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Keyword [Muscular dystrophy]
Result: 41 - 60 | Page: 3 of 10
41. The Analysis Of Clinical And Muscle Pthlogcial Characteristcics Of Limb-girdle Mhscular Dystrophy
42. The Accessment Research Of Myocardial Damage In Duchenne Muscular Dystrophy With Gated Myocardial Perfusion Imaging
43. Gene Diagnosis Of DMD And SMA By Multiplex Ligation-dependent Probe Amplification Combined With DNA/cDNA Sequencing
44. The Expression Of MuRF-1 And MAFbx In Duchenne Muscular Dystrophy And To Analysis Clinical And Pathological Features
45. Gene Diagnosis Of Dmd And Sma By Multiplex Ligation-dependent Probe Amplification Combined With Dna/cdna Sequencing
46. False Duchenne Muscular Dystrophy, Muscle Fiber Typing Of Quantitative Research
47. Three Duchenne Muscular Dystrophy
48. The Natural History Of Clinical And Pathological Features Of Duchenne Muscular Dystrophy
49. The Value Of99Tcm–MIBI SPECT Gated Myocardial Perfusion Tomography In The Progressive Muscle Malnutrition,s Myocardial Involvement
50. Clinical Research On Differen-tiation And Treatment Of Spleen-stomach Deficiency Syndrome Of Duchenne Muscular Dystrophy By Renshenzengli Oral Liquid
51. Molecular Biological And Clinical Study Of Dystrophinopathy
52. Effects Of Salidroside On Weightlessness-induced Muscle Atrophy And Duchenne Muscular Dystrophy As Well As Their
53. The Mechanism Of Cardiac Dysfunction In Burn And Muscular Dystrophy
54. The Clinical, Pathological And Genetic Characteristics Of Oculopharyngeal Myopathy Syndrome
55. Analysis Of The Genetic Characterization Of SSLP-D4Z4-4qA/qB-PLAM In Patients With FSAM And Its Association With Clinical Phenotype In Chinese Han Population
56. Investigation Of Peptide Nucleic Acid In Duchenne Muscular Dystrophy Disease Model
57. Screening, Validation And Mechanistic Studies Of Novel Formulations In Dystrophin-Deficient Mdx Mice
58. The Analysis Of Clinical And Muscle Morphological Features Of Facioscapulohumeral Muscular Dystrophy
59. The Study Of Clinic And Muscle Pathology In Patients With Becker Muscular Dystrophy
60. Mutation Analysis In330Chinese Cases With DMD/BMD And Genetic Analysis In A Fetus With Compound Heterozygous DMD Mutations
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