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Sickle cell anemia = from basic scie...
~
Costa, Fernando Ferreira.
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Sickle cell anemia = from basic science to clinical practice /
Record Type:
Electronic resources : Monograph/item
Title/Author:
Sickle cell anemia/ edited by Fernando Ferreira Costa, Nicola Conran.
Reminder of title:
from basic science to clinical practice /
other author:
Costa, Fernando Ferreira.
Published:
Cham :Springer International Publishing : : 2016.,
Description:
xv, 435 p. :ill., digital ;24 cm.
Contained By:
Springer eBooks
Subject:
Sickle cell anemia. -
Online resource:
http://dx.doi.org/10.1007/978-3-319-06713-1
ISBN:
9783319067131
Sickle cell anemia = from basic science to clinical practice /
Sickle cell anemia
from basic science to clinical practice /[electronic resource] :edited by Fernando Ferreira Costa, Nicola Conran. - Cham :Springer International Publishing :2016. - xv, 435 p. :ill., digital ;24 cm.
Although sickle cell anemia was the first molecular disease to be identified, its complex and fascinating pathophysiology is still not fully understood. A single mutation in the beta-globin gene incurs numerous molecular and cellular mechanisms that contribute to the plethora of symptoms associated with the disease. Our knowledge regarding sickle cell disease mechanisms, while still not complete, has broadened considerably over the last decades. Sickle Cell Anemia: From Basic Science to Clinical Practice aims to provide an update on our current understanding of the disease's pathophysiology and use this information as a basis to discuss its manifestations in childhood and adulthood. Current therapies and prospects for the development of new approaches for the management of the disease are also covered.
ISBN: 9783319067131
Standard No.: 10.1007/978-3-319-06713-1doiSubjects--Topical Terms:
2186963
Sickle cell anemia.
LC Class. No.: RC641.7.S5
Dewey Class. No.: 616.1527
Sickle cell anemia = from basic science to clinical practice /
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Although sickle cell anemia was the first molecular disease to be identified, its complex and fascinating pathophysiology is still not fully understood. A single mutation in the beta-globin gene incurs numerous molecular and cellular mechanisms that contribute to the plethora of symptoms associated with the disease. Our knowledge regarding sickle cell disease mechanisms, while still not complete, has broadened considerably over the last decades. Sickle Cell Anemia: From Basic Science to Clinical Practice aims to provide an update on our current understanding of the disease's pathophysiology and use this information as a basis to discuss its manifestations in childhood and adulthood. Current therapies and prospects for the development of new approaches for the management of the disease are also covered.
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based on 0 review(s)
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Items
1 records • Pages 1 •
1
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Attachments
W9278870
電子資源
11.線上閱覽_V
電子書
EB RC641.7.S5 S566 2016
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1 records • Pages 1 •
1
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