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- Objective To explore the value of immunofluorescent technique for clinical diagnosing Duchenne muscular dystrophy(DMD),Becker muscular dystrophy(BMD) and Limb-girdle muscular dystrophy(LGMD). 目的探討免疫熒光檢測對Duchenne型、Becker型和肢帶型肌營(yíng)養不良癥(DMD、BMD和LG-MD)臨床診斷的價(jià)值。
- Methods Dystrophin in the muscle tissue of 12 patients with Duchenne muscular dystrophy (DMD), 5 patients with Becker muscular dystrophy (BMD) was analysed by immunohistochemistry,and compared with muscle tissue of 6 patients without neuromuscle disease. 方法 運用免疫組化法對 12例 Duchenne型肌營(yíng)養不良癥 (DMD)患者及 5例 Becker型肌營(yíng)養不良癥 (BMD)患者的肌組織中肌營(yíng)養不良蛋白的表達進(jìn)行分析 ,并用 6例非神經(jīng)肌肉疾病患者的肌組織作為對照。
- Duchenne Becker muscular dystrophy(BMD) 進(jìn)行性肌營(yíng)養不良
- Objective To establish a normative procedure for clinical prenatal gene diagnosis of Duchenne and Becker muscular dystrophy(DMD/BMD). 目的 建立規范的假肥大型肌營(yíng)養不良癥 (DMD/BMD)產(chǎn)前基因診斷程序。
- Individuals with Duchenne muscular dystrophy usually lack dystrophin completely while thosewith Becker muscular dystrophy have dystrophinof an altered size. 是最常見(jiàn)的一類(lèi)進(jìn)行性肌營(yíng)養不良癥。
- The method of STR sequence polymorphism analysis can determine haplotypes at normal status or at risk status, it would be used in prenatal diagnosis and carrier detection in the families of Duchenne and Becker muscular dystrophy. 短串聯(lián)重復順序多態(tài)性分析方法可以準確而迅速地區分正常及風(fēng)險單體型,可用于Duchenne型或Becker型肌營(yíng)養不良家系中檢出攜帶者及產(chǎn)前診斷
- Methods: Fourteen boys with Duchenne or Becker muscular dystrophy, 6 to 11 years old, completed two treatment periods (albuterol and placebo), 12 weeks each, separated by a 12-week washout period. 基于沙丁胺醇緩釋劑治療肌營(yíng)養不良癥患兒的前期研究,作者進(jìn)行了一項隨機、雙盲、安慰劑對照的交叉設計的研究。
- Keywords Duchenne muscular dystrophy(DMD) Becker muscular dystrophy(BMD) Dystrophin Arrector pili muscle Sarcolemma; 杜興型肌營(yíng)養不良;貝克型肌營(yíng)養不良;肌營(yíng)養不良蛋白;立毛肌;肌纖維膜;
- Genetic Analysis of 60 Duchenne Muscular Dystrophy (DMD) or Becker Muscular Dystrophy (BMD) Patients Using Dystrophin cDNA 60例 DMD/BMD 患者用抗肌營(yíng)養不良 cDNA 探針的基因分析
- Duchenne and Becker muscular dystrophy 假肥大肌營(yíng)養不良
- Duchenne and Becker muscular dystrophy (DMD/BMD) Duchenne型/Becker型肌營(yíng)養不良
- Duchenne Becker muscular dystrophy BMD
- Becker muscular dystrophy(BMD) 貝氏進(jìn)行性肌營(yíng)養不良, 假肥大性肌營(yíng)養不良
- Keywords Becker muscular dystrophy;hereditary disease; 貝克氏型肌營(yíng)養不良癥;遺傳病;
- Keywords Duchenne and Becker muscular dystrophy;Dystrophin;Twins; 假肥大肌營(yíng)養不良;肌營(yíng)養不良蛋白;雙生子;
- Prenatal molecular diagnosis of Duchenne and Becker muscular dystrophy 假肥大型肌營(yíng)養不良癥的產(chǎn)前基因診斷
- Detection of Duchenne and Becker muscular dystrophy patients by DNA microarray DNA微陣列技術(shù)檢測Duchenne型/Becker型肌營(yíng)養不良患者的臨床應用研究
- Clinical application of prenatal gene diagnosis of Duchenne and Becker muscular dystrophy 假肥大型肌營(yíng)養不良癥產(chǎn)前基因診斷的臨床應用
- Pulmonary Function Characteristics and Rehabilitation Strategy for Becker Muscular Dystrophy 良性假肥大型肌營(yíng)養不良癥患者肺功能的表現特點(diǎn)與康復對策
- EXPRESSION OF DYSTROPHIN IN MUSCLE TISSSUES OF DUCHENNE AND BECKER MUSCULAR DYSTROPHY TWINS 肌營(yíng)養不良蛋白在假肥大肌營(yíng)養不良雙生子肌組織中的表達