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Journal Abstract Search

425 related items for PubMed ID: 11571218

  • 1. Respiratory muscle strength and ventilatory failure in amyotrophic lateral sclerosis.
    Lyall RA, Donaldson N, Polkey MI, Leigh PN, Moxham J.
    Brain; 2001 Oct; 124(Pt 10):2000-13. PubMed ID: 11571218
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  • 2. 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 Oct; 98(2):114-124. PubMed ID: 31018212
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  • 3. Predicting respiratory insufficiency in amyotrophic lateral sclerosis: the role of phrenic nerve studies.
    Pinto S, Turkman A, Pinto A, Swash M, de Carvalho M.
    Clin Neurophysiol; 2009 May; 120(5):941-6. PubMed ID: 19342290
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  • 4. Expiratory muscle function in amyotrophic lateral sclerosis.
    Polkey MI, Lyall RA, Green M, Nigel Leigh P, Moxham J.
    Am J Respir Crit Care Med; 1998 Sep; 158(3):734-41. PubMed ID: 9730998
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  • 6. Sniff nasal inspiratory pressure as a prognostic factor of tracheostomy or death in amyotrophic lateral sclerosis.
    Capozzo R, Quaranta VN, Pellegrini F, Fontana A, Copetti M, Carratù P, Panza F, Cassano A, Falcone VA, Tortelli R, Cortese R, Simone IL, Resta O, Logroscino G.
    J Neurol; 2015 Mar; 262(3):593-603. PubMed ID: 25522696
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  • 7. 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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  • 9. Progression from respiratory dysfunction to failure in late-onset Pompe disease.
    Berger KI, Chan Y, Rom WN, Oppenheimer BW, Goldring RM.
    Neuromuscul Disord; 2016 Aug 01; 26(8):481-9. PubMed ID: 27297666
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  • 11. Do bulbar-onset amyotrophic lateral sclerosis patients have an earlier respiratory involvement than spinal-onset amyotrophic lateral sclerosis patients?
    Pinto S, Pinto A, De Carvalho M.
    Eura Medicophys; 2007 Dec 01; 43(4):505-9. PubMed ID: 18084174
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  • 14. Respiratory measures in amyotrophic lateral sclerosis.
    Lechtzin N, Cudkowicz ME, de Carvalho M, Genge A, Hardiman O, Mitsumoto H, Mora JS, Shefner J, Van den Berg LH, Andrews JA.
    Amyotroph Lateral Scler Frontotemporal Degener; 2018 Aug 01; 19(5-6):321-330. PubMed ID: 29566571
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  • 16. Assessment and monitoring of ventilatory function and cough efficacy in patients with amyotrophic lateral sclerosis.
    Chetta A, Aiello M, Tzani P, Olivieri D.
    Monaldi Arch Chest Dis; 2007 Mar 01; 67(1):43-52. PubMed ID: 17564284
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  • 18. 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 01; 53(2):. PubMed ID: 30523161
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  • 19. 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 01; 109(6 Suppl 1):11-19. PubMed ID: 30642145
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  • 20. 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 01; 62(11):975-80. PubMed ID: 17557772
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