首页> 外文OA文献 >An Unusual Case of Distal Dominant Spinal Progressive Muscular Atrophy with Type 1 Fiber Predominance， Rimmed Vacuole， Bulbar Palsy， and Pyramidal Signs: A Variant of Juvenile Amyotrophic Lateral Sclerosis ?

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An Unusual Case of Distal Dominant Spinal Progressive Muscular Atrophy with Type 1 Fiber Predominance， Rimmed Vacuole， Bulbar Palsy， and Pyramidal Signs: A Variant of Juvenile Amyotrophic Lateral Sclerosis ?

机译：少见的远端优势性脊髓进行性肌萎缩伴1型纤维占优势，边缘液泡，球囊麻痹和金字塔形体征：少年型肌萎缩性侧索硬化症的变种？

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松崎美保子; 大澤真木子; 宍倉啓子; 新井ゆみ; 鈴木暘子; 泉達郎; 斎藤加代子; 吉田眞; 中野和俊; 平山義人; 福山幸夫; Mihoko MATSUZAKI; Makiko OSAWA; Keiko SHISHIKURA; Yumi ARAI; Haruko SUZUKI; Tatsuro IZUMI; Kayoko SAITO; Makoto YOSHIDA; Kazutoshi NAKANO; Yoshito HIRAYAMA; Yukio FUKUYAMA;
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年度 1992
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正文语种 ja
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1. Autosomal dominant juvenile amyotrophic lateral sclerosis and distal hereditary motor neuronopathy with pyramidal tract signs: synonyms for the same disorder? [J] . De Jonghe P, Auer Grumbach M, Irobi J, Brain: A journal of neurology . 2002,第Pta6期

机译：常染色体显性遗传的青少年肌萎缩性侧索硬化症和具有锥体束征的远端遗传性运动神经病：同一种疾病的同义词吗？
2. Childhood-onset spinal muscular' atrophy or juvenile amyotrophic lateral sclerosis without pontocerebellar hypoplasia caused by a novel VRK1 splice variant [J] . Sedghi M., Moslemi A., Olive M., Neuromuscular disorders: NMD . 2019,第Suppla1期

机译：儿童发病脊髓肌肉萎缩或青少年肌萎缩侧面硬化，没有Pontocerebellar发育不全的开发，由新型VRK1拼接变体引起
3. Decremental responses following repetitive nerve stimulation in spinal and bulbar muscular atrophy (SBMA) are similar to those in amyotrophic lateral sclerosis [J] . K. Tachiyama, K. Kurokawa, M. Sonoo, Journal of the Neurological Sciences: Official Bulletin of the World Federation of Neurology . 2017,第期

机译：在脊柱和泡杆肌肉萎缩（SBMA）中重复神经刺激后的衰减反应与肌营养的侧面硬化剂相似
4. Expression of androgen receptor in X-linked spinal and bulbar muscular atrophy and amyotrophic lateral sclerosis. [O] . A Ogata, T Matsuura, K Tashiro, 1994

机译：雄激素受体在X连锁脊髓和延髓性肌萎缩和肌萎缩性侧索硬化中的表达。
5. Non-progressive juvenile spinal muscular atrophy of the distal upper limb (Hirayama's disease): a clinical variant of the benign monomelic amyotrophy Atrofia muscular espinhal distal do membro superior não progressiva juvenil (doença de Hirayama): uma variante clínica da amiotrofia monomélica benigna [O] . OSVALDO J. M. NASCIMENTO, MARCOS R.G. DE FREITAS 2000

机译：上肢远端非渐进性少年脊髓性肌萎缩（平山病）：良性单体肌萎缩症的临床变体

An Unusual Case of Distal Dominant Spinal Progressive Muscular Atrophy with Type 1 Fiber Predominance， Rimmed Vacuole， Bulbar Palsy， and Pyramidal Signs: A Variant of Juvenile Amyotrophic Lateral Sclerosis ?

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