Calculation of Mitral Valve Area in Mitral Stenosis: Comparison of Continuity Equation and Pressure Half Time With Two-Dimensional Planimetry in Patients With and Without Associated Aortic or Mitral Regurgitation or Atrial Fibrillation [0.03%]
二尖瓣狭窄面积测定：对单纯二尖瓣狭窄和合并主动脉反流或左房颤患者的连续方程式和压力半时法与二维超声心动图的关系研究
Roya Sattarzadeh,Anahita Tavoosi,Mohammad Saadat et al.
Roya Sattarzadeh et al.
Accurate measurement of Mitral Valve Area (MVA) is essential to determining the Mitral Stenosis (MS) severity and to achieving the best management strategies for this disease. The goal of the present study is to compare mitral valve area (M...
Relationship Between Sleep Quality, Obstructive Sleep Apnea and Sleepiness During Day With Related Factors in Professional Drivers [0.03%]
职业司机的睡眠质量、阻塞性睡眠呼吸暂停与日间嗜睡及相关因素的关系研究
Samira Joorabbaf Motlagh,Maryam Shabany,Khosro Sadeghniiat Haghighi et al.
Samira Joorabbaf Motlagh et al.
One of the important reasons for accidents is sleepiness.With this description, the sleep disorders are associated with health and mortality, and not only affect the person but also the family and the whole society. Aim of this study was as...
The Effect of Vestibular Rehabilitation Therapy Program on Sensory Organization of Deaf Children With Bilateral Vestibular Dysfunction [0.03%]
平衡功能障碍聋儿前庭感觉再组织康复训练干预效果研究
Amir Abbas Ebrahimi,Ali Ashraf Jamshidi,Guita Movallali et al.
Amir Abbas Ebrahimi et al.
The purpose of this study was to determine the effect of vestibular rehabilitation therapy program on the sensory organization of deaf children with bilateral vestibular dysfunction. This cross-sectional and analytic study was conducted on ...
Randomized Controlled Trial
Acta medica Iranica. 2017 Nov;55(11):683-689. DOI: 2017
PDCD1 Single Nucleotide Polymorphisms in Iranian Patients With Juvenile Idiopathic Arthritis [0.03%]
伊朗幼年特发性关节炎患者的PDCD1单核苷酸多态性研究
Mahdi Mahmoudi,Alireza Rezaiemanesh,Sara Harsini et al.
Mahdi Mahmoudi et al.
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 a...
Association of Transforming Growth Factor-Beta Gene Polymorphisms in Recurrent Aphthous Stomatitis [0.03%]
转化生长因子-β基因多态性与复发性阿弗他口腔炎相关性研究
Hila Yousefi,Shamsolmoulouk Najafi,Mahsa Mohammadzadeh et al.
Hila Yousefi et al.
This study has been conducted to evaluate the allele, genotype and haplotype frequencies of the polymorphic gene coding TGF-β in recurrent aphthous stomatitis (RAS). TGF-β gene typing was done by polymerase chain reaction with sequence-sp...
Association Between IL6-174 G/C Polymorphism and Graves' Disease: A Systematic Review and Meta-Analysis [0.03%]
白细胞介素6启动子-174 G/C多态性与Graves病相关性的系统评价和 meta 分析
Danyal Imani,Ramazan Rezaei,Bahman Razi et al.
Danyal Imani et al.
Several studies have evaluated the association between interleukin-6 (IL-6) -174 G/C polymorphism and Graves' disease (GD); however, the results have been inconsistent. In the current study, a meta-analysis was performed to assess the assoc...
Nima Rezaei,Amene Saghazadeh
Nima Rezaei
A Case With Short Stature, Growth Hormone Deficiency and 46, XX, Xq27-qter Deletion [0.03%]
关于一例身材矮小、生长激素缺乏和46，XX，Xq27-qter缺失患者的报道
Şule Yıldırım,Naci Topaloğlu,Mustafa Tekin et al.
Şule Yıldırım et al.
We report a case of 11-year-old girl with growth retardation and 46, XX, Xq27-qter deletion. The endocrinologic evaluation revealed growth hormone deficiency. In karyotype analysis 46, XX, Xq27-qter deletion was determined. The deletion of ...
Case Reports
Acta medica Iranica. 2017 Oct;55(10):661-663. DOI: 2017
Denosumab Treatment of Severe Disuse Osteoporosis in a Boy With Spinal Muscular Atrophy [0.03%]
用于脊髓性肌萎缩症儿童严重废用性骨质疏松的denosumab治疗
Stepan Kutilek
Stepan Kutilek
Denosumab is a fully human recombinant monoclonal antibody to the receptor activator of nuclear factor-κB ligand. Denosumab is used in the treatment of postmenopausal osteoporosis and cancer-related bone disorders. There are only very scar...
Case Reports
Acta medica Iranica. 2017 Oct;55(10):658-660. DOI: 2017
Pericentric Inversion of Chromosome 9 in an Infant With Ambiguous Genitalia [0.03%]
染色体9臂内 inversion致婴儿外生殖器畸形
Arya Sotoudeh,Parastoo Rostami,Maryam Nakhaeimoghadam et al.
Arya Sotoudeh et al.
Pericentric inversion of Chromosome 9 is one of the most common chromosomal abnormalities, which could be associated with various manifestations in some cases. Herein, a patient is presented with ambiguous genitalia that karyotyping reveale...
Case Reports
Acta medica Iranica. 2017 Oct;55(10):655-657. DOI: 2017