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ﺑﺎﺯﮔﺸﺖ ﺑﻪ ﺻﻔﺤﻪ ﻗﺒﻠﯽ
خرید پکیج
تعداد آیتم قابل مشاهده باقیمانده: 4 مورد
نسخه الکترونیک
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Agammaglobulinemia
Clinical manifestations, epidemiology, and diagnosis of common variable immunodeficiency in adults
Clinical significance of isolated IgE deficiency
Common variable immunodeficiency in children
Gastrointestinal manifestations in primary immunodeficiency
Hyperimmunoglobulin M syndromes
IgG subclass deficiency
IgG subclasses: Physical properties, genetics, and biologic functions
Intravenous immune globulin: Adverse effects
Malignancy in inborn errors of immunity
Pathogenesis of common variable immunodeficiency
Primary humoral immunodeficiencies: An overview
Selective IgA deficiency: Clinical manifestations, pathophysiology, and diagnosis
Selective IgA deficiency: Management and prognosis
Selective IgM deficiency
Specific antibody deficiency
Treatment and prognosis of common variable immunodeficiency
Ataxia-telangiectasia
Bloom syndrome
Nijmegen breakage syndrome
Adenosine deaminase deficiency: Pathogenesis, clinical manifestations, and diagnosis
Adenosine deaminase deficiency: Treatment and prognosis
CD3/T cell receptor complex disorders causing immunodeficiency
Combined immunodeficiencies: An overview
Combined immunodeficiencies: Specific defects
Newborn screening for inborn errors of immunity
Purine nucleoside phosphorylase deficiency
Severe combined immunodeficiency (SCID) with JAK3 deficiency
Severe combined immunodeficiency (SCID): An overview
Severe combined immunodeficiency (SCID): Specific defects
T cell receptor signaling
T-B-NK+ SCID: Management
T-B-NK+ SCID: Pathogenesis, clinical manifestations, and diagnosis
X-linked severe combined immunodeficiency (X-SCID)
ZAP-70 deficiency
Approach to the adult with recurrent infections
Approach to the child with recurrent infections
Assessing antibody function as part of an immunologic evaluation
Autoimmunity in patients with inborn errors of immunity/primary immunodeficiency
Flow cytometry for the diagnosis of inborn errors of immunity
Genetic testing in patients with a suspected primary immunodeficiency or autoinflammatory syndrome
Hematopoietic cell transplantation for non-SCID inborn errors of immunity
Hematopoietic cell transplantation for severe combined immunodeficiencies
Immune and microbial mechanisms in the pathogenesis of inflammatory bowel disease
Immune function in older adults
Immune globulin therapy in inborn errors of immunity
Immunizations in patients with inborn errors of immunity
Inborn errors of immunity (primary immunodeficiencies): Classification
Inborn errors of immunity (primary immunodeficiencies): Overview of management
Laboratory evaluation of the immune system
Overview of gene therapy for inborn errors of immunity
Recognition of immunodeficiency in the first three months of life
Subcutaneous and intramuscular immune globulin therapy
Pulmonary complications of primary immunodeficiencies
Syndromic immunodeficiencies
Autoimmune lymphoproliferative syndrome (ALPS): Clinical features and diagnosis
Autoimmune lymphoproliferative syndrome (ALPS): Epidemiology and pathogenesis
Autoimmune lymphoproliferative syndrome (ALPS): Management and prognosis
Autosomal dominant hyperimmunoglobulin E syndrome
Cartilage-hair hypoplasia
Chronic mucocutaneous candidiasis
DiGeorge (22q11.2 deletion) syndrome: Clinical features and diagnosis
DiGeorge (22q11.2 deletion) syndrome: Epidemiology and pathogenesis
DiGeorge (22q11.2 deletion) syndrome: Management and prognosis
IPEX: Immune dysregulation, polyendocrinopathy, enteropathy, X-linked
Idiopathic CD4+ lymphocytopenia
Idiopathic systemic capillary leak syndrome
Mendelian susceptibility to mycobacterial diseases: An overview
Mendelian susceptibility to mycobacterial diseases: Specific defects
NK cell deficiency syndromes: Clinical manifestations and diagnosis
NK cell deficiency syndromes: Treatment
Wiskott-Aldrich syndrome
X-linked lymphoproliferative disease
Acquired disorders of the complement system
Approach to the adult with unexplained neutropenia
Chediak-Higashi syndrome
Chronic granulomatous disease: Pathogenesis, clinical manifestations, and diagnosis
Chronic granulomatous disease: Treatment and prognosis
Congenital neutropenia
Cyclic neutropenia
Immune neutropenia
Inherited disorders of the complement system
Leukocyte-adhesion deficiency
Myeloperoxidase deficiency and other enzymatic WBC defects causing immunodeficiency
Neutrophil-specific granule deficiency
Overview and clinical assessment of the complement system
Overview of neutropenia in children and adolescents
Primary disorders of phagocyte number and/or function: An overview
Safety of rheumatic disease medication use during pregnancy and lactation
Secondary immunodeficiency induced by biologic therapies

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