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199 related items for PubMed ID: 36872491

  • 1. Respiratory phenotypes in amyotrophic lateral sclerosis as determined by respiratory questions on the Amyotrophic Lateral Sclerosis Functional Rating Scale-Revised and their relation to respiratory tests.
    Pinto S, Oliveira Santos M, Gromicho M, Swash M, de Carvalho M.
    Eur J Neurol; 2023 Jun; 30(6):1594-1599. PubMed ID: 36872491
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  • 2. Impact of diabetes mellitus on the respiratory function of amyotrophic lateral sclerosis patients.
    Pinto S, Oliveira Santos M, Gromicho M, Swash M, de Carvalho M.
    Eur J Neurol; 2024 Feb; 31(2):e16129. PubMed ID: 37955564
    [Abstract] [Full Text] [Related]

  • 3. Compensatory metabolic and central respiratory drive mechanisms in ALS.
    Pinto S, Swash M, De Carvalho M.
    Amyotroph Lateral Scler Frontotemporal Degener; 2021 Nov; 22(7-8):585-587. PubMed ID: 33641560
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  • 4. 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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  • 5. Correlation between Forced Vital Capacity and Slow Vital Capacity for the assessment of respiratory involvement in Amyotrophic Lateral Sclerosis: a prospective study.
    Pinto S, de Carvalho M.
    Amyotroph Lateral Scler Frontotemporal Degener; 2017 Feb; 18(1-2):86-91. PubMed ID: 27915482
    [Abstract] [Full Text] [Related]

  • 6. Mouth occlusion pressure at 100ms (P0.1) as a respiratory biomarker in amyotrophic lateral sclerosis.
    Pinto S, Swash M, De Carvalho M.
    Amyotroph Lateral Scler Frontotemporal Degener; 2021 Feb; 22(1-2):53-60. PubMed ID: 32955378
    [Abstract] [Full Text] [Related]

  • 7. Comparison of slow and forced vital capacities on ability to predict survival in ALS.
    Pinto S, de Carvalho M.
    Amyotroph Lateral Scler Frontotemporal Degener; 2017 Nov; 18(7-8):528-533. PubMed ID: 28741375
    [Abstract] [Full Text] [Related]

  • 8. 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; 43(4):505-9. PubMed ID: 18084174
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  • 11. Ultrasonic detection of vagus, accessory, and phrenic nerve atrophy in amyotrophic lateral sclerosis: Relation to impairment and mortality.
    Walter U, Sobiella G, Prudlo J, Batchakaschvili M, Böhmert J, Storch A, Hermann A.
    Eur J Neurol; 2024 Feb; 31(2):e16127. PubMed ID: 37933884
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  • 14. Variation in noninvasive ventilation use in amyotrophic lateral sclerosis.
    Thakore NJ, Lapin BR, Pioro EP, Aboussouan LS.
    Neurology; 2019 Jul 16; 93(3):e306-e316. PubMed ID: 31182506
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  • 16. Respiratory function tests in amyotrophic lateral sclerosis: The role of maximal voluntary ventilation.
    de Carvalho M, Fernandes SR, Pereira M, Gromicho M, Santos MO, Alves I, Pinto S, Swash M.
    J Neurol Sci; 2022 Mar 15; 434():120143. PubMed ID: 35030382
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  • 18. [Respiratory domain of revised amyotrophic lateral sclerosis. Functional Rating Scale].
    Lima SE, Pessolano FA, Monteiro SG, De Vito EL.
    Medicina (B Aires); 2009 Mar 15; 69(5):547-53. PubMed ID: 19897441
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