muscular dystrophy - Globe Thesis

Keyword [muscular dystrophy] Result: 121 - 140 \| Page: 7 of 10
121.	Clinical, Imaging, Muscle Pathological And Molecular Genetics Features Of Pseudohypertrophy Muscular Dystrophy
122.	Clinic And Quantitative Skeletal Muscle MRI Study Of Children With Duchenne Muscular Dystrophy
123.	The Construction Of Duchenne And Limb Girdle Muscular Dystrophy Type Muscular Dystrophy Models In Rabbits
124.	Investigation Of Epicardial WT1~+ Cells In Dystrophic Heart And Immortalization Of Mouse Cardiosphere-derived Stem Cells
125.	Clinical And Mutational Analysis Based On A Comprehensive Database Of Duchenne Muscular Dystrophy And Dystrophin Gene Modification By CRISPR/Cas9 System
126.	Generation Of Non-integration Induced Pluripotent Stem Cells From Chorionic Villi Cells Of A Duchenne Muscular Dystrophy Fetus
127.	Clinical,Pathological And Molecular Biological Study Of Dysferlinopathy
128.	Research Of Gait Characteristics Of Duchenne/becker Muscular Dystrophy Children By Three-Dimensional Gait Analysis System
129.	A Study On The Genetic Mutation And The Protein Expression Of Dystrophin Gene
130.	Application Of MLPA In Molecular And Prenatal Diagnosis Of Ducheime Muscular Dystrophy
131.	Investigation Of Therapeutic Molecular Compounds In Duchenne Muscular Dystrophy
132.	Haplotype-Based Noninvasive Prenatal Testing For Duchenne Muscular Dystrophy And Becker's Muscular Dystrophy
133.	Clinical,Pathological And Genetic Studies Of Becker Muscular Dystrophy
134.	A Preliminary Study On The Differentiation Of Myoblasts Induced From H1cells And The Deletion Of Exon 50-51 Of The DMD Gene
135.	Observational Study On The Infection Efficiency Of Mesenchymal Stem Cells Derived From Amniotic Fluid Of A Duchenne Muscular Dystrophy Fetus By Three Viruses
136.	Clinical Observation Of Low Dose Glucocorticoid Therapy In Children With Duchenne Muscular Dystrophy
137.	The Correlation Of X Chromosome Inactivation And The Clinical Manifestions Of DMD Female Carriers
138.	Study On Pathogenicity Of A Novel Splicing Mutation For LMNA Gene Causing Limb Girdle Muscular Dystrophy 1B
139.	Association Of Phenotype-Genotype And Methylation In 4q35-D4Z4/PAS Region Of FSHD
140.	Evaluation Of Cardiac Involvement By Speckle Tracking Echocardiography In Patients With Duchenne Muscular Dystrophy
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