| no |
title |
author |
magazine |
year |
volume |
issue |
page(s) |
type |
| 1 |
A review of dysphagia in four cases of motor neurone disease
|
Scott, Amanda
|
|
1993
|
7 |
4_suppl |
p. 41-47
|
article
|
| 2 |
Bereavement - whose responsibility?
|
Oliver, David
|
|
1993
|
7 |
4_suppl |
p. 73-76
|
article
|
| 3 |
Breaking bad news in amyotrophic lateral sclerosis
|
Meininger, V.
|
|
1993
|
7 |
4_suppl |
p. 37-40
|
article
|
| 4 |
Coping with motor neurone disease — an analysis using self-regulation theory
|
Earll, Louise
|
|
1993
|
7 |
4_suppl |
p. 21-30
|
article
|
| 5 |
Decision-making in the respiratory care of amyotrophic lateral sclerosis: should home mechanical ventilation be used?
|
Oppenheimer, Edward Anthony
|
|
1993
|
7 |
4_suppl |
p. 49-64
|
article
|
| 6 |
Dying at home: a way of maintaining control for the person with ALS/M N D
|
Moore, Myrna K
|
|
1993
|
7 |
4_suppl |
p. 65-68
|
article
|
| 7 |
Editor's note
|
Kirkham, SR
|
|
1993
|
7 |
4_suppl |
p. 1
|
article
|
| 8 |
Ethical issues in palliative care - an overview
|
Oliver, David
|
|
1993
|
7 |
4_suppl |
p. 15-20
|
article
|
| 9 |
Ethics and the clinician: the daily experience with motor neurone disease
|
Carroll-Thomas, Susan
|
|
1993
|
7 |
4_suppl |
p. 11-13
|
article
|
| 10 |
Multidisciplinary management from day one: the Neuro-care approach to motor neurone disease
|
Oxtoby, Marie
|
|
1993
|
7 |
4_suppl |
p. 31-36
|
article
|
| 11 |
Palliative care and taboos within motor neurone disease
|
O'Brien, Tony
|
|
1993
|
7 |
4_suppl |
p. 69-72
|
article
|
| 12 |
Research and the associations: an era for partnership
|
Cardy, Peter
|
|
1993
|
7 |
4_suppl |
p. 3-9
|
article
|
Journal description