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Original Article

The influence of personality factors on disease progression and health‐related quality of life in people with ALS

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Pages 99-107 | Received 17 Aug 2007, Accepted 13 Dec 2007, Published online: 10 Jul 2009

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Arianna Palmieri, Johann R. Kleinbub, Francesco Pagnini, Gianni Sorarù & Sabrina Cipolletta. (2021) Empathy-based supportive treatment in amyotrophic lateral sclerosis: A pragmatic study. American Journal of Clinical Hypnosis 63:3, pages 202-216.
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Anne Hogden, David Greenfield, Peter Nugus & Matthew C Kiernan. (2012) What influences patient decision-making in amyotrophic lateral sclerosis multidisciplinary care? A study of patient perspectives. Patient Preference and Adherence 6, pages 829-838.
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Articles from other publishers (19)

Dorothée Lulé, Andrea Kübler & Albert C. Ludolph. (2019) Ethical Principles in Patient-Centered Medical Care to Support Quality of Life in Amyotrophic Lateral Sclerosis. Frontiers in Neurology 10.
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Jane A. Parkin Kullmann, Susan Hayes & Roger Pamphlett. (2018) Are people with amyotrophic lateral sclerosis (ALS) particularly nice? An international online case-control study of the Big Five personality factors. Brain and Behavior 8:10, pages e01119.
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Sabrina Cipolletta, Giorgia Rosamaria Gammino & Arianna Palmieri. (2017) Illness trajectories in patients with amyotrophic lateral sclerosis: How illness progression is related to life narratives and interpersonal relationships. Journal of Clinical Nursing 26:23-24, pages 5033-5043.
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Barbara Poletti, Laura Carelli, Annalisa Lafronza, Federica Solca, Andrea Faini, Andrea Ciammola, Monica Grobberio, Vanessa Raimondi, Rita Pezzati, Rita B. Ardito & Vincenzo Silani. (2017) Cognitive-constructivist Approach in Medical Settings: The Use of Personal Meaning Questionnaire for Neurological Patients’ Personality Investigation. Frontiers in Psychology 08.
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Annerieke C. van Groenestijn, Esther T. Kruitwagen-van Reenen, Johanna M. A. Visser-Meily, Leonard H. van den Berg & Carin D. Schröder. (2016) Associations between psychological factors and health-related quality of life and global quality of life in patients with ALS: a systematic review. Health and Quality of Life Outcomes 14:1.
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Francesco Pagnini, Gian Mauro Manzoni, Aurora Tagliaferri & Chris J Gibbons. (2014) Depression and disease progression in amyotrophic lateral sclerosis: A comprehensive meta-regression analysis. Journal of Health Psychology 20:8, pages 1107-1128.
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Johann R. Kleinbub, Arianna Palmieri, Alice Broggio, Francesco Pagnini, Enrico Benelli, Marco Sambin & Gianni Sorarù. (2015) Hypnosis-based psychodynamic treatment in ALS: a longitudinal study on patients and their caregivers. Frontiers in Psychology 6.
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Huub Creemers, Hepke Grupstra, Frans Nollet, Leonard H. van den Berg & Anita Beelen. (2014) Prognostic factors for the course of functional status of patients with ALS: a systematic review. Journal of Neurology 262:6, pages 1407-1423.
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Monique E. Hinchcliff, Jennifer L. Beaumont, Mary A. Carns, Sofia Podlusky, Krishna Thavarajah, John Varga, David Cella & Rowland W. Chang. (2015) Longitudinal Evaluation of PROMIS-29 and FACIT-Dyspnea Short Forms in Systemic Sclerosis. The Journal of Rheumatology 42:1, pages 64-72.
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Soo-Jung Park, Ho-Hyun Jeong, Eun-Su Jang, Sang-Hyuk Kim, Sung-Chul Kim & Jong-Cheon Joo. (2014) Sasang Constitutional Characteristic of Amyotrophic Lateral Sclerosis. Journal of Sasang Constitutional Medicine 26:2, pages 156-164.
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Anneli G. Ozanne & Lennart I. Persson. (2012) Correlations in health status between estimates of families of people with amyotrophic lateral sclerosis and estimates of staff. Palliative and Supportive Care 11:3, pages 183-189.
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Estela Vilhena, José Luís Pais Ribeiro, Isabel Silva, Luísa Pedro, Rute Meneses, Helena Cardoso, António Martins da Silva & Denisa Mendonça. 2013. Recent Developments in Modeling and Applications in Statistics. Recent Developments in Modeling and Applications in Statistics 31 38 .
Dorothée Lulé, Sandra Pauli, Ertan Altintas, Ulrike Singer, Thomas Merk, Ingo Uttner, Niels Birbaumer & Albert C. Ludolph. (2011) Emotional adjustment in amyotrophic lateral sclerosis (ALS). Journal of Neurology 259:2, pages 334-341.
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Louisa Ng & Fary Khan. (2011) Identification of Personal Factors in Motor Neurone Disease: A Pilot Study. Rehabilitation Research and Practice 2011, pages 1-7.
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Katja Ribbe, Heidi Friedrichs, Martin Begemann, Sabrina Grube, Sergi Papiol, Anne Kästner, Martin F Gerchen, Verena Ackermann, Asieh Tarami, Annika Treitz, Marlene Flögel, Lothar Adler, Josef B Aldenhoff, Marianne Becker-Emner, Thomas Becker, Adelheid Czernik, Matthias Dose, Here Folkerts, Roland Freese, Rolf Günther, Sabine Herpertz, Dirk Hesse, Gunther Kruse, Heinrich Kunze, Michael Franz, Frank Löhrer, Wolfgang Maier, Andreas Mielke, Rüdiger Müller-Isberner, Cornelia Oestereich, Frank-Gerald Pajonk, Thomas Pollmächer, Udo Schneider, Hans-Joachim Schwarz, Birgit Kröner-Herwig, Ursula Havemann-Reinecke, Jens Frahm, Walter Stühmer, Peter Falkai, Nils Brose, Klaus-Armin Nave & Hannelore Ehrenreich. (2010) The cross-sectional GRAS sample: A comprehensive phenotypical data collection of schizophrenic patients. BMC Psychiatry 10:1.
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Lorenzo Norris, Guinevere Que & Elham Bayat. (2010) Psychiatric Aspects of Amyotrophic Lateral Sclerosis (ALS). Current Psychiatry Reports 12:3, pages 239-245.
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Anneli G. Olsson, Inga Markhede, Susann Strang & Lennart I. Persson. (2010) Differences in quality of life modalities give rise to needs of individual support in patients with ALS and their next of kin. Palliative and Supportive Care 8:1, pages 75-82.
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. (2009) Current World Literature. Current Opinion in Supportive & Palliative Care 3:1, pages 79-89.
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Konen Obayashi, Kimiko Sato, Rie Shimazaki, Tomoko Ishikawa, Katsumasa Goto, Hidetsugu Ueyama, Teruaki Mori, Yukio Ando & Toshihide Kumamoto. (2008) Salivary Chromogranin A: Useful and Quantitative Biochemical Marker of Affective State in Patients with Amyotrophic Lateral Sclerosis. Internal Medicine 47:21, pages 1875-1879.
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