Titlebook: Benign Hematologic Disorders in Children; A Clinical Guide Deepak M. Kamat,Melissa Frei-Jones Book 2021 Springer Nature Switzerland AG 2021

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书目名称Benign Hematologic Disorders in Children影响因子(影响力)学科排名




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书目名称Benign Hematologic Disorders in Children网络公开度学科排名




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书目名称Benign Hematologic Disorders in Children被引频次学科排名




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书目名称Benign Hematologic Disorders in Children年度引用学科排名




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书目名称Benign Hematologic Disorders in Children读者反馈学科排名

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符合规定

Lead Poisoningtrated that there is no safe level of lead exposure in children. Despite efforts to reduce children’s exposure to lead, a substantial number of children continue to be exposed to lead through lead-contaminated dust, water, and soil. Lead affects all systems of the body, but it also affects the neuro

雄辩

Immune and Nonimmune Hemolytic Anemiaout 120 days in the circulation (Shemin and Rittenberg, J Biol Chem. 166:627–636, 1946). Hemolysis is therefore defined as reduced survival of circulating RBCs due to premature destruction. Under steady state conditions, the rate of RBC production equals the rate of RBC loss. As a compensatory mecha

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Alveolar-Bone

Thalassemials. Defects can arise in both the alpha and beta subunits with varying severity of symptoms. Currently most patients with severe phenotypes rely on lifelong chronic transfusions, leading to iron overload and risk for alloimmunization. New therapies are being investigated to decrease transfusion requ

stratum-corneum

Disorders of RBC Metabolismphosphate shunt and glycolytic pathway producing adenosine triphosphate (ATP) and nicotinamide adenine dinucleotide (NAD), respectively. Reduction in enzyme activity in these pathways results in hemolysis. The two most common disorders of RBC metabolism are glucose-6-phosphate dehydrogenase (G6PD) d

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CROW

Immune Thrombocytopenialdhood ITP generally follows a viral illness. Diagnosis is made by a thorough history, physical examination, complete blood count (CBC) evaluation, and peripheral smear review to rule out other diagnoses. Additional laboratory testing is usually not necessary but may be done if the clinical scenario

MILL

Inherited and Congenital Thrombocytopeniath bone marrow failure syndromes or other genetic disorders. Prompt recognition and diagnosis through algorithmic testing is key in order to provide anticipatory guidance, prevention of bleeding complications, and screening for associated syndromic medical comorbidities. Treatment is generally suppo