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Keyword [Charcot-Marie-Tooth disease]
Result: 21 - 37 | Page: 2 of 2
21. A Novel Mutation In AFAP-120 Gene Causes An Autosomal-dominant Charcot-marie-tooth Disease Type 2
22. A Novel Mutation In GJB1(c.185 G>C) In A Family With X-linked Charcot-marie-tooth Disease:Pedigree Analysis And Functional Research
23. Phenotype And Genotype Of 5 Patients With Charcot-Marie-Tooth Disease At The Onset Of Childhood
24. Identification And Functional Analysis Of NEFH Gene In A Pedigree With Charcot-Marie-Tooth Disease
25. Genetic Characteristics Of Early Onset Charcot-Marie-Tooth Disease And The Functional Study Of A Novel MPZ Mutation
26. 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
27. X-linked Charcot-marie-tooth Disease Associated With Reversible Posterior White Matter Lesions:Clinical Features And Genetic Analysis
28. Phenotypic And Genotypic Features Of X-linked Charcot-Marie-Tooth Disease Type 1 And The Study Of Mutant Cx32 Protein Expression
29. Study Of Novel Disease-causing Gene And Molecular Mechanisms For Charcot-marie-tooth Disease
30. Mutation Analyses Of Charcot-marie-tooth Disease And Functional Study Of GDAP1
31. Genetic Diagnosis And Phenotypic Correlation Of Two Hereditary Diseases:Tuberous Sclerosis Complex And Axonal Charcot-Marie-Tooth Disease
32. A Genetic Research Of An X-linked Charcot-marie-tooth Disease Pedigree
33. Study On The Pathogenic Mutations Of Two Single-gene Inherited Diseases Of The Locomotion System
34. 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
35. 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
36. A Family Report Of Charcot-Marie-Tooth Disease Type 4C Was Induced By Novel Mutations In The SH3TC2 Gene And Previous Literature Review Analysis
37. Clinical Characteristics,Gene Mutation Analysis Of Charcot-Marie-Tooth Disease And Function Study Of ATP1A1
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