Details

Textbook of Hemophilia


Textbook of Hemophilia


3. Aufl.

von: Christine A. Lee, Erik E. Berntorp, W. Keith Hoots

168,99 €

Verlag: Wiley-Blackwell
Format: PDF
Veröffentl.: 22.04.2014
ISBN/EAN: 9781118398272
Sprache: englisch
Anzahl Seiten: 560

DRM-geschütztes eBook, Sie benötigen z.B. Adobe Digital Editions und eine Adobe ID zum Lesen.

Beschreibungen

<p>Textbook of Hemophilia, 3<sup>rd</sup> edition</p> <p>Edited by<br /> <b>Christine A. Lee, MA, MD, DSc, FRCP, FRCPath, FRCOG<br /> </b>Emeritus Professor of Haemophilia, University of London, London, UK</p> <p><b>Erik E. Berntorp, MD, PhD<br /> </b>Professor of Coagulation Medicine, Lund University<br /> Malmö Centre for Thrombosis and Haemostasis, Skåne University Hospital, Malmö, Sweden</p> <p><b>W. Keith Hoots, MD<br /> </b>Director, Division of Blood Diseases and Resources, National Heart, Lung and Blood Institute<br /> National Institutes of Health, Bethesda, MD;<br /> Professor of Pediatrics and Internal Medicine, University of Texas Medical School at Houston, Houston, TX, USA</p> <p>Without doubt, <b>Textbook of Hemophilia, 3<sup>rd</sup> edition</b> is <i>the</i> definitive reference source on all aspects of haemophilia including diagnosis, management and treatment. Edited by three, world-renowned experts on haemophilia, this completely revised resource features chapters written by over 60 international contributors with international expertise in caring for haemophilia patients.</p> <p><b>Textbook of Hemophilia, 3<sup>rd</sup> edition</b></p> <ul> <li>Features eight new chapters, covering individualised dosing, vCJD and haemophilia, new drugs in the pipeline, and surgery in inhibitor patients</li> <li>Presents new developments, such as gene therapy</li> <li>Highlights controversial issues and provides advice for everyday clinical questions</li> <li>Represents essential reading for all healthcare professionals involved in the care of those with haemophilia</li> </ul> <p> <b>Titles of related interest</b></p> <p> <i>Hemophilia and Hemostasis: A Case-Based Approach to Management, 2nd Edition</i></p> <p><a href="http://eu.wiley.com/WileyCDA/Section/id-302479.html?query=Alice+D.+Ma">Ma</a>, ISBN: 9780470659762</p> <p><i>Current and Future Issues in Hemophilia Care</i></p> <p><a href="http://eu.wiley.com/WileyCDA/Section/id-302479.html?query=E.+Carlos+Rodriguez-Merchan">Rodriguez-Merchan</a>, ISBN: 9780470670576</p> <p><a href="http://www.wiley.com/go/hematology">www.wiley.com/go/hematology</a></p>
<p>Contributors ix</p> <p>Historical introduction xv<br /> <i>Christine A. Lee</i></p> <p><b>Part I: Introduction</b></p> <p>1 Overview of hemostasis 3<br /> <i>Kathleen Brummel Ziedins and Kenneth G. Mann</i></p> <p>2 Cellular processing of factor VIII and factor IX 9<br /> <i>Michael U. Callaghan and Randal J. Kaufman</i></p> <p><b>Part II: Hemophilia A</b></p> <p>3 Molecular basis of hemophilia A 23<br /> <i>Geoffrey Kemball-Cook and Keith Gomez</i></p> <p>4 Prophylaxis 33<br /> <i>Kathelijn Fischer and H. Marijke van den Berg</i></p> <p><b>Part III: Inhibitors to Factor VIII</b></p> <p>5 Inhibitors to factor VIII: immunology 43<br /> <i>Jean-Marie R. Saint-Remy and Marc G. Jacquemin</i></p> <p>6 Genetic and Environmental Risk Factors for Factor VIII inhibitor development 48<br /> <i>Jan Astermark</i></p> <p>7 Epidemiology of inhibitors in hemophilia 53<br /> <i>Alfonso Iorio</i></p> <p>8 Inhibitors to factor VIII: mild and moderate hemophilia 59<br /> <i>Kathelijne Peerlinck and Marc Jacquemin</i></p> <p>9 Inhibitors to factor VIII/IX: immune tolerance 64<br /> <i>Donna M. DiMichele</i></p> <p>10 Prophylaxis in inhibitor patients 72<br /> <i>Alessandro Gringeri</i></p> <p>11 Inhibitors to factor VIII: treatment of acute bleeds 78<br /> <i>Claude Negrier</i></p> <p><b>Part IV: Acquired Hemophilia</b></p> <p>12 Acquired inhibitors to factor VIII 87<br /> <i>Craig M. Kessler</i></p> <p><b>Part V: Hemophilia B</b></p> <p>13 Hemophilia B: molecular basis 97<br /> <i>Keith Gomez and Pratima Chowdary</i></p> <p>14 Factor IX inhibitors in hemophilia B 103<br /> <i>Meera B. Chitlur and Jeanne M. Lusher</i></p> <p>15 Treatment of inhibitors in hemophilia B 107<br /> <i>Anand Tandra and Amy D. Shapiro</i></p> <p><b>Part VI: Pharmacokinetics of Factors VIII and IX</b></p> <p>16 Pharmacokinetics 117<br /> <i>Sven Björkman</i></p> <p>17 Individualized dosing 123<br /> <i>Peter W. Collins</i></p> <p><b>Part VII: Hemophilia: Birth to Old Age</b></p> <p>18 Neonate with hemophilia 131<br /> <i>Angela E. Thomas and Elizabeth A. Chalmers</i></p> <p>19 Work-up of a bleeding child 138<br /> <i>Manuel D. Carcao and Victor S. Blanchette</i></p> <p>20 Care of the child with hemophilia 145<br /> <i>Rolf C.R. Ljung</i></p> <p>21 Hemophilia in adolescence 150<br /> <i>Pia Petrini</i></p> <p>22 Old age medicine and hemophilia 154<br /> <i>Evelien P. Mauser-Bunschoten and Roger E.G. Schutgens</i></p> <p><b>Part VIII: Products Used to Treat Hemophilia</b></p> <p>23 Products used to treat hemophilia: recombinant products 165<br /> <i>Midori Shima and Akira Yoshioka</i></p> <p>24 Products used to treat hemophilia: plasma-derived coagulation factor concentrates 174<br /> <i>Paul L.F. Giangrande</i></p> <p>25 Products used to treat hemophilia: dosing 180<br /> <i>Miguel A. Escobar</i></p> <p>26 Products used to treat hemophilia: regulation 185<br /> <i>Albert Farrugia</i></p> <p>27 New drugs in the pipeline: from concept to clinic 192<br /> <i>Leonard A. Valentino</i></p> <p><b>Part IX: Surgical management</b></p> <p>28 General surgical management of patients with hemophilia 199<br /> <i>Cindy Leissinger and Rebecca Kruse-Jarres</i></p> <p>29 Continuous infusion of coagulation products in hemophilia 204<br /> <i>Angelika Batorova and Uri Martinowitz</i></p> <p>30 Surgery in inhibitor patients 213<br /> <i>Pål Andrè Holme</i></p> <p><b>Part X: Musculoskeletal</b></p> <p>31 Joint replacement in patients with hemophilia 221<br /> <i>Nicholas Goddard</i></p> <p>32 Medical synovectomy (synoviorthesis) in hemophilia: radiosynovectomy and chemical synovectomy 228<br /> <i>E. Carlos Rodriguez-Merchan</i></p> <p>33 Pseudotumors in patients with hemophilia 233<br /> <i>Michael Heim and Uri Martinowitz</i></p> <p>34 Imaging modalities for assessment of hemophilic arthropathy 237<br /> <i>Andrea S. Doria and Björn Lundin</i></p> <p>35 Physiotherapy in the management of hemophilia 247<br /> <i>Sébastien Lobet and David Stephensen</i></p> <p>36 Outcome assessment in hemophilia 253<br /> <i>Pradeep M. Poonnoose and Alok Srivastava</i></p> <p><b>Part XI: Transfusion-transmitted Disease</b></p> <p>37 Viral hepatitis and hemophilia 265<br /> <i>Michael Makris and Geoffrey Dusheiko</i></p> <p>38 Transfusion-transmitted disease: emerging infections 272<br /> <i>Thomas R. Kreil</i></p> <p>39 vCJD and hemophilia 277<br /> <i>Carolyn M. Millar</i></p> <p><b>Part XII: Gene Therapy</b></p> <p>40 Hemophilia gene therapy: an overview 285<br /> <i>David Lillicrap</i></p> <p>41 Gene therapy trials in hemophilia A and B 291<br /> <i>Katherine A. High</i></p> <p>42 Gene therapy: molecular engineering of factor VIII and factor IX 298<br /> <i>Sundar R. Selvaraj and Steven W. Pipe</i></p> <p><b>Part XIII: Laboratory</b></p> <p>43 Laboratory and quality control of assays 311<br /> <i>Steve Kitchen</i></p> <p>44 Standardization of assays in hemophilia 318<br /> <i>Sanj Raut and Trevor W. Barrowcliffe</i></p> <p>45 Global laboratory assays in hemophilia 328<br /> <i>Benny Sørensen and Guy Young</i></p> <p><b>Part XIV: Women and Bleeding Disorders</b></p> <p>46 Obstetrics and gynecology: hemophilia 337<br /> <i>Rezan A. Kadir and Christine A. Lee</i></p> <p>47 Women and von Willebrand disease 345<br /> <i>Peter A. Kouides</i></p> <p><b>Part XV: von Willebrand Disease</b></p> <p>48 von Willebrand disease: molecular aspects 355<br /> <i>Daniel Hampshire and Anne Goodeve</i></p> <p>49 von Willebrand disease: epidemiology 362<br /> <i>Francesco Rodeghiero and Giancarlo Castaman</i></p> <p>50 von Willebrand disease: biological diagnosis 370<br /> <i>Veronica H. Flood and Robert R. Montgomery</i></p> <p>51 Classification and clinical aspects of von Willebrand disease 377<br /> <i>Augusto B. Federici</i></p> <p>52 Treatment of von Willebrand disease: desmopressin 386<br /> <i>Pier M. Mannucci</i></p> <p>53 Treatment of von Willebrand disease: therapeutic concentrates 390<br /> <i>Erik E. Berntorp</i></p> <p><b>Part XVI: Rare Bleeding Disorders</b></p> <p>54 Factor II 399<br /> <i>Jan Astermark</i></p> <p>55 Factor V and combined factor V and VIII deficiencies 403<br /> <i>Flora Peyvandi and Marzia Menegatti</i></p> <p>56 Congenital factor VII deficiency 413<br /> <i>Angelika Batorova</i></p> <p>57 Factor X and factor X deficiency 421<br /> <i>David J. Perry</i></p> <p>58 Factor XI deficiency 428<br /> <i>Paula H.B. Bolton-Maggs and Uri Seligsohn</i></p> <p>59 Factor XIII deficiency 436<br /> <i>Diane Nugent and Loan Hsieh</i></p> <p>60 Fibrinogen deficiency 445<br /> <i>Michael Laffan</i></p> <p>61 Miscellaneous rare bleeding disorders 452<br /> <i>Frederico Xavier and Amy D. Shapiro</i></p> <p><b>Part XVII: Emergency Medicine</b></p> <p>62 Emergency management of hemophilia 463<br /> <i>W. Keith Hoots</i></p> <p><b>Part XVIII: Evaluation of Hemophilia</b></p> <p>63 Clinical trials and other methodologies 473<br /> <i>Sharyne M. Donfield and Alice E. Lail</i></p> <p>64 Quality of life in hemophilia 478<br /> <i>Sylvia von Mackensen and Alessandro Gringeri</i></p> <p>65 The economics of hemophilia treatment 489<br /> <i>Katarina Steen Carlsson and Erik E. Berntorp</i></p> <p><b>Part XIX: Comprehensive Care and Delivery of Care</b></p> <p>66 Hemophilia databases 497<br /> <i>Charles R.M. Hay</i></p> <p>67 Comprehensive care and delivery of care: the developed world 502<br /> <i>Christopher A. Ludlam and Cedric R.J.R. Hermans</i></p> <p>68 Comprehensive care and delivery of care in hemophilia: the developing world 508<br /> <i>Alok Srivastava and Auro Viswabandya</i></p> <p>69 Comprehensive care and delivery of care: the global perspective 515<br /> <i>Mark W. Skinner and Alison M. Street</i></p> <p>Index 523</p> <p>Color plate section can be found facing page 202</p>
<p><strong>Christine A. Lee</strong>, MA, MD, DSc, FRCP, FRCPath, Emeritus Professor of Haemophilia, University of London; Honorary Consultant Haematologist, Oxford Haemophilia & Thrombosis Centre, Oxford, UK. <p><strong>Erik E. Berntorp</strong>, MD, PhD, Professor of Hemophilia, Lund University; Director, Department of Coagulation Disorders, Malmo University Hospital, Malmo, Sweden. <p><strong>W. Keith Hoots</strong>, MD, Professor of Pediatrics, University of Texas M.D. Anderson Cancer Center; Professor of Pediatrics and Internal Medicine, University of Texas Medical School at Houston; Medical Director, Gulf States Hemophilia and Thrombophilia Center, Houston, Texas, USA.
<p>Textbook of Hemophilia, 3<sup>rd</sup> edition</p> <p>Edited by<br /> <b>Christine A. Lee, MA, MD, DSc, FRCP, FRCPath, FRCOG<br /> </b>Emeritus Professor of Haemophilia, University of London, London, UK</p> <p><b>Erik E. Berntorp, MD, PhD<br /> </b>Professor of Coagulation Medicine, Lund University<br /> Malmö Centre for Thrombosis and Haemostasis, Skåne University Hospital, Malmö, Sweden</p> <p><b>W. Keith Hoots, MD<br /> </b>Director, Division of Blood Diseases and Resources, National Heart, Lung and Blood Institute<br /> National Institutes of Health, Bethesda, MD;<br /> Professor of Pediatrics and Internal Medicine, University of Texas Medical School at Houston, Houston, TX, USA</p> <p>Without doubt, <b>Textbook of Hemophilia, 3<sup>rd</sup> edition</b> is <i>the</i> definitive reference source on all aspects of haemophilia including diagnosis, management and treatment. Edited by three, world-renowned experts on haemophilia, this completely revised resource features chapters written by over 60 international contributors with international expertise in caring for haemophilia patients.</p> <p><b>Textbook of Hemophilia, 3<sup>rd</sup> edition</b></p> <ul> <li>Features eight new chapters, covering individualised dosing, vCJD and haemophilia, new drugs in the pipeline, and surgery in inhibitor patients</li> <li>Presents new developments, such as gene therapy</li> <li>Highlights controversial issues and provides advice for everyday clinical questions</li> <li>Represents essential reading for all healthcare professionals involved in the care of those with haemophilia</li> </ul> <p> <b>Titles of related interest</b></p> <p> <i>Hemophilia and Hemostasis: A Case-Based Approach to Management, 2nd Edition</i></p> <p><a href="http://eu.wiley.com/WileyCDA/Section/id-302479.html?query=Alice+D.+Ma">Ma</a>, ISBN: 9780470659762</p> <p><i>Current and Future Issues in Hemophilia Care</i></p> <p><a href="http://eu.wiley.com/WileyCDA/Section/id-302479.html?query=E.+Carlos+Rodriguez-Merchan">Rodriguez-Merchan</a>, ISBN: 9780470670576</p> <p><a href="http://www.wiley.com/go/hematology">www.wiley.com/go/hematology</a></p>

Diese Produkte könnten Sie auch interessieren:

Biomedical Imaging
Biomedical Imaging
von: Reiner Salzer
PDF ebook
120,99 €
Clinical Reasoning in Occupational Therapy
Clinical Reasoning in Occupational Therapy
von: Linda Robertson
PDF ebook
38,99 €
Clinical Reasoning in Occupational Therapy
Clinical Reasoning in Occupational Therapy
von: Linda Robertson
EPUB ebook
38,99 €