1、

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

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2、

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。

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3、

Electromyographic Study in Patients with Thyrotoxic Myopathy

甲状腺功能亢进性肌病肌电图的研究

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4、

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。

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5、

coenzyme q10 deficiency and isolated myopathy

辅酶Q10缺乏和孤立性肌病

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6、

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。

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7、

Nonaka myopathy with facial muscle involvement

Nonaka肌病伴面部肌肉受累

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8、

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。

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9、

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

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10、

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。

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11、

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。

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12、

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

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13、

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。

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14、

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

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15、

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。

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16、

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

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17、

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。

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18、

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。

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19、

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。

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20、

Skeletal muscle was the main target tissue of diabetic damages. The diabetic myopathy aggravated insulin resistance.

骨骼肌是全身利用葡萄糖最重要的组织之一,也是高血糖损害的主要靶位,骨骼肌病变又使外周胰岛素抵抗加重。

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