duchenne

duchenne

1. Investigation and Analysis on Fertility Condition of Female Carriers from 23 Families of Duchenne Muscular Dystro- phy.

23例假肥大型肌营养不良患者家系中女性生育情况的调查与分析

2. Genetic Analysis of 60 Duchenne Muscular Dystrophy (DMD) or Becker Muscular Dystrophy (BMD) Patients Using Dystrophin cDNA

60例 DMD/BMD 患者用抗肌营养不良 cDNA 探针的基因分析

3. Duchenne Becker muscular dystrophy

BMD

4. The muscle cell tropism of CVB 1 provides experimental basis for constructing new vector targeting to muscle cells in gene therapy of Duchenne muscular dystrophy.

CVB1 的嗜肌肉特性为在DMD等肌萎缩症的基因治疗中探索靶向载体提供了实验依据

5. The pathophysiology of dko mouse was very similar to Duchenne muscular dystrophy (DMD), and dko mouse is an ideal animal model for study of DMD clinical therapy.

dko小鼠的病理生理学表现与DMD极为相像,是DMD临床治疗研究的理想疾病动物模型。

6. Studies on Gene Deletion in Duchenne Muscular Dystrophy and Its Application in Gene Diagnosis

DMD基因缺失及其在基因诊断中的应用

7. Deletion and Duplication in Duchenne Muscular Dystrophy (DMD)Gene Studied and Applied in Gene Diagnosis

DMD基因缺失和重复及其在基因诊断中的应用

8. Detection of Duchenne and Becker muscular dystrophy patients by DNA microarray

DNA微阵列技术检测Duchenne型/Becker型肌营养不良患者的临床应用研究

9. Duchenne and Becker muscular dystrophy (DMD/BMD)

Duchenne型/Becker型肌营养不良

10. The Electrocardiographic Changes in Children with Duchenne Muscular Dystrophy and Its Clinical Significance

Duchenne型肌营养不良儿童心电图改变及其临床意义的探讨

11. A Clinical Analysis of l05 Cases of Duchenne Mascular Dystrophy and Study on Its Pathogenesis(with freeze-fractural electron microscopic observation on muscle plasma membrane of 4 cases)

Duchenne型肌营养不良症105例临床分析及其发病机制的探讨（附4例肌纤维膜冷冻断裂电镜检查）

12. Duchenne muscular dystrophy (DMD): A quantitative study of type 2C fibers and muscle satellite cells.

Duchenne型肌营养不良症:2c型纤维与肌卫星细胞的定量研究

13. A Comparative Study on the Differences of in vitro Myogenesis between Patients with Duchenne Muscular Dystrophy and Normal Person

Duchenne型肌营养不良症与正常肌组织体外成肌过程的对比研究

14. Analysis of affected muscle selectivity and laboratorial diagnosis of duchenne muscular dystrophy

Duchenne型肌营养不良症受累肌肉选择性及实验室诊断分析

15. Freeze-fracture electron microscopy observation on erythrocyte plasma membrane of carriers of duchenne muscular dystroply

Duchenne型肌营养不良症基因携带者红细胞冷冻断裂电镜观察

16. Study on the early treatment of cardiac injury caused by Duchenne muscular dystrophy

Duchenne型肌营养不良症心肌损害早期的治疗研究

17. Progress in research on the preimplantation genetic diagnosis for Duchenne muscular dystrophy

Duchenne型肌营养不良症植入前遗传学诊断研究进展

18. Study on the Gene Knockout Model Mice of Duchenne Muscular Dystrophy

Duchenne型肌营养不良症模型鼠的研究

19. Diagnosis of Duchenne muscular dystrophy by CT

Duchenne型肌营养不良症的CT诊断研究

20. A study of the prenalal gene diagnosis in Duchenne muscular dystrophy

Duchenne型肌营养不良症的产前基因诊断研究

21. Freeze-fracture Electron Microscopic Observation on Muscle Plasma Membrane of Duchenne Muscular Dystrophy

Duchenne型肌营养不良症的冷冻断裂电镜观察

22. The Detection of the Carriers with Duchenne Muscular Dystrophy

Duchenne型肌营养不良症的基因携带者的检出

23. Gene diagnosis of Duchenne muscular dystrophy

Duchenne型肌营养不良症的基因诊断

24. Cell therapy for Duchenne muscular dystrophy

Duchenne型肌营养不良症的细胞治疗

25. The study of Membrane Abnormalities in Duchenne Muscular Dystrophy

Duchenne型肌营养不良症肌细胞膜异常的研究

26. Construction of a Cellular Model for Drug Screening of Duchenne Muscular Dystrophy

Duchenne型肌营养不良症药物筛选模型的构建

27. The abnormal distribution and significance of lectin receptors in skeletal muscle of the patients with duchenne mys-cular dystrophy (DMD).

Duchenne型肌营养不良症骨骼肌凝集素受体异常分布及其意义

28. Prenatal Diagnosis of Duchenne Muscular Dystrophy (DMD) by DNA Polymorphism Analysis

Duchenne型肌营养不良症高危妊娠的产前基因诊断

29. Freeze frecture Electron Microscopic Observation?On Erythrocyte Plasma Membrane of Duchenne Muscular Dystrophy

Duchenne型肌营养不良红细胞冷冻断裂电镜观察

30. ERYTHROCYTE MEMBRANE CARBOHYDRATES, LIPIDS AND Ca~(2+)-Mg~(2+) ATPase IN DUCHENNE MUSCULAR DYSTROPHY

Duchenne型肌营养不良红细胞膜糖、脂质及Ca~(2+)-Mg~(2+)ATP酶的变化

31. Prenatal gene diagnosis in high danger families with Duchenne muscular dystrophy

Duchenne肌营养不良症高风险家系的产前基因诊断

32. Duchenne muscular dystrophy carrier detection

Duchenne肌营养不良载体检测

33. LGMD2I presenting with a characteristic Duchenne or Becker muscular dystrophy phenotype

LGMD2I是Duchenne型或Becker型肌营养不良的特征性表型

34. Duchenne's trocar

[医] 杜兴氏套针(从深部采取组织用)

35. Duchenne's attitude

[医] 杜兴氏姿势(斜方肌麻痹时的肩部姿势)

36. Duchenne's sign

[医] 杜兴氏征(膈麻痹或心包积液时的一种望诊体征)

37. Duchenne's disease

[医] 杜兴氏病(脊髓病性肌萎缩, 延髓麻痹, 运动性共济失调, 脊髓痨)

38. Duchenne's symptom

[医] 杜兴氏症状(膈肌麻痹症状)

39. Duchenne's syndrome

[医] 杜兴氏综合征(唇舌咽麻痹)

40. Duchenne's paralysis

[医] 杜兴氏麻痹(延髓性麻痹, 欧-杜二氏麻痹)

41. A STUDY ON RESTRICTION FRAGMENT LENGTHPOLYMORPHISM OF HUMAN X_p21 REGION IN A DUCHENNE MUSCULAR DYSTROPHY FAMILY

一个Duchenne型肌营养不良症家系的调查和Xp21区RFLP分析

42. Australian Neuromuscular Research Institute (ANRI) executive officer Brett Tizard says the group has designed a "genetic band-aid" to repair the muscle protein that causes Duchenne muscular dystrophy.

一个来自澳大利亚珀斯的研究小组说：他们找到了迄今为止最有希望成功治疗致病进行性肌营养不良的方法。

43. Keywords Nitric-oxide synthase;Muscle;skeletal;Immunohistochemistry;Muscular dystrophy;Duchenne;

一氧化氮合酶;肌;骨骼;免疫组织化学;肌营养不良;杜氏;

44. Detection of gene deletions in 134 cases of Duchenne and Becker muscular dystrophy with the technic of two step multiplex polymerase chain reaction (PCR)

两步-多重PCR诊断134例假肥大型进行性肌营养不良症基因缺失

45. Dystrophin, the protein missing in Duchenne muscular dystrophy patients, conducts this energy across the muscle cell's membrane, protecting the fiber.

但肌节产生的力量，如果没有向外引导的话，也会伤害肌纤维，DMD患者所缺乏的肌肉萎缩蛋白，能将这股力量传导到肌肉细胞膜上，而保护肌纤维。

46. tudies on Duchenne muscular dystrophy during the past 10 years are briefly reviewed.

作者综述了10年来对Duchenne型肌营养不良症（DMD）的研究概况。

47. Duchenne muscular dystrophy

假肥大型肌营养不良

48. Keywords Duchenne muscular dystrophy;Serum creatine kinase;Change;Regularity;Child;

假肥大型肌营养不良;血清肌酸激酶;变化;规律;儿童;

49. A clinical study on CK MM in patients with Duchenne muscular dystrophy

假肥大型肌营养不良患者肌型肌酸激酶亚型的临床研究

50. Clinical application of prenatal gene diagnosis of Duchenne and Becker muscular dystrophy

假肥大型肌营养不良症产前基因诊断的临床应用

51. Prenatal molecular diagnosis of Duchenne and Becker muscular dystrophy

假肥大型肌营养不良症的产前基因诊断

52. The Quantitative Study on Muscular Fiber Type in Duchenne Muscular Dystrophy

假肥大型进行性肌营养不良症肌纤维分型的定量研究

53. Duchenne and Becker muscular dystrophy

假肥大肌营养不良

54. Keywords Duchenne and Becker muscular dystrophy;Dystrophin;Twins;

假肥大肌营养不良;肌营养不良蛋白;双生子;

55. Keyword： Duchenne muscular dystrophy;

关 键 词： 杜氏肌营养不良;

56. Keywords Duchenne and Becker muscular dystrophy;prenatal gene diagnosis;gene linkage analysis;

关键词假肥大性肌营养不良症;产前基因诊断;基因连锁分析;

57. Keywords Duchenne muscular dystrophy;single lymphocyte;genetic diagnosis;two-time duplex PCR;

关键词肌营养不良;单个淋巴细胞;遗传学诊断;二重二次PCR;

58. As a result, in both aging and Duchenne MD, muscle fibers die and are replaced by infiltrating fibrous tissue and fat.

因此，在肌肉老化和DMD中，肌纤维同样都会死亡，并被渗入的纤维化组织和脂肪所取代。

59. First of all, mutation analysis of Duchenne muscular dystrophy (DMD) gene was carried out by CE coupled with multi-PCR technique.

在医学领域主要表现为以基因突变检测，基因家系连锁分析，特定基因的PCR产物直接检测为基础的基因诊断。

60. 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.

基于沙丁胺醇缓释剂治疗肌营养不良症患儿的前期研究，作者进行了一项随机、双盲、安慰剂对照的交叉设计的研究。

61. Approximately one in every 3,500 boys worldwide is afflicted with Duchenne muscular dystrophy with 20,000 new cases reported each year.

大约每3500男孩全世界患有杜氏肌营养不良的20000新病例每年报告。

62. Clinical pathologic studies and genetic analysis of a female Duchenne muscular dystrophy family

女性假肥大型肌营养不良症家系的临床病理和基因分析

63. female Duchenne syndrome

女性杜钦型肌营养不良综合征

64. Keywords pregnantal blood;erythroblasts;duchenne muscular dystrophy;prenatal diagnosis;

孕妇外周血;有核红细胞;杜氏进行性肌营养不良;产前诊断;

65. Carrier detection of Duchenne and Becker muscular dystrophy by quantitative multiplex PCR

定量PCR检测缺失型DMD/BMD携带者的研究

66. As for your friend's children, they have a mutation causing their Duchenne muscular dystrophy that will not be helped by the drug we are currently trialling.

对于你朋友的孩子，有个基因导致杜氏抗肌萎缩蛋白缺失，而目前的治疗并不能对这个基因有所作用。

67. The Proportion and Clinical Feature of Duchenne Muscular Dystrophy With Autosomal Recessive Inheritance

常染色体隐性遗传的类Duchenne肌营养不良临床特征及其发生比率的估计值分析

68. Intramembrane proteinic particles of muscle plasma membrane were calculated with freeze-fracture electron microscopy in 4 cases of Duchenne muscle dystrophy (DMD) .

应用冷冻断裂电镜技术对Duchenne型肌营养不良症(DMD)的骨胳肌标本4例(异常组),正常标本2例(正常组)肌细胞质膜的蛋白颗粒进行电镜观察。

69. Intramembrane protein particles of erythrocyte plasma membrane were calculated with freeze frecture electron microscopy in 5 cases of Duchenne muscular dystrophy (DMD).

应用冷冻断裂电镜技术，对5例Duchenne型肌营养不良症（DMD）的血液标本（DMD组）和3例正常标本（对照组）红细胞质膜的蛋白颗粒进行观察。

70. Detection deleted Duchenne muscular dystrophy carriers by fluorescence quantitative polymerase chain reaction.

应用荧光定量PCR检测缺失型DMD携带者的研究

71. To explore the application of erythrocyte of freeze-fracture electron microscopy in the diagnosis of carriers of Duchenne muscular dystrpphy (DMD).

探讨红细胞冷冻断裂电镜术在Duchenne型肌营养不良症基因携带者诊断中的应用。

72. Abstract: Objective To investigate the apoptosis of skeletal muscles in mdx mice,and study the effect of apoptosis on the pathogenesis in Duchenne muscular dystrophy (DMD).

摘 要：目的 研究mdx鼠体内骨骼肌细胞凋亡情况，探讨凋亡对 Duchenne型肌营养不良症（DMD）的发生发展所起的作用。

73. Abstract Objective:To study the changes of isoforms of creatine kinase-muscular model(CK-MM) in patients with Duchenne muscular dystrophy(DMD) for the purpose of early diagnosis and evaluation.

摘要目的：研究假肥大型肌营养不良(DMD)患者肌型肌酸激酶(CK-MM)亚型的变化，为早期诊断和评价病情提供依据。

74. Keywords nonsense mutation;genetic disease;Duchenne muscular dystrophy（DMD）;cystic fibrosis;PTC124;

无义突变;遗传性疾病;杜兴肌营养不良;囊性纤维病变;PTC124;

75. DEVELOPMENT OF PRENATAL UNHURT DIAGNOSIS OF X-LINKED LETHAL GENETIC-DISEASE DUCHENNE MUSCULE DYSTROPHY(DMD)

无创伤性产前基因诊断X-连锁隐性遗传病Duchenne型肌营养不良(DMD)技术的建立

76. Individuals with Duchenne muscular dystrophy usually lack dystrophin completely while thosewith Becker muscular dystrophy have dystrophinof an altered size.

是最常见的一类进行性肌营养不良症。

77. Duchenne muscular dystrophy(DMD) takes up 75%(12 cases) in 16 PMD cases,which slightly higher than reference reported.

本组16例PMD中DMD占75%(12/16),比文献报道稍高[2];

78. Duchenne's pseudohypertrophic muscular dystrophy

杜兴(氏)假性肥大性肌营养不良

79. Duchenne's type

杜兴(氏)型:假肥大型肌营养不良

80. Duchenne's type muscular dystrophy

杜兴(氏)型肌营养不良