Investigation on artificial blood or substitute blood replace the natural blood [0.03%]
人工血液或代血浆替代天然血液的研究
Sh Keyhanian,M Ebrahimifard,M Zandi
Sh Keyhanian
Blood is a liquid tissue in which dissolved with abundant chemical factors and millions of different cells The reduction of unwanted side effects, especially diseases that emerge through blood such as HIV and hepatitis, has a significant ro...
Bone density in transfusion dependent thalassemia patients in Urmia, Iran [0.03%]
伊朗乌鲁米耶市输血依赖性地中海贫血患者的骨密度
N Valizadeh,F Farrokhi,V Alinejad et al.
N Valizadeh et al.
Background: Patients with thalassemia major and intermedia are susceptible to osteopenia and osteoporosis. The mechanism of osteoporosis in these patients is multifactorial. Transfusion related iron overload in endocrine ...
Seroprovalence of herpes simplex1, 2 IgG antibodies in patients with beta thalassemia in a major tertiary care hospital located in Yazd, Iran [0.03%]
伊朗亚兹德一家大型三级护理医院β珠蛋白生成障碍性贫血患者单纯疱疹病毒1、2型IgG血清学流行率
A Atefi,F Binesh,A Hashemi et al.
A Atefi et al.
Background: Patients with beta thalassemia suffer from increased susceptibility to infections and putridity plays a major role in the patient's morbidity and mortality. The risk of transfusion-transmitted viral infection ...
Sh Ansari,A Baghersalimi,A Azarkeivan et al.
Sh Ansari et al.
Background: With modern medical management, thalassemia major is now extending into adulthood and it is expected to have a negative impact on the quality of life (QOL) of the patients. The aim of this study was to evaluat...
Medical expenses of patients with Favism admitted to 17th Shahrivar Hospital compared to G6PD enzyme screening cost, in north of Iran [0.03%]
伊朗北部 favism 病例患者的医疗费用与 g6pd 酶筛查成本的比较——以沙赫尔瓦尔医院为例
B Darbandi,M Noghbaei,F Mehrabian et al.
B Darbandi et al.
Background: Glucose-6-phosphate dehydrogenase (G6PD) enzyme deficiency is one of the prevalent disorders in Guilan province, northern Iran, causing many patients to suffer from acute hemolysis. This disease has imposed tr...
N Honar,S Kamali,M Karimi
N Honar
Background: We aimed to investigate the frequency of celiac disease in children with β-thalassemia major (B-TM) in Shiraz, southern Iran. Materials and m...
Logo therapy effect on anxiety and depression in mothers of children with cancer [0.03%]
洛伽otherapy对儿童肿瘤患者母亲焦虑抑郁的影响研究
H Delavari,M Nasirian,K Baezegar Bafrooei
H Delavari
Background: Cancer diagnosis among children can cause high stress and anxiety in parents, and they may lose their life expectancy. The present study investigated the effectiveness of Logo therapy on anxiety and depression...
Mosaic and partial monosomy of chromosome 21 in a case with low platelets count [0.03%]
嵌合体21三体及21号染色体部分单体的病例报告及低血小板分析
A Hashemi,Mh Sheikhha,Ma Manouchehri et al.
A Hashemi et al.
Background: Monosomy is defined as the presence of only one chromosome instead of two in humans. Partial monosomy occurs when only a portion of the chromosome is present in a single copy, while the rest has two copies. It...
Assessment of Thiopurine-based drugs according to Thiopurine S-methyltransferase genotype in patients with Acute Lymphoblastic Leukemia [0.03%]
急性淋巴细胞白血病患者根据硫嘌呤甲基转移酶基因型评估硫嘌呤类药物剂量响应关系的研究
F Azimi,M Jafariyan,S Khatami et al.
F Azimi et al.
For the past half century, thiopurines have earned themselves a reputation as effective anti-cancer and immunosuppressive drugs. Thiopurine S-methyltransferase (TPMT) is involved in the metabolism of all thiopurines and is one of the main e...
Family screening for a novel ATP7B gene mutation, c.2335T>G, in the South of Iran [0.03%]
伊朗南部ATP7B基因新突变c.2335T>G的家庭筛查研究
J Manoochehri,R Masoumi Dehshiri,H Faraji et al.
J Manoochehri et al.
Background: Wilson disease (WD) is a rare autosomal recessive disorder, which leads to copper metabolism, due to mutations in ATP7B gene. The gene responsible for WD consists of 21 exons that span a genomic region of abou...