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Cited by in F6Publishing
For: 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]
Number Citing Articles
1 Marco DJ, Thomas K, Ivynian S, Wilding H, Parker D, Tieman J, Hudson P. Family carer needs in advanced disease: systematic review of reviews. BMJ Support Palliat Care 2022:bmjspcare-2021-003299. [PMID: 34996834 DOI: 10.1136/bmjspcare-2021-003299] [Reference Citation Analysis]
2 Ewing G, Croke S, Rowland C, Grande G. Suitability and acceptability of the Carer Support Needs Assessment Tool (CSNAT) for the assessment of carers of people with MND: a qualitative study. BMJ Open 2020;10:e039031. [PMID: 33273047 DOI: 10.1136/bmjopen-2020-039031] [Reference Citation Analysis]
3 Shah NM, Murphy PB, Kaltsakas G. The adult multidisciplinary respiratory neuromuscular clinic. Breathe (Sheff) 2020;16:200121. [PMID: 33447275 DOI: 10.1183/20734735.0121-2020] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
4 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]
5 de Wit J, Vervoort SCJM, van Eerden E, van den Berg LH, Visser-Meily JMA, Beelen A, Schröder CD. User perspectives on a psychosocial blended support program for partners of patients with amyotrophic lateral sclerosis and progressive muscular atrophy: a qualitative study. BMC Psychol 2019;7:35. [PMID: 31202270 DOI: 10.1186/s40359-019-0308-x] [Cited by in Crossref: 5] [Cited by in F6Publishing: 2] [Article Influence: 1.7] [Reference Citation Analysis]