The DOI matches its Crossref record; 82 of the 83 references it cites were found in a registry or an index.
Psychological health in patients with amyotrophic lateral sclerosis
Abstract
Amyotrophic lateral sclerosis (ALS) is a progressive and fatal neurodegenerative disease with no known effective treatment or cure. Clinicians often expect that ALS patients will experience depression following the diagnosis because ALS is a terminal disease. The objective of the current study was to examine the evidence from the literature on psychological health in ALS patients in order to determine the prevalence and severity of depression in this population. Twenty-eight studies of ALS patients, conducted over the past 20 years, were reviewed and evaluated. The cumulative evidence suggests that clinically significant depression is neither as prevalent nor as severe as might be expected. Methodological limitations that are inherent to the measurement of depression in ALS, including the lack of appropriate instruments, small sample sizes, and reliance on cross-sectional data, have contributed to the wide range of reported results. We conclude that ALS patients are more likely to present with hopelessness and end-of-life concerns than clinically significant depression. It is important to assess a broad range of potential psychological distress early in the course of ALS, rather than focus specifically on depression, because the manner in which patients cope with their disease can affect their longevity.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“MND has been reported to be the most frequent cause of assisted suicide [5–7].”
In the citing paper
“Hopelessness is one psychological aspect which presents a significant problem for patients with MND”
From Patients experiences of maintaining mental well-being and hope within motor neuron disease: a thematic synthesis (2015) · cites this paper as Averill et al., 2007
In the citing paper
“Apart from the benefits of being connected and valued with others, interactions were also beneficial in that they provided a chance for individuals to give back or care for others (5, 16, 17, 18, 19, 27).”
From Patients experiences of maintaining mental well-being and hope within motor neuron disease: a thematic synthesis (2015) · cites this paper as [5]
In the citing paper
“Patients could also feel sadness and grief about the losses the illness had imposed on their lives (1, 5, 12).”
From Patients experiences of maintaining mental well-being and hope within motor neuron disease: a thematic synthesis (2015) · cites this paper as [5]
In the citing paper
“In a similar way, peers friends and close others became important to individuals (4, 5, 8, 12, 16, 20, 29).”
From Patients experiences of maintaining mental well-being and hope within motor neuron disease: a thematic synthesis (2015) · cites this paper as [5]
In the citing paper
“Patients highly valued maximizing the autonomy of their actions and task functions and required that they were respected within interactions (5, 7, 8, 11, 12, 14, 15, 16, 18, 19, 20, 21, 23, 24, 25, 28).”
From Patients experiences of maintaining mental well-being and hope within motor neuron disease: a thematic synthesis (2015) · cites this paper as [5]
In the citing paper
“Further to this and more generally, relationships and interaction with others was identified as important (3, 5, 11, 14, 16, 18, 19, 20, 25, 27, 29).”
From Patients experiences of maintaining mental well-being and hope within motor neuron disease: a thematic synthesis (2015) · cites this paper as [5]
In the citing paper
“Related to this, patients consistently highlighted the need for choice and autonomy given during an interaction (5, 6, 7, 9, 12, 14, 15, 20, 24, 25, 26, 28).”
From Patients experiences of maintaining mental well-being and hope within motor neuron disease: a thematic synthesis (2015) · cites this paper as [5]
In the citing paper
“Patients described the need to retain dignity and feel respected during interactions (5, 7, 12, 13, 15, 23, 25).”
From Patients experiences of maintaining mental well-being and hope within motor neuron disease: a thematic synthesis (2015) · cites this paper as [5]
In the citing paper
“The role and care given by HCPs was identified as important in that support from health care professionals influenced participants mental well-being and coping (4, 5, 12, 14, 16, 23, 26).”
From Patients experiences of maintaining mental well-being and hope within motor neuron disease: a thematic synthesis (2015) · cites this paper as [5]
In the citing paper
“Other pragmatic adaptation included individuals continuing meaningful activities (4, 5, 7, 9, 10, 12, 14, 15, 16, 17, 18, 19, 20, 25, 27, 29) or continuing being “normal” (1, 2, 5, 7, 9, 17, 18, 24) which provided access to a sense of purpose and meaning as well as valued interactions.”
From Patients experiences of maintaining mental well-being and hope within motor neuron disease: a thematic synthesis (2015) · cites this paper as [5]
In the citing paper
“A number of studies highlighted that patients required physical assistance in increasing quantities (5, 11, 16, 18).”
From Patients experiences of maintaining mental well-being and hope within motor neuron disease: a thematic synthesis (2015) · cites this paper as [5]
In the citing paper
“(c) Focusing on what could be done or achieved (2, 5, 6, 7, 11, 12, 13, 14, 27), rather than what they couldn't or what they had lost.”
From Patients experiences of maintaining mental well-being and hope within motor neuron disease: a thematic synthesis (2015) · cites this paper as [5]
In the citing paper
“Individuals consistently identified the need to search for information in order to feel more in control (2, 4, 5, 9, 10, 12, 13, 14, 15, 22, 25, 26)”
From Patients experiences of maintaining mental well-being and hope within motor neuron disease: a thematic synthesis (2015) · cites this paper as [5]
In the citing paper
“but also take action as a way of controlling aspects of their life that were controllable (2, 4, 5, 11, 12, 14, 18, 19).”
From Patients experiences of maintaining mental well-being and hope within motor neuron disease: a thematic synthesis (2015) · cites this paper as [5]
In the citing paper
“(e) Using religious faith to aid acceptance, and coping, or hoping for a miracle to occur, or life after death (5, 9, 14, 16, 20, 27, 29).”
From Patients experiences of maintaining mental well-being and hope within motor neuron disease: a thematic synthesis (2015) · cites this paper as [5]
Citations
Cites
The Hospital Anxiety and Depression Scale
Zigmond, A. S., & Snaith, R. P. (1983) · Acta Psychiatrica Scandinavica · doi:10.1111/j.1600-0447.1983.tb09716.x · Cited by 47,139
An inventory for measuring depression
BECK, A. T. (1961) · Archives of General Psychiatry · doi:10.1001/archpsyc.1961.01710120031004 · Cited by 38,032
Stress, social support, and the buffering hypothesis
Cohen, S., & Wills, T. A. (1985) · Psychological Bulletin · doi:10.1037/0033-2909.98.2.310 · Cited by 18,093
A new depression scale designed to be sensitive to change
Montgomery, S. A., & Åsberg, M. (1979) · British Journal of Psychiatry · doi:10.1192/bjp.134.4.382 · Cited by 13,962
A self-rating depression scale
ZUNG, W. W. K. (1965) · Archives of General Psychiatry · doi:10.1001/archpsyc.1965.01720310065008 · Cited by 9,813
Spitzer, R. L. (1999) · JAMA · doi:10.1001/jama.282.18.1737 · Cited by 9,802
The posttraumatic growth inventory: measuring the positive legacy of trauma
Tedeschi, R. G., & Calhoun, L. G. (1996) · Journal of Traumatic Stress · doi:10.1002/jts.2490090305 · Cited by 7,061 · cited 1×
“Tedeschi and Calhoun describe the process of rebuilding a new philosophy of life and reordering one’s priorities in the aftermath of a trauma as posttraumatic growth (69).”
BackgroundRelatives of the Impaired Elderly: Correlates of Feelings of Burden
Zarit, S. H., Reever, K. E., & Bach-Peterson, J. (1980) · The Gerontologist · doi:10.1093/geront/20.6.649 · Cited by 5,810
The measurement of pessimism: the hopelessness scale
Beck, A. T., Weissman, A., Lester, D., & Trexler, L. (1974) · Journal of Consulting and Clinical Psychology · doi:10.1037/h0037562 · Cited by 5,494
Depression. Clinical, Experimental, and Theoretical Aspects.
(1968) · Annals of Internal Medicine · doi:10.7326/0003-4819-68-2-502 · Cited by 5,233
Research works printed but not linked: 11
- 10.1037/0022-3514.56.6.958 · DOI
- Kazdin A. Methodological issues and strategies in clinical research. 2nd edn. American Psychological Association, Washington, D.C. 1998
- Karg R., Wiens A. Improving diagnostic and clinical interviewing. Psychologists desk reference, 2nd edn, G Koocher, J Norcross, S Hill. Oxford University Press, New York 2004
- American Psychiatric Association. Diagnostic and statistical manual of mental disorders, 4th edn., Text Revision. American Psychiatric Association, Washington, D.C. 2000
- McDonald E. Psycho‐spiritual overview. Amyotrophic lateral sclerosis: a comprehensive guide to treatment and management. Demos, New York 1994; 205–27
- 10.1097/00006842-200405000-00025 · DOI
- Zerssen D. Klinische selbstbeurteilungsskalen aus dem munchner psychiatrischen informationssystem: paranoid‐depressivitatsskala, depressivitatsskala – manual. 1976, Weinheim – Belt Test Gesellschaft mbH
- American Psychiatric Association. Diagnostic and statistical manual of mental disorders. 4th edn. American Psychiatric Association, Washington, D.C. 1994
- Yesavage J. Geriatric depression scale. Psychopharmacol Bull 1988; 24: 709–11
- Zuckerman M., Lubin B. Manual for the Multiple Affect Adjective Checklist. Educational and Industrial Testing Service, San Diego 1965
- McNair D., Lorr M., Droppleman L. Manual: profile of mood states. Educational and Industrial Testing Service, San Diego 1971
Cited by
Sorted by citations
Wijesekera, L. C., & Leigh, P. N. (2009) · Orphanet Journal of Rare Diseases · doi:10.1186/1750-1172-4-3 · Cited by 1,130
Frontotemporal dementia and motor neurone disease: Overlapping clinic-pathological disorders
Lillo, P., & Hodges, J. R. (2009) · Journal of Clinical Neuroscience · doi:10.1016/j.jocn.2009.03.005 · Cited by 161
DHA/EPA (Omega-3) and LA/GLA (Omega-6) as Bioactive Molecules in Neurodegenerative Diseases
Kousparou, C. A., Fyrilla, M., Stephanou, A., & Patrikios, I. S. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241310717 · Cited by 134
Metabolomic analysis of serum by (1) H NMR spectroscopy in amyotrophic lateral sclerosis
Kumar, A., Bala, L., Kalita, J., Misra, U. K., Singh, R. L., Khetrapal, C. L., & Babu, G. N. (2010) · Clinica Chimica Acta · doi:10.1016/j.cca.2010.01.016 · Cited by 107
Depression in amyotrophic lateral sclerosis
Röös, E., Mariosa, D., Ingre, C., Lundholm, C., Wirdefeldt, K., Roos, P. M., & Fang, F. (2016) · Neurology · doi:10.1212/wnl.0000000000002671 · Cited by 106
Patient-Perceived Outcomes and Quality of Life in ALS
Simmons, Z. (2014) · Neurotherapeutics · doi:10.1007/s13311-014-0322-x · Cited by 92
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. (2008) · European Journal of Neurology · doi:10.1111/j.1468-1331.2008.02303.x · Cited by 89
Health-related quality of life in ALS, myasthenia gravis and facioscapulohumeral muscular dystrophy
Winter, Y., Schepelmann, K., Spottke, A. E., Claus, D., Grothe, C., Schröder, R., Heuss, D., Vielhaber, S., Tackenberg, B., Mylius, V., et al. (2010) · Journal of Neurology · doi:10.1007/s00415-010-5549-9 · Cited by 86
The Dynamics of Quality of Life in ALS Patients and Caregivers
Roach, A. R., Averill, A. J., Segerstrom, S. C., & Kasarskis, E. J. (2009) · Annals of Behavioral Medicine · doi:10.1007/s12160-009-9092-9 · Cited by 81
Self-citationOropharyngeal dysphagia in amyotrophic lateral sclerosis alters quality of life
Paris, G., Martinaud, O., Petit, A., Cuvelier, A., Hannequin, D., Roppenneck, P., & Vérin, É. (2012) · Journal of Oral Rehabilitation · doi:10.1111/joor.12019 · Cited by 76
Depression and wish to die in a multicenter cohort of ALS patients
Rabkin, J. G., Goetz, R. R., Factor-Litvak, P. R., Hupf, J. C., McElhiney, M. C., Singleton, J., Mitsumoto, H., & The Als Cosmos Study Group (2014) · Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration · doi:10.3109/21678421.2014.980428 · Cited by 73
Depression in ALS in a large self-reporting cohort
Thakore, N. J., & Pioro, E. P. (2016) · Neurology · doi:10.1212/wnl.0000000000002465 · Cited by 64
Ferentinos, P. P., Paparrigopoulos, T. J., Rentzos, M., Zouvelou, V., Alexakis, T., & Evdokimidis, I. (2011) · Amyotrophic Lateral Sclerosis · doi:10.3109/17482968.2011.556744 · Cited by 56
Quality of life, anxiety and depression in ALS patients and their next of kin
Ozanne, A., Strang, S., & Persson, L. (2010) · Journal of Clinical Nursing · doi:10.1111/j.1365-2702.2010.03509.x · Cited by 52
Psychosocial adjustment to ALS: a longitudinal study
Matuz, T., Birbaumer, N., Hautzinger, M., & Kübler, A. (2015) · Frontiers in Psychology · doi:10.3389/fpsyg.2015.01197 · Cited by 48
Quality of life of patients with amyotrophic lateral sclerosis
Tramonti, F., Bongioanni, P., Di Bernardo, C., Davitti, S., & Rossi, B. (2012) · Psychology, Health & Medicine · doi:10.1080/13548506.2011.651149 · Cited by 47
Gould, R. L., Coulson, M. C., Brown, R. G., Goldstein, L. H., Al-Chalabi, A., & Howard, R. J. (2015) · Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration · doi:10.3109/21678421.2015.1062515 · Cited by 47
Psychological morbidity in ALS: The importance of psychological assessment beyond depression alone
Felgoise, S. H., Chakraborty, B. H., Bond, E., Rodriguez, J. L., Bremer, B. A., Walsh, S., Lai, E. C., McCluskey, L. F., & Simmons, Z. (2010) · Amyotrophic Lateral Sclerosis · doi:10.3109/17482961003667630 · Cited by 46
Laughter, crying and sadness in ALS
Thakore, N. J., & Pioro, E. P. (2017) · Journal of Neurology Neurosurgery & Psychiatry · doi:10.1136/jnnp-2017-315622 · Cited by 46
Pinto, C., Geraghty, A. W. A., Yardley, L., & Dennison, L. (2021) · BMJ Open · doi:10.1136/bmjopen-2020-044724 · Cited by 40
Death Anxiety and Depression in Amyotrophic Lateral Sclerosis Patients and Their Primary Caregivers
Grabler, M. R., Weyen, U., Juckel, G., Tegenthoff, M., & Mavrogiorgou-Juckel, P. (2018) · Frontiers in Neurology · doi:10.3389/fneur.2018.01035 · Cited by 52
Psychological health in patients with ALS is maintained as physical function declines
Cupp, J. A., Simmons, Z., Berg, A. S., Felgoise, S. H., Walsh, S., & Stephens, H. (2011) · Amyotrophic Lateral Sclerosis · doi:10.3109/17482968.2011.554555 · Cited by 43
A longer diagnostic interval is a risk for depression in amyotrophic lateral sclerosis
Caga, J., Ramsey, E., Hogden, A., Mioshi, E., & Kiernan, M. C. (2014) · Palliative & Supportive Care · doi:10.1017/s1478951514000881 · Cited by 40
van Groenestijn, A. C., van de Port, I. G. L., Schröder, C. D., Post, M. W. M., Grupstra, H. F., Kruitwagen, E. T., van der Linde, H., van Vliet, R. O., van de Weerd, M. G., van den Berg, L. H., et al. (2011) · BMC Neurology · doi:10.1186/1471-2377-11-70 · Cited by 40
Pagnini, F., Manzoni, G. M., Tagliaferri, A., & Sidey-Gibbons, C. J. (2014) · Journal of Health Psychology · doi:10.1177/1359105314530453 · Cited by 39
Jelsone-Swain, L. M., Persad, C. C., Votruba, K., Weisenbach, S. L., Johnson, T. D., Gruis, K. L., & Welsh, R. C. (2012) · Frontiers in Psychology · doi:10.3389/fpsyg.2012.00542 · Cited by 37
Soundy, A., & Condon, N. (2015) · Frontiers in Psychology · doi:10.3389/fpsyg.2015.00606 · Cited by 35
“Twenty-nine studies with 342 (175 male) unique individuals with MND were identified.”
BackgroundHealth utility decreases with increasing clinical stage in amyotrophic lateral sclerosis
Jones, A. R., Jivraj, N., Balendra, R., Murphy, C., Kelly, J., Thornhill, M., Young, C., Shaw, P. J., Leigh, P. N., Turner, M. R., et al. (2014) · Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration · doi:10.3109/21678421.2013.872149 · Cited by 35
Díaz, J. L., Sancho, J., Barreto, P., Bañuls, P., Renovell, M., & Servera, E. (2014) · Journal of Health Psychology · doi:10.1177/1359105314554819 · Cited by 37
Cluster RCT of case management on patients' quality of life and caregiver strain in ALS
Creemers, H., Veldink, J. H., Grupstra, H., Nollet, F., Beelen, A., & van den Berg, L. H. (2014) · Neurology · doi:10.1212/01.wnl.0000438227.48470.62 · Cited by 32
Plasma cortisol level in amyotrophic lateral sclerosis
Spataro, R., Volanti, P., Vitale, F. M., Meli, F., Colletti, T., Natale, A., & Bella, V. L. (2015) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2015.09.011 · Cited by 31
Suicidal Behavior and Neurological Illnesses
Coughlin Steven, S., & Sher, L. (2013) · Journal of Depression & Anxiety · doi:10.4172/2167-1044.s9-001 · Cited by 34
Barbagallo, G., Nicoletti, G., Cherubini, A., Trotta, M., Tallarico, T., Chiriaco, C., Nisticò, R., Salvino, D., Bono, F., Valentino, P., et al. (2014) · Neurological Sciences · doi:10.1007/s10072-013-1626-z · Cited by 28
Bond, L., Bowen, G., Mertens, B., Denson, K., Jordan, K., Vidakovic, B., & Mitchell, C. S. (2020) · Behavioral Sciences · doi:10.3390/bs10010033 · Cited by 27
Obayashi, K., Sato, K., Shimazaki, R., Ishikawa, T., Goto, K., Ueyama, H., Mori, T., Ando, Y., & Kumamoto, T. (2008) · Internal Medicine · doi:10.2169/internalmedicine.47.1278 · Cited by 28
Clinical screening of oropharyngeal dysphagia in patients with ALS
Paris, G., Martinaud, O., Hannequin, D., Petit, A., Cuvelier, A., Guédon, E., Roppenneck, P., & Vérin, É. (2012) · Annals of Physical and Rehabilitation Medicine · doi:10.1016/j.rehab.2012.10.005 · Cited by 27
Suicidal behavior in individuals with amyotrophic lateral sclerosis: A systematic review
Silva-Moraes, M. H., Bispo‐Torres, A. C., Barouh, J. L., de Lucena, P. H. M., Armani‐Franceschi, G., Dorea-Bandeira, I., Vieira, F., Miranda‐Scippa, Â., Quarantini, L. C., Lucena, R., et al. (2020) · Journal of Affective Disorders · doi:10.1016/j.jad.2020.08.066 · Cited by 26
Montel, S., Albertini, L., Desnuelle, C., & Spitz, É. (2012) · Journal of Palliative Medicine · doi:10.1089/jpm.2012.0162 · Cited by 26
Tröster, A. I. (2018) · Springer eBooks · doi:10.1007/978-3-319-57111-9_514 · Cited by 26
The illness experience for people with amyotrophic lateral sclerosis: A qualitative study
Yuan, M., Peng, X., Zeng, T., Wu, M., Chen, Y., Zhang, K., & Wang, X. (2021) · Journal of Clinical Nursing · doi:10.1111/jocn.15697 · Cited by 48
Ilse, B., Prell, T., Walther, M., Hartung, V., Penzlin, S., Tietz, F., Witte, O.-W., Strauss, B., & Grosskreutz, J. (2015) · Social Indicators Research · doi:10.1007/s11205-014-0621-y · Cited by 23
Association between depression and survival in Chinese amyotrophic lateral sclerosis patients
Wei, Q., Zheng, Z., Guo, X., Ou, R., Chen, X., Huang, R., Yang, J., & Shang, H. (2016) · Neurological Sciences · doi:10.1007/s10072-015-2472-y · Cited by 22
Gould, R. L., Thompson, B. J., Rawlinson, C., Kumar, P., White, D., Serfaty, M. A., Graham, C. D., McCracken, L. M., Bursnall, M., Bradburn, M., et al. (2022) · BMC Neurology · doi:10.1186/s12883-022-02950-5 · Cited by 16
The impact of physical impairment on emotional well-being in ALS
Abdulla, S., Vielhaber, S., Kollewe, K., Machts, J., Heinze, H., Dengler, R., & Petri, S. (2014) · Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration · doi:10.3109/21678421.2014.932380 · Cited by 21
A survey of artificial intelligence in gait-based neurodegenerative disease diagnosis
Rao, H., Zeng, M., Zhao, X., & Miao, C. (2025) · Neurocomputing · doi:10.1016/j.neucom.2025.129533 · Cited by 26
Psychiatric Aspects of Amyotrophic Lateral Sclerosis (ALS)
Norris, L., Que, G., & Bayat, E. (2010) · Current Psychiatry Reports · doi:10.1007/s11920-010-0118-6 · Cited by 21
Pisa, F. E., Logroscino, G., Casetta, A., Cecotti, L., Verriello, L., Bratina, A., Sartori, A., de Lorenzo, L. L., Eleopra, R., & Barbone, F. (2015) · Neuroepidemiology · doi:10.1159/000374119 · Cited by 18
Rehabilitation of motor neuron disease
Simmons, Z. (2013) · Handbook of clinical neurology · doi:10.1016/b978-0-444-52901-5.00041-1 · Cited by 20
Dying from ALS in Sweden: clinical status, setting, and symptoms
Sennfält, S., Kläppe, U., Thams, S., Samuelsson, K., Press, R., Fang, F., & Ingre, C. (2022) · Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration · doi:10.1080/21678421.2022.2096411 · Cited by 17
Mechanism of Chaihu Shugan Powder (柴胡疏肝散) for Treating Depression Based on Network Pharmacology
Liu, Y.-Y., Hu, D., Fan, Q., Zhang, X., Zhu, Y., Ni, M.-Y., Wang, Y.-M., Zhang, L., & Sheng, L. (2019) · Chinese Journal of Integrative Medicine · doi:10.1007/s11655-019-3172-x · Cited by 17
Aust, E., Linse, K., Graupner, S., Joos, M., Liebscher, D., Grosskreutz, J., Prudlo, J., Meyer, T. F., Günther, R., Pannasch, S., et al. (2022) · Journal of Neurology · doi:10.1007/s00415-022-11238-0 · Cited by 14
Mora, J. S., Salas, T., Fajardo, M. L. R., Iváñez, L., & Rodríguez-Santos, F. (2013) · Frontiers in Psychology · doi:10.3389/fpsyg.2012.00609 · Cited by 16
Anxiety and Depression in Patients with Amyotrophic Lateral Sclerosis and Their Caregivers
Pagnini, F., Lunetta, C., Banfi, P. I., Rossi, G., Gorni, K., Castelnuovo, G., Corbo, M., & Molinari, E. (2012) · Current Psychology · doi:10.1007/s12144-012-9132-7 · Cited by 15
Tröster, A. I. (2018) · Springer eBooks · doi:10.1007/978-3-319-56782-2_514-3 · Cited by 15
Tröster, A. I. (2010) · Springer eBooks · doi:10.1007/978-0-387-79948-3_514 · Cited by 14
Purpose in Life in ALS Patient–Caregiver Dyads: A Multilevel Longitudinal Analysis
Garcia, N., Morey, J. N., Kasarskis, E., & Segerstrom, S. (2017) · Health Psychology · doi:10.1037/hea0000507 · Cited by 11
Self-citationAbsence of EEG correlates of self-referential processing depth in ALS
Fomina, T., Weichwald, S., Synofzik, M., Just, J., Schöls, L. J., Schölkopf, B., & Grosse‐Wentrup, M. (2017) · PLoS ONE · doi:10.1371/journal.pone.0180136 · Cited by 12
Hu, L., Mao, S., Li, L., Bai, G., Liu, B., & Mao, J. (2022) · Neurobiology of Disease · doi:10.1016/j.nbd.2022.105749 · Cited by 13
Gould, R. L., Rawlinson, C., Thompson, B., Weeks, K., Gossage-Worrall, R., Cantrill, H., Serfaty, M. A., Graham, C. D., McCracken, L. M., White, D., et al. (2023) · Pilot and Feasibility Studies · doi:10.1186/s40814-023-01354-7 · Cited by 10
Psychological Perspectives: Quality of Life and Motivation
Kleih, S. C., & Kübler, A. (2014) · The International library of ethics, law and technology · doi:10.1007/978-94-017-8996-7_6 · Cited by 10
Rabbitte, M., Bates, U., & Keane, M. (2015) · Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration · doi:10.3109/21678421.2015.1009117 · Cited by 9
Pinto, C., Geraghty, A. W. A., Pagnini, F., Yardley, L., & Dennison, L. (2023) · Frontiers in Psychiatry · doi:10.3389/fpsyt.2023.1083196 · Cited by 7
Gold, N. D., Mallard, A. J., Hermann, J. C., Zeifman, R. J., Pagni, B. A., Bogenschutz, M. P., & Ross, S. (2023) · Journal of Palliative Medicine · doi:10.1089/jpm.2022.0604 · Cited by 6
Lapin, B. R., Mate, K., Li, Y., & Thakore, N. J. (2022) · Journal of the Neurological Sciences · doi:10.1016/j.jns.2022.120442 · Cited by 5
Wang, Z., Yang, H., Han, Y., Teng, J., Kong, X., & Qi, X. (2023) · Medicine · doi:10.1097/md.0000000000036265 · Cited by 5
Hübner, J., Hübner, I., & Kroczka, S. (2019) · Psychiatria Polska · doi:10.12740/pp/onlinefirst/103801 · Cited by 5
Nishiyama, M., Koreki, A., Isose, S., Takeda, T., Ishikawa, A., Kokubun, S., Saito, Y., Ito, K., Arai, K., Takahashi, N., et al. (2024) · Journal of Psychosomatic Research · doi:10.1016/j.jpsychores.2024.111915 · Cited by 4
Neuropsychology of Movement Disorders and Motor Neuron Disease
Tröster, A. I., & Woods, S. P. (2010) · Springer eBooks · doi:10.1007/978-1-4419-1364-7_17 · Cited by 4
Rehabilitation in Neuromuscular Disorders
Weiss, D., & Krivickas, L. S. (2010) · Elsevier eBooks · doi:10.1016/b978-1-4377-0372-6.00008-6 · Cited by 4
THEME 3 COGNITIVE AND PSYCHOLOGICAL ASSESSMENT AND SUPPORT
(2014) · Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration · doi:10.3109/21678421.2014.960176 · Cited by 4
Assessing and Managing Depression and Fatigue in Motor Neuron Disease
Sidey-Gibbons, C. J., & Young, C. A. (2012) · Neurodegenerative Disease Management · doi:10.2217/nmt.12.42 · Cited by 4
LA PRAXIS DE LA INVESTIGACIÓN CUALITATIVA
Palacios, S. (2014) · Editorial UAT · Cited by 4
The epidemiology of death and symptoms: planning for population-based palliative care
Sands, M. B., O’Connell, D. L., Piza, M., & INGHAM, J. M. (2015) · doi:10.1093/med/9780199656097.003.0006 · Cited by 4
Man, K. E., Sawula, L. J., Gurd, B. J., Taylor, S. W., Allen, M. D., & Tomasone, J. R. (2022) · Qualitative Research in Sport Exercise and Health · doi:10.1080/2159676x.2022.2128397 · Cited by 3
PSYCHOLOGY AND SOCIAL ASPECTS OF AMYOTROPHIC LATERAL SCLEROSIS: REVIEW
Abreu-Filho, A., Oliveira, A. S. B., & da Silva, H. C. A. (2019) · Psicologia Saúde & Doenças · doi:10.15309/19psd200107 · Cited by 3
The magnetic resonance imaging "wine glass" sign of amyotrophic lateral sclerosis
Parashari, U. C., Khanduri, S., Bhadury, S., Srivastava, D., & Saxena, S. (2011) · International journal of Nutrition Pharmacology Neurological Diseases · doi:10.4103/2231-0738.84217 · Cited by 3
Psychiatric Disease in Amyotrophic Lateral Sclerosis
Maiser, S., & Tiryaki, E. (2017) · Psychiatric Annals · doi:10.3928/00485713-20170413-01 · Cited by 3
Metabolomic analysis of serum by (1) H NMR spectroscopy in amyotrophic lateral sclerosis
Babu, G. N., Kumar, A., Bala, L., Kalita, J., Misra, U. K., Singh, R. L., & Khetrapal, C. L. (2010) · Clinica Chimica Acta · doi:10.1016/j.cca.2010.05.013 · Cited by 3
Bongioanni, P., Borasio, G. D., Oliver, D., Romagnoli, A. D., Kapitza, K. P., Sidle, K. C. L., & Tramonti, F. (2023) · Cochrane Database of Systematic Reviews · doi:10.1002/14651858.cd007593.pub2 · Cited by 3
The Will to Live Instead of Euthanasia
Förstl, H. (2008) · Deutsches Ärzteblatt international · doi:10.3238/arztebl.2008.0395 · Cited by 3
Amyotrophic Lateral Sclerosis: An Introduction to Treatment and Trials
Martin, H. (2012) · InTech eBooks · doi:10.5772/34020 · Cited by 2
Sasang Constitutional Characteristic of Amyotrophic Lateral Sclerosis
Park, S.-J., Jeong, H.-H., Jang, E.-S., Kim, S. H., Kim, S., & Joo, J. (2014) · Journal of Sasang Constitutional Medicine · doi:10.7730/jscm.2014.26.2.156 · Cited by 2
Tröster, A. I., Pulaski, S. J., & Woods, S. P. (2019) · Springer eBooks · doi:10.1007/978-3-030-14895-9_19 · Cited by 2
Thomas, P. T., Warrier, M. G., Arun, S., Bhuvaneshwari, B., Vengalil, S., Nashi, S., Preethish‐Kumar, V., Polavarapu, K., Rajaram, P., & Nalini, A. (2022) · Chronic Illness · doi:10.1177/17423953221097076 · Cited by 2
Creer, S., Griffiths, A. W., Hobson, E., Davies, S. M., Massey, C., Stokes, L., Waters, B., Bamber, R. W., Hastings, S., Bedford, J., et al. (2026) · Neurodegenerative Disease Management · doi:10.1080/17582024.2026.2637420 · Cited by 1
Roach, A. R. (2010) · UKnowledge (University of Kentucky) · Cited by 1
Segerstrom, S. C., & Kasarskis, E. J. (2024) · Health Psychology and Behavioral Medicine · doi:10.1080/21642850.2024.2396137 · Cited by 1
Self-citationOsafo, N., Obiri, D. D., Yeboah, K. O., & Minkah, P. A. B. (2018) · Advances in medical diagnosis, treatment, and care (AMDTC) book series · doi:10.4018/978-1-5225-5282-6.ch015 · Cited by 1
Silva, L. M. A., Paixão, I. P. S., & Oliveira, W. (2021) · Brazilian Journal of Health Review · doi:10.34119/bjhrv4n5-325 · Cited by 1
Rodriguez, J. L. (2010) · Digital Commons - PCOM (Philadelphia College of Osteopathic Medicine) · Cited by 1
A National Study of Amyotrophic Lateral Sclerosis Multidisciplinary Clinic Utilization
Young, J. (2011) · Digital Commons - PCOM (Philadelphia College of Osteopathic Medicine) · Cited by 1
Amyotrophic lateral sclerosis with depression, cognitive impairment, and mortality
Kawada, T. (2020) · Acta Neurologica Scandinavica · doi:10.1111/ane.13237 · Cited by 1
Priest, A. (2015) · Canadian Medical Association Journal · doi:10.1503/cmaj.141517
Patient Care and Treatment in Amyotrophic Lateral Sclerosis
Ikeda, K., Kano, O., Kawabe, K., & Iwasaki, Y. (2013) · Journal of Neurology Research · doi:10.4021/jnr.v3i1.176
Asymmetries of Patient Autonomy and Paternalism
Pavlović, D., & SPASSOV, A. W. (2011) · Journal of Clinical Research & Bioethics · doi:10.4172/2155-9627.1000112
Philippou, E. (2013) · University of the Witwatersrand, Johannesburg Institutional Repository on DSpace (University of the Witwatersrand, Johannesburg)
Living with ALS Perspectives of patients and next of kin
Olsson, A. G. (2010) · Gothenburg University Publications Electronic Archive (Gothenburg University)
A Study on the Anxiety Experience of Disabled Person with Progressive Rare Disease
LEEGYESEUNG (2018) · Korean Journal of Social Welfare · doi:10.20970/kasw.2018.70.2.010
Reply to: Amyotrophic lateral sclerosis with depression, cognitive impairment, and mortality
Marchi, F. D., & Mazzini, L. (2020) · Acta Neurologica Scandinavica · doi:10.1111/ane.13238
Metadata
- Authors
- Averill, A. J., Kasarskis, E. J., & Segerstrom, S. C.
- Affiliations
- University of Kentucky (US)
- Corresponding author
- Segerstrom, Suzanne C.
- Venue
- Amyotrophic Lateral Sclerosis
- Publisher
- Informa UK Limited
- Published
- 2007-01
- Volume
- 8
- Issue
- 4
- Pages
- 243-254
- ISSN
- 1471-180X (ISSN-L)
- 1748-2968
- OpenAlex
- W1976849761
- Cited by
- 110
- References
- 83
- Citations by year
- 2026: 2 · 2025: 2 · 2024: 2 · 2023: 10 · 2022: 7 · 2021: 3 · 2020: 5 · 2019: 4 · 2018: 5 · 2017: 4 · 2016: 3 · 2015: 8 · 2014: 13 · 2013: 8 · 2012: 9
- FWCI
- 4.38
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Amyotrophic Lateral Sclerosis (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Clinical Neurology › Amyotrophic Lateral Sclerosis Research
- Health Sciences › Medicine › Oncology › Cancer survivorship and care
- Health Sciences › Nursing › Research and Theory › Nursing care and research
- Keywords
- depression, mental health, psychological distress, hopelessness, depression prevalence, depression severity, neurodegenerative diseases, coping
- MeSH terms
- Amyotrophic Lateral Sclerosis, Depression, Humans, Mental Health, Review Literature as Topic, Prevalence
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review