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Encyclopedia of Medical Immunology, m. 1 Buch, m. 1 E-Book. Vol.2: Immunodeficiency Diseases
 
Product details:
ISBN13:9781461486794
ISBN10:1461486793
Binding:Unidentified
No. of pages:729 pages
Size:254x178 mm
Language:English
Illustrations: XXXVIII, 729 p. 73 illus., 60 illus. in color. Print + eReference. Illustrations, black & white
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Encyclopedia of Medical Immunology, m. 1 Buch, m. 1 E-Book. Vol.2

Immunodeficiency Diseases
 
Edition number: 1st ed. 2020
Publisher: Springer, Berlin
Date of Publication:
Number of Volumes: 1 pieces, .
 
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Short description:

606843).- CD8 alpha (CD8A) Deficiency.- Cytidine 5-Prime Triphosphate Synthase 1 (CTPS1) Deficiency (OMIM

Long description:
615897).- Dedicator of Cytokinesis 2: DOCK2 Deficiency.- DOCK8 Deficiency.- ICOS (Inducible T-Cell Costimulatory) Deficiency (OMIM
Table of Contents:

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