Lv4
548 积分 2023-03-21 加入
Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28
8天前
已完结
Endovascular treatment versus standard medical treatment for vertebrobasilar artery occlusion (BEST): an open-label, randomised controlled trial
4个月前
已完结
Genotypic-Phenotypic Correlation in HSP patients (P11-11.019)
4个月前
已关闭
Genotypic-Phenotypic Correlation in HSP patients (P11-11.019)
4个月前
已关闭
阿尔茨海默病MR检查规范中国专家共识
4个月前
已完结
Biallelic Variants in COQ4 Cause Childhood‐Onset Pure Hereditary Spastic Paraplegia
5个月前
已完结
Ears of the Lynx on Neuroimaging in a Patient with COQ4‐Associated Hereditary Spastic Paraplegia
5个月前
已完结
Clinical and genetic characteristics in a Chinese cohort of complex spastic paraplegia type 4
5个月前
已完结
[A report of atypical hypomyelinating leukodystrophy with atrophy of the basal ganglia and cerebellum caused by a de novo mutation in tubulin beta 4A (TUBB4A) gene and literature review]
5个月前
已完结
Neuroimaging to Genotype: Delineating the Spectrum of Disorders With Deficient Myelination in the Indian Population
5个月前
已完结
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