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2017 损伤，炎症和纤维化 Keystone Symposia（2017 Keystone Symposia on Injury, Inflammation and Fibrosis）
损伤 炎症 纤维化
2017/1/13
The meeting will begin on Sunday, March 26 with registration from 16:00 to 20:00 and a welcome mixer from 18:00 to 20:00. Conference events conclude on Thursday, March 30 with a closing plenary sessio...
Magnetic Resonance Elastography for Liver Fibrosis in Methotrexate Treatment
Methotrexate Hepatic Magnetic Resonance Elastography Liver Fibrosis Rheumatoid Arthritis
2013/1/31
Introduction: Hepatic magnetic resonance elastography (MRE) allows for noninvasive assessment of liver fibrosis. The purpose of this study was to evaluate the usefulness of MRE in detecting and quanti...
Infantile convulsions due to hyponatremia caused by Cystic Fibrosis
Cystic fibrosis Infantile convulsions
2009/12/31
Cystic Fibrosis (CF) is an inherited multisystem disorder of children and adults. Characterized chiefly by chronic obstruction and infection of airways, maldigestion and its consequences. It is the mo...
Neutrophil chemotaxis in acutely infected and clinically stable cystic fibrosis patients
Cystic fibrosis neutrophils chemotaxis
2009/7/1
Brochopulmonary infection in cystic fibrosis (CF) patients is associated with chronic progressive lung disease. The role of host factors, such as neutrophil functions, in the progressive pathologic pr...
Detection of Cystic Fibrosis DF508 Mutation in the Çukurova Region
Mutation Cystic Fibrosis Ç ukurova Region
2009/6/29
Cystic fibrosis (CF) is a well-known inherited multisystem disorder characterised primarily by chronic obstructive lung disease and maldigestion. The frequency of the disease varies among ethnic group...
一个常染色体显性遗传先天性眼外肌纤维化家系A Family History of Congenital Fibrosis of the Extraocular Muscle with Autosomal Dominant Inheritance
眼外肌纤维化 家系 常染色体显性遗传
2008/1/20
摘要为寻找疾病相关基因，通过随访调查、体检、病理检查等手段，发现了一眼外肌纤维化家系4代中有15人患有眼外肌纤维化综合征，主要表现先天性上眼睑下垂、下颌上举、头后仰、双眼固定下转位和被动牵拉试验阳性，眼外肌病理检查结果为肌纤维化和玻璃样变性，所有阳性体征者除眼球运动限制程度有区别外，其他眼部症状基本相同。遗传分析表明，该疾病属常染色体显性遗传。该家系可作为寻找眼外肌纤维化疾病相关基因的宝贵资源。A...
Mutation Analysis of CFTR Gene in 70 Iranian Cystic Fibrosis Patients
Cystic fibrosis Cystic fibrosis transmembrane conductance regulator Mutations Iran Single-stranded conformational polymorphism
2010/2/3
Cystic fibrosis (CF) is the most common inherited disorder in Caucasian populations, with over 1400 cystic fibrosis transmembrane conductance regulator (CFTR) mutations. The type of mutations and thei...