Physiotherapeutic conduct in amyotrophic lateral sclerosis

Andreza Martinez Pozza; Clarissa Ramirez; Laís Helena Carvalho Marino; Milene Karenine Delamura; Nelson Iguimar Valério; Neuseli Marino Lamari

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Physiotherapeutic conduct in amyotrophic lateral sclerosis

机译：肌萎缩性侧索硬化症的理疗行为

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Amyotrophic Lateral Sclerosis (ALS) is a fatal progressive neurodegenerative disease with multifactorial etiology for which, so far, there is no effective medicinal treatment. However, by means of kinesiotherapy intervention and patient guidance and care, physiotherapy can delay physical functional losses, muscle fatigue and immobility of the joint-muscle system, thereby improving the quality of life. This survey had the aim of reviewing the physiotherapeutic conduct currently used in ALS cases. Monthly monitoring is recommended, with changes in goals and conduct at each stage of the disease, activities to be pursued around the home, and emphasis on stretching, muscle strengthening, posture adequacy and respiratory kinesiotherapy.

机译：肌萎缩性侧索硬化症（ALS）是一种致死性进行性神经退行性疾病，其病因多种多样，到目前为止，尚无有效的药物治疗方法。但是，通过运动疗法的干预以及患者的指导和护理，物理疗法可以延迟身体的功能丧失，肌肉疲劳和关节肌肉系统的不活动，从而改善生活质量。这项调查的目的是审查目前在ALS病例中使用的理疗行为。建议每月进行监测，并在疾病的每个阶段改变目标和行为，在家庭中开展活动，并强调拉伸，肌肉增强，姿势适当和呼吸运动疗法。

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《Sao Paulo Medical Journal》 |2006年第6期|共5页
作者
Andreza Martinez Pozza; Clarissa Ramirez; Laís Helena Carvalho Marino; Milene Karenine Delamura; Nelson Iguimar Valério; Neuseli Marino Lamari;
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中图分类临床医学;
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1. A genetic screen identifies Tor as an interactor of VAPB in a Drosophila model of amyotrophic lateral sclerosis A genetic screen identifies Tor as an interactor of VAPB in a Drosophila model of amyotrophic lateral sclerosis A genetic screen identifies Tor as an interactor of VAPB in a Drosophila model of amyotrophic lateral sclerosis [J] . Senthilkumar Deivasigamani, Hemant Kumar Verma, Girish S. Ratnaparkhi, Biology Open . 2014,第11期

机译：遗传筛选在肌萎缩性侧索硬化症的果蝇模型中将Tor鉴定为VAPB的相互作用物遗传筛选在肌萎缩性侧索硬化症的果蝇模型中将Tor鉴定为VAPB的相互作用剂遗传筛选将Tor鉴定为果蝇模型的果蝇模型中的VAPB相互作用剂。肌萎缩性侧索硬化症
2. Amyotrophic Lateral Sclerosis Regional Variants (Brachial Amyotrophic Diplegia, Leg Amyotrophic Diplegia, and Isolated Bulbar Arnyotrophic Lateral Sclerosis) [J] . Jawdat Omar, Statland Jeffrey M., Barohn Richard J., Neurologic clinics . 2015,第4期

机译：肌萎缩性侧索硬化区域性变异（肱肌萎缩性双截瘫，腿肌萎缩性双截瘫和孤立的球囊性肌萎缩性侧索硬化）
3. Amyotrophic Lateral Sclerosis Onset Is Influenced by the Burden of Rare Variants in Known Amyotrophic Lateral Sclerosis Genes [J] . Cady Janet, Allred Peggy, Bali Taha, Annals of neurology . 2015,第1期

机译：肌萎缩性侧索硬化症的发作受到已知的肌萎缩性侧索硬化症基因的罕见变体负担的影响
4. Classification between upper and lower motor neurons in amyotrophic lateral sclerosis patients by electromyographic processing and analysis [C] . Yosra Saidane, Farid Melgani, Sofia Ben Jebara, International Symposium on Signal, Image, Video and Communications . 2021

机译：电拍摄处理和分析对肌营养的侧面硬化症患者的上下电机神经元分类
5. Electrochemical Biosensors for Neurodegenerative Disease Biomarkers: Investigations into the Origin and Diagnosis of Alzheimer’s Disease and Amyotrophic Lateral Sclerosis [D] . Wallace, William. 2021

机译：用于神经退行性疾病生物标志物的电化学生物传感器：调查阿尔茨海默病和肌营养侧面硬化的原产地和诊断
6. Diagnostic utility of the amyotrophic lateral sclerosis Functional Rating Scale—Revised to detect pharyngeal dysphagia in individuals with amyotrophic lateral sclerosis [O] . Jennifer L. Chapin, Lauren Tabor Gray, Terrie Vasilopoulos, 2020

机译：肌营养侧面硬化功能评级诊断效果规模修订以检测肌营养侧面硬化的个体咽部吞咽症
7. Physiotherapeutic conduct in amyotrophic lateral sclerosis [O] . Andreza Martinez Pozza, Milene Karenine Delamura, Clarissa Ramirez, 2006

机译：肌萎缩侧索硬化症的理疗行为
8. Summary Report: Amyotrophic Lateral Sclerosis and Multiple Sclerosis Surveillance Annual Meeting, June 24-25, 2009: Issues Related to Developing a National Surveillance System and Registries for Amyotrophic Lateral Sclerosis and Multiple Sclerosis [R] . 2009

机译：摘要报告：肌萎缩侧索硬化症和多发性硬化症监测年会，2009年6月24日至25日：与建立肌萎缩侧索硬化症和多发性硬化症的国家监测系统和登记相关的问题

Physiotherapeutic conduct in amyotrophic lateral sclerosis

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