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Keyword [Charcot-Marie-Tooth]
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1. Gene Mapping, Mutation Analysis Of Neurofilament-light Gene And Study Of Brainstem Auditory Evoked Potentials In Chinese Charcot-Marie-Tooth Disease Patients
2. Clinical, Electrophysiological, Pathological, And Genetic Study In Chinese Charcot-Marie-Tooth Disease Patients With Type 1A And X-linked
3. Cloning Of The Gene For CMT2L And Mutation Analysis Of The SIMPLE, RAB7, LMNA And MTMR2 Genes In Chinese CMT Patients
4. Clinical Features And Identification Of The Disease-Causing Genes In The Kindreds Of Hereditary Spastic Paraplegia And Charcot-Marie-Tooth Disease
5. Detect MFN2 Gene Mutation By Using Denaturing High Performance Liquid Chromatography
6. A Novel Mutation 605 (T＞A) In CX32 Gene Causes X-linked Recessive Charcot-Marie-Tooth Disease
7. Analysis Of PMP22 Duplication Mutation And Clinical Research Correlated With CMT1A
8. Molecular Pathogenesis Study Of Charcot-Marie-Tooth 2L Caused By HSP22 Variation
9. The Clinical Research Of Hereditary Motor And Sensory Neuropathy
10. Study Of A Family With A Novel Mutation Of Gap Junction Protein β1(GJB1) Gene In X-linked Charcot-Marie-Tooth Disease
11. Segmental Comparative Electrophysiological Study Of Chronic Demyelinating Neuropathies
12. Central Impairment And Functional Remodeling Of Sensory Conduction In Charcot-Marie-Tooth Disease
13. The Gene Identification And Behavioral Analysis Of CMT2L Type Transgenic Mouse Model
14. Gene Mutation Analysis Of A Special Charcot-Marie-Tooth Disease Family With Type2Diabetes Mellitus
15. Clinical And Genetic Spectrum In An Eastern Chinese Series Of Patients With Charcot-Marie-Tooth Disease
16. Genetic Diagnosis Of CMT2L Transgenic Mice And Co-localization Analysis Of HSPB8with HSPB1in Sciatic Nerve
17. The Detection Of Gene Duplication Mutations And Clinical Resesrch On Charcot-Marie-Tooth Disease
18. Identification Of The Causative Mutation For Two Families With Hereditary Neuromuscular Rare Diseases
19. Analysis On The Clinic, Pathology And PMP22Gene Of Charcot-Marie-Tooth Disease
20. Clinical, Electrophysiological And Molecular Genetic Characteristics Of59Chinese Han Patients With CMT1X
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