Lista de obras - Alireza Mahdaviani - Dominio Público Uruguay

A new ataxia-telangiectasia mutation in an 11-year-old female

artículo científico publicado en 2017

AICDA single nucleotide polymorphism in common variable immunodeficiency and selective IgA deficiency.

artículo científico publicado en 2013

Association of Mycobacterium infections in patients with Mendelian susceptibility to mycobacterial disease with venous thromboembolism.

artículo científico publicado en 2016

Autoimmunity and its association with regulatory T cells and B cell subsets in patients with common variable immunodeficiency.

artículo científico publicado en 2017

Bronchoalveolar galactomannan in invasive pulmonary aspergillosis: a prospective study in pediatric patients

artículo científico publicado en 2015

Classification of Asthma Based on Nonlinear Analysis of Breathing Pattern.

artículo científico publicado en 2016

Clinical, Immunological and Genetic Spectrum of 696 Patients with Combined Immunodeﬁciency.

artículo científico publicado en 2017

Clinical, Laboratory, and Molecular Findings for 63 Patients With Severe Combined Immunodeficiency: A Decade´s Experience.

artículo científico publicado en 2017

Clinical, immunologic, molecular analyses and outcomes of iranian patients with LRBA deficiency: A longitudinal study.

artículo científico publicado en 2017

Cohort of Iranian Patients with Congenital Agammaglobulinemia: Mutation Analysis and Novel Gene Defects

artículo científico publicado en 2016

Comparison of Common Monogenic Defects in a Large Predominantly Antibody Deficiency Cohort

artículo científico publicado en 2018

Evaluation of a new protocol for wheat desensitization in patients with wheat-induced anaphylaxis.

artículo científico publicado en 2017

Fourth Update on the Iranian National Registry of Primary Immunodeficiencies: Integration of Molecular Diagnosis

scientific article published on 09 October 2018

Fungal epidemiology in cystic fibrosis patients with a special focus on Scedosporium species complex

artículo científico publicado en 2019

Human IFN-γ immunity to mycobacteria is governed by both IL-12 and IL-23

artículo científico publicado en 2018

Human TYK2 deficiency: Mycobacterial and viral infections without hyper-IgE syndrome

artículo científico publicado en 2015

IL-10, TGF-beta, IL-2, IL-12, and IFN-gamma cytokine gene polymorphisms in asthma.

artículo científico publicado en 2008

IL-12Rβ1 deficiency in two of fifty children with severe tuberculosis from Iran, Morocco, and Turkey

artículo científico publicado en 2011

IL-2-inducible T-cell kinase deficiency with pulmonary manifestations due to disseminated Epstein-Barr virus infection.

artículo científico publicado en 2012

IgG anti-IgA antibodies in paediatric antibody-deficient patients receiving intravenous immunoglobulin.

artículo científico publicado en 2014

Inherited IL-12p40 deficiency: genetic, immunologic, and clinical features of 49 patients from 30 kindreds

artículo científico publicado en 2013

Monogenic mutations differentially affect the quantity and quality of T follicular helper cells in patients with human primary immunodeficiencies

artículo científico publicado en 2015

Novel mutation of the activation-induced cytidine deaminase gene in a Tajik family: special review on hyper-immunoglobulin M syndrome.

artículo científico publicado en 2012

Paecilomyces formosus Infection in an Adult Patient with Undiagnosed Chronic Granulomatous Disease

artículo científico publicado en 2017

Prevalence of specific immunoglobulin E and G against Aspergillus fumigatus in patients with asthma

scientific article published on 01 December 2018

Primary immunodeficiency disorders in Iran: update and new insights from the third report of the national registry.

artículo científico publicado en 2014

Proinflammatory cytokine gene polymorphisms among Iranian patients with asthma.

artículo científico publicado en 2008

Susceptibility to mycobacterial disease due to mutations in IL-12Rβ1 in three Iranian patients.

artículo científico publicado en 2017

Lista de obras de Alireza Mahdaviani

A new ataxia-telangiectasia mutation in an 11-year-old female

AICDA single nucleotide polymorphism in common variable immunodeficiency and selective IgA deficiency.

Association of Mycobacterium infections in patients with Mendelian susceptibility to mycobacterial disease with venous thromboembolism.

Autoimmunity and its association with regulatory T cells and B cell subsets in patients with common variable immunodeficiency.

Bronchoalveolar galactomannan in invasive pulmonary aspergillosis: a prospective study in pediatric patients

Classification of Asthma Based on Nonlinear Analysis of Breathing Pattern.

Clinical, Immunological and Genetic Spectrum of 696 Patients with Combined Immunodeﬁciency.

Clinical, Laboratory, and Molecular Findings for 63 Patients With Severe Combined Immunodeficiency: A Decade´s Experience.

Clinical, 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

Comparison of Common Monogenic Defects in a Large Predominantly Antibody Deficiency Cohort

Evaluation of a new protocol for wheat desensitization in patients with wheat-induced anaphylaxis.

Fourth Update on the Iranian National Registry of Primary Immunodeficiencies: Integration of Molecular Diagnosis

Fungal epidemiology in cystic fibrosis patients with a special focus on Scedosporium species complex

Human IFN-γ immunity to mycobacteria is governed by both IL-12 and IL-23

Human TYK2 deficiency: Mycobacterial and viral infections without hyper-IgE syndrome

IL-10, TGF-beta, IL-2, IL-12, and IFN-gamma cytokine gene polymorphisms in asthma.

IL-12Rβ1 deficiency in two of fifty children with severe tuberculosis from Iran, Morocco, and Turkey

IL-2-inducible T-cell kinase deficiency with pulmonary manifestations due to disseminated Epstein-Barr virus infection.

IgG anti-IgA antibodies in paediatric antibody-deficient patients receiving intravenous immunoglobulin.

Inherited IL-12p40 deficiency: genetic, immunologic, and clinical features of 49 patients from 30 kindreds

Monogenic mutations differentially affect the quantity and quality of T follicular helper cells in patients with human primary immunodeficiencies

Novel mutation of the activation-induced cytidine deaminase gene in a Tajik family: special review on hyper-immunoglobulin M syndrome.

Paecilomyces formosus Infection in an Adult Patient with Undiagnosed Chronic Granulomatous Disease

Prevalence of specific immunoglobulin E and G against Aspergillus fumigatus in patients with asthma

Primary immunodeficiency disorders in Iran: update and new insights from the third report of the national registry.

Proinflammatory cytokine gene polymorphisms among Iranian patients with asthma.

Susceptibility to mycobacterial disease due to mutations in IL-12Rβ1 in three Iranian patients.