Cited by 32Palliative Care and End-of-Life IssuesAmyotrophic Lateral Sclerosis ResearchNursing care and research

Dying at home: a way of maintaining control for the person with ALS/M N D

Moore, Myrna K·1993·Palliative Medicine

Abstract

Control is a key issue for patients with amyotrophic lateral sclerosis, and caring for them in their own homes is often an essential part of remaining in control. This goal can usually be achieved if all resources are correctly used.

Integrity signals

Registry

Crossref · 10.1177/0269216393007004s10

Cites

2 of 2 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

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?

Cites

Flagged first, then by citations

Cited by

Sorted by citations

Authors
Moore, M. K.
Affiliations
Sunnybrook Health Science Centre (CA)
Corresponding author
Moore, Myrna K
Venue
Palliative Medicine
Published
1993-10
Volume
7
Issue
4_suppl
Pages
65-68
ISSN
  • 0269-2163 (ISSN-L)
  • 1477-030X
OpenAlex
W2151857817
Cited by
32
References
2
Citations by year
2021: 1 · 2018: 1 · 2012: 1
FWCI
3.10
Type
journal article
Language
en
Open access
closed
Locations
  • Palliative Medicine (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Palliative Care and End-of-Life Issues
  • Health Sciences › Medicine › Neurology › Amyotrophic Lateral Sclerosis Research
  • Health Sciences › Health Professions › Pharmacy › Nursing care and research
Keywords
amyotrophic lateral sclerosis, motor neuron disease, home death, home care, patient control, end-of-life care, palliative care, resource allocation
MeSH terms
Amyotrophic Lateral Sclerosis, Home Care Services, Home Nursing, Humans, Ontario, Palliative Care, Patient Participation, Terminal Care, Motor Neuron Disease

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