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Hematopoietic Stem
Cell Transplantation in Clinical Practice
by Jennifer Treleaven, and A. J. Barrett |
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Cat.# EL-HEM1 |
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Published:
2008 ISBN: 9780443101472 |
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PART 1. SETTING THE SCENE
Introduction. Essential biology of stem cell
transplantation
PART 2. STEM CELL TRANSPLANTATION AS DISEASE THERAPY
Allogeneic transplantation in acute myeloid leukaemia.
Stem cell transplantation for chronic myeloid leukaemia.
Acute lymphoblastic leukemia in adults. Childhood
leukemias. The myelodysplastic syndromes. Stem cell
transplantation for myeloma. Hodgkin’s disease and
non-Hodgkin's lymphoma. Chronic lymphocytic leukaemia.
Stem cell transplantation for solid tumors in childhood.
Hematopoietic stem cell transplantation in the treatment
of breast cancer. Hematopoietic stem cell transplantation
for solid tumors in adults. Germ cell tumors. Primary
immunodeficiency diseases. Acquired aplastic anemia and
Fanconi anemia. Stem cell transplantation for thalassaemia
and sickle cell disease. Lysosomes and lysosomal function.
Hematopoietic stem cell transplantation for autoimmune
disorders
PART 3. PREPARATION FOR TRANSPLANT Patient selection:
preliminary interview, screening and selecting a donor.
Stem cell donor registries. Cord blood banks and umbilical
cord blood transplantation in children and adults. HLA
matching, compatibility testing and donor selection.
Collection and processing of marrow and blood
hematopoietic progenitor/stem cells. Vascular access.
High-dose regimens for autologous stem cell
transplantation. Myeloablative conditioning regimens for
allogeneic transplantation. Reduced-intensity conditioning
for allogeneic hematopoietic stem cell transplantation.
Transplants from unrelated or mismatched family donors.
Management of the older patient
PART 4. POST-TRANSPLANT CARE Transfusion medicine support
for hematopoietic stem cell transplantation. The
transplant pharmacopoeia. Nutrition support. Barrier
precautions, prophylaxis and neutropenic fever.
Re-immunization after hematopoietic stem cell
transplantation. Psychological and supportive care issues
in the transplant setting.
PART 5. MANAGEMENT OF POST-TRANSPLANT COMPLICATIONS Graft
failure. Acute graft-versus-host disease. Chronic
graft-versus-host disease. Management of relapse and
minimal residual disease after stem cell allografting.
Bacterial infections. Viral infections post-transplant.
Fungal infections post-transplantation. Parasitic
infections. Multiple organ failure - intensive care after
stem cell transplantation. Late effects after allogeneic
stem cell transplantation.
PART 6. THE WIDER PERSPECTIVE Starting a hemopoietic stem
cell transplant unit. Ethical and Legal Considerations in
Stem Cell Transplantation. How to build and use a stem
cell transplant database. Blood and Marrow Transplant
Organizations. Stem cell transplantation - future |
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Evidence-Based
Hematology
by Mark Crowther |
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Cat.# JW-HEM1 |
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Published:
2008 ISBN:
9781405157476 |
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This unique new book uses a series of focussed
questions, comprehensive literature evaluations and
structured grades of recommendation to provide evidence
for the treatment of hematological disorders, both
malignant and benign. With contributions from leading
international experts who have a real understanding of
evidence-based medicine the book provides comprehensive
reviews accompanied by clinical commentaries and
recommendations on the best treatment regimes to adopt for
individual patients.
The book is split into two sections: the first examines
the methodology underlying evidence based practice, and
the second concentrates on the clinical practice of
hematology, providing current "best evidence" to guide
practice in a series of well-defined clinical situations.
This clinical reference is an invaluable source of
evidence-based information distilled into guidance for
clinical practice which will be welcomed by practitioners,
trainees and associated health professionals.
Table of Contents:
About the Contributors
Preface
Part I: A Guide to the Evidence
1. Rating the quality of evidence and making
recommendations
2. An overview of systematic reviews
3. Interpreting results of clinical research
4. Finding the evidence
5. Applying EBM in clinical practice
6. Using evidence to guide the diagnosis of disease
Part II
7. Diagnosis of Deep Vein Thrombosis
8. Diagnosis of Pulmonary Embolism
9. Initial Therapy of Deep Vein Thrombosis and Pulmonary
Embolism
10. Long-term Anticoagulation in Venous Thromboembolism
11. Thrombolytic Therapy for Deep Vein Thrombosis and
Pulmonary Embolism
12. Inferior Vena Cava Interruption
13. Management of Venous Thromboembolism in Pregnancy
14. Pediatric Thrombosis
15. Bridging Anticoagulation in Patients who Require
16. Evidence-based approach to the diagnosis and
management of thrombotic thrombocytopenic purpura
17. Diagnosis and Management of Disseminated Intravascular
Coagulation
18. Diagnosis and Management of Hereditary Bleeding
Disorders
19. Diagnosis and Management of Acquired Bleeding
Disorders
20. Diagnosis and Management of Heparin-Induced
Thrombocytopenia
21. Management of Antiphospholipid Antibody Syndrome
Part III
22. Clinical Questions in iron overload
23. Aplastic Anemia
24. Acquired Anemias
25. Immune thrombocytopenic purpura
26. Neutropenia
27. Hypereosinophilia
28. Porphyrias
29. Membrane and Enzyme Abnormalities of the Erythrocyte
30. Sickle cell disease
31. Evidence-based treatment of thalassemia major
Part IV
32. Acute Lymphoblastic Leukemia in Adults
33. Acute Myeloblastic Leukemia in Adults
34. Acute Myeloid Leukemia in Adults
35. Current Areas of Controversy in the Treatment of
Patients
36. Chronic Lymphocytic Leukemia
37. Chronic Myelocytic Leukemia
38. Burkitt's Lymphoma
39. Primary Central Nervous System Lymphoma
40. Diffuse Large B-cell Lymphoma
41. Follicular Lymphoma
42. Lymphoblastic Lymphoma
43. Mantle Cell Lymphoma
44. Peripheral T-cell Lymphoma
45. Classical Hodgkin Lymphoma
46. Nodular Lymphocyte Predominant Hodgkin Lymphoma
47. Essential Thrombocythemia
48. Management of Patients with Polycythemia Vera
49. Multiple Myeloma
50. Waldenstroms Macroglobulinemia
51. Use of Hematopoietic Growth Factors for Hematologic
Malignancies
Index |
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Consultative Hemostasis and
Thrombosis
by Craig Kitchens, Barbara Alving, and
Craig Kessler |
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Cat.# EL-HEM2 |
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Published:
2007 ISBN:
9781416024019 |
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Effectively and efficiently diagnose and manage today's
full range of clotting and bleeding disorders using
clinical case studies that demonstrate real-world problems
and solutions! For each condition examined, you'll review
concise descriptions of its associated symptoms, along
with laboratory findings, diagnosis, differential
diagnosis, and treatment - all the clinical guidance you
need - at your fingertips. It's the ideal real-life
reference tool for busy physicians. A reader-friendly
design, coupled with nearly 385 illustrations and
at-a-glance tables - many new to this edition - equip you
to quickly locate the guidance you need. Abundant
laboratory protocols enable you to select and interpret
lab tests more easily.
Table of Contents: Part I: General
Information
CHAPTER 1: The Consultative Process
CHAPTER 2: A Systematic Approach to the Bleeding Patient:
Correlation of Clinical Symptoms and Signs with Laboratory
Testing
CHAPTER 3: Endothelium
Part II: Hemorrhagic Processes
CHAPTER 4: Hemophilia A and B
CHAPTER 5: Less Common Congenital Disorders of Hemostasis
CHAPTER 6: Non-hemophilic inhibitors of coagulation
CHAPTER 7: von Willebrand Disease
CHAPTER 8: General aspects of thrombocytopenia, platelet
transfusions and platelet growth factors CHAPTER 9: Immune
Thrombocytopenic Purpura
CHAPTER 10:Congenital and Acquired Disorders of Platelet
Function and Number
CHAPTER 11: Purpura and Other Hematovascular Disorders
CHAPTER 12: Disseminated Intravascular Coagulation
CHAPTER 13: The cross-talk of inflammation and coagulation
in infectious disease and their value in disseminated
intravascular coagulation
Part III: Thrombotic Processes
CHAPTER 14: Thrombophilia: Clinical and Laboratory
Assessment and Management
CHAPTER 15: Deep Vein Thrombosis and Pulmonary Embolism
CHAPTER 16: Venous Thromboses at Unusual Sites
CHAPTER 17: Prevention, Diagnosis, and Treatment of the
Postphlebitic Syndrome
CHAPTER 18: Thrombocytosis: essential thrombocythemia vs.
reactive etiologies
CHAPTER 19: The Antiphospholipid Syndrome: Clinical
Presentation, Diagnosis, and Patient Management
CHAPTER 20: Hemostatic aspects of cardiovascular medicine
CHAPTER 21: Risk factors for arterial thrombosis
CHAPTER 22: Peripheral Arterial Disease
CHAPTER 23: Thrombosis and Cancer
CHAPTER 24: Thrombotic Thrombocytopenic Purpura
CHAPTER 25: Heparin-Induced Thrombocytopenia
Part IV: Therapeutic Measures
CHAPTER 26: Antithrombotic Agents
CHAPTER 27: Blood Component And Pharmacologic Therapy of
Hemostatic Disorders
CHAPTER 28 : Thrombolytic Therapy
CHAPTER 29: Topical Hemostatic Agents for Localized
Bleeding
CHAPTER 30: Therapeutic Apheresis
CHAPTER 31: Vena Cava Filters
CHAPTER 32: Thrombosis Related to Venous Access Devices
CHAPTER 33: Dietary Supplements and Hemostasis
Part V: Issues Specific to Women
CHAPTER 34: Thrombotic Risk of Contraceptives and
Other Hormonal Therapies
CHAPTER 35: Management of Bleeding Disorders in Pregnancy
CHAPTER 36: Management of thrombophilia and APLS during
pregnancy
Part VI: Special Issues
CHAPTER 37: Surgery and Hemostasis
CHAPTER 38: Anticoagulation in the Perioperative Period
CHAPTER 39: Hemostasis Alterations in Liver Disease and
Liver Transplantation
CHAPTER 40: Outpatient Anticoagulant Therapy
CHAPTER 41: Point of Care Testing for Hemostatic Disorders
CHAPTER 42: Prevention and Treatment of Venous
Thromboembolism in Neurologic and Neurosurgical Patients
CHAPTER 43: Hematologic Interventions for Acute Central
Nervous System Disease
CHAPTER 44: Atrial Septal Abnormalities and Cryptogenic
Stroke
CHAPTER 45: Pulmonary Hypertension: Thrombotic and Non-Thrombotic
in Origin
CHAPTER 46:Hemorrhage Control and Thrombosis Following
Severe Injury
CHAPTER 47:Hemostatic Aspects of Sickle Cell Disease
CHAPTER 48: Anticoagulation for Atrial Fibrillation and
Prosthetic Cardiac Valves |
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ABC of
Clinical Haematology 3E
by Drew Provan |
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Cat.# JW-HEM2 |
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Published:
2007 ISBN: 9781405153539 |
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This ABC has established itself as a popular
introduction to Clinical Haematology, relevant both for
postgraduate students and primary care practitioners. Now
in its third edition, the ABC of Clinical Haematology has
been thoroughly revised, featuring the latest treatments
for leukaemia, antithrombotics and drugs for lymphoma and
covering the latest advances in haematology and bone
marrow transplantation.
With each chapter written by specialists in their
respective fields, this is an ideal basic text for general
practice and hospital staff with patients who have blood
related problems, in particular GPs, haematology nurses,
junior doctors, haematologists, and trainees in
haematology.
Table of Contents:
1. Iron Deficiency Anaemia
2. Macrocytic Anaemias
3. The Hereditary Anaemias
4. Polycythaemia, Essential Thrombocythaemia and
Myelofibrosis
5. Chronic Myeloid Leukaemia
6. The Acute Leukaemias
7. Platelet Disorders
8. The Myelodysplastic Syndromes
9. Multiple Myeloma and Related Conditions
10. Bleeding Disorders, Thrombosis and Anticoagulation
11. Lymphoproliferative Disorders Including Chronic
Lymphocytic Leukaemia
12. Stem Cell Transplantation
13. Haematological Disorders at the Extremes of Life
14. Haematological Emergencies
15. The Future of Haematology: the Impact of Molecular
Biology and Gene Therap
Index |
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Modern Hematology,
Biology and Clinical Management
by Reinhold Munker,
Erhard Hiller, Jonathan Glass, and Ronald
Paquette |
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Cat.# DA-HEM1 |
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Published:
2007 ISBN:
9781588295576 |
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Reinhold Munker and his distinguished colleagues have
updated and expanded Modern Hematology: Biology and
Clinical Management, now in its second edition, to
reflect the major advances in the understanding,
diagnosis, and treatment of blood disorders. Modern
Hematology: Biology and Clinical Management, Second
Edition describes the latest clinical and scientific
developments, including molecular studies used to diagnose
a variety of hematological disorders and guide their
treatment. Targeted and molecular therapies are discussed
in detail, including kinase inhibitors in
myeloproliferative disorders and humanized monoclonal
antibodies. The use of peripheral blood and umbilical cord
blood stem cells for transplantation is described, as well
as the rationale and indications for non-myeloablative
transplantation, emphasizing the preferability of
immunotherapy over cytotoxic chemotherapy. Modern
Hematology: Biology and Clinical Management, Second
Edition brings together facts, concepts, and protocols
important for the practice of hematology. In 23 chapters,
all major blood diseases are covered, as well as rare
diseases that are of scientific interest. The first two
chapters introduce the reader to the scientific basis of
blood disorders. As in the previous edition, each chapter
is illustrated by tables, figures, and a selection of
color plates. Experts in pediatric hematology, myeloma,
blood transfusion, hemoglobinopathies, pharmacology, and
infectious diseases have expanded the scope of Modern
Hematology. Comprehensive and informative, Modern
Hematology: Biology and Clinical Management, Second
Edition is an invaluable resource for medical
students, hematology trainees, residents, nurses, nurse
practitioners, and physicians in other specialties
treating patients with benign and malignant blood
disorders. |
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Haemophilia and Haemostasis:
A Case-based Approach to Management
by Harold Ross Roberts |
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Cat.# JW-HEM3 |
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Published:
2007 ISBN:
9781405167161 |
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This unique book covers the major cases one might
encounter in diagnosing, managing and treating haemophilia.
It will provide a practical and informative guide to the
broad range of topics concerning both bleeding and
clotting disorders. Haemophilia and Haemostasis: A
Case-based Approach to Management is divided into major
chapter sections by disorder. Each chapter contains
questions and cases that were originally submitted to the
online Haemostasis-forum (previously Haemophilia-forum).
Cases and questions associated with each disorder are
presented alongside practical answers from a wide range of
international contributors. Practical, clinical
questions, answered by the world's leading experts
- All case studies gathered from the Archives of the
Haemostasis/Haemophilia Forum – 1997-2006
- Covers haemophilia, Von Willebrand Disease and many
other bleeding and clotting disorders
- Over 80 case studies with practical answers
- To reflect varying practice, controversial areas
will be clearly marked and discussed throughout
Whether you are a practising clinician or trainee in
haematology, working in the fields of coagulation,
haemostasis or thrombosis, or any other health care
professional working in a haemophilia centre, this book
will provide practical clinical answers to aid in your
day to day patient care.
Table of Contents:
List of Haemostasis Forum Editors
List of Contributors
Preface
1. Hemophilia A and Hemophilia B
General Overview
Hemophilia and Immune Tolerance Therapy
The Hemophilic Ankle: An update
The Hemophilic Knee: An update
Issues with Complicated Diagnoses
Combined Hemophilia A and B Carrier
A Complex Case of Hemophilia with HIV and Hepatitis C
A Case of Hemophilia B, Mild VWD and a Factor IX
Inhibitor
Premature Infant with Hemophilia B
Hemophilic Carriers
Hemophilic Carriers and Delivery
Mild Hemophilia in Women
Treatment of the Pregnant Hemophiliac
Anticoagulation and Hemophilia
Anticoagulation for Atrial Fibrillation in a Hemophiliac
Anticoagulation for a Cardiac Valve in a Hemophiliac
Cardiac Catheterization in a Hemophiliac
Anticoagulation for a DVT in a Hemophiliac
Treatment of Hemophiliacs
DDAVP for Treatment of Mild Hemophilia during Surgery
Hemophilia and Hemodialysis
Hemophilia and Hepatitis C Treatment
Hemophilia and Physical Therapy
Hemophilia and Renal Bleeds
Hemophilia and SCUBA Diving
Hemophilia and Ventricular Septal Defect Repair
Hemophilia with Hepatitis C and Recurrent Bleeding
Isotretinoin in Hemophilia
Laser Eye Surgery in a Hemophiliac
Managing Hemophilic Pseudotumors
Continuous NovoSeven: Pros and Cons
Complications of Treatment
Hemophilia B and Immune Tolerance with Anaphylaxis
NovoSeven (rFVIIa) and DIC
Thrombosis in Prothrombin Complex Concentrates (PCCs)
vs. activated Prothrombin Complex Concentrates (APCCs)
2. Von Willebrand Disease (VWD)
Epidurals and VWD
Anticoagulation for a Cardiac Valve in a patient with
VWD type 1
VWD type 2a and Pregnancy
VWD type 2b and Pregnancy
VWD type 2b Versus Platelet Type
Prophylaxis in VWD type 3
Platelet Type VWD
3. Factor Deficiencies
Combined Factor V and VIII Deficiency
DVT Prophylaxis in FVII Deficiency
Menorrhagia in Factor VII Deficiency
Anticoagulation for Atrial Fibrillation in FX Deficiency
Management of Factor X Deficiency
Anticoagulation for Atrial Fibrillation in a patient
with Factor XI Deficiency
Factor XI Deficiency and Surgery
Prophylaxis for Patients with Factor XIII Deficiency and
Intracranial Bleeding
4. Rare Platelet and Coagulation Disorders
Coagulation Disorders
Afibrinogenemia
Dysfibrinogenemia
Hypofibrinogenemia
Gardner-Diamond Syndrome
Hereditary Hemorrhagic Telangiectasia (HHT)
Hereditary Vitamin K Dependent Coagulation Factors
Deficiency and Pregnancy
Platelet Disorders
Glanzmann’s Thrombasthenia and Gastrointestinal
Angiodysplasia
Glanzmann's Thrombasthenia and Pregnancy
NovoSeven and Wiscott-Aldrich
5. Acquired Bleeding Diatheses
Acquired Hemophilia and Second Pregnancy
Developing a Factor IX Inhibitor
Acquired Bleeding Diatheses: End-Stage Liver Disease and
Surgery
Treatment for Acute DIC
6. Miscellaneous Questions
Bleeding Time Versus PFA-100
Cocaine and DDAVP
Hyponatremia and DDAVP
The Use of the INR
Selective Serotonin Reuptake Inhibitors and Clotting
Disturbances
Work-up for Children with Intracranial Bleeding
7. Thrombotic Disorders
Are Asians genetically different from Westerners when it
comes to VTE?
Treatment of Antithrombin Deficiency
Anticardiolipin Antibody Questions
Pediatric Antiphospholipid Syndrome and Recurrent
Thrombosis
Anticoagulation for Deep Venous Thrombosis in the
Presence of an Intracranial Hemorrhage
Clinical Probability Assessment for Thromboembolic
Disease
D-dimer in Thromboembolic Disease
Progestins and Thrombosis
Unknown Thrombophilia and Surgery |
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NO IMAGE AVAILABLE |
Atlas of Clinical
Hematology
by James Armitage |
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Cat.# DA-HEM2 |
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Published:
2007 ISBN: 9781573402842 |
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Hematology is a particularly visual science. It has
always been possible to look at blood cells and their
progenitors in the bone marrow with comparative ease. Of
all the areas of medicine, Hematology is perhaps the one
most amenable to presentation in an Atlas such as this.
The Atlas of Clinical Hematology describes the exciting
advances occurring in Hematology and presents them in an
attractive and useable way. The Atlas of Clinical
Hematology describes the exciting advances occurring in
hematology and presents them in an attractive and
accessible format. Contents:
- Non-Hodgkin Lymphoma
- Hodgkin Lymphoma and Other Distinctive Lymphoid
Proliferations
- Plasma Cell Disorders
- Myeloid Disorders
- Disorders of Hemostasis and ThrombosisAnemias
- Hematopoietic Stem Cells and Cytokines
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Concise Manual of
Hematology and Oncology
by D. P. Berger, M. Engelhardt, H. Henss, R.
Mertelsmann, M. Andreeff, B. Koziner, H.
Messner, and N. Thatcher
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Cat.# DA-HEM3 |
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Published:
2007 ISBN: 9783540732761 |
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"The Concise Manual of Hematology and Oncology" is a
practice-oriented manual of medical oncology and
Hematology for day-to-day use in caring for patients'
hematologic and neoplastic diseases. It is founded on the
longstanding experience of a large specialized university
department accustomed to having to provide reliable advice
in a broad range of circumstances . We have deliberately
chosen not to give a comprehensive review of the various
subjects but have instead focused on practical methods
which have proven to be useful in our experience, with
special emphasis on standardizing chemotherapy protocols.
Contents: General
Section. Diagnostic Methods. Pharmacology and Drug
Therapy. Supportive Care. Therapeutic Methods. Hematology
and Hemostaseology. Hematological Neoplasms. Medical
Oncology. Hematological and Oncological Emergencies.
Standard Procedures. Appendix. Chemotherapy Protocols. |
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Blood
Cells: A Practical Guide 4E
by Barbara J. Bain |
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Cat.# JW-HEM4 |
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Published:
2006 ISBN:
9781405142656 |
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Blood Cells has been written with both the practising
haematologist and the trainee in mind. It aims to provide
a guide for use in the diagnostic haematology laboratory,
covering methods of collection of blood specimens, blood
film preparation and staining, the principles of manual
and automated blood counts and the assessment of the
morphological features of blood cells. The practising
haematologist should find this book sufficiently
comprehensive to be a reference source while, at the same
time, the trainee haematologist and biomedical scientist
should find it a straightforward and practical bench
manual. Enables both the haematologist and laboratory
scientist to identify blood cell features, from the most
common to the more obscure
- Provides essential information on methods of
collection, blood film preparation and staining,
together with the principles of manual and automated
blood counts
- Completely revised and updated, incorporating much
newly published information: now includes advice on
further tests when a specific diagnosis is suspected
- Four hundred high quality photographs to aid with
blood cell identification
- Highlights the purpose and clinical relevance of
haematology laboratory tests throughout
Table of Contents:
1 Blood Sampling and Blood Film Preparation and
Examination
2 Performing a Blood Count
3 Morphology of Blood Cells
4 Detecting Erroneous Blood Counts
5 Normal Ranges
6 Quantitative Changes in Blood Cells
7 Important Supplementary Tests
8 Disorders of Red Cells and Platelets
9 Disorders of White Cells
Index |
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Pediatric
Hematology 3E
by Robert J. Arceci,
Ian M. Hann, Owen P. Smith, and A. Victor
Hoffbrand
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Cat.# JW-HEM5 |
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Published:
2006 ISBN: 9781405134002 |
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Pediatric Hematology is a comprehensive and succinct
referenced text on the diagnosis and treatment of blood
diseases in childhood. It provides a ready source of
reference for all the conditions likely to be encountered
in day-to-day clinical practice. For each condition, the
authors give helpful advice on differential diagnoses and
clinical management. This third edition has been
extensively updated throughout, in light of recent
developments in this rapidly advancing area of medicine. A
well established textbook on the diagnosis and treatment
of blood disorders in childhood.
- A balanced and cutting edge referenced text on all
aspects of diagnosis and treatment
- Easy to use, practically organized, with essential
aspects of biology included within each chapter
- International editorial and contributor
team—representing a wide geographical and chronological
range
Whether you are an established sub-specialist in
pediatric hematology/oncology, a pediatrician, a trainee
or nursing specialist, this book will answer all your
questions about benign and malignant disorders of the
blood in children and young adults.
Table of Contents:
Section 1: The Scientific Basis
1. Hematopoiesis: an introduction.
Section 2: Marrow Failure Syndromes
2. Failure of red cell production
3. Inherited bone marrow failure syndromes
4. Acquired aplastic anemia
Section 3: Red Cell Disorders
5. Disorders of iron metabolism: iron deficiency, iron
overload and the sideroblastic anemias
6. Megaloblastic anemia and disorders of cobalamin and
folate metabolism
7. Nonimmune neonatal anemias
8. Immune hemolytic anemias
9. Disorders of erythrocyte metabolism including porphyria
10. Sickle cell disease
11. Hemoglobin variants and the rarer hemoglobin disorders
12. Red cell membrane abnormalities
13. Thalassemias
Section 4: Granulocyte Disorders
14. Disorders of granulopoiesis and granulocyte function
15. Histiocytic disorders
16. Acute myeloid leukemia
17. Chronic myeloid leukemia
18. Myelodysplastic syndromes
Section 5: Lymphocyte Disorders
19. Primary and acquired immunodeficiency
20. Clinical features and therapy of lymphoblastic
leukemia
21. Lymphomas
Section 6: Platelet Disorders
22. Inherited and congenital thrombocytopenia
23. Idiopathic thrombocytopenic purpura
24. Thrombocytosis
25. Platelet function disorders
Section 7: Coagulation Disorders
26. Hemophilia A and B
27. von Willebrand disease
28. Rare congenital hemorrhagic disorders
29. Acquired disorders of hemostasis
30. Bleeding in the neonate
31. Thromboembolic complications in children
Section 8: Supportive Therapy
32. Blood components and fractionated plasma products:
preparation, indications and administration
33. Hazards of transfusion
34. Management of infection in children with bone marrow
failure
Section 9: Secondary Problems
35. Hematologic effects of systemic disease and
nonhematopoietic tumors
36. Lysosomal storage disorders
37. Reference values
Index |
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Postgraduate
Haematology 5E
by A. Victor Hoffbrand,
Daniel Catovsky, and Edward G. D. Tuddenham |
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Cat.# JW-HEM6 |
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Published:
2005 ISBN:
9781405108218 |
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