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Parents’ experiences of information and decision making in the care of their child with severe spinal muscular atrophy : a population survey

(2019) JOURNAL OF CHILD NEUROLOGY. 34(4). p.210-215
Author
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Keywords
pediatrics, neonatology, SMA, palliative care, end-of-life care, LIFE-LIMITING CONDITIONS, PALLIATIVE CARE, DEATH, PLACE, END

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Citation

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MLA
Beernaert, Kim et al. “Parents’ Experiences of Information and Decision Making in the Care of Their Child with Severe Spinal Muscular Atrophy : a Population Survey.” JOURNAL OF CHILD NEUROLOGY 34.4 (2019): 210–215. Print.
APA
Beernaert, K., Lövgren, M., Jeppesen, J., Werlauff, U., Rahbek, J., Sejersen, T., & Kreicbergs, U. (2019). Parents’ experiences of information and decision making in the care of their child with severe spinal muscular atrophy : a population survey. JOURNAL OF CHILD NEUROLOGY, 34(4), 210–215.
Chicago author-date
Beernaert, Kim, Malin Lövgren, Jørgen Jeppesen, Ulla Werlauff, Jes Rahbek, Thomas Sejersen, and Ulrika Kreicbergs. 2019. “Parents’ Experiences of Information and Decision Making in the Care of Their Child with Severe Spinal Muscular Atrophy : a Population Survey.” Journal of Child Neurology 34 (4): 210–215.
Chicago author-date (all authors)
Beernaert, Kim, Malin Lövgren, Jørgen Jeppesen, Ulla Werlauff, Jes Rahbek, Thomas Sejersen, and Ulrika Kreicbergs. 2019. “Parents’ Experiences of Information and Decision Making in the Care of Their Child with Severe Spinal Muscular Atrophy : a Population Survey.” Journal of Child Neurology 34 (4): 210–215.
Vancouver
1.
Beernaert K, Lövgren M, Jeppesen J, Werlauff U, Rahbek J, Sejersen T, et al. Parents’ experiences of information and decision making in the care of their child with severe spinal muscular atrophy : a population survey. JOURNAL OF CHILD NEUROLOGY. 2019;34(4):210–5.
IEEE
[1]
K. Beernaert et al., “Parents’ experiences of information and decision making in the care of their child with severe spinal muscular atrophy : a population survey,” JOURNAL OF CHILD NEUROLOGY, vol. 34, no. 4, pp. 210–215, 2019.
@article{8589506,
  author       = {Beernaert, Kim and Lövgren, Malin and Jeppesen, Jørgen and Werlauff, Ulla and Rahbek, Jes and Sejersen, Thomas and Kreicbergs, Ulrika},
  issn         = {0883-0738},
  journal      = {JOURNAL OF CHILD NEUROLOGY},
  keywords     = {pediatrics,neonatology,SMA,palliative care,end-of-life care,LIFE-LIMITING CONDITIONS,PALLIATIVE CARE,DEATH,PLACE,END},
  language     = {eng},
  number       = {4},
  pages        = {210--215},
  title        = {Parents’ experiences of information and decision making in the care of their child with severe spinal muscular atrophy : a population survey},
  url          = {http://dx.doi.org/10.1177/0883073818822900},
  volume       = {34},
  year         = {2019},
}

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