About 18 item dissertation in line with Charcot-Marie-Tooth disease query results,the following is 1 to 50(Search took 0.096 seconds)

  1. Analysis on the Clinic, Pathology and PMP22Gene of Charcot-Marie-Tooth Disease,ShiLei/Liaoning Medical,0/14
  2. The Detection of Gene Duplication Mutations and Clinical Resesrch on Charcot-Marie-Tooth Disease,ZhangZuo/Jilin University,0/37
  3. Pathological Gene Screening and the Applicational Study of Chinese Patients with Neuromuscular Diseases,ZhaoZhe/Hebei Medical University,0/130
  4. Gene Mutation Analysis of a Special Charcot-Marie-Tooth Disease Family with Type2Diabetes Mellitus,XieTao/,0/38
  5. Identification of the Causative Mutation for Two Families with Hereditary Neuromuscular Rare Diseases,FengYaPei/Shandong University,0/26
  6. Cloning of the Gene for CMT2L and Mutation Analysis of the SIMPLE, RAB7, LMNA and MTMR2 Genes in Chinese CMT Patients,ZhaoGuoHua/Central South University,0/110
  7. Clinical, Electrophysiological, Pathological, and Genetic Study in Chinese Charcot-Marie-Tooth Disease Patients with Type 1A and X-linked,WangYi/Fudan University,1/164
  8. Clinical Features and Identification of the Disease-Causing Genes in the Kindreds of Hereditary Spastic Paraplegia and Charcot-Marie-Tooth Disease,LinPengFei/Shandong University,0/105
  9. Detect MFN2 Gene Mutation by Using Denaturing High Performance Liquid Chromatography,FuMin/Central South University,0/125
  10. Study of a Family with a Novel Mutation of Gap Junction Protein β1(GJB1) Gene in X-linked Charcot-Marie-Tooth Disease,ChenShengDong/Second Military Medical University,0/13
  11. Molecular Pathogenesis Study of Charcot-Marie-Tooth 2L Caused by HSP22 Variation,QinDaQiang/Zhejiang University,0/39
  12. The Clinical Research of Hereditary Motor and Sensory Neuropathy,HuangLiMin/Jilin University,0/51
  13. Analysis of PMP22 Duplication Mutation and Clinical Research Correlated with CMT1A,DuanXiaoHui/Peking Union Medical College , China,0/84
  14. The Study of Clinical Characteristics and Glycyl-tRNA Synthetase Gene Mutations in Adolescent-onset Myoatrophy of Bilateral Distal Upper Extremities with Knee-jerk Hyperreflexia,ZhengZuoXin/Fudan University,1/45
  15. The Electrophysiological and Pathological Analysis of CMT2L Transgenic Mouse Model,LiuZuo/Central South University,0/28
  16. Segmental Comparative Electrophysiological Study of Chronic Demyelinating Neuropathies,LiuQianYun/Fudan University,0/74
  17. Central Impairment and Functional Remodeling of Sensory Conduction in Charcot-Marie-Tooth Disease,ZhangZuoDi/Fudan University,0/44
  18. The Gene Identification and Behavioral Analysis of CMT2L Type Transgenic Mouse Model,LiuSanMei/Central South University,0/24

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