Published in J Investig Allergol Clin Immunol on January 01, 2009
Role of neutrophils in IL-17-dependent immunity to mucosal candidiasis. J Immunol (2014) 1.13
History of primary immunodeficiency diseases in iran. Iran J Pediatr (2010) 0.80
Cytokine imbalance in irritable bowel syndrome: a systematic review and meta-analysis. Neurogastroenterol Motil (2014) 1.03
Cytokine gene polymorphism in Iranian patients with chronic myelogenous leukaemia. Int J Immunogenet (2005) 0.98
The association of HLA-DRB, DQA1, DQB1 alleles and haplotype frequency in Iranian patients with pulmonary tuberculosis. Int J Tuberc Lung Dis (2004) 0.96
Necrosis of nasal cartilage due to mucormycosis in a patient with severe congenital neutropenia due to HAX1 deficiency. J Investig Allergol Clin Immunol (2008) 0.92
IL-2-inducible T-cell kinase deficiency with pulmonary manifestations due to disseminated Epstein-Barr virus infection. Int Arch Allergy Immunol (2012) 0.92
Analysis of class-switched memory B cells in patients with common variable immunodeficiency and its clinical implications. J Investig Allergol Clin Immunol (2007) 0.91
The influence of systemic therapy on the serum levels of IL-6 and IL-8 in pemphigus vulgaris. J Eur Acad Dermatol Venereol (2011) 0.89
Novel RAG2 mutation in a patient with T- B- severe combined immunodeficiency and disseminated BCG disease. J Investig Allergol Clin Immunol (2009) 0.89
Adverse reactions of prophylactic intravenous immunoglobulin; a 13-year experience with 3004 infusions in Iranian patients with primary immunodeficiency diseases. J Investig Allergol Clin Immunol (2009) 0.88
Cytokine gene polymorphisms are associated with irritable bowel syndrome: a systematic review and meta-analysis. Neurogastroenterol Motil (2012) 0.88
Pulmonary complications in primary hypogammaglobulinemia: a survey by high resolution CT scan. Monaldi Arch Chest Dis (2006) 0.87
A review of gastrointestinal disorders in patients with primary antibody immunodeficiencies during a 10-year period (1990-2000), in children hospital medical center. Iran J Allergy Asthma Immunol (2003) 0.87
The study of type 1 allergy prevalence among people of South-East of iran by skin prick test using common allergens. Iran J Allergy Asthma Immunol (2003) 0.86
Seroepidemiology of Varicella Zoster Virus among children, adolescents and medical students in a referral children medical center, Tehran, Iran. Iran J Microbiol (2012) 0.86
Multiple organ involvement with hydatid cysts. Iran J Parasitol (2010) 0.85
Genetic susceptibility to Graves' ophthalmopathy: the role of polymorphisms in proinflammatory cytokine genes. Eye (Lond) (2009) 0.83
Severe primary antibody deficiency due to a novel mutation of mu heavy chain. J Investig Allergol Clin Immunol (2012) 0.82
Interleukin-4 single nucleotide polymorphisms in juvenile systemic lupus erythematosus. Int J Immunogenet (2014) 0.82
Optic neuritis, multiple sclerosis and human leukocyte antigen: results of a 4-year follow-up study. Eur J Neurol (2005) 0.82
Molecular diagnosis of X-linked chronic granulomatous disease in Iran. Int J Hematol (2008) 0.82
Polymorphisms in IL4 and iLARA confer susceptibility to asthma. J Investig Allergol Clin Immunol (2009) 0.82
Naive CD4+ T cells and recent thymic emigrants in common variable immunodeficiency. J Investig Allergol Clin Immunol (2012) 0.82
Pediatric patients with common variable immunodeficiency: long-term follow-up. J Investig Allergol Clin Immunol (2012) 0.81
Hyper-IgE syndrome. J Postgrad Med (2010) 0.80
Adverse effects of intravenous immunoglobulin therapy in patients with antibody deficiency. Iran J Allergy Asthma Immunol (2003) 0.80
Laryngeal foreign body aspiration misdiagnosed as asthma: two case reports and a review of the literature. B-ENT (2011) 0.80
Malignancy phenotype in common variable immunodeficiency. J Investig Allergol Clin Immunol (2012) 0.80
Association between the interleukin 6 genotype at position -174 and atopic dermatitis. J Investig Allergol Clin Immunol (2013) 0.80
Health policy for common variable immunodeficiency: burden of the disease. J Investig Allergol Clin Immunol (2011) 0.80
Asthma and allergic rhinitis in a patient with BTK deficiency. J Investig Allergol Clin Immunol (2008) 0.80
Multiple independent second-site mutations in two siblings with somatic mosaicism for Wiskott-Aldrich syndrome. Clin Genet (2008) 0.79
Distribution of primary immunodeficiency disorders diagnosed in the Children's Medical Center in Iran. J Investig Allergol Clin Immunol (2005) 0.79
Altered dendritic cell function in response to sera of common variable immunodeficiency patients. Inflamm Res (2007) 0.78
Interleukin 10 and transforming growth factor beta 1 gene polymorphisms in juvenile idiopathic arthritis. Bratisl Lek Listy (2016) 0.78
Autoimmune phenotype in patients with common variable immunodeficiency. J Investig Allergol Clin Immunol (2013) 0.77
Assessment of the immune system in 55 Iranian patients with vitiligo. J Eur Acad Dermatol Venereol (2005) 0.77
Soluble CD26 and CD30 levels in patients with common variable immunodeficiency. J Investig Allergol Clin Immunol (2013) 0.77
Normal uterine size in women of reproductive age in northern Islamic Republic of Iran. East Mediterr Health J (2004) 0.77
Response to induction therapy in a pediatric population of inflammatory bowel disease. Z Gastroenterol (2010) 0.77
Correlation between common variable immunodeficiency clinical phenotypes and parental consanguinity in children and adults. J Investig Allergol Clin Immunol (2010) 0.77
Respiratory manifestations of chronic granulomatous disease; a clinical survey of patients from Iranian primary immunodeficiency registry. Iran J Allergy Asthma Immunol (2003) 0.77
Single-nucleotide polymorphisms of TNFA and IL1 in allergic rhinitis. J Investig Allergol Clin Immunol (2013) 0.76
Ataxia-telangiectasia in a patient presenting with hyper-immunoglobulin M syndrome. J Investig Allergol Clin Immunol (2010) 0.76
Common Variable Immunodeficiency or Late-Onset Combined Immunodeficiency: A New Hypomorphic JAK3 Patient and Review of the Literature. J Investig Allergol Clin Immunol (2015) 0.76
Isolated growth hormone deficiency in a patient with immunoglobulin class switch recombination deficiency. J Investig Allergol Clin Immunol (2009) 0.75
ENT manifestations in Iranian patients with primary antibody deficiencies. J Laryngol Otol (2007) 0.75
Major histocompatibility complex class I and II antigens frequencies in Baloch ethnic group living in the southeast region of Iran. Transplant Proc (2004) 0.75
Primary Antibody Deficiency in a Tertiary Referral Hospital: A 30-Year Experiment. J Investig Allergol Clin Immunol (2015) 0.75
Autoimmunity in patients with selective IgA deficiency. J Investig Allergol Clin Immunol (2015) 0.75
Genetic defects in B-cell development and their clinical consequences. J Investig Allergol Clin Immunol (2014) 0.75
A novel RAB27A mutation in a patient with Griscelli syndrome type 2. J Investig Allergol Clin Immunol (2010) 0.75
Congenital pulmonary airway malformation. Bratisl Lek Listy (2013) 0.75
NOD2 sequencing in Iranian children with Crohn's disease. Z Gastroenterol (2011) 0.75
FOXP3, RORγt and IL-10 cytokine profile in chronic heart failure. Bratisl Lek Listy (2017) 0.75
Bcgitis and vaccine-derived poliovirus infection in a patient with a novel deletion in RAG1 binding site. Int J Immunopathol Pharmacol (2013) 0.75
Renal amyloidosis in common variable immunodeficiency. Nefrologia (2010) 0.75
Association of interleukin 1 gene cluster and interleukin 1 receptor gene polymorphisms with ischemic heart failure. Bratisl Lek Listy (2016) 0.75
A novel CD40 ligand mutation in a patient with pneumonia, neutropenia, and hyperimmunoglobulin M phenotype. J Investig Allergol Clin Immunol (2013) 0.75
Prediction of future cardiac events using myocardial perfusion SPECT: a middle-term follow-up study. Rev Esp Med Nucl (2011) 0.75
Prediction of the evolution of common variable immunodeficiency: HLA typing for patients with selective IgA deficiency. J Investig Allergol Clin Immunol (2014) 0.75
Molecular characterization of Bruton's tyrosine kinase deficiency in 12 Iranian patients with presumed X-linked agammaglobulinemia. J Investig Allergol Clin Immunol (2011) 0.75
A novel deletion mutation in the human hairless (HR) gene in an Iranian family with atrichia and papular lesions. Clin Exp Dermatol (2009) 0.75
RAD50 Single-Nucleotide Polymorphism in Predominantly Antibody Deficiency. J Investig Allergol Clin Immunol (2015) 0.75