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ﺑﺎﺯﮔﺸﺖ ﺑﻪ ﺻﻔﺤﻪ ﻗﺒﻠﯽ
خرید پکیج
تعداد آیتم قابل مشاهده باقیمانده: 4 مورد
نسخه الکترونیک
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Causes and pathophysiology of vitamin B12 and folate deficiencies
Clinical manifestations and diagnosis of Fanconi anemia
Diamond-Blackfan anemia
Dyskeratosis congenita and other telomere biology disorders
Iron deficiency in infants and children <12 years: Screening, prevention, clinical manifestations, and diagnosis
Iron deficiency in infants and children <12 years: Treatment
Iron requirements and iron deficiency in adolescents
Macrocytosis/Macrocytic anemia
Management and prognosis of Fanconi anemia
Overview of causes of anemia in children due to decreased red blood cell production
Shwachman-Diamond syndrome
Treatment of acquired aplastic anemia in children and adolescents
Approach to the patient with a suspected acute transfusion reaction
Blood donor screening: Laboratory testing
Immunologic transfusion reactions
Oxygen carriers as alternatives to red blood cell transfusion
Red blood cell antigens and antibodies
Red blood cell transfusion in infants and children: Administration and complications
Red blood cell transfusion in infants and children: Indications
Red blood cell transfusion in infants and children: Selection of blood products
Therapeutic apheresis (plasma exchange or cytapheresis): Complications
Transfusion-associated graft-versus-host disease
Clinical manifestations and diagnosis of Fanconi anemia
Congenital neutropenia
Diamond-Blackfan anemia
Dyskeratosis congenita and other telomere biology disorders
Management and prognosis of Fanconi anemia
Overview of causes of anemia in children due to decreased red blood cell production
Treatment of acquired aplastic anemia in children and adolescents
Donor selection for hematopoietic cell transplantation
Hematopoietic cell transplantation for non-SCID inborn errors of immunity
Hematopoietic cell transplantation for severe combined immunodeficiencies
Hematopoietic stem cell transplantation for transfusion-dependent thalassemia
Hematopoietic stem cell transplantation in sickle cell disease
Hydroxyurea use in sickle cell disease
Investigational therapies for sickle cell disease
Overview of gene therapy for inborn errors of immunity
Thalassemia: Management after hematopoietic cell transplantation
Acquired hemophilia A (and other acquired coagulation factor inhibitors)
Acquired von Willebrand syndrome
Approach to the child with bleeding symptoms
Biology and normal function of factor VIII and factor IX
Clinical manifestations and diagnosis of hemophilia
Clinical presentation and diagnosis of von Willebrand disease
Direct oral anticoagulants (DOACs) and parenteral direct-acting anticoagulants: Dosing and adverse effects
Disseminated intravascular coagulation in infants and children
Gene therapy and other investigational approaches for hemophilia
Genetics of hemophilia A and B
Hemophilia A and B: Routine management including prophylaxis
Inhibitors in hemophilia: Mechanisms, prevalence, diagnosis, and eradication
Neonatal thrombosis: Clinical features and diagnosis
Neonatal thrombosis: Management and outcome
Overview of hemostasis
Overview of the treatment of proximal and distal lower extremity deep vein thrombosis (DVT)
Pathophysiology of von Willebrand disease
Patient perspective: von Willebrand disease
Protein C deficiency
Protein S deficiency
Prothrombin G20210A
Thrombophilia testing in children and adolescents
Treatment of bleeding and perioperative management in hemophilia A and B
Venous thrombosis and thromboembolism (VTE) in children: Risk factors, clinical manifestations, and diagnosis
Venous thrombosis and thromboembolism (VTE) in children: Treatment, prevention, and outcome
von Willebrand disease (VWD): Treatment of major bleeding and major surgery
von Willebrand disease (VWD): Treatment of minor bleeding, use of DDAVP, and routine preventive care
Acute myeloid leukemia in children and adolescents
Juvenile myelomonocytic leukemia
Overview of Hodgkin lymphoma in children and adolescents
Overview of non-Hodgkin lymphoma in children and adolescents
Overview of the clinical presentation and diagnosis of acute lymphoblastic leukemia/lymphoma in children
Introduction to recombinant hematopoietic growth factors
Overview of hematopoietic stem cells
Regulation of erythropoiesis
Regulation of myelopoiesis
Hemoglobin variants that alter hemoglobin-oxygen affinity
Hemoglobinopathy: Screening and counseling in the reproductive setting and fetal diagnosis
Methemoglobinemia
Pathogenesis of paroxysmal nocturnal hemoglobinuria
Pathophysiology of thalassemia
Protection against malaria by variants in red blood cell (RBC) genes
Structure and function of normal hemoglobins
Unstable hemoglobin variants
Alloimmune hemolytic disease of the newborn: Postnatal diagnosis and management
Autoimmune hemolytic anemia (AIHA) in children: Classification, clinical features, and diagnosis
Autoimmune hemolytic anemia (AIHA) in children: Treatment and outcome
Clinical manifestations and diagnosis of paroxysmal nocturnal hemoglobinuria
Cold agglutinin disease
Drug-induced hemolytic anemia
Hemoglobinopathy: Screening and counseling in the reproductive setting and fetal diagnosis
Management of non-RhD red blood cell alloantibodies during pregnancy
Overview of hemolytic anemias in children
Treatment and prognosis of paroxysmal nocturnal hemoglobinuria
Warm autoimmune hemolytic anemia (AIHA) in adults
Clinical manifestations and diagnosis of Fanconi anemia
Diamond-Blackfan anemia
Dyskeratosis congenita and other telomere biology disorders
Iron deficiency in infants and children <12 years: Screening, prevention, clinical manifestations, and diagnosis
Iron deficiency in infants and children <12 years: Treatment
Iron requirements and iron deficiency in adolescents
Management and prognosis of Fanconi anemia
Overview of causes of anemia in children due to decreased red blood cell production
Treatment of acquired aplastic anemia in children and adolescents
Approach to the patient with suspected iron overload
HFE and other hemochromatosis genes
Methods to determine hepatic iron content
Regulation of iron balance
Burr cells, acanthocytes, and target cells: Disorders of red blood cell membrane
Clinical use of coagulation tests
Erythropoietic protoporphyria and X-linked protoporphyria
Evaluation of bone marrow aspirate smears
Evaluation of the peripheral blood smear
Childhood lead poisoning: Clinical manifestations and diagnosis
Childhood lead poisoning: Exposure and prevention
Childhood lead poisoning: Management
Anemia of prematurity (AOP)
Approach to the child with unexplained thrombocytopenia
Causes of thrombocytopenia in children
Immune thrombocytopenia (ITP) in children: Clinical features and diagnosis
Immune thrombocytopenia (ITP) in children: Initial management
Immune thrombocytopenia (ITP) in children: Management of chronic disease
Megakaryocyte biology and platelet production
Neonatal immune-mediated thrombocytopenia
Neonatal thrombocytopenia: Clinical manifestations, evaluation, and management
Neonatal thrombocytopenia: Etiology
Platelet biology and mechanism of anti-platelet drugs
Platelet function testing
Uremic platelet dysfunction
Diagnostic approach to the patient with erythrocytosis/polycythemia
Molecular pathogenesis of congenital erythrocytoses and polycythemia vera
Neonatal polycythemia
Acute intermittent porphyria: Management
Acute intermittent porphyria: Pathogenesis, clinical features, and diagnosis
Congenital erythropoietic porphyria
Porphyrias: An overview
Acute and chronic bone complications of sickle cell disease
Approach to the child with anemia
Causes and pathophysiology of the sideroblastic anemias
Clinical manifestations and diagnosis of Fanconi anemia
Diagnosis and management of glucose-6-phosphate dehydrogenase (G6PD) deficiency
Dyskeratosis congenita and other telomere biology disorders
Genetics and pathophysiology of glucose-6-phosphate dehydrogenase (G6PD) deficiency
Hematopoietic stem cell transplantation in sickle cell disease
Hemoglobin variants including Hb C, Hb D, and Hb E
Hereditary elliptocytosis and related disorders
Hereditary spherocytosis
Hereditary stomatocytosis (HSt) and hereditary xerocytosis (HX)
Iron deficiency in infants and children <12 years: Screening, prevention, clinical manifestations, and diagnosis
Iron deficiency in infants and children <12 years: Treatment
Iron requirements and iron deficiency in adolescents
Management and prognosis of Fanconi anemia
Pyruvate kinase deficiency
Rare RBC enzyme disorders
Sideroblastic anemias: Diagnosis and management
Treatment of acquired aplastic anemia in children and adolescents
Acute and chronic bone complications of sickle cell disease
Acute stroke (ischemic and hemorrhagic) in children and adults with sickle cell disease
Diagnosis of sickle cell disorders
Evaluation and management of fever in children and adults with sickle cell disease
Hematopoietic stem cell transplantation in sickle cell disease
Hydroxyurea use in sickle cell disease
Investigational therapies for sickle cell disease
Overview of compound sickle cell syndromes
Overview of the clinical manifestations of sickle cell disease
Overview of the management and prognosis of sickle cell disease
Overview of the pulmonary complications of sickle cell disease
Pathophysiology of sickle cell disease
Priapism and erectile dysfunction in sickle cell disease
Protection against malaria by variants in red blood cell (RBC) genes
Pulmonary hypertension associated with sickle cell disease
Sickle cell disease (SCD) in adolescents and young adults (AYA): Transition from pediatric to adult care
Sickle cell disease effects on the kidney
Sickle cell disease in infancy and childhood: Routine health care maintenance and anticipatory guidance
Approach to the child with an enlarged spleen
Cervical lymphadenitis in children: Diagnostic approach and initial management
Cervical lymphadenitis in children: Etiology and clinical manifestations
Peripheral lymphadenopathy in children: Etiology
Peripheral lymphadenopathy in children: Evaluation and diagnostic approach
Clinical manifestations and diagnosis of Shiga toxin-producing Escherichia coli (STEC) hemolytic uremic syndrome (HUS) in children
HIV-associated cytopenias
Non-immune (Coombs-negative) hemolytic anemias in adults
Treatment and prognosis of Shiga toxin-producing Escherichia coli (STEC) hemolytic uremic syndrome (HUS) in children
Diagnosis of thalassemia (adults and children)
Hematopoietic stem cell transplantation for transfusion-dependent thalassemia
Hemoglobinopathy: Screening and counseling in the reproductive setting and fetal diagnosis
Management of thalassemia
Pathophysiology of thalassemia
Protection against malaria by variants in red blood cell (RBC) genes
Thalassemia: Management after hematopoietic cell transplantation
Approach to the child with lymphocytosis or lymphocytopenia
Approach to the patient with neutrophilia
Approach to the patient with unexplained eosinophilia
Clinical features and diagnosis of hemophagocytic lymphohistiocytosis
Clinical manifestations, pathologic features, and diagnosis of Langerhans cell histiocytosis
Congenital neutropenia
Cyclic neutropenia
Drug-induced neutropenia and agranulocytosis
Eosinophil biology and causes of eosinophilia
Evaluation of children with non-chemotherapy-induced neutropenia and fever
Immune neutropenia
Infectious causes of neutropenia
Management of children with non-chemotherapy-induced neutropenia and fever
Overview of neutropenia in children and adolescents
Treatment and prognosis of hemophagocytic lymphohistiocytosis

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