Titlebook: Nonmalignant Hematology; Expert Clinical Revi Syed A. Abutalib,Jean M. Connors,Margaret V. Ragni Book 2016 Springer International Publishin

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書目名稱Nonmalignant Hematology影響因子(影響力)




書目名稱Nonmalignant Hematology影響因子(影響力)學科排名




書目名稱Nonmalignant Hematology網絡公開度




書目名稱Nonmalignant Hematology網絡公開度學科排名




書目名稱Nonmalignant Hematology被引頻次




書目名稱Nonmalignant Hematology被引頻次學科排名




書目名稱Nonmalignant Hematology年度引用




書目名稱Nonmalignant Hematology年度引用學科排名




書目名稱Nonmalignant Hematology讀者反饋




書目名稱Nonmalignant Hematology讀者反饋學科排名

嫌惡

Primary Autoimmune Warm Antibody Hemolytic Anemiaslthy children aged 8 and 10 years. For a few weeks, she has been feeling weak for unknown reasons. In a laboratory examination of her blood, she had anemia with a hemoglobin of 9.0 g/dl with a normal leukocyte and platelet count.

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負擔

Iron Homeostasis and the Pathophysiology and Management of Iron DeficiencyIron is an essential element and is required for the synthesis of hemoglobin as well as multiple other proteins in all body cells. In developing countries, iron deficiency is most often the result of blood loss, although some cases result from iron malabsorption.

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Disorders of Hemoglobin Synthesis: Pathophysiology and Diagnostic EvaluationHemoglobinopathies are the most common inherited red cell disorders worldwide among which thalassemias and sickle cell syndromes constitute the two main groups. The hemoglobinopathies are commonly diffused in areas where malaria was endemic, due to the fact that mutated genes caused protection against malaria.

Inflammation

Allogeneic Hematopoietic Cell Transplant in Sickle Cell DiseaseSickle cell disease (SCD) affects approximately 100,000 people in the United States and over 25 million people worldwide. The hemoglobin S mutation in the β-globin chain leads to hemoglobin polymerization under deoxygenated conditions and results in a myriad of acute and chronic complications and early death.

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