Respiratory onset in amyotrophic lateral sclerosis: clinical features and spreading pattern

References

• de Carvalho M, Matias T, Coelho F, Evangelista T, Pinto A, Luís MLS. Motor neuron disease presenting with respiratory failure. J Neurol Sci.1996;139:117–22.
   PubMed Web of Science ®Google Scholar
• Chen R, Grand'Maison F, Strong MJ, Ramsay DA, Bolton CF. Motor neuron disease presenting as acute respiratory failure: a clinical and pathological study. J Neurol Neurosurg Psychiatry. 1996;60:455–8.
   PubMed Web of Science ®Google Scholar
• Scelsa SN, Yakubov B, Salzman SH. Dyspnea-fasciculation syndrome: early respiratory failure in ALS with minimal motor signs. Amyotroph Lateral Scler Other Motor Neuron Disord. 2002;3:239–43.
   PubMed Web of Science ®Google Scholar
• Czaplinski A, Strobel W, Gobbi C, Steck AJ, Fuhr P, Leppert D. Respiratory failure due to bilateral diaphragm palsy as an early manifestation of ALS. Med Sci Monit 2003;9:S34–S6.
   Google Scholar
• Shoesmith CL, Findlater K, Rowe A, Strong MJ. Prognosis of amyotrophic lateral sclerosis with respiratory onset. J Neurol Neurosurg Psychiatry. 2007;78:629–31.
   PubMed Web of Science ®Google Scholar
• Gautier G, Verschueren A, Monnier A, Attarian S, Salort-Campana E, Pouget J. ALS with respiratory onset: clinical features and effects of non-invasive ventilation on the prognosis. Amyotroph Lateral Scler. 2010;11:379–82.
   PubMed Web of Science ®Google Scholar
• de Carvalho M, Swash M, Pinto S. Diaphragmatic neurophysiology and respiratory markers in ALS. Front Neurol. 2019;10:143.
   PubMed Web of Science ®Google Scholar
• Ravits J, Paul P, Jorg C. Focality of upper and lower motor neuron degeneration at the clinical onset of ALS. Neurology 2007;68:1571–5.
   PubMed Web of Science ®Google Scholar
• Brooks BR. The role of axonal transport in neurodegenerative disease spread: a meta-analysis of experimental and clinical poliomyelitis compares with amyotrophic lateral sclerosis. Can J Neurol Sci. 1991;18:435–8.
   PubMed Web of Science ®Google Scholar
• Fujimura-Kiyono C, Kimura F, Ishida S, Nakajima H, Hosokawa T, Sugino M, et al. Onset and spreading patterns of lower motor neuron involvements predict survival in sporadic amyotrophic lateral sclerosis. J Neurol Neurosurg Psychiatry.2011;82:1244–9.
   PubMed Web of Science ®Google Scholar
• Brooks BR. Natural history of ALS: symptoms, strength, pulmonary function, and disability. Neurology 1996;47:71S–82S.
   PubMed Web of Science ®Google Scholar
• Körner S, Kollewe K, Fahlbusch M, Zapf A, Dengler R, Krampfl K, et al. Onset and spreading patterns of upper and lower motor neuron symptoms in amyotrophic lateral sclerosis. Muscle Nerve. 2011;43:636–42.
   PubMed Web of Science ®Google Scholar
• Gargiulo-Monachelli GM, Janota F, Bettini M, Shoesmith CL, Strong MJ, Sica RE. Regional spread pattern predicts survival in patients with sporadic amyotrophic lateral sclerosis. Eur J Neurol. 2012;19:834–41.
   PubMed Web of Science ®Google Scholar
• Walhout R, Verstraete E, van den Heuvel MP, Veldink JK, van den Berg LH. Patterns of symptom development in patients with motor neuron disease. Amyotroph Lateral Scler Frontotemporal Degener. 2018;19:21–8.
   PubMed Web of Science ®Google Scholar
• Sekiguchi T, Kanouchi T, Shibuya K, Noto Y-I, Yagi Y, Inaba A, et al. Spreading of amyotrophic lateral sclerosis lesions-multifocal hits and local propagation? J Neurol Neurosurg Psychiatry. 2014;85:85–91.
   PubMed Web of Science ®Google Scholar
• Gromicho M, Figueiral M, Uysal H, Grosskreutz J, Kuzma-Kozakiewicz M, Pinto S, et al. Spreading in ALS: the relative impact of upper and lower motor neuron involvement. Ann Clin Transl Neurol. 2020;7:1181–92.
   PubMed Web of Science ®Google Scholar
• Shefner JM, Al-Chalabi A, Baker MR, Cui L-Y, de Carvalho M, Eisen A, et al. A proposal for new diagnostic criteria for ALS. Clin Neurophysiol. 2020;131:1975–8.
   PubMed Web of Science ®Google Scholar
• Pinto S, Geraldes R, Vaz N, Pinto A, de Carvalho M. Changes of the phrenic nerve motor response in amyotrophic lateral sclerosis: longitudinal study. Clin Neurophysiol.2009;120:2082–5.
   PubMed Web of Science ®Google Scholar
• Gromicho M, Pinto S, Gisca E, Pronto-Laborinho AC, Andersen PM, de Carvalho M. Frequency of C9orf72 hexanucleotide repeat expansion and SOD1 mutations in Portuguese patients with amyotrophic lateral sclerosis. Neurobiol Aging 2018;70:325–e7.
   PubMed Web of Science ®Google Scholar
• Pinto S, Swash M, De Carvalho M. Mouth occlusion pressure at 100ms (P0. 1) as a respiratory biomarker in amyotrophic lateral sclerosis. Amyotroph Lateral Scler Frontotemporal Degener.2021;22:53–60.
   PubMed Web of Science ®Google Scholar
• de Carvalho M, Costa J, Pinto S, Pinto A. Percutaneous nocturnal oximetry in amyotrophic lateral sclerosis: periodic desaturation. Amyotroph Lateral Scler. 2009;10:154–61.
   PubMed Web of Science ®Google Scholar
• Pinto S, de Carvalho M. Breathing new life into treatment advances for respiratory failure in amyotrophic lateral sclerosis patients. Neurodegener Dis Manag. 2014;4:83–102.
   PubMedGoogle Scholar
• Traynor BJ, Alexander M, Corr B, Frost E, Hardiman O. Effect of a multidisciplinary amyotrophic lateral sclerosis (ALS) clinic on ALS survival: a population based study, 1996–2000. J Neurol Neurosurg Psychiatry.2003;74:1258–61.
   PubMed Web of Science ®Google Scholar
• Andersen Andersen PM, Abrahams S, Borasio GD, de Carvalho M, Chio A, Van Damme P, On Diagnosis and Management of Amyotrophic Lateral Sclerosis, et al. EFNS guidelines on the clinical management of amyotrophic lateral sclerosis (MALS)-revised report of an EFNS Task Force. Eur J Neurol. 2012;19:360–75.
   PubMed Web of Science ®Google Scholar
• Pinto AC, Evangelista T, Carvalho M, Alves MA, Sales Luís ML. Respiratory assistance with a non-invasive ventilator (Bipap) in MND/ALS patients: survival rates in a controlled trial. J Neurol Sci.1995;129:19–26.
   PubMed Web of Science ®Google Scholar
• Bourke SC, Tomlinson M, Williams TL, Bullock RE, Shaw PJ, Gibson GJ. Effects of non-invasive ventilation on survival and quality of life in patients with amyotrophic lateral sclerosis: a randomised controlled trial. Lancet Neurol. 2006;5:140–7.
   PubMed Web of Science ®Google Scholar