نتایج جستجو برای: sma dissection

تعداد نتایج: 60736  

برزگر, محمد, جبارپور بنیادی, مرتضی, عمرانی, امید,

Background and Objectives: The neuromuscular degenerative disorder, known as spinal muscular atrophy (SMA), is a common fatal disease in neonates. In most patients with SMA, exon 7 and/or exon 8 of SMN1 gene is deleted. It is reported that the deletion of exon 5 from NAIP gene may be involved in the severity of SMA disease. The present study was aimed to evaluate the genotype- phenotype correla...

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: :Cirugia espanola 2014
Mercedes Rubio-Manzanares Dorado Luis Miguel Marín Gómez Juan Serrano Díez-Canedo Javier Padillo Ruiz Miguel Ángel Gómez Bravo

Hepatic arterial vascularization presents great anatomic variability. The vascular configuration described as normal is found in only 55%–75.5% of cases, which means that a large percentage of patients present an anatomic variation. Amongst them, the most frequent variation is the right hepatic artery (RHA), branch of the superior mesenteric artery (SMA). This variation can involve a single rig...

Journal: :Annals of thoracic and cardiovascular surgery : official journal of the Association of Thoracic and Cardiovascular Surgeons of Asia 2002
Satoshi Yamashiro Yukio Kuniyoshi Kazufumi Miyagi Mitsuyoshi Shiumoji Toru Uezu Katsuya Arakaki Kageharu Koja

We report a case of acute type A dissection with ischemic enterocolitis due to blood flow insufficiency in the superior mesenteric artery. A 67 year-old man, with medicated ischemic heart disease and hypertension, presented to another hospital with chest pain radiating to the back and epigastrium. Contrast-enhanced computed tomography revealed a type A dissecting aneurysm, that extended from th...

Journal: :European journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery 2009
Naomichi Uchida Hidenori Shibamura Akira Katayama Norimitsu Shimada Miwa Sutoh

OBJECTIVE To describe the fate of the false lumen remaining in the descending thoracic aorta after extensive primary repair of the thoracic aorta by the modified elephant trunk technique with a stent graft for acute type A aortic dissection, particularly the changes of the false lumen on enhanced CT scanning. METHODS The subjects were 65 consecutive patients who received arch replacement with...

2013
Toshihiko Masui Toyonari Kubota Keiko Aoki Yasutaka Nakanishi Takumi Miyamoto Junko Nagata Koshiro Morino Atsushi Fukugaki Michio Takamura Shinichi Sugimoto Hideyuki Onuma Atsuo Tokuka

Pancreatic cancer patients with para-aortic lymph node metastasis have a poor prognosis and patients living longer than 3 years are rare. We had a patient with pancreatic cancer who survived for more than 10 years after removal of the para-aortic lymph node metastasis. A 57-year-old woman was diagnosed with pancreatic head cancer and underwent a pancreaticoduodenectomy with subtotal gastric res...

پایان نامه :وزارت علوم، تحقیقات و فناوری - دانشگاه گیلان - دانشکده فنی 1393

مخلوط آسفالت گرم با استخوان بندی سنگدانه ای(sma) یک نوع آسفالت گرم با دانه بندی گسسته است که دارای مقاومت بالا در برابر خرابی ها و مناسب برای راه های دارای بار ترافیکی سنگین می باشد. قیر لاستیکی یکی از انواع قیر های دارای ویسکوزیته بالا می باشد. در این پژوهش با استفاده از آزمایش مارشال رفتار استاتیکی مخلوط sma حاوی خرده لاستیک مورد ارزیابی قرار گرفت. از سوی دیگر مقاومت در برابر شیار شدگی، مدول ...

2009
Djamila Bouhalouan Nassima Aissani Bouziane Beldjilali

Résumé. Le principe d’un ordonnancement coopératif selon une modélisation multi-agents résulte du rapprochement des domaines de l’Ordonnancement et de l’Intelligence Artificielle Distribuée. Le travail que nous présentons dans ce papier a pour objectif l’étude de l’adéquation des métaheuristiques avancées dans un SMA dans le cadre de la résolution d’un problème d’optimisation bien défini qui es...

Journal: :medical journal of islamic republic of iran 0
seyed reza kazemi nezhad department of genetics, faculty of science, shahid chamran universityof ahvaz, ahvaz, iran.سازمان اصلی تایید شده: دانشگاه شهید چمران (shahid chamran university) fatemeh mosavi department of genetics, faculty of science, shahid chamran university of ahvaz, ahvaz, iran.سازمان اصلی تایید شده: دانشگاه شهید چمران (shahid chamran university) ali akbar momen ahvaz jundishapur university of medical sciences, iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی جندی شاپور اهواز (ahvaz jundishapur university of medical sciences) hamid galehdari department of genetics, faculty of science, shahid chamran university of ahvaz, ahvaz, iran.سازمان اصلی تایید شده: دانشگاه شهید چمران (shahid chamran university) gholamreza mohamadian genetic counseling centre, khuzestan welfare organization, ahvaz, iran.سازمان های دیگر: khuzestan welfare organization

background: spinal muscular atrophy (sma) is the second most common lethal autosomal recessive disease. it is a neuromuscular disorder caused by degenerative of lower motor neurons and occasionally bulbar neurons leading to progressive limb paralysis and muscular atrophy. the smn1 gene is recognized as a sma causing gene while naip has been characterized as a modifying factor for the clinical s...

Journal: :genetics in the 3rd millennium 0
امید آریانی omid ariani مرتضی بنیادی morteza bonyadi center of excellence for molecular analysis of smn gene biodiversity, department of genetics, faculty of natural sciences, university of tabriz, tabriz, iran محمد برزگر mohammad barzegar

spinal muscular atrophy (sma) is an autosomal recessive neuromuscular disorder characterized by degeneration of spinal cord anterior horn cells, leading to muscular atrophy. sma is clinically classified into three sub-groups based on the age of onset and severity. the majority of patients with sma have homozygous deletions of exons 7 and 8 of the survival motor neuron (smn) gene. the purpose of ...

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