脑白质病,Leukoencephalopathy
1)Leukoencephalopathy脑白质病
1.CT and MRI Diagnosis of Leukoencephalopathy in Adults;成人脑白质病的CT及MRI诊断
2.Analysis of imaging and clinical feature of leukoencephalopathy with hearing loss first complaint首诊为听力下降的脑白质病患者影像学及临床特征分析
英文短句/例句

1.CT and Clinical Analysis of Arteriosclerosis Disease of Tapetum White Matter动脉硬化性脑白质病的CT与临床分析
2.Clinical Risk Factors of White Matter Lesions in Patients with Ischemic Cerebral Disease缺血性脑血管病患者脑白质病变的临床相关因素分析
3.Rank correlation between white matter lesions and intracranial atherosclerosis脑白质病变与颅内动脉硬化的相关性研究
4.Correlation between Leukoencephalopathy and Atherosclerosis脑白质病变与动脉粥样硬化的相关性分析
5.PML lesions are found in white matter and at the corticomedullary junction of cerebral and cerebellar cortex.PML病变见于脑和小脑的白质和皮质-白质交界处。
6.Clinical analysis of the patients with cerebrovascular disease accompanied leukoaraiosis;脑血管病伴发脑白质疏松症临床分析
7.Clinical and EIF2B Gene Mutations in Patients with Vanishing White Matter;白质消融性白质脑病临床与EIF2B基因突变研究
8.A Study of Pathomechanism of Cerebral Small Vessel in Leukoaraiosis (White Matter Lesions)脑白质疏松(白质损伤)的小血管病理机制研究
9.Functional Study on EIF2B5 Gene Mutations in Vanishing White Matter Disease白质消融性白质脑病致病基因EIF2B5突变蛋白功能研究
10.Such lesions are most common in basal ganglia, deep white matter, and brain stem.此病变多位于基底节、白质深部、脑干。
11.Alexander disease and Canavan disease亚历山大病及海绵状脑白质营养不良
12.Advance research on proteomics in cerebral ischemia disease脑缺血性疾病的蛋白质组学研究进展
13.The Clinical Study of Leukoarasis in Patients with Cerebral Vascular Disease;对脑血管病患者脑白质疏松的临床研究
14.The Epidemiological Study of Heroin Spongiform Leucoencephalopathy in Drug Users;广州市海洛因海绵状白质脑病流行病学调查
15.Study on Neuropathology and Detection of Myelin Basic Protein and Its Antibody in Heroin Spongiform Leukoencephalopathy;海洛因海绵状白质脑病病理与髓鞘碱性蛋白及其抗体检测的研究
16.Eukaryotic translation initiation factor 2B and leukoencephalopathy with vanishing white matter真核细胞翻译启动因子2B与白质消融性白质脑病
17.Study on Neural Pathology and Oligodendrocyte Apoptosis in Heroin Spongiform Leucoencephalopathy Pathogenesis海洛因海绵状白质脑病神经病理及少突胶质细胞凋亡机制研究
18.The so-called mad Cow disease is caused by abnormal proteins coming into contact with neurons in the Brain所谓“疯牛病 ”,是异常蛋白质侵入脑神经原的结果
相关短句/例句

leukoencephalopathy白质脑病
1.Clinical and imaging features of reversible posterior leukoencephalopathy syndrome;可逆性后部白质脑病综合征的临床及影像学特点
2.Imaging diagnosis of reversible posterior leukoencephalopathy syndrome;可逆性后部白质脑病综合征的影像学表现
3.Objective To analyse and investigate the clinical characters, diagnostic criteria, pathogenesis and prevention of heroin leukoencephalopathy (HLE).目的 分析和探讨海络因白质脑病 (heroin leukoencephalopathy,HLE)的临床特点、诊断规律、发病机制及防治经验。
3)white matter lesions脑白质病变
1.Comparison of visual rating scales for white matter lesions on magnetic resonance imaging;脑白质病变MRI视觉分级方法的比较
4)Leukoencephalopathy脑白质病变
1.Exploring into MRI Diagnosis for Child Leukoencephalopathy;MRI诊断儿童脑白质病变的初步探讨
2.The object of this research is normal neonates or children and neonates or children who suspiciously leukoencephalopathy by clinical manifestation or abnormal long T2-WI signal at white matter, to study quantitative ADC values of Diffusion-Weighted Imaging using Siemens 3.本组研究以正常新生儿及儿童或临床上或影像学表现可疑为新生儿或儿童脑白质病变的新生儿或儿童患者为研究对象,应用西门子3。
3.Objective To investigate the correlation between leukoencephalopathy and atherosclerosis.目的研究脑白质病变与动脉粥样硬化的关系。
5)megalencephalic leukoencephalopathy巨脑性白质脑病
6)viral leukoncephalopathy病毒性脑白质病
延伸阅读

X-连锁肾上腺脑白质营养不良X-连锁肾上腺脑白质营养不良 是肾上腺脑白质营养不良较多见的一种类型。致病基因在X染色体上,位于Xq28。本病的酶异常是二十四酰辅酶A连接酶的缺陷,生化特点是极长链脂肪酸分解障碍。病理改变神经系统有广泛的中枢性和周围性白质脱髓鞘,肾上腺皮质有萎缩和发育不良。起病年龄可于儿童和成人,临床症状轻重不等,有的可能长期不出现症状。还有介于儿童型和成人型之间的过渡类型。儿童起病的X-连锁ALD最多见。多在4~10岁间的男孩起病。临床特点是神经、心理、行为异常。神经症状和肾上腺症状可同时或相继出现,并可能单独存在。神经系统症状可见多动、攻击行为、智力低下、学习困难、记忆障碍、退缩等,运动障碍有步态不稳、痉挛性瘫痪。还可见癫痫发作,视、听障碍,视神经萎缩等。肾上腺皮质功能不全时表现为轻重不等的皮肤和黏膜色素增加,变黑,以及失盐征。病程为进行性,多在15岁以内死亡。CT和MRI可查出大脑白质病变,脑脊液可有蛋白和细胞数稍增高,局部有γ球蛋白产生。实验室诊断:血浆和皮肤成纤维细胞中极长链脂肪酸增高,特别是C26脂肪酸增高,C26/C22比值增加。在发生肾上腺皮质功能不全的艾迪生危象时,血中皮质醇减低,不发生危象时,用ACTH刺激试验才能发现肾上腺储备减少。治疗困难。发生肾上腺皮质功能不全时可给以类固醇激素行替代疗法。但对神经系统症状的进展并无影响。