Charcot-Marie-Tooth - Globe Thesis

Keyword [Charcot-Marie-Tooth] Result: 21 - 40 \| Page: 2 of 3
21.	Function Disability And Genetics Research In Pediatric Charcot-marie-tooth Patients
22.	MPZ Gene Mutation Detection And The Phenotype Analysis In Chinese CMT Patients
23.	The Protective Effects Of Dl-3-n-butylphthalide Against Mitochondrial Injury Caused By HSPB8K141N Mutation
24.	Clinical Features Retrospectively Analysis Of 24 Cases Children Charcot-Marie-Tooth Disease
25.	A Novel Mutation In AFAP-120 Gene Causes An Autosomal-dominant Charcot-marie-tooth Disease Type 2
26.	A Novel Mutation In GJB1(c.185 G>C) In A Family With X-linked Charcot-marie-tooth Disease:Pedigree Analysis And Functional Research
27.	Phenotype And Genotype Of 5 Patients With Charcot-Marie-Tooth Disease At The Onset Of Childhood
28.	Identification And Functional Analysis Of NEFH Gene In A Pedigree With Charcot-Marie-Tooth Disease
29.	Genetic Characteristics Of Early Onset Charcot-Marie-Tooth Disease And The Functional Study Of A Novel MPZ Mutation
30.	Contact Heat Evoked Potential:Normal Value And Use In Virtual Realty;Study Of Charcot-Marie-Tooth Disease In China And Effect Of Mesencephalic Astrocyte-derived Neurotrophic Factor In Endoplasmic Reticulum Stress Of RT4-D6P2T With MPZ Mutation
31.	X-linked Charcot-marie-tooth Disease Associated With Reversible Posterior White Matter Lesions:Clinical Features And Genetic Analysis
32.	Phenotypic And Genotypic Features Of X-linked Charcot-Marie-Tooth Disease Type 1 And The Study Of Mutant Cx32 Protein Expression
33.	Study Of Novel Disease-causing Gene And Molecular Mechanisms For Charcot-marie-tooth Disease
34.	Mutation Analyses Of Charcot-marie-tooth Disease And Functional Study Of GDAP1
35.	Genetic Diagnosis And Phenotypic Correlation Of Two Hereditary Diseases:Tuberous Sclerosis Complex And Axonal Charcot-Marie-Tooth Disease
36.	A Genetic Research Of An X-linked Charcot-marie-tooth Disease Pedigree
37.	Study On The Pathogenic Mutations Of Two Single-gene Inherited Diseases Of The Locomotion System
38.	Kinetic analysis of tyrosyl-tRNA synthetase variants associated with dominant-intermediate Charcot-Marie-Tooth type C
39.	Glycyl-tRNA synthetase mutations cause Charcot-Marie-Tooth disease type 2D and distal spinal muscular atrophy type V: A potentially novel disease mechanism for human peripheral neuropathies
40.	The effects of resistance training and oral creatine supplementation on muscle fiber morphology, strength and activities of daily living in patients with Charcot-Marie-Tooth disease
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