目的对一个遗传性异常纤维蛋白原血症家系进行表型和基因型分析。
Objective To analyze the phenotype and genotype of a family with inherited dysfibrinogenemia.
表明纤维蛋白原结合唾液酸的水平可作为诊断肝硬化获得性异常纤维蛋白血症的理想指标。
Polymerization of fibrin monomer was inverse ratio with fibrinogen bound sialic acid. It suggests that fibrinogen boud sialic acid levels may be diagnostic index acquired dysfibrinogenaemia.
还有其他一些夫妇在他们做出决定或计划之前，他们想获得婴儿是否有唐氏综合症、囊胞性纤维症或其他遗传异常疾病。
Still other couples want to be armed with the information that their unborn child will have Down's syndrome cystic fibrosis or other genetic abnormalities before they make decisions or plans.
纤维细胞积聚不足或者过多都能导致组织功能异常。
Either inadequate or excessive accumulation of fibroblasts could result in abnormal tissue function.
饮食中摄入纤维较少的人群发生异常高血糖水平的风险越高。
And those who got little fiber in their diets were at greater risk of developing abnormally high blood sugar levels.
还有其他一些夫妇在他们做出决定或计划之前，他们想获得婴儿是否有唐氏综合症、囊胞性纤维症或其他遗传异常疾病。
Still other couples want to be armed with the information that their unborn child will have Down's syndrome, cystic fibrosis or other genetic abnormalities before they make decisions or plans.
骨骼肌活检病理检查可见破碎样红纤维及异常线粒体。
The biopsy in the skeletal muscle showed ragged red fiber and abnormal mitochondria.
材料与方法：收集45例由手术病理证实的骨纤维异常增殖症的X线、CT和MRI表现特点。
Materials and Methods: Collects 45 cases of fibrous dysplasia of bone which confirms by the surgery pathology X, ct, and MRI performance characteristic.
本报告认为该肾动脉肌纤维发育异常是后天的，可能不是先天性的。
The report suggests that fibromuscular dysplasia of the renal arteries is acquired and may not be presented from birth.
报告4例全身性骨纤(选自一组356例骨纤维异常增殖症，发病率约占1%)，3例以病理证实，病变侵犯全身所有长、短、扁骨和不规则骨。
This is to report 4 cases of systemic fibrous dysplasia selected from a group of 356 cases of the disease with a incidence of 1%. 3 of them were proved pathologically.
硬皮病其他常见的影像学表现包括：肺纤维化、消化道蠕动异常（最常见于食管）。
Other common radiologic findings in scleroderma include pulmonary fibrosis and dilation and dysmotility of the gastrointestinal tract (most commonly affecting the esophagus).
骨纤维异常增殖可以药物治疗，也可以手术植骨或者固定。
Fibrous dysplasia may be treated medically with bisphosphanates or surgically with bone graft or fixation.
纤维连接蛋白和层粘连蛋白低表达在血窦壁异常结构形成中有重要作用。
The low expression of Fibronectin and Laminin plays an important role in the pathogenesis of the abnormal sinusoid wall in OCH.
结节硬化的颅内异常与基因上存在异常的神经元沿异常的放射冠神经交织纤维的移行异常有关。
The intracranial abnormalities of tuberous sclerosis are thought to be associated with disordered migration of dysgenetic neurons along abnormal radial glial fibers.
目的：评价磁共振弥散张量纤维束成像技术在大脑胶质瘤所导致的大脑白质纤维异常改变中的价值。
Objective: To evaluate the usefulness of diffusion tensor tracking in abnormal cerebral white matter induced by cerebral gliomas.
在未来的造纸工业中，提高废纸在纤维原料中的比重异常重要。
It is important to raise the proportion which waste paper holds in the fiber materials in future papermaking industry.
因此，创伤后成纤维细胞出现异常必将影响创伤愈合过程，甚至引起创伤难愈。
Therefore, fibroblasts are the most important cell types during wound healing, its abnormalities will inevitably impair wound healing.
结果11例患者中颅底肿瘤6例，颅底骨纤维异常增生症3例，脑膜脑膨出2例。
Results Among 11 patients, there were 6 patients with skull base tumor, 3 patients with fibrosis hyperplasia, 2 patients with encephalomeningocele.
目的：分析骨纤维异常增殖症的MRI与CT特点，探讨其特点与病理之间的关系。
Purpose: to analysis the MRI and CT features of fibrous dysplasia of bone, to evaluate the correlation between the MRI and pathologic findings.
骨质纤维的发育异常影响到多处骨头。
肥厚也可使大量肌纤维产生异常高的压力。
Hypertrophy also allows the abnormally high pressure to be developed by a greater number of myofibrils.
随访期间未发生肺纤维化、继发肿瘤及生长发育异常等不良事件。
No pulmonary fibrosis, secondary malignancies and abnormity of growth and development were found during follow-up.
阐明淀粉样纤维的毒性机制对于研制用于治疗淀粉样疾病的药物显得异常重要。
It is essential to elucidate the cytotoxic mechanism of amyloid fibrils for developing novel medicines for the treatment of amyloid diseases.
结论多纤维分叉异常是导致部分各向异性降低的原因之一，但多纤维分叉现象并不一定影响部分各向异性FA值。
Conclusion Abnormal crossing of multi-fiber within a voxel is one of reasons to cause diffusion anisotropy change. Abnormal crossing of multi-fiber may not affect the FA value.
前言：目的：探讨螺旋CT在诊断骨纤维异常增殖症中的价值。
Objective: To evaluate the worth of spiral ct in diagnosis of fibrous dysplasia of bone.
肝纤维化是各种致病因素导致肝内结缔组织异常增生的肝内弥散性细胞外基质过度沉积的病理过程。
Hepatic fibrosis was caused by intrahepatic connective tissue dysplasia due to many pathological factors, Which was a massive diffuse ECM deposition pathological process in human body.
单体素内多纤维分叉异常不一定会影响白质纤维的部分各向异性；
Multi-fiber within a voxel might not result in white matter abnormalities;
单体素内多纤维分叉异常不一定会影响白质纤维的部分各向异性；
Multi-fiber within a voxel might not result in white matter abnormalities;
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