jennifer, 1949- |
| author_sort | Ochs, Hans D., 1936- |
| building | Verbundindex |
| bvnumber | localFWS |
| callnumber-first | R - Medicine |
| callnumber-label | RC606 |
| callnumber-raw | RC606 .G46 2007eb |
| callnumber-search | RC606 .G46 2007eb |
| callnumber-sort | RC 3606 G46 42007EB |
| callnumber-subject | RC - Internal Medicine |
| collection | ZDB-4-EBA |
| 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. 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. 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. |
| ctrlnum | (OCoLC)76909372 |
| dewey-full | 616.97/9042 |
| dewey-hundreds | 600 - Technology (Applied sciences) |
| dewey-ones | 616 - Diseases |
| dewey-raw | 616.97/9042 |
| dewey-search | 616.97/9042 |
| dewey-sort | 3616.97 49042 |
| dewey-tens | 610 - Medicine and health |
| discipline | Medizin |
| edition | 2nd ed. |
| format | Electronic eBook |
| fullrecord | <?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>08829cam a2200745 a 4500</leader><controlfield tag="001">ZDB-4-EBA-ocm76909372 </controlfield><controlfield tag="003">OCoLC</controlfield><controlfield tag="005">20241004212047.0</controlfield><controlfield tag="006">m o d </controlfield><controlfield tag="007">cr cnu---unuuu</controlfield><controlfield tag="008">061208s2007 nyuaf ob 001 0 eng d</controlfield><datafield tag="010" ind1=" " ind2=" "><subfield code="z"> 2005027951</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">N$T</subfield><subfield code="b">eng</subfield><subfield code="e">pn</subfield><subfield code="c">N$T</subfield><subfield code="d">YDXCP</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">OCLCG</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">N$T</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">IDEBK</subfield><subfield code="d">OKC</subfield><subfield code="d">DKDLA</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">NLGGC</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">TOA</subfield><subfield code="d">AGLDB</subfield><subfield code="d">OCLCO</subfield><subfield code="d">PIFAG</subfield><subfield code="d">OCLCO</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">WY@</subfield><subfield code="d">OCLCO</subfield><subfield code="d">OCLCA</subfield><subfield code="d">LUE</subfield><subfield code="d">OCLCO</subfield><subfield code="d">STF</subfield><subfield code="d">OCLCO</subfield><subfield code="d">VNS</subfield><subfield code="d">UAB</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">VTS</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">REC</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">M8D</subfield><subfield code="d">OCLCO</subfield><subfield code="d">OCLCA</subfield><subfield code="d">VLY</subfield><subfield code="d">OCLCO</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">INARC</subfield><subfield code="d">OCLCL</subfield><subfield code="d">OCLCQ</subfield><subfield code="d">OCLCL</subfield></datafield><datafield tag="016" ind1="7" ind2=" "><subfield code="z">101257982</subfield><subfield code="2">DNLM</subfield></datafield><datafield tag="019" ind1=" " ind2=" "><subfield code="a">144222136</subfield><subfield code="a">427962335</subfield><subfield code="a">482023971</subfield><subfield code="a">666967197</subfield><subfield code="a">1162007393</subfield></datafield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">9780199747962</subfield><subfield code="q">(electronic bk.)</subfield></datafield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">0199747962</subfield><subfield code="q">(electronic bk.)</subfield></datafield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">019514774X</subfield><subfield code="q">(alk. paper)</subfield></datafield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">9780195147742</subfield><subfield code="q">(alk. paper)</subfield></datafield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">9786610564279</subfield></datafield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">6610564272</subfield></datafield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">1429420456</subfield></datafield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">9781429420457</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(OCoLC)76909372</subfield><subfield code="z">(OCoLC)144222136</subfield><subfield code="z">(OCoLC)427962335</subfield><subfield code="z">(OCoLC)482023971</subfield><subfield code="z">(OCoLC)666967197</subfield><subfield code="z">(OCoLC)1162007393</subfield></datafield><datafield tag="050" ind1=" " ind2="4"><subfield code="a">RC606</subfield><subfield code="b">.G46 2007eb</subfield></datafield><datafield tag="060" ind1=" " ind2="4"><subfield code="a">WD 308</subfield><subfield code="b">P9523 2006</subfield></datafield><datafield tag="072" ind1=" " ind2="7"><subfield code="a">MED</subfield><subfield code="x">044000</subfield><subfield code="2">bisacsh</subfield></datafield><datafield tag="072" ind1=" " ind2="7"><subfield code="a">HEA</subfield><subfield code="x">027000</subfield><subfield code="2">bisacsh</subfield></datafield><datafield tag="072" ind1=" " ind2="7"><subfield code="a">HEA</subfield><subfield code="x">039090</subfield><subfield code="2">bisacsh</subfield></datafield><datafield tag="082" ind1="7" ind2=" "><subfield code="a">616.97/9042</subfield><subfield code="2">22</subfield></datafield><datafield tag="049" ind1=" " ind2=" "><subfield code="a">MAIN</subfield></datafield><datafield tag="245" ind1="0" ind2="0"><subfield code="a">Primary immunodeficiency diseases :</subfield><subfield code="b">a molecular and genetic approach /</subfield><subfield code="c">edited by Hans D. Ochs, C.I. Edvard Smith, Jennifer M. Puck.</subfield></datafield><datafield tag="250" ind1=" " ind2=" "><subfield code="a">2nd ed.</subfield></datafield><datafield tag="260" ind1=" " ind2=" "><subfield code="a">New York :</subfield><subfield code="b">Oxford University Press,</subfield><subfield code="c">2007.</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">1 online resource (xvii, 726 pages, 32 unnumbered pages of plates) :</subfield><subfield code="b">illustrations (some color)</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="a">text</subfield><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="a">computer</subfield><subfield code="b">c</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="a">online resource</subfield><subfield code="b">cr</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="504" ind1=" " ind2=" "><subfield code="a">Includes bibliographical references and index.</subfield></datafield><datafield tag="505" ind1="0" ind2=" "><subfield code="a">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].</subfield></datafield><datafield tag="505" ind1="0" ind2=" "><subfield code="a">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.</subfield></datafield><datafield tag="505" ind1="0" ind2=" "><subfield code="a">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.</subfield></datafield><datafield tag="505" ind1="0" ind2=" "><subfield code="a">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.</subfield></datafield><datafield tag="588" ind1="0" ind2=" "><subfield code="a">Print version record.</subfield></datafield><datafield tag="520" ind1=" " ind2=" "><subfield code="a">This book will present the principles of immunology, genetics, and molecular biology as they pertain to the primary immunodeficiency diseases; the hallmark of these diseases is an increased susceptbility to infections. The major authorities in the field address both the scientific aspects and the practical, clinical aspects of these disorders, including therapeutic strategies. The second edition features 11 new chapters as well as a significant updating of all the first edition material in this fast-developing field. The book should appeal to geneticists, pediatricians, immunologists, infectio.</subfield></datafield><datafield tag="546" ind1=" " ind2=" "><subfield code="a">English.</subfield></datafield><datafield tag="650" ind1=" " ind2="0"><subfield code="a">Immunological deficiency syndromes</subfield><subfield code="x">Genetic aspects.</subfield></datafield><datafield tag="650" ind1=" " ind2="2"><subfield code="a">Immunologic Deficiency Syndromes</subfield><subfield code="x">genetics</subfield></datafield><datafield tag="650" ind1=" " ind2="6"><subfield code="a">Syndromes de déficit immunitaire</subfield><subfield code="x">Aspect génétique.</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">MEDICAL</subfield><subfield code="x">Immunology.</subfield><subfield code="2">bisacsh</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">HEALTH & FITNESS</subfield><subfield code="x">Allergies.</subfield><subfield code="2">bisacsh</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">HEALTH & FITNESS</subfield><subfield code="x">Diseases</subfield><subfield code="x">Immune System.</subfield><subfield code="2">bisacsh</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Ochs, Hans D.,</subfield><subfield code="d">1936-</subfield><subfield code="1">https://id.oclc.org/worldcat/entity/E39PBJghjjChHbFhxDhwvjmPQq</subfield><subfield code="0">http://id.loc.gov/authorities/names/n97803607</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Smith, C. I. Edvard,</subfield><subfield code="d">1951-</subfield><subfield code="1">https://id.oclc.org/worldcat/entity/E39PCjwfvjfbHb7qcFbvT8qvVy</subfield><subfield code="0">http://id.loc.gov/authorities/names/n97803608</subfield></datafield><datafield tag="700" ind1="1" ind2=" "><subfield code="a">Puck, Jennifer,</subfield><subfield code="d">1949-</subfield><subfield code="1">https://id.oclc.org/worldcat/entity/E39PCjKFgtWjd8MGYBbG6kTBHd</subfield><subfield code="0">http://id.loc.gov/authorities/names/n97803609</subfield></datafield><datafield tag="758" ind1=" " ind2=" "><subfield code="i">has work:</subfield><subfield code="a">Primary immunodeficiency diseases (Text)</subfield><subfield code="1">https://id.oclc.org/worldcat/entity/E39PCFRPm7dDFYYrGkc6XmXC43</subfield><subfield code="4">https://id.oclc.org/worldcat/ontology/hasWork</subfield></datafield><datafield tag="776" ind1="0" ind2="8"><subfield code="i">Print version:</subfield><subfield code="t">Primary immunodeficiency diseases.</subfield><subfield code="b">2nd ed.</subfield><subfield code="d">New York : Oxford University Press, 2007</subfield><subfield code="z">9780195147742</subfield><subfield code="w">(DLC) 2005027951</subfield><subfield code="w">(OCoLC)61745545</subfield></datafield><datafield tag="776" ind1="0" ind2="8"><subfield code="i">Print version:</subfield><subfield code="t">Primary immunodeficiency diseases.</subfield><subfield code="b">2nd ed.</subfield><subfield code="d">New York : Oxford University Press, 2007</subfield><subfield code="z">019514774X</subfield><subfield code="z">9780195147742</subfield><subfield code="w">(DLC) 2005027951</subfield><subfield code="w">(OCoLC)61745545</subfield></datafield><datafield tag="856" ind1="4" ind2="0"><subfield code="l">FWS01</subfield><subfield code="p">ZDB-4-EBA</subfield><subfield code="q">FWS_PDA_EBA</subfield><subfield code="u">https://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&AN=167565</subfield><subfield code="3">Volltext</subfield></datafield><datafield tag="938" ind1=" " ind2=" "><subfield code="a">Internet Archive</subfield><subfield code="b">INAR</subfield><subfield code="n">primaryimmunodef0000unse_h6g5</subfield></datafield><datafield tag="938" ind1=" " ind2=" "><subfield code="a">EBSCOhost</subfield><subfield code="b">EBSC</subfield><subfield code="n">167565</subfield></datafield><datafield tag="938" ind1=" " ind2=" "><subfield code="a">ProQuest MyiLibrary Digital eBook Collection</subfield><subfield code="b">IDEB</subfield><subfield code="n">56427</subfield></datafield><datafield tag="938" ind1=" " ind2=" "><subfield code="a">YBP Library Services</subfield><subfield code="b">YANK</subfield><subfield code="n">2495777</subfield></datafield><datafield tag="938" ind1=" " ind2=" "><subfield code="a">YBP Library Services</subfield><subfield code="b">YANK</subfield><subfield code="n">3288981</subfield></datafield><datafield tag="994" ind1=" " ind2=" "><subfield code="a">92</subfield><subfield code="b">GEBAY</subfield></datafield><datafield tag="912" ind1=" " ind2=" "><subfield code="a">ZDB-4-EBA</subfield></datafield><datafield tag="049" ind1=" " ind2=" "><subfield code="a">DE-863</subfield></datafield></record></collection> |
| id | ZDB-4-EBA-ocm76909372 |
| illustrated | Illustrated |
| indexdate | 2024-11-27T13:15:59Z |
| institution | BVB |
| isbn | 9780199747962 0199747962 019514774X 9780195147742 9786610564279 6610564272 1429420456 9781429420457 |
| language | English |
| oclc_num | 76909372 |
| open_access_boolean | |
| owner | MAIN DE-863 DE-BY-FWS |
| owner_facet | MAIN DE-863 DE-BY-FWS |
| physical | 1 online resource (xvii, 726 pages, 32 unnumbered pages of plates) : illustrations (some color) |
| psigel | ZDB-4-EBA |
| publishDate | 2007 |
| publishDateSearch | 2007 |
| publishDateSort | 2007 |
| publisher | Oxford University Press, |
| record_format | marc |
| spelling | Primary immunodeficiency diseases : a molecular and genetic approach / edited by Hans D. Ochs, C.I. Edvard Smith, Jennifer M. Puck. 2nd ed. New York : Oxford University Press, 2007. 1 online resource (xvii, 726 pages, 32 unnumbered pages of plates) : illustrations (some color) text txt rdacontent computer c rdamedia online resource cr rdacarrier Includes bibliographical references and index. 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. 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. 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. Print version record. This book will present the principles of immunology, genetics, and molecular biology as they pertain to the primary immunodeficiency diseases; the hallmark of these diseases is an increased susceptbility to infections. The major authorities in the field address both the scientific aspects and the practical, clinical aspects of these disorders, including therapeutic strategies. The second edition features 11 new chapters as well as a significant updating of all the first edition material in this fast-developing field. The book should appeal to geneticists, pediatricians, immunologists, infectio. English. Immunological deficiency syndromes Genetic aspects. Immunologic Deficiency Syndromes genetics Syndromes de déficit immunitaire Aspect génétique. MEDICAL Immunology. bisacsh HEALTH & FITNESS Allergies. bisacsh HEALTH & FITNESS Diseases Immune System. bisacsh Ochs, Hans D., 1936- https://id.oclc.org/worldcat/entity/E39PBJghjjChHbFhxDhwvjmPQq http://id.loc.gov/authorities/names/n97803607 Smith, C. I. Edvard, 1951- https://id.oclc.org/worldcat/entity/E39PCjwfvjfbHb7qcFbvT8qvVy http://id.loc.gov/authorities/names/n97803608 Puck, Jennifer, 1949- https://id.oclc.org/worldcat/entity/E39PCjKFgtWjd8MGYBbG6kTBHd http://id.loc.gov/authorities/names/n97803609 has work: Primary immunodeficiency diseases (Text) https://id.oclc.org/worldcat/entity/E39PCFRPm7dDFYYrGkc6XmXC43 https://id.oclc.org/worldcat/ontology/hasWork 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 FWS01 ZDB-4-EBA FWS_PDA_EBA https://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&AN=167565 Volltext |
| spellingShingle | Primary immunodeficiency diseases : a molecular and genetic approach / 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. 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. 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. Immunological deficiency syndromes Genetic aspects. Immunologic Deficiency Syndromes genetics Syndromes de déficit immunitaire Aspect génétique. MEDICAL Immunology. bisacsh HEALTH & FITNESS Allergies. bisacsh HEALTH & FITNESS Diseases Immune System. bisacsh |
| title | Primary immunodeficiency diseases : a molecular and genetic approach / |
| title_auth | Primary immunodeficiency diseases : a molecular and genetic approach / |
| title_exact_search | Primary immunodeficiency diseases : a molecular and genetic approach / |
| title_full | Primary immunodeficiency diseases : a molecular and genetic approach / edited by Hans D. Ochs, C.I. Edvard Smith, Jennifer M. Puck. |
| title_fullStr | Primary immunodeficiency diseases : a molecular and genetic approach / edited by Hans D. Ochs, C.I. Edvard Smith, Jennifer M. Puck. |
| title_full_unstemmed | Primary immunodeficiency diseases : a molecular and genetic approach / edited by Hans D. Ochs, C.I. Edvard Smith, Jennifer M. Puck. |
| title_short | Primary immunodeficiency diseases : |
| title_sort | primary immunodeficiency diseases a molecular and genetic approach |
| title_sub | a molecular and genetic approach / |
| topic | Immunological deficiency syndromes Genetic aspects. Immunologic Deficiency Syndromes genetics Syndromes de déficit immunitaire Aspect génétique. MEDICAL Immunology. bisacsh HEALTH & FITNESS Allergies. bisacsh HEALTH & FITNESS Diseases Immune System. bisacsh |
| topic_facet | Immunological deficiency syndromes Genetic aspects. Immunologic Deficiency Syndromes genetics Syndromes de déficit immunitaire Aspect génétique. MEDICAL Immunology. HEALTH & FITNESS Allergies. HEALTH & FITNESS Diseases Immune System. |
| url | https://search.ebscohost.com/login.aspx?direct=true&scope=site&db=nlebk&AN=167565 |
| work_keys_str_mv | AT ochshansd primaryimmunodeficiencydiseasesamolecularandgeneticapproach AT smithciedvard primaryimmunodeficiencydiseasesamolecularandgeneticapproach AT puckjennifer primaryimmunodeficiencydiseasesamolecularandgeneticapproach |