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Journal Abstract Search

327 related items for PubMed ID: 17128109

  • 1. [Amyotrophic lateral sclerosis (ALS): evaluation of respiratory function].
    Perez T.
    Rev Neurol (Paris); 2006 Jun; 162 Spec No 2():4S188-4S194. PubMed ID: 17128109
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  • 2. [Neuromuscular disorders - assessment of the respiratory muscles].
    Perez T.
    Rev Neurol (Paris); 2006 Apr; 162(4):437-44. PubMed ID: 16585904
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  • 5. Assessment of ventilatory function in patients with neuromuscular disease.
    Rochester DF, Esau SA.
    Clin Chest Med; 1994 Dec; 15(4):751-63. PubMed ID: 7867289
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  • 7. [Hypodynamic respiratory insufficiency. Diagnostic investigation].
    Wiis J, Mortensen J, Jacobsen E.
    Ugeskr Laeger; 2002 Dec 30; 165(1):15-20. PubMed ID: 12529942
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  • 8. 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 30; 12(6):458-63. PubMed ID: 21745123
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  • 10. 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 Nov 30; 98(2):114-124. PubMed ID: 31018212
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  • 11. Percutaneous nocturnal oximetry in amyotrophic lateral sclerosis: periodic desaturation.
    de Carvalho M, Costa J, Pinto S, Pinto A.
    Amyotroph Lateral Scler; 2009 Jun 30; 10(3):154-61. PubMed ID: 18763180
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  • 12. The cortico-diaphragmatic pathway involvement in amyotrophic lateral sclerosis: neurophysiological, respiratory and clinical considerations.
    Miscio G, Gukov B, Pisano F, Mazzini L, Baudo S, Salvadori A, Mauro A.
    J Neurol Sci; 2006 Dec 21; 251(1-2):10-6. PubMed ID: 17078971
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  • 13. Respiratory muscle strength and ventilatory failure in amyotrophic lateral sclerosis.
    Lyall RA, Donaldson N, Polkey MI, Leigh PN, Moxham J.
    Brain; 2001 Oct 21; 124(Pt 10):2000-13. PubMed ID: 11571218
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  • 15. [A study of bulbar, upper extremity, and lower extremity motor function preservation at the time that respiratory symptoms appear in ALS].
    Kimura F, Fujimura C, Ishida S, Hosokawa T, Sato T, Nakajima H, Furutama D, Sugino M.
    Rinsho Shinkeigaku; 2007 Apr 21; 47(4):140-6. PubMed ID: 17511283
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  • 17. 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 21; 62(11):975-80. PubMed ID: 17557772
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  • 18. The Borg dyspnoea score: a relevant clinical marker of inspiratory muscle weakness in amyotrophic lateral sclerosis.
    Just N, Bautin N, Danel-Brunaud V, Debroucker V, Matran R, Perez T.
    Eur Respir J; 2010 Feb 21; 35(2):353-60. PubMed ID: 19741023
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  • 19. Sniff nasal pressure: a sensitive respiratory test to assess progression of amyotrophic lateral sclerosis.
    Fitting JW, Paillex R, Hirt L, Aebischer P, Schluep M.
    Ann Neurol; 1999 Dec 21; 46(6):887-93. PubMed ID: 10589541
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