Buch, Englisch, 729 Seiten, Book + Online Access, Format (B × H): 178 mm x 254 mm
Buch, Englisch, 729 Seiten, Book + Online Access, Format (B × H): 178 mm x 254 mm
ISBN: 978-1-4614-8679-4
Verlag: Palgrave MacMillan UK
An outstanding new resource of immense value to a wide range of medical researchers and practitioners, the encyclopedia features a user-friendly subdivision of diseases according to their affective locus in the human body. The sections cover integumentary, skeletal, respiratory, digestive, urinary, and reproductive transmissible pathogens. This high-profile encyclopedia will be an essential addition to academic libraries worldwide.
Zielgruppe
Research
Autoren/Hrsg.
Fachgebiete
- Medizin | Veterinärmedizin Medizin | Public Health | Pharmazie | Zahnmedizin Medizin, Gesundheitswesen Public Health, Gesundheitsmanagement, Gesundheitsökonomie, Gesundheitspolitik
- Medizin | Veterinärmedizin Medizin | Public Health | Pharmazie | Zahnmedizin Klinische und Innere Medizin Infektionskrankheiten
- Medizin | Veterinärmedizin Medizin | Public Health | Pharmazie | Zahnmedizin Medizinische Fachgebiete Medizinische Mikrobiologie & Virologie
- Medizin | Veterinärmedizin Medizin | Public Health | Pharmazie | Zahnmedizin Klinische und Innere Medizin Immunologie
Weitere Infos & Material
Complement Deficiencies: C1 Deficiency and Associated Disorders.- C5b-C9 Deficiency.- Complement C3 Deficiency.- Complement Component C2 Deficiency.- Associated with Atypical Hemolytic Uremic Syndrome.- Complete Deficiency of Complement C4.- Ficolin-3.- Hereditary Deficiency of C1 Inhibitor and Angioedema.- Mannose-Binding Lectin-Associated Serine Protease-2 (MASP-2) Deficiency.- Primary and Secondary CD59 Deficiency.- Properdin Deficiency.- Dysregulation-CD27 Deficiency.- DKC1, Dyskeratosis Congenita/Hoyeraal-Hreidarsson Syndrome.- FAAP24 Deficiency.- PRF1 Deficiency.- STX11 Deficiency.- STXBP2 Deficiency.- TERC Deficiency.- TERT.- UNC13D Deficiency.- XIAP Deficiency.- Defects in Innate Immunity: Anhidrotic Ectodermal Dysplasia with Immunodeficiency (EDA-ID), Autosomal-Dominant.- Anhidrotic Ectodermal Dysplasia with Immunodeficiency (EDA-ID), X-linked.- APOL-1 Variants, Susceptibility and Resistance to Trypanosomiasis.- CARD9 Deficiency.- Chronic Mucocutaneous Candidiasis, ACT1 Deficiency.- Chronic Mucocutaneous Candidiasis, IL-17F Deficiency.- Chronic Mucocutaneous Candidiasis, STAT1 Gain of Function.- Chronic Mucocutaneous Candidiasis: IL-17RA Deficiency.- EVER1 and EVER2 Mutations in Epidermodysplasia Verruciformis.- IRF3 Deficiency.- Isolated Congenital Asplenia (ICA) and Mutations in RPSA.- Predisposition to Severe Viral Infection, MCM4 Deficiency.- Predisposition to Severe Viral Infection, STAT2 Deficiency.- TBK1 Deficiency.- TIR Signaling Pathway Deficiency, HOIL1 Deficiency.- TIR Signaling Pathway Deficiency, IRAK-4 Deficiency.- TIR Signaling Pathway Deficiency, MyD88 Deficiency.- TLR3 Deficiency.- TRAF3 Deficiency.- TRIF Deficiency.- UNC93B1 Deficiency.- Warts, Hypogammaglobulinemia, Infections, Myelokathexis (WHIM) Syndrome.- Combined Immunodeficiencies: B Cell Lymphoma/Leukemia 10 Deficiency.- Caspase Recruitment Domain 11, CARD11.- CD3d,e and z Deficiencies.- CD40 Deficiency, Hyper-IgM Syndrome Type 3 (OMIM # 606843).- CD8 alpha (CD8A) Deficiency.- Cytidine 5-Prime Triphosphate Synthase 1 (CTPS1) Deficiency (OMIM # 615897).- Dedicator of Cytokinesis 2: DOCK2 Deficiency.- DOCK8 Deficiency.- ICOS (Inducible T-Cell Costimulatory) Deficiency (OMIM # 607594).- IKBKB Deficiency.- IL21, Deficiency of.- IL21Receptor, Deficiency of.- ITK Deficiency.- LRBA (Lipopolysaccharide-Responsive and Beige-Like Anchor Protein) Deficiency (OMIM# 614700).- Lymphocyte Specific Protein Tyrosine Kinase, LCK.- MAGT1 Deficiency.- MALT1 Deficiency.- Mammalian sterile 20-like 1 (MST1) deficiency.- MHC Class I, A Deficiency of.- MHC Class II, Deficiency of.- NF-kappa B-Inducing Kinase (NIK).- Omenn Deficiency.- OX40 Deficiency.- Ras Homolog Family Member H (RHOH) Deficiency.- TCR- alpha Deficiency.- X-Linked Hyper-IgM Syndrome: CD40Ligand Deficiency (OMIM # 308230).- ZAP70 Deficiency (OMIM # 176947).- Combined Immunodeficiencies with Associated or Syndromic Features: ADA and PNP Deficiency.- Telangiectasia (ATM).- Ataxia-Telangiectasia-Like Disorder (ATLD).- Autosomal Dominant Anhidrotic Ectodermal Dysplasia with Immunodeficiency (AD-EDA-ID).- Autosomal Dominant Hyper IgE Syndrome.- Bloom Syndrome.- Calcium Channel Defects (STIM1 and ORAI1).- Cartilage Hair Hypoplasia (RMRP).- CHARGE Syndrome (CHD7, SEMA3E).- Clinical Presentation of Polymerase E1 (POLE1) and Polymerase E2 (POLE2) Deficiencies.- Comel-Netherton Syndrome (SPINK5).- Defects in B12 and Folate Metabolism (TCN2, SLC46A1 (PCFT Deficiency), MTHFD1).- DiGeorge Anomaly (del22q11).- Down Syndrome.- Hepatic Veno-occlusive Disease with Immunodeficiency (VODI).- IKAROS (IKZF1) Deficiency.- Immunodeficiency with Multiple Intestinal Atresias (TTC7A).- Immunodeficiency, Centromeric Instability, and Facial Dysmorphism (ICF Syndrome) (ICF1-DNMT3B, ICF-2 ZBTB24).- Jacobsen Syndrome.- Kabuki Syndrome.- LUBAC Deficiencies.- MCM4 Deficiency.- Nijmegen Breakage Syndrome (NBS1).- PGM3-deficiency.- PMS2 Deficiency.- RIDDLE Syndrome (RNF168).- Schimke Immuno-osseous Dysplasia.- Short Telomere Syndromes.- STAT5b Deficiency, AR.- TCN2 D