[1]
|
Maksymowicz-Sliwinska, A., Lule, D., Nieporecki, K., et al. (2023) The Quality of Life and Depression in Primary Caregivers of Patients with Amyotrophic Lateral Sclerosis Is Affected by Patient-Related and Culture-Specific Conditions. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 24, 317-326.
https://doi.org/10.1080/21678421.2022.2126322
|
[2]
|
Galvin, M., Gavin, T., Mays, I., et al. (2020) Individual Quality of Life in Spousal ALS Patient-Caregiver Dyads. Health and Quality of Life Outcomes, 18, Article No. 371. https://doi.org/10.1186/s12955-020-01551-5
|
[3]
|
Makkonen, T., Ruottinen, H., Puhto, R., et al. (2018) Speech Deterioration in Amyotrophic Lateral Sclerosis (ALS) after Manifestation of Bulbar Symptoms. International Journal of Language & Communication Disorders, 53, 385- 392. https://doi.org/10.1111/1460-6984.12357
|
[4]
|
Thomas, K. (2020) Percutaneous Endoscopic Gastrostomy Tube Placement in Amyotrophic Lateral Sclerosis: A Case Series with a Multidisciplinary, Team-Based Approach. Annals of Gastroenterology, 33, 1-5.
https://doi.org/10.20524/aog.2020.0517
|
[5]
|
Hardiman, O., Al-Chalabi, A., Chio, A., et al. (2017) Amyotrophic Lateral Sclerosis. Nature Reviews Disease Primers, 3, Article No. 17071. https://doi.org/10.1038/nrdp.2017.71
|
[6]
|
Peggion, C., Scalcon, V., Massimino, M.L., et al. (2022) SOD1 in ALS: Taking Stock in Pathogenic Mechanisms and the Role of Glial and Muscle Cells. Antioxidants, 11, Article 614. https://doi.org/10.3390/antiox11040614
|
[7]
|
Liu, T., Woo, J.A., Bukhari, M.Z., et al. (2020) CHCHD10-Regulated OPA1-Mitofilin Complex Mediates TDP-43- Induced Mitochondrial Phenotypes Associated with Frontotemporal Dementia. FASEB Journal, 34, 8493-8509.
https://doi.org/10.1096/fj.201903133RR
|
[8]
|
Candelise, N., Salvatori, I., Scaricamazza, S., et al. (2022) Mechanis-tic Insights of Mitochondrial Dysfunction in Amyotrophic Lateral Sclerosis: An Update on a Lasting Relationship. Me-tabolites, 12, Article 233.
https://doi.org/10.3390/metabo12030233
|
[9]
|
Castellanos-Montiel, M.J., Chaineau, M. and Durcan, T.M. (2020) The Neglected Genes of ALS: Cytoskeletal Dynamics Impact Synaptic Degeneration in ALS. Frontiers in Cellular Neu-roscience, 14, Article 594975.
https://doi.org/10.3389/fncel.2020.594975
|
[10]
|
Chio, A., Logroscino, G., Hardiman, O., et al. (2009) Prognostic Factors in ALS: A Critical Review. Amyotrophic Lateral Sclerosis, 10, 310-323. https://doi.org/10.3109/17482960802566824
|
[11]
|
Elamin, M., Bede, P., Montuschi, A., et al. (2015) Predicting Prognosis in Amyotrophic Lateral Sclerosis: A Simple Algorithm. Journal of Neurology, 262, 1447-1454. ttps://doi.org/10.1007/s00415-015-7731-6
|
[12]
|
Daghlas, I., Lever, T.E. and Leary, E. (2018) A Retrospective Investiga-tion of the Relationship between Baseline Covariates and Rate of ALSFRS-R Decline in ALS Clinical Trials. Amyo-trophic Lateral Sclerosis and Frontotemporal Degeneration, 19, 206-211. https://doi.org/10.1080/21678421.2017.1418001
|
[13]
|
Lee, J., Madhavan, A., Krajewski, E., et al. (2021) Assess-ment of Dysarthria and Dysphagia in Patients with Amyotrophic Lateral Sclerosis: Review of the Current Evidence. Muscle & Nerve, 64, 520-531.
https://doi.org/10.1002/mus.27361
|
[14]
|
Rooney, J., Byrne, S., Heverin, M., et al. (2015) A Multidisciplinary Clinic Approach Improves Survival in ALS: A Comparative Study of ALS in Ireland and Northern Ireland. Journal of Neurol-ogy, Neurosurgery & Psychiatry, 86, 496-501. https://doi.org/10.1136/jnnp-2014-309601
|
[15]
|
Jani, M.P. and Gore, G.B. (2016) Swallowing Characteristics in Amyotrophic Lateral Sclerosis. NeuroRehabilitation, 39, 273-276. https://doi.org/10.3233/NRE-161357
|
[16]
|
Ngo, S.T., Wang, H., Henderson, R.D., et al. (2021) Ghrelin as a Treatment for Amyotrophic Lateral Sclerosis. Journal of Neuroendocrinology, 33, e12938. https://doi.org/10.1111/jne.12938
|
[17]
|
Tomik, B. and Guiloff, R.J. (2010) Dysarthria in Amyotrophic Lateral Scle-rosis: A Review. Amyotrophic Lateral Sclerosis, 11, 4-15. https://doi.org/10.3109/17482960802379004
|
[18]
|
Makkonen, T., Korpijaakko-Huuhka, A., Ruottinen, H., et al. (2016) Oral Motor Functions, Speech and Communication before a Definitive Diagnosis of Amyotrophic Lateral Sclero-sis. Journal of Communication Disorders, 61, 97-105.
https://doi.org/10.1016/j.jcomdis.2016.04.002
|
[19]
|
Waito, A.A., Valenzano, T.J., Peladeau-Pigeon, M., et al. (2017) Trends in Research Literature Describing Dysphagia in Motor Neuron Diseases (MND): A Scoping Review. Dysphagia, 32, 734-747.
https://doi.org/10.1007/s00455-017-9819-x
|
[20]
|
Murono, S., Hamaguchi, T., Yoshida, H., et al. (2015) Evaluation of Dysphagia at the Initial Diagnosis of Amyotrophic Lateral Sclerosis. Auris Nasus Larynx, 42, 213-217. https://doi.org/10.1016/j.anl.2014.10.012
|
[21]
|
Plowman, E.K., Tabor, L.C., Robison, R., et al. (2016) Discriminant Ability of the Eating Assessment Tool-10 to Detect Aspiration in Individuals with Amyotrophic Lateral Sclerosis. Neu-rogastroenterology & Motility, 28, 85-90.
https://doi.org/10.1111/nmo.12700
|
[22]
|
Plowman, E.K., Watts, S.A., Robison, R., et al. (2016) Voluntary Cough Airflow Differentiates Safe versus Unsafe Swallowing in Amyotrophic Lateral Sclerosis. Dysphagia, 31, 383-390. https://doi.org/10.1007/s00455-015-9687-1
|
[23]
|
Tremolizzo, L., Susani, E., Lunetta, C., et al. (2014) Primitive Re-flexes in Amyotrophic Lateral Sclerosis: Prevalence and Correlates. Journal of Neurology, 261, 1196-1202. https://doi.org/10.1007/s00415-014-7342-7
|
[24]
|
Couratier, P., Lautrette, G., Luna, J.A., et al. (2021) Phenotypic Variability in Amyotrophic Lateral Sclerosis. Revue Neurologique, 177, 536-543. https://doi.org/10.1016/j.neurol.2021.03.001
|
[25]
|
Marin-Medina, D.S., Gaspar-Toro, J.M. and Munoz-Rosero, A.M. (2023) Clinical Examination of the Cranial Nerves. The New England Journal of Medicine, 389, 1057-1058. https://doi.org/10.1056/NEJMc2309338
|
[26]
|
Reese, V., Das, J.M. and Al Khalili, Y. (2023) Cranial Nerve Testing. StatPearls, Treasure Island.
|
[27]
|
Sonoo, M., Kuwabara, S., Shimizu, T., et al. (2009) Utility of Trapezius EMG for Di-agnosis of Amyotrophic Lateral Sclerosis. Muscle & Nerve, 39, 63-70. https://doi.org/10.1002/mus.21196
|
[28]
|
Tankisi, H., Otto, M., Pugdahl, K., et al. (2013) Spontaneous Electromyo-graphic Activity of the Tongue in Amyotrophic Lateral Sclerosis. Muscle Nerve, 48, 296-298. https://doi.org/10.1002/mus.23781
|
[29]
|
Risi, B., Cotti Piccinelli, S., Gazzina, S., et al. (2023) Prognostic Useful-ness of Motor Unit Number Index (MUNIX) in Patients Newly Diagnosed with Amyotrophic Lateral Sclerosis. Journal of Clinical Medicine, 12, Article 5036.
https://doi.org/10.3390/jcm12155036
|
[30]
|
Bede, P. and Hardiman, O. (2014) Lessons of ALS Imaging: Pitfalls and Future Directions—A Critical Review. NeuroImage: Clinical, 4, 436-443. https://doi.org/10.1016/j.nicl.2014.02.011
|
[31]
|
Rajagopalan, V., Chaitanya, K.G. and Pioro, E.P. (2023) Quantita-tive Brain MRI Metrics Distinguish Four Different ALS Phenotypes: A Machine Learning Based Study. Diagnostics, 13, Article 1521.
https://doi.org/10.3390/diagnostics13091521
|
[32]
|
van der Graaff, M.M., Sage, C.A., Caan, M.W.A., et al. (2011) Upper and Extra-Motoneuron Involvement in Early Motoneuron Disease: A Diffusion Tensor Imaging Study. Brain, 134, 1211-1228. https://doi.org/10.1093/brain/awr016
|
[33]
|
Plowman, E.K., Tabor, L.C., Wyme, J. and Pattee, G. (2017) The Evaluation of Bulbar Dysfunction in Amyotrophic Lateral Sclerosis: Survey of Clinical Practice Patterns in the Unit-ed States. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 18, 351-357. https://doi.org/10.1080/21678421.2017.1313868
|
[34]
|
Rooney, J., Burke, T., Vajda, A., et al. (2017) What Does the ALSFRS-R Really Measure? A Longitudinal and Survival Analysis of Functional Dimension Subscores in Amyo-trophic Lateral Sclerosis. Journal of Neurology, Neurosurgery & Psychiatry, 88, 381-385. https://doi.org/10.1136/jnnp-2016-314661
|
[35]
|
Smith, R.A., Macklin, E.A., Myers, K.J., et al. (2018) Assessment of Bulbar Function in Amyotrophic Lateral Sclerosis: Validation of a Self-Report Scale (Center for Neurologic Study Bulbar Function Scale). European Journal of Neurology, 25, 907-e66. https://doi.org/10.1111/ene.13638
|
[36]
|
Smith, R., Pioro, E., Myers, K., et al. (2017) Enhanced Bulbar Function in Amyotrophic Lateral Sclerosis: The Nuedexta Treatment Trial. Neurotherapeutics, 14, 762-772. https://doi.org/10.1007/s13311-016-0508-5
|
[37]
|
Appel, V., Stewart, S.S., Smith, G. and Appel, S.H. (1987) A Rating Scale for Amyotrophic Lateral Sclerosis: Description and Preliminary Experience. Annals of Neurology, 22, 328-333. https://doi.org/10.1002/ana.410220308
|
[38]
|
Hillel, A.D., Miller, R.M., Yorkston, K., et al. (1989) Amy-otrophic Lateral Sclerosis Severity Scale. Neuroepidemiology, 8, 142-150. https://doi.org/10.1159/000110176
|
[39]
|
Kidney, D., Alexander, M., Corr, B., et al. (2009) Oropharyngeal Dyspha-gia in Amyotrophic Lateral Sclerosis: Neurological and Dysphagia Specific Rating Scales. Amyotrophic Lateral Sclerosis and Other Motor Neuron Disorders, 5, 150-153. https://doi.org/10.1080/14660820410019675
|
[40]
|
Donohue, C., Tabor Gray, L., Anderson, A., et al. (2022) Discriminant Ability of the Eating Assessment Tool-10 to Detect Swallowing Safety and Efficiency Impairments. The Laryngoscope, 132, 2319-2326.
https://doi.org/10.1002/lary.30043
|
[41]
|
Abdelnour-Mallet, M., Tezenas Du Montcel, S., Cazzolli, P.A., et al. (2012) Validation of Robust Tools to Measure Sialorrhea in Amyotrophic Lateral Sclerosis: A Study in a Large French Cohort. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 14, 302-307. https://doi.org/10.3109/21678421.2012.735238
|
[42]
|
Bede, P., Bokde, A., Elamin, M., et al. (2013) Grey Matter Correlates of Clinical Variables in Amyotrophic Lateral Sclerosis (ALS): A Neuroimaging Study of ALS Motor Pheno-type Heterogeneity and Cortical Focality. Journal of Neurology, Neurosurgery & Psychiatry, 84, 766-773. https://doi.org/10.1136/jnnp-2012-302674
|
[43]
|
Beukelman, D., Fager, S. and Nordness, A. (2011) Communication Support for People with ALS. Neurology Research International, 2011, Article ID: 714693. https://doi.org/10.1155/2011/714693
|
[44]
|
Rong, P., Yunusova, Y., Wang, J., et al. (2015) Predicting Early Bulbar Decline in Amyotrophic Lateral Sclerosis: A Speech Subsystem Approach. Behavioural Neurology, 2015, Article ID: 183027. https://doi.org/10.1155/2015/183027
|
[45]
|
Allison, K.M., Yunusova, Y., Campbell, T.F., et al. (2017) The Diagnostic Utility of Patient-Report and Speech-Lan- guage Pathologists’ Ratings for Detecting the Early Onset of Bulbar Symptoms Due to ALS. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration, 18, 358-366. https://doi.org/10.1080/21678421.2017.1303515
|
[46]
|
Rong, P., Yunusova, Y., Richburg, B. and Green, J.R. (2018) Automatic Extraction of Abnormal Lip Movement Features from the Alternating Motion Rate Task in Amyotrophic Lat-eral Sclerosis. International Journal of Speech-Lan- guage Pathology, 20, 610-623. https://doi.org/10.1080/17549507.2018.1485739
|