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Journal of Clinical Immunology, ISSN 0271-9142, 1/2018, Volume 38, Issue 1, pp. 129 - 143
Since the 1990s, the International Union of Immunological Societies (IUIS) PID expert committee (EC), now called Inborn Errors of Immunity Committee, has... 
Medical Microbiology | Biomedicine | Immunology | Primary immunodeficiencies | IUIS | Classification | Infectious Diseases | Internal Medicine | Inborn errors of immunity | Phenotypic | DISEASES | IMMUNOLOGY | Immunodeficiency | Hypersensitivity | Malignancy | Original
Journal Article
Journal of Clinical Immunology, ISSN 0271-9142, 1/2017, Volume 37, Issue 1, pp. 1 - 2
Journal Article
Journal of Clinical Immunology, ISSN 0271-9142, 8/2013, Volume 33, Issue 6, pp. 1078 - 1087
Journal Article
Journal of Clinical Immunology, ISSN 0271-9142, 4/2016, Volume 36, Issue 3, pp. 187 - 194
X-linked agammagobulinemia (XLA) is a primary immunodeficiency caused by Bruton’s tyrosine kinase (BTK) gene defect. XLA patients have absent or reduced number... 
Medical Microbiology | north african population | Biomedicine | Immunology | novel mutations | BTK | Infectious Diseases | Internal Medicine | XLA | GENOTYPE-PHENOTYPE CORRELATION | GENE-MUTATIONS | GENOMIC ORGANIZATION | IMMUNOLOGY | IDENTIFICATION | B-CELLS | BRUTONS TYROSINE KINASE | FAMILIES | AGAMMAGLOBULINEMIA XLA | Agammaglobulinemia - immunology | Agammaglobulinemia - genetics | Humans | Child, Preschool | Genetic Diseases, X-Linked - complications | Agammaglobulinemia - diagnosis | Infant | Male | Genetic Counseling | Protein-Tyrosine Kinases - immunology | Protein-Tyrosine Kinases - genetics | Morocco | Adult | Genetic Diseases, X-Linked - genetics | Algeria | Opportunistic Infections - immunology | B-Lymphocytes - pathology | Child | Tunisia | Opportunistic Infections - complications | Gene Expression | Agammaglobulinemia - complications | Genetic Association Studies | Gene Frequency | Opportunistic Infections - genetics | Sequence Analysis, DNA | Genetic Diseases, X-Linked - diagnosis | Opportunistic Infections - diagnosis | Genetic Diseases, X-Linked - immunology | B-Lymphocytes - immunology | Age of Onset | Alleles | Heterozygote | Mutation | Genetic research | Genetic aspects | B cells | Index Medicus | Agammaglobulinemia/diagnosis | Protein-Tyrosine Kinases/genetics | Agammaglobulinemia/complications | Life Sciences | Agammaglobulinemia/genetics | Genetic Diseases, X-Linked/complications | Opportunistic Infections/complications | Biochemistry, Molecular Biology | Agammaglobulinemia/immunology | Genetic Diseases, X-Linked/immunology | B-Lymphocytes/pathology | Genetic Diseases, X-Linked/diagnosis | Opportunistic Infections/diagnosis | B-Lymphocytes/immunology | Protein-Tyrosine Kinases/immunology | Agammaglobulinaemia Tyrosine Kinase | Opportunistic Infections/immunology | Opportunistic Infections/genetics | Genetic Diseases, X-Linked/genetics
Journal Article
Annals of the New York Academy of Sciences, ISSN 0077-8923, 11/2011, Volume 1238, Issue 1, pp. 42 - 52
Journal Article
Journal of Clinical Immunology, ISSN 0271-9142, 5/2014, Volume 34, Issue 4, pp. 452 - 458
Journal Article
The Pan African Medical Journal, 01/2017, Volume 26
Le Syndrome hyper IgM est un déficit immunitaire héréditaire bien connu, décrit pour la première fois en 1961. Il est causé par un défaut au niveau des... 
Journal Article
La Tunisie medicale, ISSN 0041-4131, 10/2018, Volume 96, Issue 10-11, pp. 672 - 677
Primary Immunodeficiency (PIDs) is a set of 330 rare hereditary diseases that increase susceptibility to infections, allergies, autoimmunity, and neoplasia.... 
Journal Article
08/2014, ISBN 0124115543
To identify patients with primary immunodeficiency disorders (PID) in countries with high infant mortality, frequent bacterial, fungal, parasitic and viral... 
Middle East | Africa | History | Latin America | Primary immunodeficiency
Book Chapter
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