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Sickle cell anemia[electronic resour...

Conran, Nicola.

Sickle cell anemia[electronic resource] :from basic science to clinical practice /

紀錄類型:	書目-語言資料,印刷品 : Monograph/item
杜威分類號:	616.1527
書名/作者:	Sickle cell anemia : from basic science to clinical practice // edited by Fernando Ferreira Costa, Nicola Conran.
其他作者:	Costa, Fernando Ferreira.
出版者:	Cham : : Springer International Publishing :, 2016.
面頁冊數:	xv, 435 p. : : ill., digital ;; 24 cm.
Contained By:	Springer eBooks
標題:	Internal Medicine.
標題:	Medical Biochemistry.
標題:	Medicine/Public Health, general.
標題:	Sickle cell anemia.
標題:	Medicine & Public Health.
標題:	Hematology.
ISBN:	9783319067131
ISBN:	9783319067124
摘要、提要註:	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.
電子資源:	http://dx.doi.org/10.1007/978-3-319-06713-1

Sickle cell anemia[electronic resource] :from 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

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

341979
Internal Medicine.

LC Class. No.: RC641.7.S5

Dewey Class. No.: 616.1527

Sickle cell anemia[electronic resource] :from basic science to clinical practice /
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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 463494
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700 1 $a Conran, Nicola. $3 639878
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