Spinocerebellar ataxia - Globe Thesis

Keyword [Spinocerebellar ataxia] Result: 61 - 80 \| Page: 4 of 5
61.	The Study On The Causative Gene Of Common Spinocerebellar Ataxia Subtypes In Guangxi Zhuang Normal Population
62.	Clinical Characteristics Of Spinocerebellar Ataxia 2(SCA2) And Multiple System Atrophy (MSA) And Analysis Of ATXN2 Gene Mutation
63.	Study On The Clinical Features And Genetic Mutation Of Spinocerebellar Ataxia Type 1 From A Kazakh Family
64.	The Value Of EAS-EMG And US-EMG In The Diagnosis And Differential Diagnosis Of Multiple System Atrophy
65.	Clinical Features And Genetic Analysis Of Pathogenic Dynamic Mutation Of Patients With Spinocerebellar Ataxia
66.	Clinical Research In Chinese Patients With Spinocerebellar Ataxia Type 3 And Generation Of A New BAC-SCA3 Mice Model
67.	Role Of CHIP In Pathogenesis Of Spinocerebellar Ataxia Type 3
68.	Combination Of Ancient Literature On Encephalopathy And Study On The Effect Of Zishen Yisui Jiannao Recipe On Encephalopathy With Kidney Deficiency And Marrow Deficiency
69.	Study On The Zhuang Family Of Spinocerebellar Ataxia Type 3
70.	Assiocation Between CAG Repeat Length And Age At Onset Of Spinocerebellar Ataxia Type 3:A Meta-Analysis
71.	A Study Of The Non-ataxia Clinical Symptoms And The Correlation Between The Onset Age And Abnormal Number Of CAG Repetitions In Spinocerebellar Ataxia Type 3
72.	Clinical And Molecular Biological Study On A Chinese Family Of Spinocerebellar Ataxia Type1
73.	Spinocerebellar Ataxia Type 2 In A Family With Different Phenotypes:A Case Report And Literature Review
74.	The Discussion Of TGM6 As A Specific Causative Gene For Spinocerebellar Ataxia 35
75.	Familial Spinal Cerebellar Ataxia11 In China
76.	The Efficacy Of Repetitive Transcranial Magnetic Stimulation In The Treatment Of Spinocerebellar Ataxia
77.	Ataxin-7 conserved motifs determine the severity of the neurodegenerative disorder spinocerebellar ataxia type 7 in transgenic mice and influence lifespan in yeast
78.	RNA gain of function effects in spinocerebellar ataxia type 8
79.	Pin1 Regulates The Monoubiquitination And Activity Of CHIP Via UbE2W
80.	The Establishment Of Genetic Diagnosis Platform For Hereditary Cerebellar Ataxia And Mapping And Cloning Of Novel Causative Genes For Hereditary Cerebellar Ataxia
<<First <Prev Next> Last>> Jump to