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Keyword [Spinocerebellar ataxia]
Result: 41 - 60 | Page: 3 of 5
41. Clinical Manifestation, Imaging Characteristics, And Gen Mutation Analysis Of One Pedigree Of The Spinocerebellar Ataxia With Severe Cataract
42. Serum Insulin-like System Alterations In Patients With Spinocerebellar Ataxia
43. Clinical Heterogeneity And Gene Diagnosis Of Spinocerebellar Ataxia Type3
44. The Research Of Genetic Typing Of Patients With Spinocerebellar Ataxia In Guangxi Region
45. Cases Report And Clinical Analysis Of Spinocerebellar Ataxia Type2(SCA2)
46. The Cell-based Functional Study Of TGM6, A Causative Gene Of Spinocerebellar Ataxia Type35
47. Gene Diagnosis And Clinical Characteristics Research Of Spinocerebellar Ataxia Type3/Machado-joseph Disease In Yunnan Province
48. Studies On Clinical And Electrophysiological Characteristics Of Spinocerebellar Ataxia Type3in A Pedigree
49. To Study The Abnormal Phenotype In SCA Drosophila Model Caused By Gene X
50. Clinical Characteristics Of Spinocerebellar Ataxia Type2in Chinese Han Population And Analysis Of ATXN2Gene Mutation
51. Functional Study Of The Spinocerebellar Ataxia-related Gene Atx-3in C. Elegans
52. The Study Of The Resting-state Functional Magnetic Resonance Imaging In Spinocerebellar Ataxia Type3Patients
53. The Expression Of PGC-1α In The Peripheral Tissue Of Spinocerebellar Ataxia Type 6 Patients
54. Study Of Cerebral White Matter Fiber Bundles By Diffusion Tensor Imaging Of Hereditary Spinocerebellar Ataxia Type 3 In Yunnan Province
55. To Analyze The Clinical Phenotype And The Image Of 6 Spinocerebellar Ataxia Type 2 And 3 Patients
56. The Correlation Between Cognitive Impairment And The Volume Change Of The Subcortical Nuclei In Spinocerebellar Ataxia Patients
57. Identification Of The Causative Mutations For Two Families With Monogenic Diseases
58. Peripheral Nerve Involvement In Type 3 Spinocerebellar Ataxia
59. EEG Study And Bioinformatics Analysis Of SCA3 Mice
60. Mechanism Of Learning And Memory In Spinocerebellar Ataxia Type 3 Mice
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