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机译:经典婴儿型群患者的肌肉MRI:脂肪替代和水肿的变化
C Mondino Natl Neurol Inst Neuroradiol Dept Via Mondino 2 I-27100 Pavia Italy;
Univ Pavia Dept Brain &
Behav Sci Child Neuropsychiat Unit Pavia Italy;
Univ Milan Dept Neurosci Fdn IRCCS Ca Granda Osped Maggiore Policlin Unit Neuroradiol Milan;
Bambino Gesu Pediat Hosp Neuroradiol Unit Rome Italy;
Univ Pavia Dept Brain &
Behav Sci Neurol Unit Pavia Italy;
San Gerardo Hosp Unit Rare Metab Dis Monza Italy;
Univ Milan Fdn IRCCS Ca Granda Osped Maggiore Policlin Dept Pathophysiol &
Transplantat Pediat;
Azienda Osped Univ Unit Metab Dis Padua Italy;
Azienda Osped Univ Unit Metab Dis Padua Italy;
AOU Meyer Hosp Metab &
Neuromuscular Unit Florence Italy;
AOU Meyer Hosp Metab &
Neuromuscular Unit Florence Italy;
Univ Naples Federico II Sect Pediat Dept Translat Med Naples Italy;
Univ Naples Federico II Sect Pediat Dept Translat Med Naples Italy;
Bambino Gesu Pediat Hosp Unit Metab Rome Italy;
Bambino Gesu Pediat Hosp Unit Metab Rome Italy;
Giannina Gaslini Inst Dept Pediat Unit Rare Dis Genoa Italy;
glycogenosis II; infantile-onset Pompe disease; muscle MRI; Pompe disease; STIR; T2;
机译:经典婴儿型群患者的肌肉MRI:脂肪替代和水肿的变化
机译:用酶疗法治疗的典型婴儿庞贝氏病患者常见面部肌肉无力,言语障碍和吞咽困难。
机译:经酶疗法治疗的典型婴儿庞贝氏病患者常见面部肌肉无力,言语障碍和吞咽困难
机译:CLN2经典晚期婴儿NCL
机译:患儿特异性iPS细胞的小儿发作性庞贝病的骨骼肌模型
机译:远端肌肉弱点是长期酶治疗的经典婴儿婴儿婴儿群体患者的常见和早期特征
机译:经酶疗法治疗的典型婴儿庞贝氏病患者常见面部肌肉无力,言语障碍和吞咽困难