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Sickle cell anemiafrom basic science...

Conran, Nicola.

Sickle cell anemiafrom basic science to clinical practice /

Record Type:	Electronic resources : Monograph/item
Title/Author:	Sickle cell anemiaedited 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$q(electronic bk.)

Sickle cell anemiafrom basic science to clinical practice /
Sickle cell anemiafrom 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$q(electronic bk.)

Standard No.: 10.1007/978-3-319-06713-1doiSubjects--Topical Terms:

742235
Sickle cell anemia.

LC Class. No.: RC641.7.S5

Dewey Class. No.: 616.1527

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245 0 0 $a Sickle cell anemia $h [electronic resource] : $b from basic science to clinical practice / $c edited by Fernando Ferreira Costa, Nicola Conran.
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520 $a 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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650 2 4 $a Medicine/Public Health, general. $3 273879
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