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

作者: 拿著錫    時間: 2025-3-21 16:23
書目名稱Benign Hematologic Disorders in Children影響因子(影響力)




書目名稱Benign Hematologic Disorders in Children影響因子(影響力)學(xué)科排名




書目名稱Benign Hematologic Disorders in Children網(wǎng)絡(luò)公開度




書目名稱Benign Hematologic Disorders in Children網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Benign Hematologic Disorders in Children被引頻次




書目名稱Benign Hematologic Disorders in Children被引頻次學(xué)科排名




書目名稱Benign Hematologic Disorders in Children年度引用




書目名稱Benign Hematologic Disorders in Children年度引用學(xué)科排名




書目名稱Benign Hematologic Disorders in Children讀者反饋




書目名稱Benign Hematologic Disorders in Children讀者反饋學(xué)科排名





作者: Pantry    時間: 2025-3-21 21:26

作者: 符合規(guī)定    時間: 2025-3-22 00:59
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
作者: 雄辯    時間: 2025-3-22 07:09
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
作者: OFF    時間: 2025-3-22 09:39

作者: Alveolar-Bone    時間: 2025-3-22 13:26
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
作者: stratum-corneum    時間: 2025-3-22 20:19
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
作者: 地殼    時間: 2025-3-23 00:58

作者: CROW    時間: 2025-3-23 04:43
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
作者: MILL    時間: 2025-3-23 09:30
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
作者: Estimable    時間: 2025-3-23 12:00

作者: anagen    時間: 2025-3-23 13:56

作者: JAMB    時間: 2025-3-23 19:05

作者: thalamus    時間: 2025-3-23 23:01

作者: 自由職業(yè)者    時間: 2025-3-24 02:43

作者: Eosinophils    時間: 2025-3-24 06:47

作者: Erythropoietin    時間: 2025-3-24 11:24

作者: 人類    時間: 2025-3-24 15:18
Marla C. Dubinsky MD,Stephan R. Targan MDdic or chronic transfusions, folic acid supplementation, or even splenectomy in certain situations. This chapter will review the pathophysiology of these disorders as well as their diagnosis and clinical management, including the recognition and management of hemolytic anemia.
作者: output    時間: 2025-3-24 22:11

作者: 能夠支付    時間: 2025-3-24 23:39
Red Blood Cell Membrane Defectsdic or chronic transfusions, folic acid supplementation, or even splenectomy in certain situations. This chapter will review the pathophysiology of these disorders as well as their diagnosis and clinical management, including the recognition and management of hemolytic anemia.
作者: 增長    時間: 2025-3-25 04:35
Book 2021ular anomalies and complement dysregulation syndromes..Written by experts in the field,?.Benign Hematologic Disorders in Children: A Clinical Guide?.is a valuable resourcefor clinicians and practitioners who treat children afflicted with these disorders..
作者: 惡心    時間: 2025-3-25 08:09
Lead Poisoninglogical, hematological, and renal systems most prominently. Iron deficiency appears to increase the risk of lead absorption, but anemia due to lead poisoning is uncommon. Although children with lead poisoning require appropriate medical and public health intervention, efforts should be directed at primary prevention of lead exposure.
作者: meritorious    時間: 2025-3-25 14:39

作者: Introduction    時間: 2025-3-25 17:38

作者: GORGE    時間: 2025-3-25 20:47
https://doi.org/10.1007/978-94-009-0371-5lobin F levels has resulted in increased survival to adulthood for children with access to these therapies. This chapter focuses on expanding knowledge of the pathophysiology of SCD, advances in prevention, and treatment and novel curative therapies.
作者: palliate    時間: 2025-3-26 01:38
https://doi.org/10.1007/978-1-60327-433-3nt. Medical interventions are recommended in case of mucosal bleeding, parental anxiety, or high activity level of the child. Serious, life-threatening hemorrhagic events are rare in childhood ITP. In an office setting, pediatricians can manage ITP with serial CBC evaluations and physical examinations to rule out major bleeding symptoms.
作者: Orgasm    時間: 2025-3-26 07:10

作者: Toxoid-Vaccines    時間: 2025-3-26 12:26

作者: 截斷    時間: 2025-3-26 12:45

作者: Cabinet    時間: 2025-3-26 20:20
Disorders of Granulocyte Functionsnostic tests. The key to the successful management of phagocyte disorders include early diagnosis and early initiation of antibiotic to prevent and treat infections. In some disorders, treatments such as prophylactic antibiotics, granulocyte colony-stimulating factor infusions, and hematopoietic cell transplantation maybe necessary.
作者: compose    時間: 2025-3-27 00:55

作者: ALE    時間: 2025-3-27 03:58
https://doi.org/10.1007/978-94-009-7439-5eficiency and pyruvate kinase (PK) deficiency. G6PD deficiency predominantly results in acute episodic hemolysis in response to exposure to oxidative stress. PK deficiency results in chronic non-spherocytic hemolytic anemia. Treatment of both disorders is supportive with a focus of avoiding offending agents in G6PD deficiency.
作者: 雄偉    時間: 2025-3-27 08:06
Vikram Kanagala M.D.,Daniel J. Stein M.D.iatric myeloproliferative disorder with distinct biological and clinical features when compared to adult essential thrombocytosis. In this chapter, we will provide an overview of primary and secondary causes of thrombocytosis.
作者: 符合你規(guī)定    時間: 2025-3-27 12:54

作者: Prostaglandins    時間: 2025-3-27 14:50

作者: 驚惶    時間: 2025-3-27 20:15

作者: 罵人有污點    時間: 2025-3-28 01:39
Isabel Roitman,Anjali Mone,Arun Swaminathnticipatory guidance, prevention of bleeding complications, and screening for associated syndromic medical comorbidities. Treatment is generally supportive, and prognosis depends on the underlying cause.
作者: Projection    時間: 2025-3-28 05:16
https://doi.org/10.1007/978-3-319-75022-4Diagnosis lies in the careful assessment of the patient’s clinical features, and occasionally targeted genetic testing, as well as the timing and pattern of the neutropenia. Management varies from observation to use of colony-stimulating factors.
作者: enhance    時間: 2025-3-28 06:21

作者: 露天歷史劇    時間: 2025-3-28 10:51
Thalassemiafelong chronic transfusions, leading to iron overload and risk for alloimmunization. New therapies are being investigated to decrease transfusion requirements; however, only hematopoietic stem cell transplant and recent gene therapy are able to completely eliminate the need for transfusions.
作者: 牽索    時間: 2025-3-28 18:00

作者: legislate    時間: 2025-3-28 20:20
NeutropeniaDiagnosis lies in the careful assessment of the patient’s clinical features, and occasionally targeted genetic testing, as well as the timing and pattern of the neutropenia. Management varies from observation to use of colony-stimulating factors.
作者: 相容    時間: 2025-3-29 02:12

作者: 手工藝品    時間: 2025-3-29 05:17
https://doi.org/10.1007/978-1-84628-933-0mmon nutritional anemia but also the most common cause of anemia in infancy and childhood. Iron deficiency anemia has important health ramifications including effects on neurodevelopment. Dietary modifications can prevent iron deficiency, and if iron deficiency develops, simple interventions help pr
作者: Infelicity    時間: 2025-3-29 09:08

作者: Chameleon    時間: 2025-3-29 13:20

作者: THROB    時間: 2025-3-29 16:55
https://doi.org/10.1007/978-94-009-0371-5 100,000 individuals in the United States. The bulk of the disease burden is found outside the United States with an estimated 300,000 babies born annually in sub-Saharan Africa, the Middle East, and Indian subcontinent affected by SCD. The use of preventive strategies including penicillin prophylax
作者: Fibrinogen    時間: 2025-3-29 23:32

作者: Gyrate    時間: 2025-3-30 01:11
https://doi.org/10.1007/978-94-009-7439-5phosphate 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
作者: hematuria    時間: 2025-3-30 06:27

作者: 騙子    時間: 2025-3-30 10:53

作者: 平躺    時間: 2025-3-30 13:30

作者: 感染    時間: 2025-3-30 18:46
https://doi.org/10.1007/978-3-030-81780-0r quantitative defects. These disorders may also be associated with either macrothrombocytopenia or microthrombocytopenia; however, the majority of disorders show normal platelet size and morphology. Bleeding severity is variable but generally consists of mild-to-moderate mucocutaneous bleeding incl
作者: exophthalmos    時間: 2025-3-30 22:58





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