Primary immunodeficiency and autoimmunity: A comprehensive review
The primary immunodeficiency diseases (PIDs) include many genetic disorders that affect different components of the innate and adaptive responses. The number of distinct genetic PIDs has increased exponentially with improved methods of detection and advanced laboratory methodology. Patients with PID...
- Autores:
- Tipo de recurso:
- Fecha de publicación:
- 2019
- Institución:
- Universidad del Rosario
- Repositorio:
- Repositorio EdocUR - U. Rosario
- Idioma:
- eng
- OAI Identifier:
- oai:repository.urosario.edu.co:10336/22264
- Acceso en línea:
- https://doi.org/10.1016/j.jaut.2019.01.011
https://repository.urosario.edu.co/handle/10336/22264
- Palabra clave:
- Cytotoxic T lymphocyte antigen 4
Interleukin 2 receptor alpha
STAT protein
Allergy
Ataxia telangiectasia
Autoimmune disease
Autoimmune lymphoproliferative syndrome
Autoimmune polyendocrinopathy candidiasis ectodermal dystrophy
Autoimmunity
Chronic granulomatous disease
Common variable immunodeficiency
Complement deficiency
Digeorge syndrome
Disease predisposition
Endocrine system
Gastrointestinal tract
Gene rearrangement
Genetic disorder
Human
Hyper ige syndrome
Hyper igm syndrome
Immune deficiency
Immunological tolerance
Molecular mimicry
Omenn syndrome
Pathophysiology
Phagocytosis
Polyendocrinopathy
Prevalence
Priority journal
Recurrent infection
Regulatory T lymphocyte
Review
Th17 cell
Wiskott Aldrich syndrome
X linked agammaglobulinemia
Autoimmune diseases
Autoimmunity
Immunodeficiencies
Immunologic deficiency syndromes
Primary immunodeficiency
- Rights
- License
- Abierto (Texto Completo)