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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

331 related items for PubMed ID: 29181534

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  • 2. Relationships between slow vital capacity and measures of respiratory function on the ALSFRS-R.
    Jackson C, De Carvalho M, Genge A, Heiman-Patterson T, Shefner JM, Wei J, Wolff AA.
    Amyotroph Lateral Scler Frontotemporal Degener; 2018 Nov; 19(7-8):506-512. PubMed ID: 30379086
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  • 3. 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. The prognostic value of spirometric tests in Amyotrophic Lateral Sclerosis patients.
    Pirola A, De Mattia E, Lizio A, Sannicolò G, Carraro E, Rao F, Sansone V, Lunetta C.
    Clin Neurol Neurosurg; 2019 Sep; 184():105456. PubMed ID: 31382080
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  • 8. Mechanical ventilation for amyotrophic lateral sclerosis/motor neuron disease.
    Radunovic A, Annane D, Rafiq MK, Brassington R, Mustfa N.
    Cochrane Database Syst Rev; 2017 Oct 06; 10(10):CD004427. PubMed ID: 28982219
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  • 9. The amyotrophic lateral sclerosis functional rating scale predicts survival time in amyotrophic lateral sclerosis patients on invasive mechanical ventilation.
    Lo Coco D, Marchese S, La Bella V, Piccoli T, Lo Coco A.
    Chest; 2007 Jul 06; 132(1):64-9. PubMed ID: 17475635
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  • 10. Prognostic role of slow vital capacity in amyotrophic lateral sclerosis.
    Calvo A, Vasta R, Moglia C, Matteoni E, Canosa A, Mattei A, La Mancusa C, Focaraccio L, Mazzini L, Chiò A, D'Ovidio F, Manera U.
    J Neurol; 2020 Jun 06; 267(6):1615-1621. PubMed ID: 32052165
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  • 12. Comparison of Slow and Forced Vital Capacity on Ability to Evaluate Respiratory Function in Bulbar-Involved Amyotrophic Lateral Sclerosis.
    Huang X, Du C, Yang Q, Fan D.
    Front Neurol; 2022 Jun 06; 13():938256. PubMed ID: 35837231
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  • 13. Classifying Patients with Amyotrophic Lateral Sclerosis by Changes in FVC. A Group-based Trajectory Analysis.
    Ackrivo J, Hansen-Flaschen J, Jones BL, Wileyto EP, Schwab RJ, Elman L, Kawut SM.
    Am J Respir Crit Care Med; 2019 Dec 15; 200(12):1513-1521. PubMed ID: 31322417
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  • 15. [Clinical characteristics of elderly Japanese patients with amyotrophic lateral sclerosis; with special reference to the development of respiratory failure].
    Terao S, Miura N, Osano Y, Adachi K, Sobue G.
    Rinsho Shinkeigaku; 2006 Jun 15; 46(6):381-9. PubMed ID: 16986698
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  • 16. Effects of early introduction of non-invasive positive pressure ventilation based on forced vital capacity rate of change: Variation across amyotrophic lateral sclerosis clinical phenotypes.
    Elamin EM, Wilson CS, Sriaroon C, Crudup B, Pothen S, Kang YC, White KT, Anderson WM.
    Int J Clin Pract; 2019 Jan 15; 73(1):e13257. PubMed ID: 30230161
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  • 20. Gamma aminobutyric acid (GABA) modulators for amyotrophic lateral sclerosis/motor neuron disease.
    Diana A, Pillai R, Bongioanni P, O'Keeffe AG, Miller RG, Moore DH.
    Cochrane Database Syst Rev; 2017 Jan 09; 1(1):CD006049. PubMed ID: 28067943
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