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Book Categories |
1 | Overview of hemostasis | 1 |
2 | Cellular processing of factors VIII and IX | 5 |
3 | Work-up of a bleeding adult | 13 |
4 | Molecular basis of hemophilia A | 19 |
5 | Hemophilia A : role of factor VIII in coagulation | 27 |
6 | Natural history of inhibitor development in children with severe hemophilia A treated with factor VIII products | 34 |
7 | Prophylaxis | 39 |
8 | Continuous infusion of coagulation products in hemophilia | 46 |
9 | Inhibitors to factor VIII - immunology | 53 |
10 | Inhibitors to factor VIII - molecular basis | 59 |
11 | Inhibitors to factor VIII - epidemiology and treatment | 64 |
12 | Inhibitors to factor VIII - mild and moderate hemophilia | 71 |
13 | Inhibitors to factor VIII/IX : treatment of inhibitors - immune tolerance induction | 74 |
14 | Inhibitors of factor VIII : treatment of acute bleeds | 80 |
15 | Acquired inhibitors to factor VIII | 86 |
16 | Hemophilia B - molecular basis | 91 |
17 | Inhibitors in hemophilia B | 97 |
18 | Treatment of inhibitors in hemophilia B | 101 |
19 | Pharmacokinetics | 106 |
20 | Work-up of a bleeding child | 112 |
21 | Care of the child with hemophilia | 120 |
22 | The neonate with hemophilia | 125 |
23 | Products used to treat hemophilia : evolution of treatment for hemophilia A and B | 131 |
24 | Products used to treat hemophilia : recombinant products | 136 |
25 | Products used to treat hemophilia : plasma-derived coagulation factor concentrates | 142 |
26 | Products used to treat hemophilia : recombinant factor VIIa | 147 |
27 | Products used to treat hemophilia : dosing | 153 |
28 | Products used to treat hemophilia : regulation | 158 |
29 | Joint replacement | 164 |
30 | Synoviorthesis in hemophilia | 169 |
31 | Pseudotumors in patients with hemophilia | 174 |
32 | Radiology | 177 |
33 | Magnetic resonance imaging/joint outcome assessment | 182 |
34 | Physiotherapy in the management of hemophilia | 193 |
35 | Transfusion transmitted disease : history of epidemics (focus on HIV) | 200 |
36 | Transfusion transmitted disease : hepatitis C virus infection and liver transplantation | 207 |
37 | Gene therapy : introduction and overview | 214 |
38 | Gene therapy for hemophilia B | 220 |
39 | Gene therapy for hemophilia A | 226 |
40 | Gene therapy : molecular engineering of factor VIII and factor IX | 229 |
41 | Laboratory assays in hemophilia | 235 |
42 | Standardization of assays | 242 |
43 | Obstetrics and gynecology : hemophilia | 249 |
44 | von Willebrand disease : molecular aspects | 257 |
45 | von Willebrand disease : epidemiology | 265 |
46 | von Willebrand disease : biological diagnosis | 272 |
47 | Classification and clinical aspects of von Willebrand disease | 279 |
48 | Treatment of von Willebrand disease : desmopressin | 285 |
49 | Treatment of von Willebrand disease : therapeutic concentrates | 289 |
50 | Women and von Willebrand disease | 296 |
51 | Factor II | 302 |
52 | Factor V and combined factor V and VIII deficiencies | 306 |
53 | Congenital factor VII deficiency | 311 |
54 | Factor X and factor X deficiency | 315 |
55 | Factor XI deficiency | 321 |
56 | Factor XIII | 328 |
57 | Fibrinogen | 332 |
58 | Miscellaneous rare bleeding disorders | 338 |
59 | Quality of life in hemophilia | 345 |
60 | The economics of hemophilia treatments | 351 |
61 | Comprehensive care and delivery of care : the developed world | 359 |
62 | Comprehensive care and delivery of care : the developing world | 366 |
63 | Comprehensive care and delivery of care : the global perspective | 371 |
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Add Textbook of Hemophilia, Covering how to asses both bleeding children and adults, Hemophilia A and B, molecular basis of the disease, the role of factors in coagulation, epidemiology, pharmacokinetics, and treatment of inhibitors. There is a section on musculoskeletal aspects of , Textbook of Hemophilia to the inventory that you are selling on WonderClubX
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Add Textbook of Hemophilia, Covering how to asses both bleeding children and adults, Hemophilia A and B, molecular basis of the disease, the role of factors in coagulation, epidemiology, pharmacokinetics, and treatment of inhibitors. There is a section on musculoskeletal aspects of , Textbook of Hemophilia to your collection on WonderClub |