MARC details
| 000 -LEADER |
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| fixed length control field |
04321cam a2200325 4500 |
| 001 - CONTROL NUMBER |
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| control field |
9780470988398 |
| 008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION |
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| fixed length control field |
180406t2004 xxu||||| |||| 00| 0 eng d |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER |
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| ISBN |
9780470988398 |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER |
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| ISBN |
1405107804 |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER |
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| ISBN |
0470988398 |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER |
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| ISBN |
1405140208 |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER |
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| ISBN |
9781405140201 |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER |
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| ISBN |
1280199660 |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER |
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| ISBN |
9781280199660 |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER |
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| ISBN |
1405107804 |
| 020 ## - INTERNATIONAL STANDARD BOOK NUMBER |
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| ISBN |
9781405107808 |
| 100 ## - MAIN ENTRY--PERSONAL NAME |
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| Personal author |
Okpala, Iheanyi E. |
| 245 #0 - TITLE STATEMENT |
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| Title |
Practical management of haemoglobinopathies |
| Medium |
[E-Book] |
| 260 ## - PUBLICATION INFORMATION |
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| Place of publication |
Malden, Mass. : |
| Publisher |
Blackwell Pub., |
| Date |
2004 |
| 300 ## - PHYSICAL DESCRIPTION |
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| Physical description |
1 online resource (xi, 244 pages) : illustrations (some color) |
| 505 ## - CONTENTS |
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| Contents |
text |
| 505 ## - CONTENTS |
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| Contents |
The concept of comprehensive care of sickle cell disease / I.E. Okpala -- Haemoglobinopathy diagnostic tests (1): blood counts, sickle solubility test, haemoglobin electrophoresis, & high performance liquid chromatography / Yvonne Daniel -- Haemoglobinopathy diagnostic tests (2): isoelectric focusing, mass spectrometry, & DNA analysis / Barbara Wild -- Epidemiology, genetics and pathophysiology of sickle cell disease / I.E. Okpala -- The genetics & multiple phenotypes of beta-thalassaemia / Swee Lay Thein -- The diagnosis & significance of alpha-thalassaemia / A. Stephens -- Morbid anatomy & autopsy findings in sickle cell disease & sickle cell trait / Sebastian Lucas -- Sickle cell crisis / I.E. Okpala -- Treatment modalities for pain in sickle cell disease / I.E. Okpala -- Childhood sickle cell disease & thalassaemia / Moira Dick. |
| 505 ## - CONTENTS |
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| Contents |
Acute chest syndrome in sickle cell disease / Josh Wright -- Blood transfusion therapy for haemoglobinopathies / Nay Win -- Management of pregnancy in sickle cell disease & thalassaemia / Susan Bewley -- Hepato-biliary complications of the sickle cell diseases / C.S. Johnson -- Pulmonary hypertension / I.E. Okpala -- Stroke in sickle cell disease / Kwaku Ohene-Frempong -- Clinical management of beta-thalassaemia / Kornelia Cinkotai -- Iron chelation therapy in thalassaemia & sickle cell disease / B. Wonke -- Renal disease in sickle cell disease / Ian Abbs -- Assessment of prognosis & hydroxyurea therapy in sickle cell disease / I.E. Okpala. |
| 505 ## - CONTENTS |
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| Contents |
Haemopoietic stem cell transplantation for thalassaemia & sickle cell disease / Irene Roberts & Christina Halsey -- Practical guidelines, antibiotic therapy, exchange blood transfusion / I.E. Okpala -- Drug dependence in sickle cell disease / I.K. Azuonye -- The roles & function of a community sickle cell & thalassaemia centre / C. Rochester-Peart -- Community nursing care for people with thalassaemia & sickle cell disease / Sadie Daley -- Counselling people affected by sickle cell disease & thalassaemia / C. Onyedinma-Ndubueze -- Sickle cell disease & thalassaemia: the challenge for health professionals / Elizabeth Anionwu. |
| 520 ## - ABSTRACT |
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| Abstract |
Remote |
| 520 ## - ABSTRACT |
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| Abstract |
Includes bibliographical references and index. |
| 520 ## - ABSTRACT |
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| Abstract |
Though knowledge of thalassaemia and sickle cell disease has improved steadily for half a century, these inherited haemoglobulinopathies still present a highly significant public health challenge, particularly in the developing world. Though some important advances in specific therapies such as stem cell transplantation have increased the potential for a cure, improvements in daily management remain central to improving the quality of life of patients. This is a postgraduate text, which will be invaluable to trainees and residents in haematology, haematologists in practice and healthcare professionals treating those with sickle cell disease and thalassaemia. The contributors cover basic science and epidemiological aspects of the public health challenge, but maintain a focus on the day to day issues encountered in dealing with affected people. A comprehensive picture of care management is presented, including diagnostic, therapeutic, and psychosocial aspects. Also included is a separate section of self-assessment questions designed to help candidates prepare for examinations in haematology.; Containing clear, practical advice, this text is an essential, practical resource to bridge the gap between expensive reference texts and smaller manuals. |
| 710 ## - ADDED CORPORATE NAME |
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| Added corporate author |
Wiley InterScience (Online service) |
| 856 ## - ONLINE RESOURCE |
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| Uniform Resource Identifier |
<a href="http://dx.doi.org/10.1002/9780470988398">http://dx.doi.org/10.1002/9780470988398</a> |
| Link text |
[Wiley Online Library] |