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Keyword [ataxia]
Result: 41 - 60 | Page: 3 of 9
41. The Analysis Of FMR1 Gene Permutation In Sporadic Spinocerebellar Ataxia And Multiple System Atrophy Patients
42. Development Of A Dural-color Multiplex Ligation Dependent Probe Amplification And Its Application In Diagnosis Of Spinocerebellar Ataxia
43. Analysis On The Gene Mutation Of SCA3 And SCA7 In Two SCAs Families
44. The Diffusion Tensor Imaging Characteristics Of Spinocerebellar Ataxia 2 Patients And Clinical Analysis
45. Clinical And Gene Diagnosis Of Spinocerebellar Ataxia Type3
46. Studies On The Genetic Mutation Of Spinocerebellar Ataxia Type 12 And Clinical Characteristics From A Uygur Nationality Parentage
47. The Clinical Feature, Neuroimaging Feature And Genotyping Of Five Pedigrees With Spinocerebellar Ataxia In Shandong
48. Clinical And Gene Diagnosis Of Myotonic Dystrophy
49. BOLD-fMRI Quantitive Analysis Of Hand Coordination Function Adjustment Motor Cortex In Ataxia
50. Effects And Mechanisms Of Human Umbilical Cord Mesenchymal Stem Cell Transplantation On Spinocerebellar Ataxia Mice
51. The Effect Of MicroRNA-18a On ATM Gene Expression And Autophagy Process In HCT116Colon Cancer Cells
52. Causative Gene Localization For Two Kinds Of Monogenic Disorders And Prenatal Diagnosis
53. Anti-oxidative Effects Of Ataxin-3
54. Study Of The Role Of SUMOylation On Phenotype Of SCA3/MJD Drosophila Model And Its Mechanism
55. Studies On The Genetic Mutation, Microstructure Damage Imaging Characteristics On White Matter Brain, Serum α-Synuclein Expression Level Of Spinocerebellar Ataxia Type12
56. Study On Cognitive Impairment In Spinocerebellar Ataxia Type1,2,3,12
57. Sensory Ataxia Form Of Chronic Inflammatory Demyelinating Polyneuropathy:a Case Report And Literature Review
58. Clinical And Molecular Features Of A Chinese Family With Spinocerebellar Ataxia Type6
59. Different Type Of Imaging Findings Of Olivopontocerebellar Atrophy And Clinical Correlative Factors Analysis
60. 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
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