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1.Methods Thirty-three biopsy-proved PMD patients underwent MRI of face, scapular, thigh, and leg, including 16 cases of Duchenne muscular dystrophy (DMD), 2 cases of Beck er′s muscular dystrophy, 5 cases of limb-girdle muscular dystrophy, and 10 c ases o f facioscapulohumeral muscular dystrophy. Spin echo sequence, fast spin echo seq uence, and STIR sequence were utilized.
方法 选择头部、肩胛部、骨盆、双侧大腿及双侧小腿肌肉 ,对 3 3例经病理活检证实的PMD患者行MRI检查 ,其中假大型PMD(Duchenne型PMD ,DMD) 16例、肢带型PMD 5例、良性型PMD(Becker型肌病 ) 2例 ,肩肱型PMD 10例。收藏指正
2.Materials and Methods: Four normal controls and 53 cases with biopsy proved muscular diseases, including 16 cases of Duchenne muscular dystrophy?DMD?, 5 cases of limb girdle muscular dystrophy, 10 cases of facioscapulohumeral muscular dystrophy, 9 cases with polymyositis, 9 cases with tipid storage myopathy, and 4 cases of neurogenic myopathy, underwent MRI of thigh and leg.
材料和方法:选择骨盆、双侧大腿及双侧小腿肌肉,对53例经病理活检证实的肌肉疾病患者及4例健康人行MRI检查,进行性肌营养不良症(PMD)31例,其中假大型进行性肌营养不良症(Duchenne型PMD,DMD)16例,肢带型PMD5例,肩肱型PMD10例; 多发性肌炎(PM)9例;收藏指正
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