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Sickle cell disease

Author: Graham R Serjeant; Beryl E Serjeant
Publisher: Oxford ; New York : Oxford University Press, 2001.
Series: Oxford medical publications.
Edition/Format:   Print book : English : 3rd edView all editions and formats
Summary:

This new edition contains many new references and incorporates the latest thinking on the biology of the disease and the best practice in its management.

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Additional Physical Format: Online version:
Serjeant, Graham R.
Sickle cell disease.
Oxford : New York : Oxford University Press, 2001
(OCoLC)606596789
Online version:
Serjeant, Graham R.
Sickle cell disease.
Oxford : New York : Oxford University Press, 2001
(OCoLC)608991982
Material Type: Internet resource
Document Type: Book, Internet Resource
All Authors / Contributors: Graham R Serjeant; Beryl E Serjeant
ISBN: 0192630369 9780192630360
OCLC Number: 46650664
Description: xix, 772 pages : illustrations, maps ; 24 cm.
Contents: Ch. 1. Basic concepts --
Ch. 2. Distribution of sickle cell disease --
Ch. 3. Nomenclature and genetics of sickle cell disease --
Ch. 4. Diagnosis of sickle cell disease --
Ch. 5. Pathophysiology of sickle cell disease --
Ch. 6. Historical aspects --
Ch. 7. The bone marrow --
Ch. 8. The blood --
Ch. 9. The liver and gallbladder --
Ch. 10. The spleen --
Ch. 11. The immune system --
Ch. 12. The gut and abdomen --
Ch. 13. Cardiovascular system --
Ch. 14. Pulmonary system --
Ch. 15. Leg ulceration --
Ch. 16. Bone and joint lesions --
Ch. 17. The painful crisis --
Ch. 18. Renal manifestations --
Ch. 19. Priapism --
Ch. 20. The nervous system --
Ch. 21. The eyes --
Ch. 22. Physical and sexual development --
Ch. 23. Pregnancy and contraception --
Ch. 24. Endocrine system, metabolism, and nutrition --
Ch. 25. Homozygous sickle cell disease --
Ch. 26. Sickle cell-haemoglobin C disease --
Ch. 27. Sickle cell-[beta] thalassaemia --
Ch. 28. Other forms of sickle cell disease --
Ch. 29. Sickle cell --
hereditary persistence of fetal haemoglobin --
Ch. 30. The sickle cell trait --
Ch. 31. General supportive measures --
Ch. 32. Transfusion --
Ch. 33. Attempts to inhibit sickling --
Ch. 34. Surgery and anaesthesia --
Ch. 35. Screening and sickle cell clinics --
Ch. 36. Age and patterns of clinical involvement --
Ch. 37. Causes of death --
Ch. 38. Natural history.
Series Title: Oxford medical publications.
Responsibility: Graham R. Serjeant and Beryl E. Serjeant.
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" . . . this remains an excellent overview of sickle cell disease. It is well written and easy to read . . . I would consider this an excellent purchase for those with an interest in sickle cell Read more...

 
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