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Lista de obras de Asghar Aghamohammadi

A Comparison of Clinical and Immunologic Phenotypes in Familial and Sporadic Forms of Common Variable Immunodeficiency

artículo científico

A Novel TTC7A Deficiency Presenting With Combined Immunodeficiency and Chronic Gastrointestinal Problems

artículo científico publicado en 2018

A Review on Defects of Dendritic Cells in Common Variable Immunodeficiency

artículo científico publicado en 2017

A hypomorphic recombination-activating gene 1 (RAG1) mutation resulting in a phenotype resembling common variable immunodeficiency.

artículo científico publicado en 2014

A new case of congenital ficolin-3 deficiency with primary immunodeficiency

artículo científico publicado en 2020

A novel CD40 ligand mutation in a patient with pneumonia, neutropenia, and hyperimmunoglobulin M phenotype

artículo científico publicado el 1 de enero de 2013

A review of gastrointestinal disorders in patients with primary antibody immunodeficiencies during a 10-year period (1990-2000), in children hospital medical center

artículo científico publicado en 2003

A review on guidelines for management and treatment of common variable immunodeficiency

artículo científico

A single center 14 years study of infectious complications leading to hospitalization of patients with primary antibody deficiencies

A single center 14 years study of infectious complications leading to hospitalization of patients with primary antibody deficiencies

artículo científico publicado en 2010

A study of malnutrition in Iranian patients with primary antibody deficiency.

artículo científico publicado en 2004

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

artículo científico publicado en 2013

Abnormality of regulatory T cells in common variable immunodeficiency.

artículo científico publicado en 2016

Adverse effects of intravenous immunoglobulin therapy in patients with antibody deficiency.

artículo científico publicado en 2003

Adverse reactions of prophylactic intravenous immunoglobulin infusions in Iranian patients with primary immunodeficiency

artículo científico publicado en 2004

Adverse reactions of prophylactic intravenous immunoglobulin; a 13-year experience with 3004 infusions in Iranian patients with primary immunodeficiency diseases.

artículo científico publicado en 2009

Adverse reactions to Mycobacterium bovis bacille Calmette-Guérin vaccination against tuberculosis in Iranian children

artículo científico publicado en 2015

Agammaglobulinemia: comorbidities and long-term therapeutic risks

Alteration in frequency and function of CD4⁺CD25⁺FOXP3⁺ regulatory T cells in patients with immune thrombocytopenic purpura

artículo científico publicado en 2014

Altered dendritic cell function in response to sera of common variable immunodeficiency patients.

artículo científico publicado en 2007

Analysis of class-switched memory B cells in patients with common variable immunodeficiency and its clinical implications.

artículo científico publicado en 2007

Analysis of switched memory B cells in patients with IgA deficiency

artículo científico publicado en 2011

Antibiotic resistance in patients with primary immunodeficiency disorders versus immunocompetent patients

artículo científico publicado en 2015

Antibody response to pneumococcal capsular polysaccharide vaccination in patients with chronic kidney disease

artículo científico publicado en 2009

Approach to the Management of Autoimmunity in Primary Immunodeficiency.

artículo científico publicado en 2016

Assessment of immune response following immunization with DTP/Td and MMR vaccines in children treated for acute lymphoblastic leukemia

artículo científico publicado en 2014

Association between single nucleotide polymorphisms of the interleukin-4 gene and atopic dermatitis

artículo científico publicado en 2015

Association between the interleukin 6 genotype at position -174 and atopic dermatitis

artículo científico publicado el 1 de enero de 2013

Association of HLA class II alleles with childhood asthma and Total IgE levels

artículo científico publicado en 2008

Association of IL-4 and IL-10 gene promoter polymorphisms with common variable immunodeficiency

artículo científico publicado en 2009

Association of single nucleotide polymorphisms of interleukin-1 family with atopic dermatitis.

artículo científico publicado en 2012

Asthma and Allergic Diseases in a Selected Group of Patients With Common Variable Immunodeficiency

artículo científico publicado en 2016

Ataxia telangiectasia syndrome: moonlighting ATM.

artículo científico publicado en 2017

Ataxia-telangiectasia in Iran: clinical and laboratory features of 104 patients

artículo científico publicado en 2007

Ataxia-telangiectasia or neurologic Wilson's disease: when strong family history becomes a diagnostic bias

artículo científico publicado en 2012

Ataxia-telangiectasia: A review of clinical features and molecular pathology

article

Ataxia-telangiectasia: Epidemiology, Pathogenesis, Clinical Phenotype, Diagnosis, Prognosis and Management

scientific article published on 13 August 2020

Atopic Manifestations: Dermatitis, Allergic Rhinitis and Asthma in Patients With Hypogammaglobulinemia

artículo científico publicado en 2015

Autism in a child with common variable immunodeficiency

artículo científico publicado en 2013

Autoimmune phenotype in patients with common variable immunodeficiency

artículo científico publicado en 2013

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

artículo científico publicado en 2017

Autoimmunity in Common Variable Immunodeficiency: A Systematic Review and Meta-Analysis

scientific article published on 18 November 2020

Autoimmunity in Primary Antibody Deficiencies.

artículo científico publicado en 2016

Autoimmunity in X-linked agammaglobulinemia: Kawasaki disease and review of the literature

artículo científico

Autoimmunity in a cohort of 471 patients with primary antibody deficiencies.

artículo científico publicado en 2017

Autoimmunity in common variable immunodeficiency: epidemiology, pathophysiology and management.

artículo científico publicado en 2016

Autoimmunity in patients with selective IgA deficiency

artículo científico publicado en 2015

Autoimmunity in primary T-cell immunodeficiencies.

artículo científico publicado en 2016

Autosomal recessive agammaglobulinemia: a novel non-sense mutation in CD79a

artículo científico publicado en 2014

B-cell–T-cell activation and interaction in common variable immunodeficiency

artículo científico publicado en 2010

BAK, BAX, and NBK/BIK proapoptotic gene alterations in Iranian patients with ataxia telangiectasia

artículo científico publicado en 2009

Bacillus Calmette-Guérin (BCG) complications associated with primary immunodeficiency diseases

artículo científico publicado en 2012

Behavior abnormality following intravenous immunoglobulin treatment in patients with primary antibody deficiencies

artículo científico publicado en 2010

Bilateral basal ganglia involvement in a patient with Griscelli syndrome.

artículo científico publicado en 2006

Blood pressure nomograms for school children in Iran

artículo científico publicado en 2003

Bronchiectasis in common variable immunodeficiency: A systematic review and meta-analysis

scientific article published on 13 December 2019

CD40 ligand expression on stimulated T-helper lymphocytes in patients with common variable immunodeficiency

artículo científico publicado en 2007

Candidiasis associated with very early onset inflammatory bowel disease: First IL10RB deficient case from the National Iranian Registry and review of the literature

artículo científico publicado en 2019

Cellular and molecular mechanisms of immune dysregulation and autoimmunity

artículo científico publicado en 2016

Cernunnos deficiency associated with BCG adenitis and autoimmunity: First case from the national Iranian registry and review of the literature.

artículo científico publicado en 2017

Characterization of 11 new cases of leukocyte adhesion deficiency type 1 with seven novel mutations in the ITGB2 gene

artículo científico publicado en 2010

Chromosomal radiosensitivity in patients with common variable immunodeficiency

artículo científico publicado en 2007

Chronic granulomatous disease: a clinical survey of 41 patients from the Iranian primary immunodeficiency registry

artículo científico publicado en 2004

Class Switch Recombination Process in Ataxia Telangiectasia Patients with Elevated Serum Levels of IgM

Clearing Vaccine-Derived Poliovirus Infection Following Hematopoietic Stem Cell Transplantation: a Case Report and Review of Literature

artículo científico publicado en 2018

Clinical Manifestations, Immunological Characteristics and Genetic Analysis of Patients with Hyper-Immunoglobulin M Syndrome in Iran

artículo científico publicado en 2019

Clinical and immunological features of 65 Iranian patients with common variable immunodeficiency

artículo científico publicado en 2005

Clinical and laboratory findings in Iranian children with cyclic neutropenia.

artículo científico publicado en 2004

Clinical and laboratory findings in hyper-IgM syndrome with novel CD40L and AICDA mutations.

artículo científico publicado en 2009

Clinical implications of systematic phenotyping and exome sequencing in patients with primary antibody deficiency

artículo científico publicado en 2018

Clinical phenotype classification for selective immunoglobulin A deficiency

artículo científico

Clinical recommendations for oral management of patients with primary antibody deficiencies

artículo científico publicado en 2016

Clinical, Immunologic, and Molecular Spectrum of Patients with LPS-Responsive Beige-Like Anchor Protein Deficiency: A Systematic Review

artículo científico publicado en 2019

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

artículo científico publicado en 2017

Clinical, Immunological and Genetic findings in Patients with UNC13D Deficiency (FHL3): a Systematic Review

artículo científico publicado en 2020

Clinical, Immunological and Molecular Characteristics of 37 Iranian Patients with X-Linked Agammaglobulinemia

artículo científico publicado en 2006

Clinical, Immunological, and Genetic Features in Patients with Activated PI3Kδ Syndrome (APDS): a Systematic Review

artículo científico publicado en 2019

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

artículo científico publicado en 2017

Clinical, laboratory and imaging findings of the patients with disseminated bacilli Calmette-Guerin disease

artículo científico publicado en 2014

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

artículo científico publicado en 2016

Combined immunodeficiency and Epstein-Barr virus-induced B cell malignancy in humans with inherited CD70 deficiency

scientific article published on 23 December 2016

Combined immunodeficiency presenting with vaccine-associated paralytic poliomyelitis: a case report and narrative review of literature.

artículo científico publicado en 2013

Common variable immunodeficiency: a heterogeneous group needs further subclassification

artículo científico publicado en 2009

Comparison of Bone Mineral Density in Common variable immunodeficiency and X-Linked Agammaglobulinaemia Patients

artículo científico publicado en 2017

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

artículo científico publicado en 2018

Comparison of clinical and immunological features and mortality in common variable immunodeficiency and agammaglobulinemia patients

scientific article published on 03 May 2019

Comparison of pulmonary diseases in common variable immunodeficiency and X-linked agammaglobulinaemia

article

Comparison of various classifications for patients with common variable immunodeficiency (CVID) using measurement of B-cell subsets

artículo científico publicado en 2016

Comprehensive assessment of respiratory complications in patients with common variable immunodeficiency

scientific article published on 30 January 2020

Congenital neutropenia and primary immunodeficiency disorders: a survey of 26 Iranian patients

artículo científico publicado en 2005

Consanguinity in Primary Immunodeficiency Disorders; the Report from Iranian Primary Immunodeficiency Registry

scientific article published on 01 August 2006

Correlation between common variable immunodeficiency clinical phenotypes and parental consanguinity in children and adults

artículo científico publicado en 2010

Costs of Hospital Admission on Primary Immunodeficiency Diseases

artículo científico publicado en 2017

Cutaneous Granulomatosis and Class Switching Defect as a Presenting Sign in Ataxia-Telangiectasia: First Case from the National Iranian Registry and Review of the Literature

scientific article published on 25 November 2019

Cutaneous granulomas in common variable immunodeficiency: case report and review of literature

scientific article published on January 2010

Cytokine gene polymorphisms in common variable immunodeficiency

artículo científico publicado en 2009

Cytokines in common variable immunodeficiency as signs of immune dysregulation and potential therapeutic targets - a review of the current knowledge

artículo científico

Debilitating progressive encephalitis in a patient with BTK deficiency

artículo científico publicado en 2012

Deleterious mutations in LRBA are associated with a syndrome of immune deficiency and autoimmunity

artículo científico publicado en 2012

Detection of Epstein-Barr virus DNA in plasma and lymph node biopsy samples of pediatric and adult patients with Hodgkin lymphoma

artículo científico publicado en 2010

Diagnostic Approach to the Patients with Suspected Primary Immunodeficiency

scientific article published on 01 January 2020

Different brands of intravenous immunoglobulin for primary immunodeficiencies: how to choose the best option for the patient?

artículo científico

Disease Evolution and Response to Rapamycin in Activated Phosphoinositide 3-Kinase δ Syndrome: The European Society for Immunodeficiencies-Activated Phosphoinositide 3-Kinase δ Syndrome Registry. ⬇️

artículo científico publicado en 2018

Distribution of primary immunodeficiency disorders diagnosed in a tertiary referral center,Tehran, Iran (2006-2013).

artículo científico publicado en 2014

Dystonia in Ataxia Telangiectasia: A Case Report with Novel Mutations

artículo científico publicado en 2020

ENT manifestations in Iranian patients with primary antibody deficiencies

artículo científico publicado en 2007

Early onset steroid induced posterior subcapsular cataract in a patient with common variable immunodeficiency: case reports and review of literature

artículo científico publicado en 2016

Echocardiographic abnormalities and their correlation with bronchiectasis score in primary antibody deficiencies

artículo científico publicado en 2010

Economic burden of common variable immunodeficiency: annual cost of disease

artículo científico publicado en 2015

Effect of Class Switch Recombination Defect on the Phenotype of Ataxia-Telangiectasia Patients

artículo científico publicado en 2020

Effect of anti-epileptic drugs on serum immunoglobulin levels in children.

artículo científico publicado en 2010

Effect of anti-epileptic drugs on serum level of IgG subclasses ⬇️

artículo científico publicado el 1 de septiembre de 2010

Effect of regular intravenous immunoglobulin therapy on prevention of pneumonia in patients with common variable immunodeficiency

artículo científico publicado en 2006

Efficacy of an Attachment-Based Intervention Model on Health Indices in Children with Chronic Disease and Their Mothers

artículo científico publicado en 2018

Efficacy of intravenous immunoglobulin on the prevention of pneumonia in patients with agammaglobulinemia

artículo científico publicado en 2004

Epidemiology and pathophysiology of malignancy in common variable immunodeficiency?

artículo científico publicado en 2017

Erratum to: BAK, BAX, and NBK/BIK Proapoptotic Gene Alterations in Iranian Patients with Ataxia Telangiectasia

article

Evaluation of CD4+CD25+FOXP3+ regulatory T cells function in patients with common variable immunodeficiency

artículo científico publicado en 2013

Evaluation of Expression of LRBA and CTLA-4 Proteins in Common Variable Immunodeficiency Patients

scientific article published on 15 November 2020

Evaluation of Immunoglobulin Levels and Infection Rate in Patients with Common Variable Immunodeficiency After Immunoglobulin Replacement Therapy

artículo científico publicado en 2010

Evaluation of Known Defective Signaling-Associated Molecules in Patients Who Primarily Diagnosed as Common Variable Immunodeficiency

artículo científico publicado en 2016

Evaluation of Natural Regulatory T Cells in Subjects with Selective IgA Deficiency: From Senior Idea to Novel Opportunities

artículo científico publicado en 2012

Evaluation of antibody response to polysaccharide vaccine and switched memory B cells in pediatric patients with inflammatory bowel disease

scientific article published on 14 August 2013

Evaluation of class switch recombination in B lymphocytes of patients with common variable immunodeficiency.

artículo científico publicado en 2013

Evaluation of humoral immune function in patients with bronchiectasis

artículo científico publicado en 2008

Evaluation of humoral immune function in patients with chronic idiopathic thrombocytopenic purpura.

artículo científico publicado en 2013

Evaluation of infectious and non-infectious complications in patients with primary immunodeficiency

artículo científico publicado en 2017

Evaluation of physicians' awareness of pediatric diseases in iran.

artículo científico publicado en 2014

Evaluation of pulmonary complications in patients with primary immunodeficiency disorders

artículo científico publicado en 2017

Evaluation of respiratory complications in patients with X-linked and autosomal recessive agammaglobulinemia

artículo científico publicado en 2020

Evaluation of serum IgA levels in Iranian patients with type 1 diabetes mellitus

artículo científico publicado en 2010

Evaluation of the TLR negative regulatory network in CVID patients

artículo científico publicado en 2018

Expanding Clinical Phenotype and Novel Insights into the Pathogenesis of ICOS Deficiency

scientific article published on 20 December 2019

Expression of activation-induced cytidine deaminase gene in B lymphocytes of patients with common variable immunodeficiency

artículo científico publicado en 2013

Family study of pediatric patients with primary antibody deficiencies

artículo científico publicado en 2013

Features and roles of T helper 9 cells and interleukin 9 in immunological diseases

artículo científico publicado en 2018

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

scientific article published on 09 October 2018

Frequency and Clinical Manifestations of Patients with Primary Immunodeficiency Disorders in Iran: Update from the Iranian Primary Immunodeficiency Registry

artículo científico publicado en 2006

Frequency and expression of inhibitory markers of CD4(+) CD25(+) FOXP3(+) regulatory T cells in patients with common variable immunodeficiency.

artículo científico publicado en 2013

Frequency of Allergic Rhinitis in School-age Children (7-18 Years) in Tehran

artículo científico publicado en 2003

G2-lymphocyte chromosomal radiosensitivity in patients with LPS responsive beige-like anchor protein (LRBA) deficiency

scientific article published on 13 February 2019

Gastrointestinal manifestations in patients with common variable immunodeficiency

artículo científico publicado en 2007

Genetic defects in B-cell development and their clinical consequences

artículo científico

Genetic mutations and immunological features of severe combined immunodeficiency patients in Iran

artículo científico publicado en 2019

Genotype-phenotype correlation in Bruton's tyrosine kinase deficiency

artículo científico publicado en 2008

Graft versus host disease and microchimerism in a JAK3 deficient patient

scientific article published on 22 August 2019

HLA-DRB1,-DQA1 and -DQB1 allele and haplotype frequencies in female patients with early onset breast cancer

artículo científico publicado en 2011

HODGKIN LYMPHOMA IN TWO SIBLINGS WITH COMMON VARIABLE IMMUNODEFICIENCY

artículo científico publicado en 2007

Health policy for common variable immunodeficiency: burden of the disease

article

Health-related quality of life in primary antibody deficiency

artículo científico publicado en 2011

Health-related quality of life in primary immune deficient patients

artículo científico publicado en 2006

High production of IL-18 by dendritic cells induced by sera from patients with primary antibody deficiency

artículo científico publicado en 2007

Histocompatibility Complex Status and Mendelian Randomization Analysis in Unsolved Antibody Deficiency

artículo científico publicado en 2020

History of primary immunodeficiency diseases in iran ⬇️

artículo científico publicado el 1 de marzo de 2010

Home-based subcutaneous immunoglobulin versus hospital-based intravenous immunoglobulin in treatment of primary antibody deficiencies: systematic review and meta analysis

artículo científico

Hyper-IgE syndrome

scientific article published on 01 April 2010

IL-10 induces TGF-β secretion, TGF-β receptor II upregulation, and IgA secretion in B cells

scientific article published on 01 September 2019

Identification of an SH2D1A mutation in a hypogammaglobulinemic male patient with a diagnosis of common variable immunodeficiency

scientific article published on 01 July 2003

IgA deficiency and the MHC: assessment of relative risk and microheterogeneity within the HLA A1 B8, DR3 (8.1) haplotype

artículo científico publicado en 2009

IgA deficiency: correlation between clinical and immunological phenotypes

artículo científico publicado en 2008

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

artículo científico publicado en 2014

Immunoglobulin class switch recombination deficiency type 1 or CD40 ligand deficiency: from bedside to bench and back again

artículo científico publicado en 2013

Immunologic evaluation of patients with recurrent ear, nose, and throat infections

artículo científico publicado en 2008

Immunomodulatory effect of G2013 (a-L-Guluronic acid) on theTLR2 and TLR4 in human mononuclear cells.

artículo científico

Impact of IgE-mediated Food Allergy on Parental Quality of Life in Iranian Patients

artículo científico publicado en 2016

Impact of delayed diagnosis in children with primary antibody deficiencies

artículo científico publicado en 2011

Impaired Akt phosphorylation in B-cells of patients with common variable immunodeficiency.

artículo científico publicado en 2016

Important Factors Influencing Severity of Common Variable Immunodeficiency

artículo científico publicado en 2016

Important differences in the diagnostic spectrum of primary immunodeficiency in adults versus children

artículo científico

In vitro chromosomal radiosensitivity in patients with common variable immunodeficiency

scientific article published on 30 June 2018

Increased serum levels of soluble CD30 in patients with common variable immunodeficiency and its clinical implications

artículo científico publicado en 2007

Indications and safety of intravenous and subcutaneous immunoglobulin therapy

artículo científico publicado en 2011

Individual Radiosensitivity Assessment of the Families of Patients by G2-Checkpoint Abrogation

Infectious and Noninfectious Pulmonary Complications in Patients With Primary Immunodeficiency Disorders.

artículo científico publicado en 2017

Inflammation, a significant player of Ataxia-Telangiectasia pathogenesis?

artículo científico publicado en 2018

Interleukin-4 and Transforming Growth Factor-Beta Single Nucleotide Genes Polymorphisms Confer Susceptibility To Atopic Dermatitis

article

Interleukin-6 and tumor necrosis factor-alpha gene polymorphisms in chronic idiopathic urticaria

artículo científico publicado en 2013

Investigation of underlying primary immunodeficiencies in patients with severe atopic dermatitis

artículo científico publicado en 2013

Is there a need to redefine the diagnostic criteria for common variable immunodeficiency?

artículo científico publicado en 2013

LPS-Responsive Beige-Like Anchor Gene Mutation Associated With Possible Bronchiolitis Obliterans Organizing Pneumonia Associated With Hypogammaglobulinemia and Normal IgM Phenotype and Low Number of B Cells

artículo científico publicado en 2016

Leishmaniasis and Autoimmunity in Patient with LPS-Responsive Beige-Like Anchor Protein (LRBA) Deficiency

artículo científico publicado en 2020

Long-term evaluation of a historical cohort of Iranian common variable immunodeficiency patients

artículo científico publicado en 2014

Long-term follow-up of ninety eight Iranian patients with primary immune deficiency in a single tertiary centre

artículo científico publicado en 2016

Long-term outcome of LRBA deficiency in 76 patients after various treatment modalities as evaluated by the immune deficiency and dysregulation activity (IDDA) score

scientific article published on 27 December 2019

Long-term outcomes of 176 patients with X-linked hyper-IgM syndrome treated with or without hematopoietic cell transplantation

artículo científico publicado en 2016

Lymphocytic Interstitial Pneumonitis: An Unusual Presentation of X-Linked Hyper Ig M Syndrome.

artículo científico publicado en 2016

Lymphoma of mucosa-associated lymphoid tissue in common variable immunodeficiency.

artículo científico publicado en 2006

Major histocompatibility complex class I and II antigens frequencies in Baloch ethnic group living in the southeast region of Iran

scientific article published on 01 June 2004

Malignancy in common variable immunodeficiency: a systematic review and meta-analysis

artículo científico publicado en 2019

Managing patients with side effects and adverse events to immunoglobulin therapy

artículo científico publicado en 2015

Mannose-binding lectin polymorphisms in common variable immunodeficiency

artículo científico publicado en 2009

Mannose-binding lectin protein deficiency among patients with primary immunodeficiency disease receiving IVIG therapy

artículo científico publicado en 2017

Measurement of Health-Related Quality of Life in Primary Antibody-Deficient Patients.

artículo científico publicado en 2017

Monogenic mutations associated with IgA deficiency

artículo científico publicado en 2016

Monogenic polyautoimmunity in primary immunodeficiency diseases

scholarly article by Gholamreza Azizi et al published October 2018 in Autoimmunity Reviews

Morbidity and mortality of Iranian patients with hyper IgM syndrome: a clinical analysis

artículo científico publicado en 2014

Mortality and Morbidity in Common Variable Immunodeficiency

artículo científico publicado en 2006

Mortality and morbidity in patients with X-linked agammaglobulinaemia

artículo científico publicado en 2014

Mortality in primary immunodeficient patients, registered in Iranian primary immunodeficiency registry.

artículo científico publicado en 2004

Neutropenia and primary immunodeficiency diseases

artículo científico publicado en 2009

Neutropenia associated with X-linked Agammaglobulinemia in an Iranian referral center

artículo científico publicado en 2009

Neutropenia in Iranian patients with primary immunodeficiency disorders.

artículo científico publicado en 2005

Neutropenia in patients with primary antibody deficiency disorders

artículo científico publicado en 2004

New insights into physiopathology of immunodeficiency-associated vaccine-derived poliovirus infection; systematic review of over 5 decades of data

artículo científico publicado en 2018

New therapeutic approach by sirolimus for enteropathy treatment in patients with LRBA deficiency.

artículo científico publicado en 2017

Novel Mutation of ZAP-70-related Combined Immunodeficiency: First Case from the National Iranian Registry and Review of the Literature.

artículo científico publicado en 2016

Novel Mutations in TACI (TNFRSF13B) Causing Common Variable Immunodeficiency

artículo científico publicado en 2009

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

Novel mutations in TNFRSF7/CD27: Clinical, immunologic, and genetic characterization of human CD27 deficiency

artículo científico

Ocular involvement in primary immunodeficiency diseases

artículo científico publicado en 2013

Oral and dental health status in patients with primary antibody deficiencies

artículo científico publicado en 2011

Oral manifestations in selective IgA deficiency

artículo científico publicado en 2004

Otological findings in pediatric patients with hypogammaglobulinemia

artículo científico publicado en 2014

Outcomes and Treatment Strategies for Autoimmunity and Hyperinflammation in Patients with RAG Deficiency

scientific article published on 12 March 2019

Overweight and obesity and their associated factors in adolescents in Tehran, Iran, 2004-2005.

artículo científico publicado en 2006

PIK3R1 Mutation Associated with Hyper IgM (APDS2 Syndrome): A Case Report and Review of the Literature

scientific article published on 01 January 2019

Patients with Primary Immunodeficiencies Are a Reservoir of Poliovirus and a Risk to Polio Eradication

artículo científico publicado en 2017

Pediatric patients with common variable immunodeficiency: long-term follow-up

artículo científico publicado en 2012

Physicians awareness on primary immunodeficiency disorders in Iran

artículo científico publicado en 2012

Polyautoimmunity in Patients with LPS-Responsive Beige-Like Anchor (LRBA) Deficiency

artículo científico publicado en 2018

Polymorphisms Of Genes Encoding Interleukin-4 and Its Receptor Are Associated With Chronic Idiopathic Urticaria

article

Prediction of the evolution of common variable immunodeficiency: HLA typing for patients with selective IgA deficiency

article published in 2014

Predominantly Antibody Deficiency

Preference of Genetic Diagnosis of CXCR4 Mutation Compared with Clinical Diagnosis of WHIM Syndrome

Presence of Idiopathic Thrombocytopenic Purpura and autoimmune hemolytic anemia in the patients with common variable immunodeficiency.

artículo científico publicado en 2008

Prevalence of asthma related to BMI in adolescents in Tehran, Iran, 2004-2005

artículo científico publicado en 2006

Primary Antibody Deficiency in a Tertiary Referral Hospital: A 30-Year Experiment

artículo científico publicado en 2015

Primary Immunodeficiencies and Cancers

Primary Immunodeficiency Diseases and Bacillus Calmette-Guérin (BCG)-Vaccine-Derived Complications: A Systematic Review

artículo científico publicado en 2020

Primary ciliary dyskinesia in six patients with bronchiectasis

artículo científico publicado en 2016

Primary immunodeficiencies: a decade of shifting paradigms, the current status and the emergence of cutting-edge therapies and diagnostics

artículo científico publicado en 2014

Primary immunodeficiency diseases associated with increased susceptibility to viral infections and malignancies

artículo científico publicado en 2011

Primary immunodeficiency diseases associated with neurologic manifestations

artículo científico

Primary immunodeficiency diseases in Northern Iran.

artículo científico publicado en 2017

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

artículo científico publicado en 2014

Primary immunodeficiency in Iran: first report of the National Registry of PID in Children and Adults

scientific article published on 01 November 2002

Progression of Selective IgA Deficiency to Common Variable Immunodeficiency

artículo científico publicado en 2008

Proinflammatory cytokine gene single nucleotide polymorphisms in common variable immunodeficiency

artículo científico publicado en 2009

Protein Kinase C-Delta Defect in Autoimmune Lymphoproliferative Syndrome-Like Disease: First Case from the National Iranian Registry and Review of the Literature

artículo científico publicado en 2020

Psychiatric aspects of primary immunodeficiency diseases: the parental study

artículo científico publicado en 2013

RAC2 loss-of-function mutation in 2 siblings with characteristics of common variable immunodeficiency

artículo científico publicado en 2014

Recurrent Gallbladder Hydrops and Sclerosing Cholangitis in 11-Year-Old Male with Hyper IgM Syndrome

artículo científico publicado en 2013

Recurrent Infections

Recurrent infections and bilateral uveitis in a patient with CD8 deficiency

artículo científico publicado en 2005

Renal amyloidosis in common variable immunodeficiency

artículo científico publicado en 2010

Report on the First Survey of Iranian Patients with Hereditary Angioedema.

artículo científico publicado en 2015

Respiratory Complications in Patients with Hyper IgM Syndrome

scientific article published on 11 June 2019

Respiratory manifestations of chronic granulomatous disease; a clinical survey of patients from Iranian primary immunodeficiency registry

artículo científico publicado en 2003

Response to polysaccharide vaccination amongst pediatric patients with common variable immunodeficiency correlates with clinical disease

artículo científico publicado en 2008

Rheumatologic complications in a cohort of 227 patients with common variable immunodeficiency

artículo científico publicado en 2018

Risk factors leading to hospital admission in Iranian asthmatic children

artículo científico publicado en 2007

Role of Apoptosis in the Pathogenesis of Common Variable Immunodeficiency (CVID).

artículo científico publicado en 2017

Role of apoptosis in common variable immunodeficiency and selective immunoglobulin A deficiency.

artículo científico publicado en 2016

Selective IgA Deficiency: Epidemiology, Pathogenesis, Clinical Phenotype, Diagnosis, Prognosis and Management.

artículo científico publicado en 2016

Selective immunoglobulin A deficiency in Iranian blood donors: prevalence, laboratory and clinical findings

artículo científico publicado en 2008

Serum bactericidal antibody response 1 year after meningococcal polysaccharide vaccination of patients with common variable immunodeficiency

artículo científico publicado en 2010

Serum bactericidal antibody response to serogroup C polysaccharide meningococcal vaccination in children with primary antibody deficiencies

artículo científico publicado en 2007

Serum bactericidal antibody responses to meningococcal polysaccharide vaccination as a basis for clinical classification of common variable immunodeficiency

artículo científico publicado en 2008

Severe combined immunodeficiency: a cohort of 40 patients

artículo científico publicado en 2007

Severe congenital neutropenia or hyper-IgM syndrome? A novel mutation of CD40 ligand in a patient with severe neutropenia.

artículo científico publicado en 2008

Single nucleotide polymorphisms of IL-2, but not IL-12 and IFN-γ, are associated with increased susceptibility to chronic spontaneous urticaria

artículo científico publicado en 2017

Single nucleotide polymorphisms of the genes encoding IL-10 and TGF-β1 in Iranian children with atopic dermatitis

artículo científico publicado en 2018

Soluble CD26 and CD30 levels in patients with common variable immunodeficiency

artículo científico publicado el 1 de enero de 2013

Soluble molecules in intravenous immunoglobulin: benefits and limitations

artículo científico publicado en 2015

Spectrum of Phenotypes Associated with Mutations in LRBA.

artículo científico

Spectrum of bone marrow failures of myeloid series: new report of neutropenic patients from a referral pediatric center in Iran

artículo científico publicado en 2013

Study of SH2D1A gene mutation in paediatric patients with B-cell lymphoma

artículo científico publicado en 2015

Successful management of neutropenia in a patient with CD40 ligand deficiency by immunoglobulin replacement therapy.

artículo científico publicado en 2007

Systematic investigation for underlying causes of recurrent infections in children: surveillance of primary immunodeficiency

artículo científico publicado en 2017

T- helper 1 and 2 cytokine assay in patients with common variable immunodeficiency.

artículo científico publicado en 2008

T-Cell Abnormalities in Common Variable Immunodeficiency

artículo científico publicado en 2016

TNF-alpha single nucleotide polymorphisms in atopic dermatitis

artículo científico publicado en 2012

The Clinical, Immunohematological, and Molecular Study of Iranian Patients with Severe Congenital Neutropenia

artículo científico publicado en 2007

The First Iranian Cohort of Pediatric Patients with Activated Phosphoinositide 3-Kinase-δ (PI3Kδ) Syndrome (APDS)

artículo científico publicado en 2021

The First Purine Nucleoside Phosphorylase Deficiency Patient Resembling IgA Deficiency and a Review of the Literature

scientific article published on 19 March 2019

The Heterogeneous Pathogenesis of Selective Immunoglobulin A Deficiency

scientific article published on 15 May 2019

The Use of Immunoglobulin Therapy in Primary Immunodeficiency Diseases

artículo científico publicado en 2016

The approach to children with recurrent infections.

artículo científico

The circulating T helper subsets and regulatory T cells in patients with common variable immunodeficiency with no known monogenic disease.

artículo científico publicado en 2018

The clinical and immunological features of patients with primary antibody deficiencies.

artículo científico publicado en 2018

The clinical and laboratory survey of Iranian patients with Hyper-IgE syndrome

scientific article published on 01 January 2006

The clinical significance of complete class switching defect in Ataxia telangiectasia patients

artículo científico publicado en 2017

The demographics of primary immunodeficiency diseases across the unique ethnic groups in Iran, and approaches to diagnosis and treatment

artículo científico publicado en 2011

The evaluation of neutropenia in common variable immune deficiency patients

artículo científico publicado en 2019

The first cohort of Iranian patients with hyper immunoglobulin E syndrome: A long-term follow-up and genetic analysis

scientific article published on 15 May 2019

The hyper IgM syndromes: Epidemiology, pathogenesis, clinical manifestations, diagnosis and management

artículo científico publicado en 2018

The imbalance of circulating T helper subsets and regulatory T cells in patients with LRBA deficiency: Correlation with disease severity

scientific article published on 28 May 2018

The persian version of the chronic urticaria quality of life questionnaire: factor analysis, validation, and initial clinical findings

artículo científico publicado en 2014

The role of toll-like receptors in B-cell development and immunopathogenesis of common variable immunodeficiency

artículo científico publicado en 2015

The uncommon combination of common variable immunodeficiency, macrophage activation syndrome, and cytomegalovirus retinitis

artículo científico publicado en 2012

Toward the stratification and personalization of common variable immunodeficiency treatment

Tuberculosis: a new look at an old disease

scholarly article by Nima Rezaei et al published March 2011 in Expert Review of Clinical Immunology

Two Faces of LRBA Deficiency in Siblings: Hypogammaglobulinemia and Normal Immunoglobulin Levels.

artículo científico publicado en 2018

Vaccine-Derived Poliovirus Infection among Patients with Primary Immunodeficiency and Effect of Patient Screening on Disease Outcomes, Iran

scientific article published on 01 November 2019

Vaccine-Derived Polioviruses and Children with Primary Immunodeficiency, Iran, 1995-2014.

artículo científico publicado en 2016

Vaccine-associated paralytic poliomyelitis in immunodeficient children, Iran, 1995-2008.

artículo científico publicado en 2010

X-linked agammaglobulinemia: a survey of 33 Iranian patients

artículo científico publicado en 2004

X-linked lymphoproliferative syndrome: a genetic condition typified by the triad of infection, immunodeficiency and lymphoma.

artículo científico publicado en 2010

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