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For: Soundy A, Condon N. Patients experiences of maintaining mental well-being and hope within motor neuron disease: a thematic synthesis. Front Psychol. 2015;6:606. [PMID: 26029142 DOI: 10.3389/fpsyg.2015.00606] [Cited by in Crossref: 14] [Cited by in F6Publishing: 13] [Article Influence: 2.0] [Reference Citation Analysis]
Number Citing Articles
1 Holkham L, Soundy A. The experience of informal caregivers of patients with motor neurone disease: A thematic synthesis. Palliat Support Care 2018;16:487-96. [PMID: 28931454 DOI: 10.1017/S1478951517000852] [Cited by in Crossref: 8] [Cited by in F6Publishing: 4] [Article Influence: 1.6] [Reference Citation Analysis]
2 Gunton A, Hansen G, Schellenberg KL. Photovoice as a Participatory Research Tool in Amyotrophic Lateral Sclerosis. J Neuromuscul Dis 2021;8:91-9. [PMID: 32986680 DOI: 10.3233/JND-200537] [Reference Citation Analysis]
3 Olsman E. Hope in Health Care: A Synthesis of Review Studies. In: van den Heuvel SC, editor. Historical and Multidisciplinary Perspectives on Hope. Cham: Springer International Publishing; 2020. pp. 197-214. [DOI: 10.1007/978-3-030-46489-9_11] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
4 Anestis E, Eccles FJR, Fletcher I, Simpson J. Neurologists' current practice and perspectives on communicating the diagnosis of a motor neurodegenerative condition: a UK survey. BMC Neurol 2021;21:34. [PMID: 33482753 DOI: 10.1186/s12883-021-02062-6] [Reference Citation Analysis]
5 Hamama-Raz Y, Norden Y, Buchbinder E. The double sides of hope: The meaning of hope among amyotrophic lateral sclerosis (ALS) patients. Death Stud 2021;45:238-47. [PMID: 31192774 DOI: 10.1080/07481187.2019.1626946] [Reference Citation Analysis]
6 Rose A, Rosewilliam S, Soundy A. Shared decision making within goal setting in rehabilitation settings: A systematic review. Patient Educ Couns 2017;100:65-75. [PMID: 27486052 DOI: 10.1016/j.pec.2016.07.030] [Cited by in Crossref: 67] [Cited by in F6Publishing: 57] [Article Influence: 11.2] [Reference Citation Analysis]
7 Overbeck G, Davidsen AS, Kousgaard MB. Enablers and barriers to implementing collaborative care for anxiety and depression: a systematic qualitative review. Implement Sci. 2016;11:165. [PMID: 28031028 DOI: 10.1186/s13012-016-0519-y] [Cited by in Crossref: 40] [Cited by in F6Publishing: 39] [Article Influence: 6.7] [Reference Citation Analysis]
8 Pinto C, Geraghty AWA, Yardley L, Dennison L. Emotional distress and well-being among people with motor neurone disease (MND) and their family caregivers: a qualitative interview study. BMJ Open 2021;11:e044724. [PMID: 34404695 DOI: 10.1136/bmjopen-2020-044724] [Reference Citation Analysis]
9 Weeks KR, Gould RL, Mcdermott C, Lynch J, Goldstein LH, Graham CD, McCracken L, Serfaty M, Howard R, Al-Chalabi A, White D, Bradburn M, Young T, Cooper C, Shaw DPJ, Lawrence V. Needs and preferences for psychological interventions of people with motor neuron disease. Amyotroph Lateral Scler Frontotemporal Degener 2019;20:521-31. [PMID: 31298054 DOI: 10.1080/21678421.2019.1621344] [Cited by in Crossref: 6] [Cited by in F6Publishing: 5] [Article Influence: 2.0] [Reference Citation Analysis]
10 Soundy A. Psycho-emotional content of illness narrative master plots for people with chronic illness: Implications for assessment. World J Psychiatr 2018; 8(3): 79-82 [PMID: 30254977 DOI: 10.5498/wjp.v8.i3.79] [Cited by in CrossRef: 6] [Cited by in F6Publishing: 4] [Article Influence: 1.5] [Reference Citation Analysis]
11 Yaghoobzadeh A, Pahlevan Sharif S, Ong FS, Soundy A, Sharif Nia H, Moradi Bagloee M, Sarabi M, Goudarzian AH, Morshedi H. Cross-Cultural Adaptation and Psychometric Evaluation of the Herth Hope Index Within a Sample of Iranian Older Peoples. Int J Aging Hum Dev 2019;89:356-71. [PMID: 30569732 DOI: 10.1177/0091415018815239] [Cited by in Crossref: 6] [Cited by in F6Publishing: 2] [Article Influence: 1.5] [Reference Citation Analysis]
12 van Eenennaam RM, Koppenol LS, Kruithof WJ, Kruitwagen-van Reenen ET, Pieters S, van Es MA, van den Berg LH, Visser-Meily JMA, Beelen A. Discussing Personalized Prognosis Empowers Patients with Amyotrophic Lateral Sclerosis to Regain Control over Their Future: A Qualitative Study. Brain Sci 2021;11:1597. [PMID: 34942899 DOI: 10.3390/brainsci11121597] [Reference Citation Analysis]
13 Ando H, Cousins R, Young CA. Exploring and Addressing 'Concerns' for Significant Others to Extend the Understanding of Quality of Life With Amyotrophic Lateral Sclerosis: A Qualitative Study. J Cent Nerv Syst Dis 2019;11:1179573519859360. [PMID: 31312086 DOI: 10.1177/1179573519859360] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 1.3] [Reference Citation Analysis]
14 Morgan DD, Marston C, Barnard E, Farrow C. Conserving dignity and facilitating adaptation to dependency with intimate hygiene for people with advanced disease: A qualitative study. Palliat Med 2021;35:1366-77. [PMID: 34044651 DOI: 10.1177/02692163211017388] [Reference Citation Analysis]