References
- Preux PM, Couratier P, Boutros-Toni F, Salle JY, Tabaraud F, Bernet-Bernady P, . Survival Prediction in Sporadic Amyotrophic Lateral Sclerosis. Age and Clinical Form at Onset Are Independent Risk Factors. Neuroepidemiology. 1996;15:153–60.
- Chiò A, Logroscino G, Hardiman O, Swingler R, Mitchell D, Beghi E, . Prognostic factors in ALS: a critical review. Amyotroph Lateral Scler. 2009;10:310–23.
- Paillisse C, Lacomblez L, Dib M, Bensimon G, Garcia Acosta S, Meininger V. Prognostic factors for survival in amyotrophic lateral sclerosis patients treated with riluzole. Amyotroph Lateral Scler. 2005;6:37–44.
- McDonald ER, Wiedenfeld SA, Carpenter CL, Walter RA. Survival in Amyotrophic Lateral Sclerosis: The Role of Psychological Factors. Arch Neurol. 1994;51:17–23.
- Johnston M, Earll L, Giles M, Mcclenahan R, Val Morrison DS. Mood as a predictor of disability and survival in patients newly diagnosed with ALS/MND. British Journal of Health Psychology. 1999;4:127–36.
- Lazarus R, Folkman S. Stress, appraisal and coping. Springer, 1984.
- Montel S, Albertini L, Spitz E. Coping strategies as related to medical and demographic data in ALS. Acta Neurol Scand. 2012;125:136–41.
- Montel S, Albertini L, Spitz E. Coping strategies in relation with quality of life in ALS. J Muscle & Nerve. 2012; 45:131–4.
- Brooks BR, Miller RG, Swash M, Munsat TL. El Elscorial revisited: revised criteria for the diagnosis of amyotrophic lateral sclerosis. Amyotroph Lateral Scler. 2000;1:193–9.
- Cedarbaum JM, Stambler N, Malta E, Fuller C, Hilt D, Thurmond B, . The ALSFRS-R: a revised ALS functional rating scale that incorporates assessments of respiratory function. Neurol Sci. 1999;169:13–21.
- Muller L, Spitz E. Multidimensional assessment of coping: validation of the Brief COPE among French population. Encephale. 2003;29:507–18.
- Goodchild ME, Ducan-Jones P. Chronicity and the General Health Questionnaire. Brit J Psychiatry. 1985;146:55–61.
- Elamin M, Phukan J, Bede P, Jordan N, Byrne S, Pender N, . Executive dysfunction is a negative prognostic indicator in patients with ALS without dementia. Neurology. 2011;76:1263–9.