myopathy的例句大全

The Experiment of Emergency Treatment and Nursing in 4 Cases of Acute Thyrotoxic Myopathy

4例急性甲亢肌病的抢救护理体会

19 Cases of chronic thyrotoxic myopathy ( CTM) are reported.

对19例慢性甲状腺机能亢进性肌病，进行了回顾性研究。

Electromyographic Study in Patients with Thyrotoxic Myopathy

甲状腺功能亢进性肌病肌电图的研究

We experimentalize in order to investigate these factors whether express in alcoholic myopathy or not.

本实验旨在研究慢性酒精性肌病的发病过程中这些因子是否有表达。

coenzyme q10 deficiency and isolated myopathy

辅酶Q10缺乏和孤立性肌病

Have Raynaud's phenomenon, arthritis, swollen hands, inflammatory myopathy, weakened esophageal peristalsis, such as reduced lung diffusing capacity.

有雷诺现象，关节炎，肿胀手，炎性肌病，食管蠕动减弱，肺弥散功能降低等。

Nonaka myopathy with facial muscle involvement

Nonaka肌病伴面部肌肉受累

Objective To study the mitochondrial DNA deletion of mitochondrial myopathy and mitochondrial encephalomyopathy.

目的为了检测线粒体肌病和脑肌病患者的骨骼肌细胞的线粒体DNA的缺失情况。

Congenital hypertrophic cardiomyopathy, cataract, mitochondrial myopathy and defec-tive oxidative phosphorylation in two sib-lings with Sengers-like syndrome

在2例患有新格斯样综合征的同胞兄弟身上的先天性肥大心肌症、白内障、线粒性肌病和氧化磷酸化反应缺陷

Objective To discuss the clinical and pathologic features as well as pathogenesis of nemaline myopathy.

目的探讨杆状体肌病（NM）临床、病理特点及发病机制。

Conclusions Adult form nemaline myopathy is clinically nonspecific.

结论成人型杆状体肌病临床缺乏特征性。

Adult form nemaline myopathy: two cases report with clinicopathological and ultrastructural study

成人型杆状体肌病二例临床病理和超微结构研究

Objective To investigate the clinical and pathological features of adult form nemaline myopathy.

目的探讨成人型杆状体肌病的临床病理和超微结构特点。

Adult-onset nemaline myopathy and monoclonal gammopathy

成人发病的杆状体肌病伴发单克隆丙球蛋白病

Objective To investigate the clinical manifestations and pathological features of nemaline myopathy ( NM).

目的探讨杆状体肌病的临床表现和病理特点。

Characterization of the muscle involvement in dynamin 2-related centronuclear myopathy

动力蛋白-2相关性中央核肌病的肌肉受累特征

Objective To report the clinical and pathological features of centronuclear myopathy in three Chinese children.

目的报道3例中央核肌病的临床和病理特点，讨论其分类和可能的发病机制。

A clinical and ultrasounic examination was made on 120 sites of voluntary muscle from 29 cases with neuromuscular diseases, including varied muscular dystrophy, polymyositis, diversified neuro-genic myopathy and DMD possible carrier.

对29例神经肌肉疾病（包括多种肌营养不良，多发性肌炎，多种神经原性肌肉病变与DMD可能递体）的120处随意肌进行了临床与超声检查。

Methods By using total mtDNA abstracted from skeletal muscles in the patient with mitochondrial myopathy and encephalomyopathy.

方法从1例线粒体肌病和1例脑肌病（MERRF）患者骨骼肌活检标本中，提取总DNA，以限制性内切酶PvuⅡ酶切，与mtDNA全长探针进行分子杂交。

In pure mitochondrial myopathy and CPEO group, none had the 5 point mutations.

单纯型线粒体肌病组和CPEO组均未发现以上5个位点的突变。