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[資源]
2015年新著——遺傳性血紅蛋白�。ㄓ⑽陌妫�
"Inherited Hemoglobin Disorders" ed. by Anjana Munshi
InTAvE | 2015 | ISBN: 9535121987 9789535121985 | 191 pages | PDF | 7 MB
This book describes the genetic defects of hemoglobins, disease complications, and therapeutic strategies. The book serves as an important resource and review to the researchers in the field of hemoglobinopathies.
This book has two distinct sections.
The first theme includes seven chapters devoted to the types of hemoglobinopathies, mutation spectrum, diagnostic methods, and disease complications, and the second theme includes three chapters focusing on various treatment strategies.
The content of the chapters presented in the book is guided by the knowledge and experience of the contributing authors.
Contents
Preface
1 Hemoglobinopathy Approach Diagnosis and Treatment Policy
2 Thalassemia — From Genotype to Phenotype
3 Sickle Cell Disease (SCD)
4 Interaction between Erythropoiesis and Iron Metabolism in Human β-thalassemia - Recent Advances and New Therapeutic Approaches
5 Acute Splenic Sequestration Crisis
6 Comparative Study of the Amount of Re-released Hemoglobin from α-Thalassemia and Hereditary Spherocytosis Erythrocytes
7 Modifiers of γ-Globin Gene Expression and Treatment of β-Thalassemia
8 Novel Therapy Approaches in β-Thalassemia Syndromes — A Role of Genetic Modifiers
9 Sickle Cell Disease – Current Treatment and New Therapeutical Approaches![2015年新著——遺傳性血紅蛋白病（英文版）]()
InTAvE | 2015 | ISBN: 9535121987 9789535121985 | 191 pages | PDF | 7 MB |
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2015-11-23 15:43:36, 7.43 M
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