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Keyword [Spinocerebellar ataxia]
Result: 21 - 40 | Page: 2 of 5
21. Detection Of FGF14 Gene Mutation In Spinocerebellar Ataxia Patients
22. Clinical And Genetic Study Of Spinocerebellar Ataxia
23. Casein Kinase 2 Interacts With And Phosphorylates Ataxin-3
24. The Research Of Clinical Features And Gene Mutation Of Five Families With Spinocerebellar Ataxia In Shangdong
25. The Analysis Of FMR1 Gene Permutation In Sporadic Spinocerebellar Ataxia And Multiple System Atrophy Patients
26. Development Of A Dural-color Multiplex Ligation Dependent Probe Amplification And Its Application In Diagnosis Of Spinocerebellar Ataxia
27. Analysis On The Gene Mutation Of SCA3 And SCA7 In Two SCAs Families
28. The Diffusion Tensor Imaging Characteristics Of Spinocerebellar Ataxia 2 Patients And Clinical Analysis
29. Clinical And Gene Diagnosis Of Spinocerebellar Ataxia Type3
30. Studies On The Genetic Mutation Of Spinocerebellar Ataxia Type 12 And Clinical Characteristics From A Uygur Nationality Parentage
31. The Clinical Feature, Neuroimaging Feature And Genotyping Of Five Pedigrees With Spinocerebellar Ataxia In Shandong
32. Effects And Mechanisms Of Human Umbilical Cord Mesenchymal Stem Cell Transplantation On Spinocerebellar Ataxia Mice
33. Causative Gene Localization For Two Kinds Of Monogenic Disorders And Prenatal Diagnosis
34. Anti-oxidative Effects Of Ataxin-3
35. Study Of The Role Of SUMOylation On Phenotype Of SCA3/MJD Drosophila Model And Its Mechanism
36. Studies On The Genetic Mutation, Microstructure Damage Imaging Characteristics On White Matter Brain, Serum α-Synuclein Expression Level Of Spinocerebellar Ataxia Type12
37. Study On Cognitive Impairment In Spinocerebellar Ataxia Type1,2,3,12
38. Clinical And Molecular Features Of A Chinese Family With Spinocerebellar Ataxia Type6
39. Summary In The Special Clinical Features Of Patients With Spinocerebellar Ataxias In Chinese Population And Analysis In Clinical Manifestations Of Patients With Huntington’s Disease Ever Misdiagnosed As Spinocerebellar Ataxia
40. Analysis Of Clinical Manifestation, Imaging And Gene Mutation In Two Korean Nationality Pedigrees From Liaoning Province Suffering From Spinocerebellar Ataxia
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