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ﺑﺎﺯﮔﺸﺖ ﺑﻪ ﺻﻔﺤﻪ ﻗﺒﻠﯽ
خرید پکیج
تعداد آیتم قابل مشاهده باقیمانده: 4 مورد
نسخه الکترونیک
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Acquired pure red cell aplasia in adults
Aplastic anemia: Pathogenesis, clinical manifestations, and diagnosis
Approach to the adult with pancytopenia
Dyskeratosis congenita and other telomere biology disorders
Hematopoietic cell transplantation for aplastic anemia in adults
Treatment of acquired aplastic anemia in children and adolescents
Treatment of aplastic anemia in adults
Clinical manifestations and diagnosis of polycythemia vera
Diagnostic approach to the patient with erythrocytosis/polycythemia
Kidney transplantation in adults: Posttransplant erythrocytosis
Molecular pathogenesis of congenital erythrocytoses and polycythemia vera
Prognosis and treatment of polycythemia vera and secondary polycythemia
Red blood cell membrane: Structure and dynamics
Regulation of erythropoiesis
Anemia of chronic disease/anemia of inflammation
Burr cells, acanthocytes, and target cells: Disorders of red blood cell membrane
Causes of anemia in patients with cancer
Clonal hematopoiesis of indeterminate potential (CHIP) and related disorders of clonal hematopoiesis
Diagnosis of hemolytic anemia in adults
Diagnostic approach to anemia in adults
Elective (diagnostic or therapeutic) splenectomy
Evaluation and management of anemia and iron deficiency in adults with heart failure
Idiopathic and clonal cytopenias of uncertain significance (ICUS and CCUS)
Macrocytosis/Macrocytic anemia
Red blood cell survival: Normal values and measurement
Role of erythropoiesis-stimulating agents in the treatment of anemia in patients with cancer
Splenomegaly and other splenic disorders in adults
Acute stroke (ischemic and hemorrhagic) in children and adults with sickle cell disease
Fetal hemoglobin (Hb F) in health and disease
Hemoglobin variants including Hb C, Hb D, and Hb E
Hemoglobin variants that alter hemoglobin-oxygen affinity
Hemoglobinopathy: Screening and counseling in the reproductive setting and fetal diagnosis
Methemoglobinemia
Methods for hemoglobin analysis and hemoglobinopathy testing
Pathophysiology of thalassemia
Prevention of stroke (initial or recurrent) in sickle cell disease
Protection against malaria by variants in red blood cell (RBC) genes
Structure and function of normal hemoglobins
Unstable hemoglobin variants
Anemia in malaria
Cold agglutinin disease
Diagnosis and management of glucose-6-phosphate dehydrogenase (G6PD) deficiency
Diagnosis of hemolytic anemia in adults
Diagnosis of immune TTP
Diagnostic approach to suspected TTP, HUS, or other thrombotic microangiopathy (TMA)
Drug-induced hemolytic anemia
Drug-induced thrombotic microangiopathy (DITMA)
Genetics and pathophysiology of glucose-6-phosphate dehydrogenase (G6PD) deficiency
Hereditary elliptocytosis and related disorders
Hereditary spherocytosis
Hereditary stomatocytosis (HSt) and hereditary xerocytosis (HX)
Hereditary thrombotic thrombocytopenic purpura (hTTP)
Immune TTP: Initial treatment
Management of non-RhD red blood cell alloantibodies during pregnancy
Non-immune (Coombs-negative) hemolytic anemias in adults
Paroxysmal cold hemoglobinuria
Pathophysiology of TTP and other primary thrombotic microangiopathies (TMAs)
Patient perspective: Thrombotic thrombocytopenic purpura (TTP)
Pyruvate kinase deficiency
Rare RBC enzyme disorders
Red blood cell survival: Normal values and measurement
RhD alloimmunization in pregnancy: Management
RhD alloimmunization in pregnancy: Overview
RhD alloimmunization: Prevention in pregnant and postpartum patients
Warm autoimmune hemolytic anemia (AIHA) in adults
Causes and diagnosis of iron deficiency and iron deficiency anemia in adults
Iron requirements and iron deficiency in adolescents
Patient perspective: Iron deficiency anemia
Regulation of iron balance
Treatment of iron deficiency anemia in adults
Approach to the patient with suspected iron overload
Arthritis and bone disease associated with hereditary hemochromatosis
Clinical manifestations and diagnosis of hereditary hemochromatosis
HFE and other hemochromatosis genes
Iron chelators: Choice of agent, dosing, and adverse effects
Management and prognosis of hereditary hemochromatosis
Methods to determine hepatic iron content
Regulation of iron balance
Automated complete blood count (CBC)
Evaluation of the peripheral blood smear
Microcytosis/Microcytic anemia
Red blood cell survival: Normal values and measurement
Causes and pathophysiology of vitamin B12 and folate deficiencies
Clinical manifestations and diagnosis of vitamin B12 and folate deficiency
Treatment of vitamin B12 and folate deficiencies
Hematologic complications of alcohol use
Hematologic complications of rheumatoid arthritis
Clinical manifestations and diagnosis of paroxysmal nocturnal hemoglobinuria
Pathogenesis of paroxysmal nocturnal hemoglobinuria
Treatment and prognosis of paroxysmal nocturnal hemoglobinuria
ALA dehydratase porphyria
Acute intermittent porphyria: Management
Acute intermittent porphyria: Pathogenesis, clinical features, and diagnosis
Congenital erythropoietic porphyria
Erythropoietic protoporphyria and X-linked protoporphyria
Hereditary coproporphyria
Porphyria cutanea tarda and hepatoerythropoietic porphyria: Management and prognosis
Porphyria cutanea tarda and hepatoerythropoietic porphyria: Pathogenesis, clinical manifestations, and diagnosis
Porphyrias: An overview
Variegate porphyria
Anemia in pregnancy
Management of non-RhD red blood cell alloantibodies during pregnancy
RhD alloimmunization in pregnancy: Management
RhD alloimmunization in pregnancy: Overview
RhD alloimmunization: Prevention in pregnant and postpartum patients
Acute and chronic bone complications of sickle cell disease
Acute chest syndrome (ACS) in sickle cell disease (adults and children)
Acute stroke (ischemic and hemorrhagic) in children and adults with sickle cell disease
Acute vaso-occlusive pain management in sickle cell disease
Diagnosis of sickle cell disorders
Disease-modifying therapies to prevent pain and other complications of sickle cell disease
Evaluation and management of fever in children and adults with sickle cell disease
Evaluation of acute pain in sickle cell disease
Gene test interpretation: Sickle cell variant in the hemoglobin beta locus (HBB)
Hematopoietic stem cell transplantation in sickle cell disease
Hemoglobinopathy: Screening and counseling in the reproductive setting and fetal diagnosis
Hepatic manifestations of 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
Patient perspective: Sickle cell disease
Prevention of stroke (initial or recurrent) in sickle cell disease
Priapism and erectile dysfunction in sickle cell disease
Pulmonary hypertension associated with sickle cell disease
Red blood cell transfusion in sickle cell disease: Indications and transfusion techniques
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
Sickle cell disease in sub-Saharan Africa
Sickle cell disease: Obstetric considerations
Sickle cell trait
Transfusion in sickle cell disease: Management of complications including iron overload
Causes and pathophysiology of the sideroblastic anemias
Clinical manifestations, diagnosis, and classification of myelodysplastic syndromes (MDS)
Myelodysplastic syndromes/neoplasms (MDS): Management of hematologic complications in lower-risk MDS
Prognosis of myelodysplastic neoplasms/syndromes (MDS) in adults
Sideroblastic anemias: Diagnosis and management
Treatment of high or very high risk myelodysplastic syndromes
Treatment of lower-risk myelodysplastic syndromes (MDS)
Alpha thalassemia major: Prenatal and postnatal management
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
Molecular genetics of the thalassemia syndromes
Pathophysiology of thalassemia
Public health issues in the thalassemic syndromes
Thalassemia: Management after hematopoietic cell transplantation

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