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A Novel Recessive Mutation of Interferon-γ Receptor 1 in a Patient with Mycobacterium tuberculosis in Bone Marrow Aspirate

artículo científico publicado en 2019

A gain-of-function mutation of STAT1: A novel genetic factor contributing to chronic mucocutaneous candidiasis

artículo científico publicado en 2017

A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activity

scientific article published on 01 June 2018

APRIL gene polymorphism and serum sAPRIL levels in children with systemic lupus erythematosus

artículo científico publicado en 2016

Association of IL4 single-nucleotide polymorphisms with febrile seizures.

artículo científico publicado en 2014

Association of TGFB, but not IL10, single nucleotide polymorphisms with febrile seizures.

artículo científico publicado en 2015

Association of interleukin-1 family gene polymorphisms with juvenile idiopathic arthritis in Iranian population

artículo científico publicado en 2016

Association of interleukin-6 single nucleotide polymorphisms with juvenile idiopathic arthritis

artículo científico publicado en 2016

Association of tumour necrosis factor-alpha G/A -238 and G/A -308 single nucleotide polymorphisms with juvenile idiopathic arthritis

artículo científico publicado en 2016

Cytokine Secretion Pattern in Treatment of Lymphocytes of Multiple Sclerosis Patients with Fumaric Acid Esters ⬇️

artículo científico publicado el 21 de abril de 2011

Exome sequencing revealed C1Q homozygous mutation in Pediatric Systemic Lupus Erythematosus.

artículo científico publicado en 2018

Hypomorphic DOCK8 deletion causes hypereosinophilic syndrome

scientific article published on 20 November 2019

MHC class II deficiency: Report of a novel mutation and special review

artículo científico publicado en 2017

Non-variant specific antibody responses to the C-terminal region of merozoite surface protein-1 of Plasmodium falciparum (PfMSP-119) in Iranians exposed to unstable malaria transmission ⬇️

artículo científico publicado el 16 de septiembre de 2010

Novel AICDA mutation in a case of autosomal recessive hyper-IgM syndrome, growth hormone deficiency and autoimmunity.

artículo científico publicado en 2016

Polymorphisms of genes encoding interleukin-4 and its receptor in Iranian patients with juvenile idiopathic arthritis

artículo científico publicado en 2016

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

Specific immunotherapy in ovarian cancer: a systematic review.

artículo científico publicado en 2016

The cytoskeletal regulator HEM1 governs B cell development and prevents autoimmunity

scientific article published on 01 July 2020

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