Works matching Amyotrophic lateral sclerosis
Results: 5000
IMPACTO DO TRATAMENTO COM RILUZOL NA EFICIÊNCIA E REGRESSÃO DA ESCLEROSE LATERAL AMIOTRÓFICA.
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- Revista Foco (Interdisciplinary Studies Journal), 2023, v. 16, n. 11, p. 1, doi. 10.54751/revistafoco.v16n11-127
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Respiratory physiotherapy in patients with Amyotrophic Lateral Sclerosis. A systematic review.
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- Archivos de Neurociencias, 2020, v. 25, n. 4, p. 9, doi. 10.31157/archneurosciencesmex.v25i4.213
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筋萎縮性側索硬化症と認知機能障害.
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- Japanese Journal of Cognitive Neuroscience, 2023, v. 24, n. 2, p. 49
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- Article
干细胞治疗肌萎缩侧索硬化症：细胞来源、数量、修饰手段及给药途径.
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- Chinese Journal of Tissue Engineering Research / Zhongguo Zuzhi Gongcheng Yanjiu, 2025, v. 29, n. 19, p. 4083, doi. 10.12307/2025.054
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Translation of the Preference-Based Amyotrophic Lateral Sclerosis Scale into French.
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- Canadian Journal of Neurological Sciences, 2025, v. 52, n. 1, p. 129, doi. 10.1017/cjn.2024.18
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Correlação entre independência funcional e qualidade de vida de pacientes com esclerose lateral amiotrófica.
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- Cadernos de Terapia Ocupacional da UFSCar, 2014, v. 22, n. 3, p. 507, doi. 10.4322/cto.2014.071
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Assessment of a multiple biomarker panel for diagnosis of amyotrophic lateral sclerosis.
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- 2016
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- journal article
Oropharyngeal dysphagia in amyotrophic lateral sclerosis alters quality of life.
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- Journal of Oral Rehabilitation, 2013, v. 40, n. 3, p. 199, doi. 10.1111/joor.12019
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Respiratory phenotypes in amyotrophic lateral sclerosis as determined by respiratory questions on the Amyotrophic Lateral Sclerosis Functional Rating Scale–Revised and their relation to respiratory tests.
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- European Journal of Neurology, 2023, v. 30, n. 6, p. 1594, doi. 10.1111/ene.15765
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Assessment of bulbar function in amyotrophic lateral sclerosis: validation of a self‐report scale (Center for Neurologic Study Bulbar Function Scale).
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- European Journal of Neurology, 2018, v. 25, n. 7, p. 907, doi. 10.1111/ene.13638
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Multipoint incremental motor unit number estimation versus amyotrophic lateral sclerosis functional rating scale and the medical research council sum score as an outcome measure in amyotrophic lateral sclerosis.
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- Annals of Indian Academy of Neurology, 2014, v. 17, n. 3, p. 336, doi. 10.4103/0972-2327.138522
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Clinical and Genetic Aspects of Juvenile Amyotrophic Lateral Sclerosis: A Promising Era Emerges.
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- Genes, 2024, v. 15, n. 3, p. 311, doi. 10.3390/genes15030311
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Passive Versus Active Circuit During Invasive Mechanical Ventilation in Subjects With Amyotrophic Lateral Sclerosis.
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- Respiratory Care, 2018, v. 63, n. 9, p. 1132, doi. 10.4187/respcare.05866
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不同途径神经干细胞移植对肌萎缩侧索硬化神经炎症的影响.
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- Chinese Journal of Tissue Engineering Research / Zhongguo Zuzhi Gongcheng Yanjiu, 2023, v. 27, n. 15, p. 2363, doi. 10.12307/2023.371
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Amyotrophic lateral sclerosis in Beijing: Epidemiologic features and prognosis from 2010 to 2015.
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- Brain & Behavior, 2018, v. 8, n. 11, p. N.PAG, doi. 10.1002/brb3.1131
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Translation and Psychometric Evaluation of a Korean Version of the Amyotrophic Lateral Sclerosis-Specific Quality of Life – Revised.
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- Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, 2017, v. 18, n. 1/2, p. 92, doi. 10.1080/21678421.2016.1249885
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Ethnic and demographic incidence of amyotrophic lateral sclerosis (ALS) in Brazil: A population based study.
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- Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration, 2016, v. 17, n. 3/4, p. 275, doi. 10.3109/21678421.2016.1140210
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- Article
Case report: Flail leg syndrome in familial amyotrophic lateral sclerosis with L144S SOD1 mutation.
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- Frontiers in Neurology, 2023, v. 14, p. 1, doi. 10.3389/fneur.2023.1138668
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Hippocampal aggregation signatures of pathogenic UBQLN2 in amyotrophic lateral sclerosis and frontotemporal dementia.
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- Brain: A Journal of Neurology, 2024, v. 147, n. 10, p. 3547, doi. 10.1093/brain/awae140
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The multifaceted role of kinases in amyotrophic lateral sclerosis: genetic, pathological and therapeutic implications.
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- 2020
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- journal article
Experiences with advance care planning in amyotrophic lateral sclerosis: Qualitative longitudinal study with people with amyotrophic lateral sclerosis and their family carers.
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- Palliative Medicine, 2024, v. 38, n. 5, p. 572, doi. 10.1177/02692163241242320
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How to manage exacerbation of respiratory failure in a patient diagnosed with amyotrophic lateral sclerosis.
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- Palliative Medicine in Practice, 2020, v. 14, n. 1, p. 44, doi. 10.5603/PMPI.2020.0006
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- Article
Η γενετική της πλαγίας μυατροφικής σκλήρυνσης Νεότερα δεδομένα
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- Archives of Hellenic Medicine / Arheia Ellenikes Iatrikes, 2019, v. 36, n. 2, p. 166
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The effect of social support on the emotional well-being of people with amyotrophic lateral sclerosis: Exploring the mediating role of spirituality.
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- Palliative & Supportive Care, 2024, v. 22, n. 6, p. 1932, doi. 10.1017/S1478951524000610
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An Exploratory Trial of EPI-589 in Amyotrophic Lateral Sclerosis (EPIC-ALS): Protocol for a Multicenter, Open-Labeled, 24-Week, Single-Group Study.
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- JMIR Research Protocols, 2023, v. 12, n. 1, p. 819, doi. 10.2196/42032
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Assistive Robots for Patients With Amyotrophic Lateral Sclerosis: Exploratory Task-Based Evaluation Study With an Early-Stage Demonstrator.
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- JMIR Rehabilitation & Assistive Technologies, 2022, v. 9, n. 3, p. 1, doi. 10.2196/35304
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ESCLEROSE LATERAL AMIOTRÓFICA (ELA): MECANISMOS, DIAGNÓSTICO E POSSÍVEIS TRATAMENTOS.
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- Revista Foco (Interdisciplinary Studies Journal), 2023, v. 16, n. 5, p. 1, doi. 10.54751/revistafoco.v16n5-058
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Clinical and epidemiological characteristics of amyotrophic lateral sclerosis in an Egyptian cohort.
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- Neurological Sciences, 2025, v. 46, n. 3, p. 1225, doi. 10.1007/s10072-024-07760-w
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Safety and efficacy of lithium in patients with amyotrophic lateral sclerosis: a systematic review and meta-analysis of randomized controlled trials.
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- Neurological Sciences, 2023, v. 44, n. 9, p. 3029, doi. 10.1007/s10072-023-06814-9
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Psychoeducational groups for people with Amyotrophic Lateral Sclerosis and their caregiver: a qualitative study.
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- 2022
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- journal article
Validation of the revised Amyotrophic Lateral Sclerosis Functional Rating Scale in Poland and its reliability in conditions of the medical experiment.
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- Neurological Sciences, 2021, v. 42, n. 3, p. 943, doi. 10.1007/s10072-020-04565-5
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Recumbent stepping aerobic exercise in amyotrophic lateral sclerosis: a pilot study.
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- 2019
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Efficacy and safety of edaravone in treatment of amyotrophic lateral sclerosis-a systematic review and meta-analysis.
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- 2019
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Association between alcohol consumption and amyotrophic lateral sclerosis: a meta-analysis of five observational studies.
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- 2016
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Association between the Angiogenin (ANG) K17I variant and amyotrophic lateral sclerosis risk in Caucasian: a meta-analysis.
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- 2015
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An exploratory study of serum creatinine levels in patients with amyotrophic lateral sclerosis.
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- Neurological Sciences, 2014, v. 35, n. 10, p. 1591, doi. 10.1007/s10072-014-1807-4
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Cross-cultural adaptation and validation for the Brazilian population of the instrument Amyotrophic Lateral Sclerosis-Specific Quality of Life-Short Form (ALSSQOL-SF).
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- 2020
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- journal article
Intact single muscle fibres from SOD1<sup>G93A</sup> amyotrophic lateral sclerosis mice display preserved specific force, fatigue resistance and training‐like adaptations.
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- Journal of Physiology, 2019, v. 597, n. 12, p. 3133, doi. 10.1113/JP277456
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Efficacy of non-pharmacological interventions for individuals with amyotrophic lateral sclerosis: systematic review and network meta-analysis of randomized control trials.
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- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-62213-w
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Negotiating the Beginning of Care: A Grounded Theory Study of Health Services for Amyotrophic Lateral Sclerosis.
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- Brain Sciences (2076-3425), 2022, v. 12, n. 12, p. 1623, doi. 10.3390/brainsci12121623
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Emotional Processing and Experience in Amyotrophic Lateral Sclerosis: A Systematic and Critical Review.
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- Brain Sciences (2076-3425), 2021, v. 11, n. 10, p. 1356, doi. 10.3390/brainsci11101356
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Informal Caregiving in Amyotrophic Lateral Sclerosis (ALS): A High Caregiver Burden and Drastic Consequences on Caregivers' Lives.
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- Brain Sciences (2076-3425), 2021, v. 11, n. 6, p. 748, doi. 10.3390/brainsci11060748
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Diabetes Mellitus and Amyotrophic Lateral Sclerosis: A Systematic Review.
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- Biomolecules (2218-273X), 2021, v. 11, n. 6, p. 867, doi. 10.3390/biom11060867
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Methodology Aspects of Colony Maintain for a Murine Model of Amyotrophic Lateral Sclerosis (ALS) TDP-43 Proteinopathy.
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- Animals (2076-2615), 2020, v. 10, n. 12, p. 2329, doi. 10.3390/ani10122329
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Comparing methods to combine functional loss and mortality in clinical trials for amyotrophic lateral sclerosis.
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- Clinical Epidemiology, 2018, v. 10, p. 333, doi. 10.2147/CLEP.S153196
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Exosomal TAR DNA binding protein 43 profile in canine model of amyotrophic lateral sclerosis: a preliminary study in developing blood-based biomarker for neurodegenerative diseases.
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- Annals of Medicine, 2023, v. 55, n. 1, p. 34, doi. 10.1080/07853890.2022.2153162
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Expression of hepatocyte growth factor in the skin of amyotrophic lateral sclerosis.
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- Acta Neurologica Scandinavica, 2012, v. 125, n. 6, p. 389, doi. 10.1111/j.1600-0404.2011.01579.x
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Incidence of amyotrophic lateral sclerosis in the Faroe Islands.
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- Acta Neurologica Scandinavica, 2012, v. 126, n. 1, p. 62, doi. 10.1111/j.1600-0404.2011.01611.x
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Pulmonary function tests and diaphragmatic compound muscle action potential in patients with sporadic amyotrophic lateral sclerosis.
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- Acta Neurologica Scandinavica, 2010, v. 121, n. 6, p. 400, doi. 10.1111/j.1600-0404.2009.01199.x
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In vitro neurotoxic properties and excitatory aminoacids concentration in the cerebrospinal fluid of amyotrophic lateral sclerosis patients. Relationship with the degree of certainty of disease diagnoses.
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- Acta Neurologica Scandinavica, 2010, v. 121, n. 2, p. 120, doi. 10.1111/j.1600-0404.2009.01200.x
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- Article