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Version October 2024
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Agammaglobulinemia
Clinical manifestations, epidemiology, and diagnosis of common variable immunodeficiency in adults
IgG subclass deficiency
IgG subclasses: Physical properties, genetics, and biologic functions
Pathogenesis of common variable immunodeficiency
Selective IgA deficiency: Clinical manifestations, pathophysiology, and diagnosis
Selective IgM deficiency
Specific antibody deficiency
Transient hypogammaglobulinemia of infancy
Antigen-presenting cells
Apoptosis and autoimmune disease
Immunology of the maternal-fetal interface
Mast cells: Development, identification, and physiologic roles
The adaptive cellular immune response: T cells and cytokines
Toll-like receptors: Roles in disease and therapy
Bloom syndrome
Nijmegen breakage syndrome
Adenosine deaminase deficiency: Pathogenesis, clinical manifestations, and diagnosis
Adenosine deaminase deficiency: Treatment and prognosis
Combined immunodeficiencies: An overview
Combined immunodeficiencies: Specific defects
Immunizations in patients with inborn errors of immunity
Inborn errors of immunity (primary immunodeficiencies): Overview of management
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
Acute phase reactants
Overview of autoimmunity
Human leukocyte antigens (HLA): A roadmap
Agammaglobulinemia
Immunoglobulin genetics
Overview of therapeutic monoclonal antibodies
Primary humoral immunodeficiencies: An overview
Structure of immunoglobulins
The adaptive humoral immune response
Flow cytometry for the diagnosis of inborn errors of immunity
Immune globulin therapy in inborn errors of immunity
Laboratory evaluation of the immune system
Approach to the child with recurrent infections
Autoinflammatory diseases mediated by NFkB and/or aberrant TNF activity
Autoinflammatory diseases mediated by inflammasomes and related IL-1 family cytokines (inflammasomopathies)
Autoinflammatory diseases mediated by interferon production and signaling (interferonopathies)
Autoinflammatory diseases mediated by miscellaneous mechanisms
Deficiency of adenosine deaminase 2 (DADA2)
Hyperimmunoglobulin D syndrome: Clinical manifestations and diagnosis
Hyperimmunoglobulin D syndrome: Management
Hyperimmunoglobulin D syndrome: Pathophysiology
Periodic fever with aphthous stomatitis, pharyngitis, and adenitis (PFAPA syndrome)
The autoinflammatory diseases: An overview
Tumor necrosis factor receptor-1 associated periodic syndrome (TRAPS)
Autosomal dominant hyperimmunoglobulin E syndrome
Cartilage-hair hypoplasia
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
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
Chediak-Higashi syndrome
Chronic granulomatous disease: Pathogenesis, clinical manifestations, and diagnosis
Chronic granulomatous disease: Treatment and prognosis
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
Primary disorders of phagocyte number and/or function: An overview
CD3/T cell receptor complex disorders causing immunodeficiency
Syndromic immunodeficiencies
Hematopoietic cell transplantation for non-SCID inborn errors of immunity
Hematopoietic cell transplantation for severe combined immunodeficiencies
Overview of gene therapy for inborn errors of immunity
Pathogenesis of graft-versus-host disease (GVHD)
Transplantation immunobiology
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