Cargando…

Textbook of Hemophilia

Detalles Bibliográficos
Autor principal: Lee, Christine A.
Formato: Electrónico eBook
Idioma:Inglés
Publicado: Newark : John Wiley & Sons, Incorporated, 2014.
Colección:New York Academy of Sciences Ser.
Acceso en línea:Texto completo

MARC

LEADER 00000cam a2200000Mu 4500
001 EBOOKCENTRAL_on1347029813
003 OCoLC
005 20240329122006.0
006 m o d
007 cr cnu||||||||
008 230209s2014 xx o ||| 0 eng d
040 |a EBLCP  |b eng  |c EBLCP  |d DXU  |d OCLCQ  |d OCLCO  |d EBLCP  |d OCLCQ  |d OCLCL 
066 |c (S 
020 |a 9781118398272 
020 |a 1118398270 
035 |a (OCoLC)1347029813 
082 0 4 |a 616.1/572  |q OCoLC  |2 23/eng/20230216 
049 |a UAMI 
100 1 |a Lee, Christine A. 
245 1 0 |a Textbook of Hemophilia  |h [electronic resource]. 
260 |a Newark :  |b John Wiley & Sons, Incorporated,  |c 2014. 
300 |a 1 online resource (570 p.). 
490 1 |a New York Academy of Sciences Ser. 
500 |a Description based upon print version of record. 
505 0 |a Cover -- Title page -- Copyright page -- Contents -- Contributors -- Historical introduction -- Early history -- Treatment -- Human immunodeficiency virus -- Hepatitis C virus -- New products -- Variant Creutzfeldt-Jakob disease -- The future -- Notes on this edition -- References -- PART I: Introduction -- CHAPTER 1: Overview of hemostasis -- Introduction -- Importance of complex assembly to coagulation -- Extrinsic pathway to blood coagulation -- Attenuation of the procoagulant response -- Conclusion -- Acknowledgment -- References 
505 8 |a Mutation nomenclature -- Disease severity -- References -- CHAPTER 4: Prophylaxis -- Rationale for prophylaxis -- Introduction of prophylaxis -- Prophylaxis in children -- When to start prophylaxis -- Prophylaxis in adults -- Prophylaxis versus on-demand therapy: issues of cost-effectiveness -- Optimal treatment regimen for prophylaxis -- Future issues in prophylaxis -- Conclusion -- References -- PART III: Inhibitors to factor VIII -- CHAPTER 5: Inhibitors to factor VIII: immunology -- Introduction -- Homeostasis of the antifactor VIII immune response -- Lessons from animal models 
505 8 |a Clinical observations -- Characterization of antifactor VIII antibodies -- Factor VIII-specific T cells -- Future perspectives -- References -- CHAPTER 6: Genetic and environmental risk factors for factor VIII inhibitor development -- Introduction -- Genetic factors -- Type of causative mutation -- Major histocompatibility complex -- Immune-regulatory molecules -- Environmental factors -- Factor concentrate-related factors -- Conclusion -- References -- CHAPTER 7: Epidemiology of inhibitors in hemophilia -- Introduction -- Definitions of epidemiology terms 
500 |a Definitions relating to inhibitor terms 
590 |a ProQuest Ebook Central  |b Ebook Central Academic Complete 
758 |i has work:  |a Textbook of hemophilia (Text)  |1 https://id.oclc.org/worldcat/entity/E39PCGWwwCqxYmmkKTwR7MVW8P  |4 https://id.oclc.org/worldcat/ontology/hasWork 
776 0 8 |i Print version:  |a Lee, Christine A.  |t Textbook of Hemophilia  |d Newark : John Wiley & Sons, Incorporated,c2014  |z 9781118398241 
830 0 |a New York Academy of Sciences Ser. 
856 4 0 |u https://ebookcentral.uam.elogim.com/lib/uam-ebooks/detail.action?docID=7103607  |z Texto completo 
880 8 |6 505-00/(S  |a CHAPTER 2: Cellular processing of factor VIII and factor IX -- Factor VIII and hemophilia A -- Factor VIII expression -- Domain structure of factor VIII -- Disulfide bond formation -- Asparagine- and serine/threonine-linked glycosylation -- Chaperone-assisted factor VIII folding -- Tyrosine sulfation -- Phosphorylation of serine and threonine residues -- Proteolytic processing -- Summary -- Factor IX and hemophilia B -- Domain structure of factor IX -- Disulfide bond formation -- Asparagine- and serine/threonine-linked glycosylation -- γ-Carboxylation of glutamic acid residues 
880 8 |6 505-00/(S  |a β-Hydroxylation of aspartic acid and asparagine -- Tyrosine sulfation -- Phosphorylation of serine and threonine residues -- Factor IX Padua -- Proteolytic processing -- Summary -- Acknowledgments -- References -- PART II: Hemophilia A -- CHAPTER 3: Molecular basis of hemophilia A -- Introduction -- Structure and function of the factor VIII gene (F8) and protein -- F8 gene -- Production of factor VIII protein -- F8 gene defects found in hemophilia A -- Gene rearrangements -- Single-base substitutions in the F8 gene -- Sequence insertions and deletions -- Conclusion -- Public database 
938 |a ProQuest Ebook Central  |b EBLB  |n EBL7103607 
994 |a 92  |b IZTAP