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Association between Body Composition and Disease Severity in Patients with Motor Neuron Disease / Amyotrophic Lateral Sclerosis

机译：运动神经元疾病/肌营养侧面硬化症患者身体成分和疾病严重程度的关系

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1. “Switchboard” malfunction in motor neuron diseases: Selective pathology of thalamic nuclei in amyotrophic lateral sclerosis and primary lateral sclerosis [J] . Rangariroyashe H. Chipika, Eoin Finegan, Stacey Li Hi Shing, NeuroImage: Clinical . 2020,第1期

机译：电机神经元疾病中的“切换器”故障：肌营养侧面硬化和原发性外壳中的丘脑核的选择性病理学
2. Progressive brainstem pathology in motor neuron diseases: Imaging data from amyotrophic lateral sclerosis and primary lateral sclerosis [J] . Peter Bede, Rangariroyashe H. Chipika, Eoin Finegan, Data in Brief . 2020,第2期

机译：运动神经元疾病中的渐进性脑干病理：来自肌萎缩外壳和原发性侧向硬化的成像数据
3. Identification and outcomes of clinical phenotypes in amyotrophic lateral sclerosis/motor neuron disease: Australian National Motor Neuron Disease observational cohort [J] . Richard Macdonnell, Paul Talman, Merrilee Needham, BMJ Open . 2016,第9期

机译：肌萎缩性侧索硬化/运动神经元疾病的临床表型的鉴定和结果：澳大利亚国家运动神经元疾病观察队列
4. Cytoskeletal defects in amyotrophic lateral sclerosis (motor neuron disease) [C] . Jean-Pierre Julien, Stephanie Millecamps, Jasna Kri Novartis Foundation symposium on Nuclear organization in development and disease . 2005

机译：肌营养侧面硬化症（运动神经元疾病）细胞骨骼缺陷
5. Targeting Motor Neuron - Immune System Crosstalk to Modulate the Disease Progression in Amyotrophic Lateral Sclerosis Mouse Model [D] . Trolese, Maria Chiara. 2020

机译：靶向运动神经元 - 免疫系统串扰调节肌营养侧面硬化小鼠模型中的疾病进展
6. Progressive brainstem pathology in motor neuron diseases: Imaging data from amyotrophic lateral sclerosis and primary lateral sclerosis [O] . Peter Bede, Rangariroyashe H. Chipika, Eoin Finegan, 2020

机译：运动神经元疾病的进展性脑干病理：肌萎缩性侧索硬化症和原发性侧索硬化症的影像资料
7. “Switchboard” malfunction in motor neuron diseases: Selective pathology of thalamic nuclei in amyotrophic lateral sclerosis and primary lateral sclerosis [O] . Rangariroyashe H. Chipika, Eoin Finegan, Stacey Li Hi Shing, 2020

机译：电机神经元疾病中的“切换器”故障：肌营养侧面硬化和原发性外壳中的丘脑核的选择性病理学

Association between Body Composition and Disease Severity in Patients with Motor Neuron Disease / Amyotrophic Lateral Sclerosis

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