机译:带有和不带有PANK2突变的伴有脑铁蓄积的神经退行性变的脑MRI
Departments of Molecular and Medical Genetics, School of Medicine, Oregon Health & Science University, Portland, Ore|Pediatrics and Neurology, School of Medicine, Oregon Health & Science University, Portland, Ore;
Departments of Radiology, University of Wisconsin, Madison, Wis;
Departments of Molecular and Medical Genetics, School of Medicine, Oregon Health & Science University, Portland, Ore;
Howard Hughes Medical Institute and Departments of Medicine and Pediatrics, University of California, San Francisco, Calif;
Departments of Radiology, University of Wisconsin, Madison, Wis|Neurology, University of Wisconsin, Madison, Wis;
机译:PANK2和C19orf12突变是脑铁积聚导致神经退行性变的常见原因
机译:PAMP2和C19ORF12突变是脑铁累积的神经变性的常见原因
机译:PANK2基因分析证实了具有脑铁积聚(NBIA)的神经退行性疾病的遗传异质性,但突变在其他类型的成人神经退行性疾病中很少见。
机译:表现为人脑中铁变性(NBIA)的神经退行性病变中的铁含量的表征
机译:敏感性加权MRI,用于评估镰状细胞疾病的脑氧合和脑铁
机译:带有和不带有PANK2突变的伴有脑铁蓄积的神经退行性变的脑MRI
机译:具有脑铁累积的特发性神经变性的成人展示案,没有PANG2和PLA2G6基因的突变