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Journal Abstract Search

130 related items for PubMed ID: 22819354

  • 1. Balancing between autonomy and support: coping strategies by patients with amyotrophic lateral sclerosis.
    Tramonti F, Bongioanni P, Fanciullacci C, Rossi B.
    J Neurol Sci; 2012 Sep 15; 320(1-2):106-9. PubMed ID: 22819354
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  • 2. Amyotrophic lateral sclerosis and assisted ventilation: how patients decide.
    Lemoignan J, Ells C.
    Palliat Support Care; 2010 Jun 15; 8(2):207-13. PubMed ID: 20557668
    [Abstract] [Full Text] [Related]

  • 3. The impact of active coping strategies on survival in ALS: the first pilot study.
    Montel S, Albertini L, Desnuelle C, Spitz E.
    Amyotroph Lateral Scler; 2012 Oct 15; 13(6):599-601. PubMed ID: 22881411
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  • 4. Coping strategies as related to medical and demographic data in amyotrophic lateral sclerosis.
    Montel S, Albertini L, Spitz E.
    Acta Neurol Scand; 2012 Feb 15; 125(2):136-41. PubMed ID: 21470190
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  • 7. Living with amyotrophic lateral sclerosis/motor neurone disease (ALS/MND): decision-making about 'ongoing change and adaptation'.
    King SJ, Duke MM, O'Connor BA.
    J Clin Nurs; 2009 Mar 15; 18(5):745-54. PubMed ID: 19239541
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  • 8. A permanent emergency: a longitudinal study on families coping with amyotrophic lateral sclerosis.
    Tramonti F, Barsanti I, Bongioanni P, Bogliolo C, Rossi B.
    Fam Syst Health; 2014 Sep 15; 32(3):271-9. PubMed ID: 24749678
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  • 9. [Assessment of "coping with disease" in patients with amyotrophic lateral sclerosis (ALS): on the use of an interviewer assessment rating scale].
    Böcker FM, Seibold I.
    Psychother Psychosom Med Psychol; 1990 Aug 15; 40(8):285-92. PubMed ID: 2236471
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  • 10. Ventilator dependence and expressions of need: a study of patients with amyotrophic lateral sclerosis in Japan.
    Hirano YM, Yamazaki Y, Shimizu J, Togari T, Bryce TJ.
    Soc Sci Med; 2006 Mar 15; 62(6):1403-13. PubMed ID: 16263201
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  • 12. Coping with amyotrophic lateral sclerosis; from diagnosis and during disease progression.
    Jakobsson Larsson B, Nordin K, Nygren I.
    J Neurol Sci; 2016 Feb 15; 361():235-42. PubMed ID: 26810549
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  • 13. Caregiver burden and patients' perception of being a burden in ALS.
    Chiò A, Gauthier A, Calvo A, Ghiglione P, Mutani R.
    Neurology; 2005 May 24; 64(10):1780-2. PubMed ID: 15911811
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  • 14. [Emotions and amyotrophic lateral sclerosis: a psychopathological perspective].
    Bungener C.
    Geriatr Psychol Neuropsychiatr Vieil; 2012 Mar 24; 10(1):57-64. PubMed ID: 22414400
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  • 15. Long-term management of respiratory failure in amyotrophic lateral sclerosis.
    Sivak ED, Gipson WT, Hanson MR.
    Ann Neurol; 1982 Jul 24; 12(1):18-23. PubMed ID: 6810747
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  • 17. Differences in quality of life modalities give rise to needs of individual support in patients with ALS and their next of kin.
    Olsson AG, Markhede I, Strang S, Persson LI.
    Palliat Support Care; 2010 Mar 24; 8(1):75-82. PubMed ID: 20163763
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  • 18. Perceptions of quality of life in people with ALS: effects of coping and health care.
    Foley G, O'Mahony P, Hardiman O.
    Amyotroph Lateral Scler; 2007 Jun 24; 8(3):164-9. PubMed ID: 17538778
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  • 20. The family support group in the treatment of amyotrophic lateral sclerosis.
    Finger S.
    Neurol Clin; 1987 Feb 24; 5(1):83-100. PubMed ID: 3561383
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