about
Human TYK2 deficiency: Mycobacterial and viral infections without hyper-IgE syndromeIL-12Rβ1 deficiency in two of fifty children with severe tuberculosis from Iran, Morocco, and TurkeyA new ataxia-telangiectasia mutation in an 11-year-old femaleNovel mutation of the activation-induced cytidine deaminase gene in a Tajik family: special review on hyper-immunoglobulin M syndrome.Classification of Asthma Based on Nonlinear Analysis of Breathing Pattern.Inherited IL-12p40 deficiency: genetic, immunologic, and clinical features of 49 patients from 30 kindredsMonogenic mutations differentially affect the quantity and quality of T follicular helper cells in patients with human primary immunodeficienciesClinical, immunologic, molecular analyses and outcomes of iranian patients with LRBA deficiency: A longitudinal study.Cohort of Iranian Patients with Congenital Agammaglobulinemia: Mutation Analysis and Novel Gene Defects.Autoimmunity and its association with regulatory T cells and B cell subsets in patients with common variable immunodeficiency.IL-2-inducible T-cell kinase deficiency with pulmonary manifestations due to disseminated Epstein-Barr virus infection.Association of Mycobacterium infections in patients with Mendelian susceptibility to mycobacterial disease with venous thromboembolism.IgG anti-IgA antibodies in paediatric antibody-deficient patients receiving intravenous immunoglobulin.Clinical, Immunological and Genetic Spectrum of 696 Patients with Combined Immunodeficiency.Susceptibility to mycobacterial disease due to mutations in IL-12Rβ1 in three Iranian patients.Evaluation of a new protocol for wheat desensitization in patients with wheat-induced anaphylaxis.Paecilomyces formosus Infection in an Adult Patient with Undiagnosed Chronic Granulomatous Disease.Clinical, Laboratory, and Molecular Findings for 63 Patients With Severe Combined Immunodeficiency: A Decade´s Experience.Primary immunodeficiency disorders in Iran: update and new insights from the third report of the national registry.Bronchoalveolar galactomannan in invasive pulmonary aspergillosis: a prospective study in pediatric patients.AICDA single nucleotide polymorphism in common variable immunodeficiency and selective IgA deficiency.IL-10, TGF-beta, IL-2, IL-12, and IFN-gamma cytokine gene polymorphisms in asthma.Proinflammatory cytokine gene polymorphisms among Iranian patients with asthma.Fourth Update on the Iranian National Registry of Primary Immunodeficiencies: Integration of Molecular DiagnosisHuman IFN-γ immunity to mycobacteria is governed by both IL-12 and IL-23Comparison of Common Monogenic Defects in a Large Predominantly Antibody Deficiency CohortFungal epidemiology in cystic fibrosis patients with a special focus on Scedosporium species complexPrevalence of specific immunoglobulin E and G against Aspergillus fumigatus in patients with asthma
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P50
description
Forscher
@de
chercheur
@fr
investigador
@es
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
研究者
@zh
name
Alireza Mahdaviani
@ast
Alireza Mahdaviani
@en
Alireza Mahdaviani
@es
Alireza Mahdaviani
@nl
type
label
Alireza Mahdaviani
@ast
Alireza Mahdaviani
@en
Alireza Mahdaviani
@es
Alireza Mahdaviani
@nl
prefLabel
Alireza Mahdaviani
@ast
Alireza Mahdaviani
@en
Alireza Mahdaviani
@es
Alireza Mahdaviani
@nl
P106
P1153
24734528900
P31
P496
0000-0001-6224-4797