Antibody therapy : substitution -- immunomodulation -- monoclonal immunotherapy /: substitution -- immunomodulation -- monoclonal immunotherapy. ([2018])
- Record Type:
- Book
- Title:
- Antibody therapy : substitution -- immunomodulation -- monoclonal immunotherapy /: substitution -- immunomodulation -- monoclonal immunotherapy. ([2018])
- Main Title:
- Antibody therapy : substitution -- immunomodulation -- monoclonal immunotherapy
- Further Information:
- Note: Paul Imbach, editor.
- Editors:
- Imbach, Paul
- Contents:
- Intro; Foreword; Contents; About the Editor; Introduction; 1: The Clinical Translation of Intravenous Immunoglobulin from Substitution to Immunomodulation; 1.1 History of New Observations; 1.2 The Translation of IVIG From ITP to Other Autoimmune Disorders; 1.3 The Bridge of Polyclonal and Monoclonal Antibodies; References; Further Reading; Part I: Update of Substitutive and Immunomodulatory Antibodies/ Drugs Indications; 2: From Immune Substitution to Immuno-modulation; 2.1 History; 2.2 IgG for Replacement: How Much?; 2.3 Immunomodulation in Autoimmune Diseases. 2.4 Immunomodulation in Alloimmune Diseases2.5 Immunomodulation in Inflammatory Diseases; 2.6 Expansion to New Indications; References; 3: Manual of Primary and Secondary Immunodeficiencies; 3.1 Introduction; 3.2 X-Linked (Bruton's) Agammaglobulinemia; 3.2.1 Definition and Prevalence; 3.2.2 Pathophysiology; 3.2.3 Clinical Manifestations; 3.2.4 Diagnostics; 3.2.5 Differential Diagnosis; 3.2.6 Therapy; 3.2.7 Prognosis; 3.3 Severe Combined Immunodeficiency (SCID); 3.3.1 Definition and Prevalence; 3.3.2 Pathophysiology; 3.3.2.1 Different Forms; T-B + Variants; T-B-Variants. 3.3.3 Clinical Manifestations3.3.4 Diagnostics; 3.3.5 Treatment; 3.4 Hyper-IgM Syndromes; 3.4.1 Pathogenesis; 3.4.2 Clinical Presentation; 3.4.3 Treatment; 3.5 Common Variable Immunodeficiency (CVID); 3.5.1 Incidence and Diagnosis; 3.5.2 Clinical Manifestations; 3.5.3 Treatment; 3.6 Selective Antibody Deficiency; 3.6.1 Definition and Diagnosis; 3.6.2Intro; Foreword; Contents; About the Editor; Introduction; 1: The Clinical Translation of Intravenous Immunoglobulin from Substitution to Immunomodulation; 1.1 History of New Observations; 1.2 The Translation of IVIG From ITP to Other Autoimmune Disorders; 1.3 The Bridge of Polyclonal and Monoclonal Antibodies; References; Further Reading; Part I: Update of Substitutive and Immunomodulatory Antibodies/ Drugs Indications; 2: From Immune Substitution to Immuno-modulation; 2.1 History; 2.2 IgG for Replacement: How Much?; 2.3 Immunomodulation in Autoimmune Diseases. 2.4 Immunomodulation in Alloimmune Diseases2.5 Immunomodulation in Inflammatory Diseases; 2.6 Expansion to New Indications; References; 3: Manual of Primary and Secondary Immunodeficiencies; 3.1 Introduction; 3.2 X-Linked (Bruton's) Agammaglobulinemia; 3.2.1 Definition and Prevalence; 3.2.2 Pathophysiology; 3.2.3 Clinical Manifestations; 3.2.4 Diagnostics; 3.2.5 Differential Diagnosis; 3.2.6 Therapy; 3.2.7 Prognosis; 3.3 Severe Combined Immunodeficiency (SCID); 3.3.1 Definition and Prevalence; 3.3.2 Pathophysiology; 3.3.2.1 Different Forms; T-B + Variants; T-B-Variants. 3.3.3 Clinical Manifestations3.3.4 Diagnostics; 3.3.5 Treatment; 3.4 Hyper-IgM Syndromes; 3.4.1 Pathogenesis; 3.4.2 Clinical Presentation; 3.4.3 Treatment; 3.5 Common Variable Immunodeficiency (CVID); 3.5.1 Incidence and Diagnosis; 3.5.2 Clinical Manifestations; 3.5.3 Treatment; 3.6 Selective Antibody Deficiency; 3.6.1 Definition and Diagnosis; 3.6.2 Treatment; 3.7 Transient Hypogammaglobulinemia of Infancy; 3.7.1 Definition and Diagnosis; 3.7.2 Management; 3.8 Isolated IgG 1-3 Subclass Deficiency; 3.8.1 Management. 3.9 Selective IgA Deficiency with or without IgG2 Deficiency3.10 Wiskott-Aldrich Syndrome (WAS); 3.10.1 Pathogenesis/Etiology; 3.10.2 Clinical Manifestations; 3.10.3 Treatment; 3.11 Ataxia Telangiectasia; 3.11.1 Pathophysiology/Etiology; 3.11.2 Clinical Manifestation; 3.11.3 Treatment; 3.12 Secondary Immunodeficiency; 3.12.1 Chronic Lymphocytic Leukemia (CLL), Multiple Myeloma (MM) and Treatment of Related Secondary Immunodeficiency in Patients with Hematologic or with Solid Tumor Malignancy with or without Transplantation; 3.12.2 Specific Aspects; 3.12.2.1 CLL and MM. 3.12.2.2 Hematopoietic Stem Cell Transplantation HSCT3.12.2.3 Solid Organ Transplantation; 3.12.3 HIV Infection in Children; 3.12.4 Preterm Infants; 3.12.5 Geriatrics: Immunosenescence; 3.13 Other Combined Immunodeficiency; 4: Manual of Intravenous and Subcutaneous IgG Indications in Autoimmune Diseases; 4.1 Introduction; 4.2 General Characteristics of Autoimmune Disorders; 4.3 General Characteristics of IVIG as an Immunomodulatory Biological Agent; 4.4 Clinical Categorization of IVIG Indications of Autoimmune and Inflammatory Disorders; 4.5 Hematology. … (more)
- Publisher Details:
- Cham, Switzerland : Springer
- Publication Date:
- 2018
- Copyright Date:
- 2018
- Extent:
- 1 online resource
- Subjects:
- 616.0792
Medicine
Immunoglobulins -- Therapeutic use
HEALTH & FITNESS -- Diseases -- General
MEDICAL -- Clinical Medicine
MEDICAL -- Diseases
MEDICAL -- Evidence-Based Medicine
MEDICAL -- Internal Medicine
Immunoglobulins -- Therapeutic use
Immunoglobulin G -- therapeutic use
Antibodies, Monoclonal -- therapeutic use
Immunologic Factors
Immunomodulation
Oncology
Medical -- Immunology
Medical -- Oncology
Immunology
Oncology
Hematology
Immunology
Oncology
Medical -- Hematology
Haematology
Electronic books - Languages:
- English
- ISBNs:
- 9783319680385
3319680382
3319680374
9783319680378 - Related ISBNs:
- 9783319680378
- Notes:
- Note: Includes bibliographical references.
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- British Library HMNTS - ELD.DS.373707
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