N. Parvaneh

N. Rezaei, A. Aghamohammadi, M. Moin, 2008, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Impact of delayed diagnosis in children with primary antibody deficiencies.

N. Rezaei, A. Aghamohammadi, N. Parvaneh, 2011, Journal of microbiology, immunology, and infection = Wei mian yu gan ran za zhi.

Assessment of Pubertal Development in Iranian Girls

A. Salavati, M. Mohammadi, K. Mohammad, 2010, Iranian journal of pediatrics.

Pubertal Development in a Random Sample of 4,020 Urban Iranian Girls

A. Salavati, K. Mohammad, M. Karbakhsh, 2008, Journal of pediatric endocrinology & metabolism : JPEM.

Mortality and morbidity in common variable immunodeficiency.

A. Salavati, N. Pouladi, N. Rezaei, 2006, Journal of tropical pediatrics.

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

A. Aghamohammadi, N. Parvaneh, H. Alimadadi, 2018, Journal of investigational allergology & clinical immunology.

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

N. Rezaei, K. Moazzami, A. Aghamohammadi, 2010, Journal of investigational allergology & clinical immunology.

Common variable immunodeficiency: a heterogeneous group needs further subclassification

N. Rezaei, A. Aghamohammadi, N. Parvaneh, 2009, Expert review of clinical immunology.

Inherited IL-12p40 Deficiency: Genetic, Immunologic, and Clinical Features of 49 Patients From 30 Kindreds (vol 92, pg 109, 2013)

Sami Al-Hajjar, C. Picard, L. Abel, 2013 .

Autoimmune phenotype in patients with common variable immunodeficiency.

N. Rezaei, A. Aghamohammadi, N. Parvaneh, 2013, Journal of investigational allergology & clinical immunology.

TNFAIP3 mutation causing haploinsufficiency of A20 with a hemophagocytic lymphohistiocytosis phenotype: a report of two cases

F. Shahram, V. Ziaee, N. Parvaneh, 2022, Pediatric Rheumatology.

Disparity in Access to Care and Its Impact on Diagnosis and Outcomes of Allergic Diseases

N. Parvaneh, 2020 .

Acute Flaccid Paralysis: A Registry-based Study of Demographic, Clinical, and Diagnostic Characteristics of Children in a Referral Center in Iran

N. Parvaneh, A. Tavasoli, Sayna Bagheri, 2020 .

The Efficacy of Anti-Tumor Necrosis Factor Therapy in Cryopyrin-Associated Periodic Syndromes: A Report of Two Cases

F. Tahghighi, V. Ziaee, N. Parvaneh, 2022, Case reports in genetics.

Different phenotypes of the same XIAP mutation in a family: A case of XIAP deficiency with juvenile idiopathic arthritis

M. Shabani, N. Parvaneh, H. Alimadadi, 2019, Pediatric blood & cancer.

Characterization of six novel mutations in CYBA: the gene causing autosomal recessive chronic granulomatous disease *

S. Teimourian, C. Kannengiesser, N. Parvaneh, 2008, British journal of haematology.

Effective anti-mycobacterial treatment for BCG disease in patients with Mendelian Susceptibility to Mycobacterial Disease (MSMD): a case series

J. Casanova, A. Velayati, J. Bustamante, 2021, Annals of clinical microbiology and antimicrobials.

Post-mortem Diagnosis of Heme Oxygenase-1 Deficiency by Whole Exome Sequencing in an Iranian Child

F. Tahghighi, V. Ziaee, N. Parvaneh, 2019, International journal of molecular and cellular medicine.

Vitamin D insufficiency among children and adolescents living in Tehran, Iran.

S. Alavian, A. Salavati, M. Motlagh, 2009, Journal of tropical pediatrics.

Evaluation of Antibody Response to Polysaccharide Vaccine and Switched Memory B Cells in Pediatric Patients with Inflammatory Bowel Disease

N. Rezaei, A. Aghamohammadi, N. Parvaneh, 2013, Gut and liver.

Timing of puberty in Iranian girls according to their living area: a national study

R. Kelishadi, M. Motlagh, G. Ardalan, 2011, Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences.

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

L. Hammarström, N. Rezaei, R. Sherkat, 2014, Expert review of clinical immunology.

Associations of Behavioral Disorders with Asthma in Iranian Children.

M. Effatpanah, N. Parvaneh, M. Zaki-Dizaji, 2019, Iranian journal of allergy, asthma, and immunology.

Lymphoma of mucosa-associated lymphoid tissue in common variable immunodeficiency

N. Rezaei, A. Aghamohammadi, N. Parvaneh, 2006, Leukemia & lymphoma.

The risk of hemophagocytic lymphohistiocytosis in Hermansky-Pudlak syndrome type 2.

Sebastian F N Bode, K. Schwarz, C. Klein, 2013, Blood.

Isolation of a type 3 vaccine-derived poliovirus (VDPV) from an Iranian child with X-linked agammaglobulinemia.

Qi Chen, S. Teimourian, O. Kew, 2008, Virus research.

Vaccine-associated paralytic poliomyelitis in a patient with MHC class II deficiency.

O. Kew, N. Parvaneh, S. Mamishi, 2007, Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology.

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

A. Salavati, M. Vodjgani, N. Rezaei, 2007, Journal of investigational allergology & clinical immunology.

Evaluation of liver diseases in Iranian patients with primary antibody deficiencies.

N. Pouladi, N. Rezaei, S. Teimourian, 2009, Annals of hepatology.

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

N. Pouladi, N. Rezaei, K. Moazzami, 2009, Journal of investigational allergology & clinical immunology.

Infectious and NonInfectious Complications among Undiagnosed Patients with Common Variable Immunodeficiency

M. Tavassoli, N. Rezaei, K. Moazzami, 2009 .

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

A. Aghamohammadi, M. Gouya, N. Parvaneh, 2019, Emerging infectious diseases.

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

A. Aghamohammadi, N. Parvaneh, H. Abolhassani, 2014, Immunological investigations.

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

M. Mohammadpour, A. Aghamohammadi, N. Parvaneh, 2010, Emerging infectious diseases.

Polymorphism in the First Intron of Interferon-Gamma Gene (+874T/A) in Patients with BCG Adenitis

A. Salavati, H. Ashraf, N. Parvaneh, 2009 .

Tumefactive Multiple Sclerosis Variants: Report of Two Cases of Schilder and Balo Diseases

N. Parvaneh, A. Tavasoli, H. Alizadeh, 2017, Iranian journal of child neurology.

Molecular and clinical characterization of autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy syndrome (APECED) in Iranian non-Jewish patients: report of two novel AIRE gene pathogenic variants

N. Parvaneh, H. Akhavan-Niaki, F. Sayarifard, 2022, Orphanet Journal of Rare Diseases.

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

V. Lougaris, A. Plebani, H. Ochs, 2019, The journal of allergy and clinical immunology. In practice.

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

M. Tavassoli, L. Hammarström, N. Rezaei, 2018, Journal of Clinical Immunology.

Intermittent Neutropenia as an Early Feature of Mild Mevalonate Kinase Deficiency

I. Touitou, V. Ziaee, N. Parvaneh, 2013, Journal of Clinical Immunology.

Inherited human ITK deficiency impairs IFN-γ immunity and underlies tuberculosis

J. Casanova, J. Uitto, L. Abel, 2022, The Journal of experimental medicine.

Detection of Epstein-Barr virus infection in lymphoma: ELISA and PCR method.

M. Izadyar, N. Parvaneh, B. Pourakbari, 2010 .

Invasive aspergillosis in chronic granulomatous disease: report of 7 cases

A. Salavati, M. Yeganeh, N. Parvaneh, 2006, European Journal of Pediatrics.

Genetic Mutations and Immunological Features of Severe Combined Immunodeficiency Patients in Iran.

N. Rezaei, A. Aghamohammadi, M. Keramatipour, 2019, Immunology letters.

Serum sickness-like reactions in Iranian children: a registry-based study in a referral center.

M. Saatchi, A. Aghamohammadi, N. Parvaneh, 2020, Allergologia et immunopathologia.

Inborn errors of metabolism underlying primary immunodeficiencies

J. Casanova, P. Quartier, P. Lonlay, 2014, Journal of Clinical Immunology.

Novel BTK mutation presenting with vaccine-associated paralytic poliomyelitis

A. Salavati, Y. Gheisari, S. Teimourian, 2008, European Journal of Pediatrics.

Analysis of Switched Memory B Cells in Patients with IgA Deficiency

N. Rezaei, K. Moazzami, A. Aghamohammadi, 2011, International Archives of Allergy and Immunology.

Progression of Selective IgA Deficiency to Common Variable Immunodeficiency

Lennart Hammarstrom, N. Rezaei, A. Aghamohammadi, 2008, International Archives of Allergy and Immunology.

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

N. Rezaei, K. Moazzami, A. Aghamohammadi, 2010, Acta dermatovenerologica Croatica : ADC.

Gastrointestinal Manifestations in Patients with Common Variable Immunodeficiency

A. Salavati, N. Rezaei, A. Aghamohammadi, 2007, Digestive Diseases and Sciences.

Effects of Coronavirus Disease 2019 (COVID-19) on Peripheral Blood Lymphocytes and Their Subsets in Children: Imbalanced CD4+/CD8+ T Cell Ratio and Disease Severity

N. Parvaneh, S. Mahmoudi, A. Navaeian, 2021, Frontiers in Pediatrics.

Etiology and Antimicrobial Susceptibility of Bacerial Septic Arthritis and Osteomyelitis

N. Parvaneh, M. Taherikalani, S. Mamishi, 2007 .

Treatment of pemphigus vulgaris with mycophenolate mofetil as a steroid-sparing agent.

F. Farshidfar, C. Chams‐Davatchi, N. Parvaneh, 2008, European journal of dermatology : EJD.

Fatal invasive aspergillosis in a child with chronic granulomatous disease.

N. Parvaneh, S. Ansari, B. Ahmadi, 2022, Journal of wound care.

Periodic Fever and Neutrophilic Dermatosis: Is It Sweet's Syndrome?

V. Ziaee, N. Parvaneh, R. Assari, 2014, Case reports in immunology.

Revisiting Human IL-12R&bgr;1 Deficiency: A Survey of 141 Patients From 30 Countries

Smita Y. Patel, A. Al-ghonaium, Sami Al-Hajjar, 2010, Medicine.

Invasive Rasamsonia argillacea infection in chronic granulomatous disease: Report of a new case and literature review.

L. Moradi, N. Parvaneh, H. Eshaghi, 2020, Journal de mycologie medicale.

A Variety of Alu-Mediated Copy Number Variations Can Underlie IL-12Rβ1 Deficiency

J. Casanova, C. Picard, C. Deswarte, 2018, Journal of clinical immunology.

Clinical features of Candidiasis in patients with inherited interleukin 12 receptor β1 deficiency.

J. Casanova, J. Franco, C. Picard, 2014, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America.

Hematologically important mutations: leukocyte adhesion deficiency (first update).

A. Fischer, S. Holland, T. Kuijpers, 2012, Blood cells, molecules & diseases.

NCKAP1L defects lead to a novel syndrome combining immunodeficiency, lymphoproliferation, and hyperinflammation

M. Konantz, C. Lengerke, Zhichao Miao, 2020, The Journal of experimental medicine.

Clinical, immunologic, and genetic spectrum of 696 patients with combined immunodeficiency

M. Afarideh, A. Ghajar, R. Geha, 2017, The Journal of allergy and clinical immunology.

Clinical presentation and outcome in infantile Sandhoff disease: a case series of 25 patients from Iranian neurometabolic bioregistry with five novel mutations

J. Zschocke, N. Parvaneh, Z. Rezaei, 2018, Orphanet Journal of Rare Diseases.

IgA Deficiency: Correlation Between Clinical and Immunological Phenotypes

N. Rezaei, A. Aghamohammadi, M. Moin, 2008, Journal of Clinical Immunology.

A Variety of Alu-Mediated Copy Number Variations Can Underlie IL-12Rβ1 Deficiency

J. Casanova, C. Picard, C. Deswarte, 2018, Journal of Clinical Immunology.

IL-12Rβ1 Deficiency in Two of Fifty Children with Severe Tuberculosis from Iran, Morocco, and Turkey

J. Casanova, A. Bousfiha, L. Abel, 2011, PloS one.

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

N. Pouladi, N. Rezaei, K. Moazzami, 2008, Iranian journal of allergy, asthma, and immunology.

Demographic, clinical, immunological, and molecular features of iranian national cohort of patients with defect in DCLRE1C gene

Z. Chavoshzadeh, A. Fahimzad, N. Parvaneh, 2023, Allergy, Asthma & Clinical Immunology.

Natural Killer Cells from Patients with Recombinase-Activating Gene and Non-Homologous End Joining Gene Defects Comprise a Higher Frequency of CD56bright NKG2A+++ Cells, and Yet Display Increased Degranulation and Higher Perforin Content

L. Notarangelo, J. Walter, V. Lougaris, 2017, Front. Immunol..

Genetic defects in B-cell development and their clinical consequences.

L. Hammarström, A. Aghamohammadi, N. Parvaneh, 2014, Journal of investigational allergology & clinical immunology.

Human papillomavirus detected in esophageal squamous cell carcinoma in Iran.

S. Akiba, A. Behzadi, N. Parvaneh, 2012, European journal of internal medicine.

Inherited and acquired immunodeficiencies underlying tuberculosis in childhood

J. Casanova, A. Bousfiha, F. Ailal, 2015, Immunological reviews.

Mandibuloacral Dysplasia in An Iranian Girl

M. Mehdizadeh, N. Parvaneh, A. Rabbani, 2006 .

Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease

Phillip A. Richmond, A. Hoischen, J. Casanova, 2022, medRxiv.

Analysis of RAB27A Gene in Griscelli Syndrome type 2: Novel Mutations Including a Deletion Hotspot

M. Yeganeh, F. Mahjoub, M. Modarressi, 2008, Journal of Clinical Immunology.

Ocular Manifestations of Chronic Granulomatous Disease: First Report of Coats’ Disease and Literature Review

M. Shabani, N. Parvaneh, M. Parvin, 2020, Journal of Clinical Immunology.

UNC13D Deficiency Associated With Epileptic Seizures and Antibody Deficiency: The First Case from the Iranian National Registry.

N. Rezaei, A. Aghamohammadi, N. Parvaneh, 2019, Journal of investigational allergology & clinical immunology.

Consensus Middle East and North Africa Registry on Inborn Errors of Immunity

R. Geha, A. Bousfiha, W. Al-Herz, 2021, Journal of Clinical Immunology.

Bacillus Calmette–Guérin (BCG)‐associated hemophagocytic lymphohistiocytosis in the setting of IFN‐γR1 deficiency: A diagnostic dilemma

N. Parvaneh, L. Parvaneh, M. Shahrooei, 2020, EJHaem.

Hematologically important mutations: Leukocyte adhesion deficiency (second update).

K. Schwarz, H. Kanegane, C. Klein, 2023, Blood cells, molecules & diseases.

DOCK8 deficiency in six Iranian patients

M. Houshmand, B. Grimbacher, M. Moin, 2016, Clinical case reports.

Primary Immunodeficiency Disorders in Iran: Update and New Insights from the Third Report of the National Registry

N. Rezaei, R. Sherkat, A. Aghamohammadi, 2014, Journal of Clinical Immunology.

Novel UBR1 gene mutation in a patient with typical phenotype of Johanson–Blizzard syndrome

N. Rezaei, M. Zenker, N. Parvaneh, 2011, European Journal of Pediatrics.

A novel RAB27A mutation in a patient with Griscelli syndrome type 2.

N. Rezaei, Z. Pourpak, N. Parvaneh, 2010, Journal of investigational allergology & clinical immunology.

Characterization of 11 New Cases of Leukocyte Adhesion Deficiency Type 1 with Seven Novel Mutations in the ITGB2 Gene

N. Rezaei, R. Sherkat, A. Aghamohammadi, 2010, Journal of Clinical Immunology.

Inherited IL-12p40 Deficiency

Sami Al-Hajjar, J. Casanova, C. Picard, 2013, Medicine.

A Novel STK4 Mutation Presenting with Juvenile Idiopathic Arthritis and Epidermodysplasia Verruciformis

V. Ziaee, N. Parvaneh, M. Ahadi, 2019, Journal of Clinical Immunology.

Molecular diagnosis of X-linked chronic granulomatous disease in Iran

Z. Rezvani, S. Teimourian, M. Moin, 2008, International journal of hematology.

Novel CYBA mutation in a family with BCGitis.

N. Rezaei, N. Parvaneh, M. Shahrooei, 2019, Acta microbiologica et immunologica Hungarica.

Primary immunodeficiencies: a rapidly evolving story.

J. Casanova, L. Notarangelo, M. Conley, 2013, The Journal of allergy and clinical immunology.

Graft versus host disease and microchimerism in a JAK3 deficient patient

H. Rahimi, A. Aghamohammadi, M. Hamid, 2019, Allergy, Asthma & Clinical Immunology.

Recurrent Infections and Easy Bruising

N. Parvaneh, 2019, Pediatric Immunology.

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

M. Tavassoli, L. Hammarström, N. Rezaei, 2018, Journal of Clinical Immunology.

Chediak Higashi Syndrome with Hemophagocytic Lymphohistiocytosis

N. Parvaneh, Moeinadin Safavi, 2022, Fetal and pediatric pathology.

Griscelli syndrome type 2; a pediatric case with immunodeficiency.

F. Mahjoub, N. Parvaneh, T. Cheraghi, 2007, Iranian journal of allergy, asthma, and immunology.

Diffuse dermal melanocytosis in two patients with Sandhoff disease and mucopolysaccharidosis VI

N. Parvaneh, S. Shiva, A. Tavasoli, 2014, International journal of dermatology.

Mutation spectra of the ITGB2 gene in Iranian families with leukocyte adhesion deficiency type 1.

V. Yassaee, N. Parvaneh, Sara Boosaliki, 2016, Human immunology.

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

N. Rezaei, K. Moazzami, M. Mohammadpour, 2010, Respirology.

National Consensus on Diagnosis and Management Guidelines for Primary Immunodeficiency

M. Tavassoli, N. Rezaei, M. Eslamian, 2019 .

Epidermodysplasia verruciformis associated with plasmablastic lymphoma and hepatitis B virus infection.

M. Mohammadpour, N. Parvaneh, K. Azadmanesh, 2012, Acta dermatovenerologica Croatica : ADC.

Human IL-23 is essential for IFN-γ-dependent immunity to mycobacteria

J. Casanova, S. Tangye, F. Sallusto, 2023, Science Immunology.

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

A. Aghamohammadi, B. Negahdari, N. Parvaneh, 2017, European annals of allergy and clinical immunology.

Candidate Predisposition Variants in Kaposi Sarcoma as Detected by Whole-Genome Sequencing

J. Casanova, L. Aaltonen, L. Abel, 2019, Open forum infectious diseases.

The frequency of Helicobacter pylori infection in patients with primary antibody deficiencies

R. Malekzadeh, S. Merat, L. Moradi, 2019 .

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

A. Salavati, L. Notarangelo, A. Plebani, 2006, International Archives of Allergy and Immunology.

2q34-qter duplication and 4q34.2-qter deletion in a patient with developmental delay.

A. Reymond, L. Harewood, N. Parvaneh, 2012, European journal of medical genetics.

NOD2 Sequencing in Iranian Children with Crohn’s Disease

K. Moazzami, N. Parvaneh, F. Motamed, 2011, Zeitschrift für Gastroenterologie.

Autoimmune lymphoproliferative syndrome: meticulous care for diagnosis.

A. Aghamohammadi, M. Yeganeh, N. Parvaneh, 2005, Iranian journal of allergy, asthma, and immunology.

Ataxia-telangiectasia in a patient presenting with hyper-immunoglobulin M syndrome.

O. Ohara, N. Rezaei, K. Moazzami, 2010, Journal of investigational allergology & clinical immunology.

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

V. Lougaris, A. Plebani, S. Giliani, 2016, Expert review of clinical immunology.

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

R. Amin, M. Afarideh, A. Ghajar, 2015, Journal of investigational allergology & clinical immunology.

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.

N. Rezaei, A. Aghamohammadi, T. Hirschmugl, 2016, Acta medica Iranica.

Neonatal Marfan Syndrome: Report of Two Cases

N. Parvaneh, Y. Ghandi, Keyhan S.Zanjani, 2013, Iranian Journal of Pediatrics.

Phenotypic analysis of Pyrin-Associated Autoinflammation with Neutrophilic Dermatosis patients during treatment.

C. Wouters, J. J. van den Oord, A. Liston, 2021, Rheumatology.

Impaired IL-23–dependent induction of IFN-γ underlies mycobacterial disease in patients with inherited TYK2 deficiency

J. Casanova, A. Bousfiha, S. Ehl, 2022, The Journal of experimental medicine.

Homozygous MEFV Gene Variant and Pyrin-Associated Autoinflammation With Neutrophilic Dermatosis: A Family With a Novel Autosomal Recessive Mode of Inheritance.

J. Uitto, V. Ziaee, M. Yousefi, 2021, JAMA dermatology.

Evaluation of interleukin-12 receptor β1 and interferon gamma receptor 1 deficiency in patients with disseminated BCG infection.

N. Parvaneh, S. Mahmoudi, B. Pourakbari, 2019, Allergologia et immunopathologia.

Intermittent Neutropenia as an Early Feature of Mild Mevalonate Kinase Deficiency

I. Touitou, V. Ziaee, N. Parvaneh, 2013, Journal of Clinical Immunology.

Selective antibody deficiency and its relation to the IgG2 and IgG3 subclass titers in recurrent respiratory infections.

R. Sherkat, N. Parvaneh, A. Babak, 2013, Iranian journal of immunology : IJI.

Clinical and Laboratory Findings in Hyper-IgM Syndrome with Novel CD40L and AICDA Mutations

A. Imanzadeh, L. Hammarström, N. Rezaei, 2009, Journal of Clinical Immunology.

Complement deficiency in pediatric-onset systemic lupus erythematosus

V. Ziaee, B. Moazzami, N. Parvaneh, 2018, Journal of Laboratory Physicians.

Immunodeficiency with susceptibility to lymphoma with complex genotype affecting energy metabolism (FBP1, ACAD9) and vesicle trafficking (RAB27A)

W. Klapper, S. Ehl, H. Hennies, 2023, Frontiers in Immunology.

A. Imanzadeh, M. Tavassoli, S. Pourjabbar, 2011, Iranian journal of allergy, asthma, and immunology.

Novel mutations of NP in two patients with purine nucleoside phosphorylase deficiency.

V. Micheli, S. Teimourian, M. Bertelli, 2008, Clinical biochemistry.

Successful Desensitization to Idursulfase in a Patient with Type II Mucopolysaccharidosis ( Hunter syndrome )

N. Rezaei, A. Aghamohammadi, S. Shahkarami, 2011 .

Molecular characterization of Bruton's tyrosine kinase deficiency in 12 Iranian patients with presumed X-linked agammaglobulinemia.

N. Rezaei, A. Aghamohammadi, S. Shahkarami, 2011, Journal of investigational allergology & clinical immunology.

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

A. Imanzadeh, N. Rezaei, K. Moazzami, 2010, Human psychopharmacology.

Inherited ARPC5 mutations cause an actinopathy impairing cell motility and disrupting cytokine signaling

J. Casanova, S. Pittaluga, L. Notarangelo, 2023, Nature communications.

Tuberculosis: a new look at an old disease

J. Casanova, N. Rezaei, A. Aghamohammadi, 2011, Expert review of clinical immunology.

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

N. Rezaei, A. Aghamohammadi, B. Moazzami, 2019, International Archives of Allergy and Immunology.

Progressive multifocal leukoencephalopathy in purine nucleoside phosphorylase deficiency

N. Pouladi, M. Yeganeh, N. Parvaneh, 2007, Brain and Development.

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

N. Rezaei, A. Aghamohammadi, N. Parvaneh, 2010, The Brazilian journal of infectious diseases : an official publication of the Brazilian Society of Infectious Diseases.

ENDGAME OF POLIO ERADICATION INITIATIVE AND OPV ADVERSE EVENT; A CASE REPORT OF IMMUNODEFICIENT VACCINE DERIVED POLIO VIRUS

N. Parvaneh, Gouya Mohammad Mahdi, S. Mamishi, 2007 .

Two Novel Biallelic RASGRP1 Mutations Presenting with Immunodeficiency, Hodgkin’s Lymphoma, and Autoimmunity

R. Sherkat, I. Meyts, X. Bossuyt, 2022, Journal of Clinical Immunology.

Clinical, Immunological, and Genetic Findings in Iranian Patients with MHC-II Deficiency: Confirmation of c.162delG RFXANK Founder Mutation in the Iranian Population.

J. Casanova, L. Abel, R. Sherkat, 2023, Journal of clinical immunology.

Corrigendum: Natural Killer Cells from Patients with Recombinase-Activating Gene and Non-Homologous End Joining Gene Defects Comprise a Higher Frequency of CD56bright NKG2A+++ Cells, and Yet Display Increased Degranulation and Higher Perforin Content

L. Notarangelo, J. Walter, V. Lougaris, 2017, Front. Immunol..

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

M. Mohammadpour, A. Aghamohammadi, N. Parvaneh, 2010, Emerging infectious diseases.

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

N. Rezaei, K. Moazzami, A. Aghamohammadi, 2010, Journal of investigational allergology & clinical immunology.

Revisiting Human IL-12R&bgr;1 Deficiency: A Survey of 141 Patients From 30 Countries

Smita Y. Patel, A. Al-ghonaium, Sami Al-Hajjar, 2010, Medicine.

Clinical and immunological characteristics of 69 leukocyte adhesion deficiency‐I patients

L. Moradi, A. Kazemnejad, N. Sabetkish, 2023, Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology.

Human MCTS1-dependent translation of JAK2 is essential for IFN-γ immunity to mycobacteria

A. Teleman, D. Rinchai, Y. Seeleuthner, 2023, Cell.

Human germline heterozygous gain-of-function STAT6 variants cause severe allergic disease

Phillip A. Richmond, A. Hoischen, W. Wasserman, 2023, The Journal of experimental medicine.

A Variety of Alu-Mediated Copy Number Variations Can Underlie IL-12Rβ1 Deficiency

J. Casanova, C. Picard, C. Deswarte, 2018, Journal of Clinical Immunology.

Impaired in-vitro responses to IL-12 and IFN-γ in Iranian patients with Mendelian susceptibility to mycobacterial disease.

N. Parvaneh, S. Mamishi, G. Khotaei, 2015, Allergologia et immunopathologia.

Autoantibodies against type I IFNs in humans with alternative NF-κB pathway deficiency

J. Derisi, F. Rieux-Laucat, J. Fellay, 2023, Nature.

Successful Treatment of Fungal Osteomyelitis with Voriconazole in a Patient with Chronic Granulomatous Disease

M. Mohammadpour, Z. Pourpak, N. Parvaneh, 2010, Iranian Journal of Pediatrics.

The immunopathological landscape of human pre-TCRα deficiency: from rare to common variants

Chaim A. Schramm, J. Kelsen, C. Deswarte, 2024, Science.

A Novel Non-frameshift ADA Deletion Detected by Whole Exome Sequencing in an Iranian Family with Severe Combined Immunodeficiency.

X. Bossuyt, N. Parvaneh, Hassan Rokni-Zadeh, 2020, Iranian journal of allergy, asthma, and immunology.

A Rare Case of Hyper IgE Syndrome with Vocal Cords Involvement.

N. Parvaneh, M. Movahedi, M. Gharagozlou, 2019, Iranian journal of allergy, asthma, and immunology.

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

N. Pouladi, K. Moazzami, A. Aghamohammadi, 2009, Journal of investigational allergology & clinical immunology.

Effects of Coronavirus Disease 2019 (COVID-19) on Peripheral Blood Lymphocytes and Their Subsets in Children: Imbalanced CD4+/CD8+ T Cell Ratio and Disease Severity

N. Parvaneh, S. Mahmoudi, B. Pourakbari, 2020, Frontiers in Pediatrics.

Functional characterization of two RAB27A missense mutations found in Griscelli syndrome type 2

M. Mohammadpour, M. Fukuda, N. Parvaneh, 2010, Pigment cell & melanoma research.

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