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Journal Abstract Search

744 related items for PubMed ID: 28743265

  • 21. Measuring vital capacity in amyotrophic lateral sclerosis: Effects of interfaces and reproducibility.
    Pellegrino GM, Sferrazza Papa GF, Centanni S, Corbo M, Kvarnberg D, Tobin MJ, Laghi F.
    Respir Med; 2021 Jan; 176():106277. PubMed ID: 33310203
    [Abstract] [Full Text] [Related]

  • 22. Heterogeneity of predictors of nocturnal hypoventilation in amyotrophic lateral sclerosis.
    Crescimanno G, Sorano A, Greco F, Canino M, Abbate A, Marrone O.
    Amyotroph Lateral Scler Frontotemporal Degener; 2021 Feb; 22(1-2):46-52. PubMed ID: 32897112
    [Abstract] [Full Text] [Related]

  • 23. Factors related to respiration influencing survival and respiratory function in patients with amyotrophic lateral sclerosis: a retrospective study.
    Leonardis L, Dolenc Grošelj L, Vidmar G.
    Eur J Neurol; 2012 Dec; 19(12):1518-24. PubMed ID: 22594630
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  • 24. Respiratory muscle testing in amyotrophic lateral sclerosis: a practical approach.
    Sferrazza Papa GF, Pellegrino GM, Shaikh H, Lax A, Lorini L, Corbo M.
    Minerva Med; 2018 Dec; 109(6 Suppl 1):11-19. PubMed ID: 30642145
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  • 25. Changes of the phrenic nerve motor response in amyotrophic lateral sclerosis: longitudinal study.
    Pinto S, Geraldes R, Vaz N, Pinto A, de Carvalho M.
    Clin Neurophysiol; 2009 Dec; 120(12):2082-2085. PubMed ID: 19833553
    [Abstract] [Full Text] [Related]

  • 26. Daytime Mouthpiece for Continuous Noninvasive Ventilation in Individuals With Amyotrophic Lateral Sclerosis.
    Bédard ME, McKim DA.
    Respir Care; 2016 Oct; 61(10):1341-8. PubMed ID: 27354681
    [Abstract] [Full Text] [Related]

  • 27. Respiratory Muscle Strength as a Predictive Biomarker for Survival in Amyotrophic Lateral Sclerosis.
    Polkey MI, Lyall RA, Yang K, Johnson E, Leigh PN, Moxham J.
    Am J Respir Crit Care Med; 2017 Jan 01; 195(1):86-95. PubMed ID: 27494149
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  • 30. How respiratory muscle strength correlates with cough capacity in patients with respiratory muscle weakness.
    Park JH, Kang SW, Lee SC, Choi WA, Kim DH.
    Yonsei Med J; 2010 May 01; 51(3):392-7. PubMed ID: 20376892
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  • 32. Monitoring respiratory muscle strength assists in early diagnosis of respiratory dysfunction as opposed to the isolated use of pulmonary function evaluation in amyotrophic lateral sclerosis.
    Fregonezi G, Araújo PR, Macêdo TL, Dourado Junior ME, Resqueti VR, Andrade Ade F.
    Arq Neuropsiquiatr; 2013 Mar 01; 71(3):146-52. PubMed ID: 23563713
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  • 35. Tolerance of Volume Control Noninvasive Ventilation in Subjects With Amyotrophic Lateral Sclerosis.
    Martínez D, Sancho J, Servera E, Marín J.
    Respir Care; 2015 Dec 01; 60(12):1765-71. PubMed ID: 26420900
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  • 36. Transcutaneous CO2 monitoring as indication for inpatient non-invasive ventilation initiation in patients with amyotrophic lateral sclerosis.
    Quigg KH, Wilson MW, Choi PJ.
    Muscle Nerve; 2022 Apr 01; 65(4):444-447. PubMed ID: 34761401
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  • 37. A comparison of maximal inspiratory pressure and forced vital capacity as potential criteria for initiating non-invasive ventilation in amyotrophic lateral sclerosis.
    Mendoza M, Gelinas DF, Moore DH, Miller RG.
    Amyotroph Lateral Scler; 2007 Apr 01; 8(2):106-11. PubMed ID: 17453639
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  • 38. Association between low sniff nasal-inspiratory pressure (SNIP) and sleep disordered breathing in amyotrophic lateral sclerosis: Preliminary results.
    Carratù P, Cassano A, Gadaleta F, Tedone M, Dongiovanni S, Fanfulla F, Resta O.
    Amyotroph Lateral Scler; 2011 Nov 01; 12(6):458-63. PubMed ID: 21745123
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  • 39. Factors predicting survival following noninvasive ventilation in amyotrophic lateral sclerosis.
    Peysson S, Vandenberghe N, Philit F, Vial C, Petitjean T, Bouhour F, Bayle JY, Broussolle E.
    Eur Neurol; 2008 Nov 01; 59(3-4):164-71. PubMed ID: 18230874
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  • 40. Does timing of initiation influence acceptance and adherence to NIV in patients with ALS?
    Vitacca M, Banfi P, Montini A, Paneroni M.
    Pulmonology; 2020 Nov 01; 26(1):45-48. PubMed ID: 31175073
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