Geha Raif, Notarangelo Luigi (eds.) Case Studies In Immunology: A Clinical Companion

7th edition. — Garland Science, 2016. — 385 p. — ISBN: 9780815345121Case Studies in Immunology,Seventh Edition is intended for medical students and undergraduate and graduate students in immunology. It presents major topics of immunology through a selection of clinical cases that reinforce and extend the basic science. Each case history is preceded by essential scientific facts about the immunological mechanisms of that specific disorder. The cases themselves demonstrate how immunological problems are deconstructed in the clinic and each one is followed by a concise summary of the clinical finding and questions which can serve as discussion points.X-linked Agammaglobulinemia
CD40 Ligand Deficiency
Activation-Induced Cytidine Deaminase Deficiency
Common Variable Immunodeficiency
X-linked Severe Combined Immunodeficiency
Adenosine Deaminase Deficiency
Omenn Syndrome
MHC Class II Deficiency
DiGeorge Syndrome
Acquired Immune Deficiency Syndrome (AIDS)
Graft-Versus-Host Disease
MHC Class I Deficiency
X-linked Lymphoproliferative Syndrome
Hemophagocytic Lymphohistiocytosis
Chediak–Higashi Syndrome
Wiskott–Aldrich Syndrome
Autoimmune Polyendocrinopathy–Candidiasis–Ectodermal Dystrophy (APECED)
Immune Dysregulation, Polyendocrinopathy, Enteropathy X-linked Disease
Autoimmune Lymphoproliferative Syndrome (ALPS)
Hyper IgE Syndrome
Ataxia Telangiectasia
Warts, Hypogammaglobulinemia, Infections, and Myelokathexis Syndrome (WHIM Syndrome)
X-linked Hypohidrotic Ectodermal Dysplasia and Immunodeficiency
Interferon-γ Receptor Deficiency
Severe Congenital Neutropenia
Chronic Granulomatous Disease
Leukocyte Adhesion Deficiency
Recurrent Herpes Simplex Encephalitis
Interleukin 1 Receptor-Associated Kinase 4 Deficiency
Congenital Asplenia
Hereditary Angioedema
Deficiency of the C8 Complement Component
Hereditary Periodic Fever Syndromes
Systemic Juvenile Idiopathic Arthritis
Rheumatoid Arthritis
Systemic Lupus Erythematosus
Systemic Lupus Erythematosus
Multiple Sclerosis
Autoimmune Hemolytic Anemia
Myasthenia Gravis
Pemphigus Vulgaris
Celiac Disease
Acute Infectious Mononucleosis
Hemolytic Disease of the Newborn
Toxic Shock Syndrome
Lepromatous Leprosy
Allergic Asthma
Drug-induced Serum Sickness
Contact Sensitivity to Poison Ivy
Dedicator of Cytokinesis 8 Deficiency
Activated PI3KD Syndrome (APDS)
Increased Susceptibility toCandidaInfections
LPS-Responsive Beige-Like Anchor (LRBA) Deficiency
T Cell Signaling Defects
Channelopathies