تالیفات

 

PDCD1 Single Nucleotide Polymorphisms in Iranian Patients With Juvenile Idiopathic Arthritis

مولف: Mahdi Mahmoudi1, 2, Alireza Rezaiemanesh1, 3, Sara Harsini4, 5, Arash Salmaninejad6, Shiva Poursani1, Tayyeb Bahrami7, Vahid Ziaee8, 9, and Nima Rezaei3, 5, 6

خلاصه: Abstract- Juvenile idiopathic arthritis (JIA) is a clinically heterogeneous cluster of complex diseases, in which both the genetic and environmental factors seem to play a role in the development of the disease. The current study aims to assess the association of programmed cell death 1 (PDCD1, also called PD-1) gene variants with JIA vulnerability in Iranian population. In this case-control association study, we investigated a group of 50 Iranian patients ... سال انتشار: 2017
 

HLA-DRB and HLA-DQB Allele and Haplotype Frequencies in Iranian Patients with Recurrent Aphthous Stomatitis

Authers: Shamsolmoulouk Najafi1, Mahsa Mohammadzadeh2, Alireza Zare Bidoki3, 4, Ghasem Meighani5, Saeed Aslani6, 7, Mahdi Mahmoudi6, and Nima Rezaei7, 8, 9

Abstract: Recurrent aphthous stomatitis (RAS) is known as the most common chronic disease of the oral cavity, which affects a range of 5-25% of the population. RAS appears to be associated with some human leukocyte antigen (HLA) class II alleles and haplotypes. This study attempts to survey the distribution of HLA-DRB and -DQB alleles among Iranian RAS patients and healthy controls. In order to evaluate the association of HLA-DR and DQ alleles ... سال انتشار: 2016
 

Gene Expression Profiling of Toll-Like Receptor 4 and 5 in Peripheral Blood Mononuclear Cells in Rheumatic Disorders: Ankylosing Spondylitis and Rheumatoid Arthritis

Authers: Iran J Allergy Asthma Immunol February 2016; 15(1):87-92.

Abstract: Spondyloarthropathies (SpA), defined by inflammatory situations, are a category of rheumatic diseases with mainly involvement of the spine, enthuses, and peripheral joints.1 Ankylosing spondylitis (AS), as the prototype of this category, is an autoimmune disease with a chronic inflammatory arthritis which is characterized by axial skeletal ankylosis, inflammation at the entheses, and arthritis of the peripheral limbs.2 AS shows a strong association with Human Leucocyte Antigen (HLA)-B27 hereditary, and the ... سال انتشار: 2016
 

Consensus classification criteria for paediatric Behçet’s disease from a prospective observational cohort: PEDBD

Authers: Isabelle Koné-Paut, 1 Fahrad Shahram, 2 Martha Darce-Bello, 1 Luca Cantarini, 3 Rolando Cimaz, 4 Marco Gattorno, 5 Jordi Anton, 6 Michael Hofer, 7 Bouchra Chkirate, 8 Kenza Bouayed, 9 Ilknur Tugal-Tutkun, 10 Jasmin Kuemmerle-Deschner, 11 Hélène Agostini,

Abstract: We aimed to describe the main features of Behçet’s disease (BD) in children in the largest prospective cohort to date and to propose a classification. Methods An international expert consensus group was formed to define a data set of minimal symptoms for the inclusion of patients. Patients were entered prospectively during 66 months. Experts classified patients on a consensus basis. The concordance of two international classifications was analysed in confirmed patients with BD. Comparisons of subgroups of patients helped define consensus ... سال انتشار: 2015
 

ملاس يگدنز كبس ذاختا رد روحم يروئت يشزومآ همانرب ريثأتينيلاب ييامزآراك هعلاطم كي :وناز زورترآ هب نايلاتبم رد

مولف: 217-209 :1393 زییاپ ،3 هرامش ،32 هرود ،ناريا يملاسا يروهمج يكشزپ ماظن نامزاس يملع هلجم

خلاصه: یتلکسا ینلاضع متسیس هدننک ناوتان تلالاتخا نیرتلوادتم زا وناز یگدییاس :هنیمز ملاس يگدنز كبس ذاحتا .دوش یم لاتبم دارفا یمسج ییاناوتان و درد بجوم هک تسا نيرت مهم وناز زورترا يتظفاحم ياهراتفر هب نا�سر بيسآ ياهراتفر رييغت هلزنم هب يشزومآ همانرب ريثأت يسررب هعلاطم نيا زا فده .تسا لكشم نيا زا يريگ�شيپ هار.تسا وناز زورترآ هب نايلاتبم رد ملاس يگدنز كبس ذاختا رد روحم يروئت لاتبم ناراميب زا رفن 168 ... سال انتشار: 2015
 

The International Criteria for Behcet’s Disease (ICBD): a collaborative study of 27 countries on the sensitivity and specificity of the new criteria

Authers: F. Davatchi, 1, *, † S. Assaad-Khalil, 2, † K.T. Calamia, 3, † J.E. Crook, 4, † B. Sadeghi-Abdollahi, 1, † M. Schirmer, 5, † T. Tzellos, 6, † C.C. Zouboulis, 6, 7, 8, *, † M. Akhlagi, 1 A. Al-Dalaan, 9 Z.S. Alekberova, 10 A.A. Ali, ،A.R. Jamshidi،A. Nadji،F. Shahram،H. Shams،N. Ziaei1

Abstract: Behcet’s disease (BD) is a chronic, relapsing, inflammatory vascular disease with no pathognomonic test. Low sensitivity of the currently applied International Study Group (ISG) clinical diagnostic criteria led to their reassessment. Methods An International Team for the Revision of the International Criteria for BD (from 27 countries) submitted data from 2556 clinically diagnosed BD patients and 1163 controls with BD-mimicking diseases or presenting at least one major BD sign. These were randomly divided into ... سال انتشار: 2013