نتایج جستجو برای: sma dissection

تعداد نتایج: 60736  

ژورنال: پژوهش در پزشکی 2004
آرش محمدی توفیق, , ابوالفضل افشار فرد, , محمد مظفر, ,

  Superior mesenteric artery (SMA) aneurysm is one of the rare visceral aneurysm with different clinical manifestations. There are few reported cases worldwide, each being reported in a specific situation. In this paper, a rare case of disease with fistulization of SMA to jejunum, causing massive GI bleeding is reported. Having DSA studies completed, the patient was operated and SMA was ligated...

Journal: :civil engineering infrastructures journal 0
mohammad hooshmand m.sc. graduate, young researchers and elite club, tabriz branch, islamic azad university, tabriz, iran behzad rafezy associate professor, department of civil engineering, sahand university of technology, tabriz, iran yousef hosseinzadeh associate professor, faculty of civil engineering, university of tabriz, tabriz, iran hamid ahmadi assistant professor, faculty of civil engineering, university of tabriz, tabriz, iran

the seismic performance of hybrid braces composed of steel and shape memory alloy (sma) was investigated in this paper. six types of hybrid braces were used, constituted by sma content of 0, 20, 40, 60, 80, and 100%. a nonlinear dynamic analysis was performed under el centro earthquake records, with the maximum acceleration of 0.6g and 0.9g. our results showed that the seismic performance, i.e....

Journal: :Saudi medical journal 2012
Eman E Emam Ali S Sawan Soha R Al-Tamimi Rihab M Molah

Malignant spiradenoma/cylindroma of the vulva is an extremely rare adnexal tumor. We report the clinicopathological features of a 58-year-old woman who presented with malignant spiradenoma/cylindroma originating in the vulva and metastasized to the inguinal lymph nodes. Surgical excision with adequate margins and lymph node dissection was performed. Sections from the case were stained with Peri...

Journal: :iranian journal of child neurology 0
afrooz rashnonejad 1.young researchers and elites club, north tehran branch, islamic azad university, tehran, iran huseyin onay 2. department of medical genetics, faculty of medicine, ege university, izmir, turkey tahir atik 3. department of pediatrics, faculty of medicine, ege university, izmir, turkey ozlem atan sahin 4. department of molecular biology and biochemistry, health sciences institute, acibadem university, istanbul, tureky sarenur gokben 5. division of child neurology, department of pediatrics, faculty of medicine, ege university, izmir, turkey hasan tekgul 5. division of child neurology, department of pediatrics, faculty of medicine, ege university, izmir, turkey

how to cite this article: rashnonejad a, onay h, atik t, atan sahin o, gokben s, tekgul h, ozkinay f. molecular genetic analysis of survival motor neuron gene in 460 turkish cases with suspicious spinal muscular atrophy disease. iran j child neurol. autumn 2016; 10(4):30-35. abstract objective to describe 12 yr experience of molecular genetic diagnosis of spinal muscular atrophy (sma) in 460 ca...

2017
Adama Zongo Pawan Khera Mahamadou Sawadogo Yaduru Shasidhar Manda Sriswathi Manish K. Vishwakarma Philippe Sankara Bonny R. Ntare Rajeev K. Varshney Manish K. Pandey Haile Desmae

Groundnut (Arachis hypogaea L.) is an important oilseed and food crop of the world. Breeding for disease resistance is one of major objectives in groundnut breeding. Early leaf spot (ELS) is one of the major destructive diseases worldwide and in West Africa, particularly in Burkina Faso causing significant yield losses. Conventional breeding approaches have been employed to develop improved var...

Journal: :iranian journal of child neurology 0
m.r. salehi omran pediatric neurologist,babol university of medical sciences a. ghabeli juibary general physician

abstract objective autosomal recessive spinal muscular atrophy (sma) is, after cystic fibrosis, the second most common fatal monogenic disorder and the second most common hereditary neuromuscular disease after duchenne dystrophy. the disease is characterized by degeneration of anterior horn cells leading to progressive paralysis with muscular atrophy. depending on the clinical type (werdnig- ho...

2015
Li‐Xin Jia Wen‐Mei Zhang Hong‐Jia Zhang Tao‐Tao Li Yue‐Li Wang Yan‐Wen Qin Hong Gu Jie Du

Thoracic aortic aneurysm/dissection (TAAD) is characterized by excessive smooth muscle cell (SMC) loss, extracellular matrix (ECM) degradation and inflammation. In response to certain stimuli, endoplasmic reticulum (ER) stress is activated and regulates apoptosis and inflammation. Excessive apoptosis promotes aortic inflammation and degeneration, leading to TAAD. Therefore, we studied the role ...

ژورنال: :پژوهش در پزشکی 0
نور امیر مظفری گروه میکروبشناسی و ویروس شناسی، دانشگاه علوم پزشکی ایران هما فروهش تهرانی علیرضا سالک مقدم محمد روستایی بهرام روادگر منیژه قاسمی

سابقه و هدف : اسهال یکی از علل مهم مرگ و میر کودکان در کشورهای جهان سوم می باشد. طبق آمار منتشره از طرف سازمان بهداشت جهانی (who) سالانه حدود 12 میلیون کودک در سراسر جهان بر اثر ابتلاء به بیماریهای مختلف جان خود را از دست می دهند که سهم بیماری اسهال ، 5 میلیون نفر در سال می باشد.باکتری ها با مکانیسم های مختلفی در ایجاد اسهال نقش دارند. یکی از مهمترین مکانیس ها تولید انتروتوکسین از جمله انتروتوک...

Journal: :iranian journal of otorhinolaryngology 0
ali bagherihagh department of otorhinolaryngology, baqiyatallah university of medical sciences, tehran, iran. seyed mousa sadr hosseini department of otorhinolaryngology, tehran university of medical sciences, tehran, iran.

introduction:cold dissection (cd) and bipolar cautery dissection (bcd) techniques are two common surgical tonsillectomy procedures used in the clinic. obstruction has become more prevalent as the major surgical indication and is most prominently observed in younger children.case report:  in this report, we aimed to explain the abovementioned surgical techniques in detail and compare the results...

2017
Xiang Lin Jin-Jing Li Wen-Jing Qian Qi-Jie Zhang Zhong-Feng Wang Ying-Qian Lu En-Lin Dong Jin He Ning Wang Li-Xiang Ma Wan-Jin Chen

Spinal muscular atrophy (SMA) is a devastating motor neuron disease caused by mutations of the survival motor neuron 1 (SMN1) gene. SMN2, a paralogous gene to SMN1, can partially compensate for the loss of SMN1. On the basis of age at onset, highest motor function and SMN2 copy numbers, childhood-onset SMA can be divided into three types (SMA I-III). An inverse correlation was observed between ...

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