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机译:常染色体隐性遗传性痉挛性截瘫的MR影像学表现
Departments of Diagnostic Radiology, American University of Beirut Medical Center, Beirut, Lebanon;
Internal Medicine–Neurology Division, American University of Beirut Medical Center, Beirut, Lebanon;
Internal Medicine–Neurology Division, American University of Beirut Medical Center, Beirut, Lebanon;
Departments of Diagnostic Radiology, American University of Beirut Medical Center, Beirut, Lebanon;
Internal Medicine–Neurology Division, American University of Beirut Medical Center, Beirut, Lebanon;
机译:常染色体隐性遗传性痉挛性截瘫的MR影像学表现
机译:由于捷克患者的FA2H基因新型变异,常染色体隐性遗传性痉挛截瘫型SPG35
机译:SPTAN1变体作为常染色体隐性遗传性痉挛性截瘫患者的潜在原因
机译:遗传痉挛性截瘫术中的步态分析参数的试验 - 重复性分析
机译:果蝇突变M1 Spastin在遗传性痉挛性截瘫治疗中毒性作用的果蝇模型的开发和操纵。
机译:由SPG11突变引起的常染色体隐性遗传性痉挛性截瘫的中国家庭
机译:常染色体隐性遗传性痉挛性截止截瘫的先生成像发现