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Journal Abstract Search

165 related items for PubMed ID: 18005051

  • 1. ALS patients and caregivers communication preferences and information seeking behaviour.
    Chiò A, Montuschi A, Cammarosano S, De Mercanti S, Cavallo E, Ilardi A, Ghiglione P, Mutani R, Calvo A.
    Eur J Neurol; 2008 Jan; 15(1):55-60. PubMed ID: 18005051
    [Abstract] [Full Text] [Related]

  • 2. Information needs and information-seeking preferences of ALS patients and their carers.
    Abdulla S, Vielhaber S, Machts J, Heinze HJ, Dengler R, Petri S.
    Amyotroph Lateral Scler Frontotemporal Degener; 2014 Dec; 15(7-8):505-12. PubMed ID: 25007829
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  • 3. Breaking the news: a survey of ALS patients and their caregivers.
    McCluskey L, Casarett D, Siderowf A.
    Amyotroph Lateral Scler Other Motor Neuron Disord; 2004 Sep; 5(3):131-5. PubMed ID: 15512900
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  • 5. A longitudinal study on quality of life and depression in ALS patient-caregiver couples.
    Gauthier A, Vignola A, Calvo A, Cavallo E, Moglia C, Sellitti L, Mutani R, Chiò A.
    Neurology; 2007 Mar 20; 68(12):923-6. PubMed ID: 17372127
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  • 7. Anxiety undermines quality of life in ALS patients and caregivers.
    Vignola A, Guzzo A, Calvo A, Moglia C, Pessia A, Cavallo E, Cammarosano S, Giacone S, Ghiglione P, Chiò A.
    Eur J Neurol; 2008 Nov 20; 15(11):1231-6. PubMed ID: 18803649
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  • 10. Interviews with patients, family, and caregivers in amyotrophic lateral sclerosis: comparing needs.
    Bolmsjö I, Hermerén G.
    J Palliat Care; 2001 Nov 20; 17(4):236-40. PubMed ID: 11813340
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  • 12. Experiences of truth disclosure in terminally ill cancer patients in palliative home care.
    Friedrichsen M, Lindholm A, Milberg A.
    Palliat Support Care; 2011 Jun 20; 9(2):173-80. PubMed ID: 24468485
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  • 13. The provision of assistive devices and home adaptations to patients with ALS in the Netherlands: patients' perspectives.
    Creemers H, Beelen A, Grupstra H, Nollet F, van den Berg LH.
    Amyotroph Lateral Scler Frontotemporal Degener; 2014 Sep 20; 15(5-6):420-5. PubMed ID: 24899120
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  • 15. Aggressiveness, sexuality, and obsessiveness in late stages of ALS patients and their effects on caregivers.
    Marconi A, Meloni G, Fossati F, Lunetta C, Bastianello S, Melazzini M, Banfi P, Rossi G, Corbo M.
    Amyotroph Lateral Scler; 2012 Sep 20; 13(5):452-8. PubMed ID: 22871080
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  • 17. Trends and determinants of end-of-life practices in ALS in the Netherlands.
    Maessen M, Veldink JH, Onwuteaka-Philipsen BD, de Vries JM, Wokke JH, van der Wal G, van den Berg LH.
    Neurology; 2009 Sep 22; 73(12):954-61. PubMed ID: 19770471
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  • 18. Attitudes towards hastened death in ALS: a prospective study of patients and family caregivers.
    Stutzki R, Weber M, Reiter-Theil S, Simmen U, Borasio GD, Jox RJ.
    Amyotroph Lateral Scler Frontotemporal Degener; 2014 Mar 22; 15(1-2):68-76. PubMed ID: 24070371
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  • 19. Religiousness is positively associated with quality of life of ALS caregivers.
    Calvo A, Moglia C, Ilardi A, Cammarosano S, Gallo S, Canosa A, Mastro E, Montuschi A, Chiò A.
    Amyotroph Lateral Scler; 2011 May 22; 12(3):168-71. PubMed ID: 21348787
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  • 20. Neurobehavioral symptoms in ALS are negatively related to caregivers' burden and quality of life.
    Chiò A, Vignola A, Mastro E, Giudici AD, Iazzolino B, Calvo A, Moglia C, Montuschi A.
    Eur J Neurol; 2010 Oct 22; 17(10):1298-303. PubMed ID: 20402747
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