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Journal Abstract Search

246 related items for PubMed ID: 23563713

  • 1. 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; 71(3):146-52. PubMed ID: 23563713
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  • 2. Motor responses of the sternocleidomastoid muscle in patients with amyotrophic lateral sclerosis.
    Pinto S, de Carvalho M.
    Muscle Nerve; 2008 Oct; 38(4):1312-7. PubMed ID: 18785186
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  • 3. Muscle impairment in neuromuscular disease using an expiratory/inspiratory pressure ratio.
    Fregonezi G, Azevedo IG, Resqueti VR, De Andrade AD, Gualdi LP, Aliverti A, Dourado-Junior ME, Parreira VF.
    Respir Care; 2015 Apr; 60(4):533-9. PubMed ID: 25587161
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  • 4. Assessing Inspiratory Muscle Strength for Early Detection of Respiratory Failure in Motor Neuron Disease: Should We Use MIP, SNIP, or Both?
    Janssens JP, Adler D, Iancu Ferfoglia R, Poncet A, Genton Graf L, Leuchter I, Escher Imhof M, Héritier Barras AC.
    Respiration; 2019 Apr; 98(2):114-124. PubMed ID: 31018212
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  • 6. The predictive value of respiratory function tests for non-invasive ventilation in amyotrophic lateral sclerosis.
    Tilanus TBM, Groothuis JT, TenBroek-Pastoor JMC, Feuth TB, Heijdra YF, Slenders JPL, Doorduin J, Van Engelen BG, Kampelmacher MJ, Raaphorst J.
    Respir Res; 2017 Jul 25; 18(1):144. PubMed ID: 28743265
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  • 7. The value of multiple tests of respiratory muscle strength.
    Steier J, Kaul S, Seymour J, Jolley C, Rafferty G, Man W, Luo YM, Roughton M, Polkey MI, Moxham J.
    Thorax; 2007 Nov 25; 62(11):975-80. PubMed ID: 17557772
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  • 9. 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 25; 51(3):392-7. PubMed ID: 20376892
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  • 11. Noninvasive assessment of respiratory muscle strength and activity in Myotonic dystrophy.
    Evangelista MA, Dias FAL, Dourado Júnior MET, do Nascimento GC, Sarmento A, Gualdi LP, Aliverti A, Resqueti V, Fregonezi GAF.
    PLoS One; 2017 May 25; 12(6):e0177318. PubMed ID: 28594857
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  • 12. Myelodysplastic syndrome patients present more severe respiratory muscle impairment and reduced forced vital capacity: Is disordered inflammatory signaling the culprit?
    Okubo BM, Matos AG, Ribeiro Junior HL, Borges DP, Oliveira RTG, de Castro MF, Martins MRA, Gonçalves RP, Bruin PFC, Pinheiro RF, Magalhães SMM.
    PLoS One; 2017 May 25; 12(9):e0184079. PubMed ID: 28877261
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  • 15. Maximal values of sniff nasal inspiratory pressure in healthy subjects.
    Uldry C, Fitting JW.
    Thorax; 1995 Apr 25; 50(4):371-5. PubMed ID: 7785009
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  • 16. Human diaphragm atrophy in amyotrophic lateral sclerosis is not predicted by routine respiratory measures.
    Guimarães-Costa R, Similowski T, Rivals I, Morélot-Panzini C, Nierat MC, Bui MT, Akbar D, Straus C, Romero NB, Michel PP, Menegaux F, Salachas F, Gonzalez-Bermejo J, Bruneteau G, RespiStimALS team, contributors to the RespiStimALS study were:.
    Eur Respir J; 2019 Feb 25; 53(2):. PubMed ID: 30523161
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  • 18. Heart Failure Results in Inspiratory Muscle Dysfunction Irrespective of Left Ventricular Ejection Fraction.
    Spiesshoefer J, Henke C, Kabitz HJ, Bengel P, Schütt K, Nofer JR, Spieker M, Orwat S, Diller GP, Strecker JK, Giannoni A, Dreher M, Randerath WJ, Boentert M, Tuleta I.
    Respiration; 2021 Feb 25; 100(2):96-108. PubMed ID: 33171473
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  • 20. 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 25; 176():106277. PubMed ID: 33310203
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