Family caregiver perspectives on symptoms and treatments for patients dying from complications of cystic fibrosis
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ATS Core Curriculum 2015: Part III. Pediatric Pulmonary Medicine.Palliation of dyspnea in pediatrics.Palliative care for people with non-malignant lung disease: summary of current evidence and future direction.Evaluation of Pain, Dyspnea, and Goals of Care Among Adults With Cystic Fibrosis: A Comprehensive Palliative Care Survey.A Cross-Sectional Examination of the Association Between Dyspnea and Distress as Experienced by Palliative Home Care Clients and Their Informal Caregivers.Pediatric lung transplantation and end of life care in cystic fibrosis: Barriers and successful strategies.Fatigue in cystic fibrosis: a novel prospective study investigating subjective and objective factors associated with fatigue.
P2860
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P2860
Family caregiver perspectives on symptoms and treatments for patients dying from complications of cystic fibrosis
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on 17 September 2010
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
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vědecký článek
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name
Family caregiver perspectives ...... mplications of cystic fibrosis
@en
Family caregiver perspectives ...... plications of cystic fibrosis.
@nl
type
label
Family caregiver perspectives ...... mplications of cystic fibrosis
@en
Family caregiver perspectives ...... plications of cystic fibrosis.
@nl
prefLabel
Family caregiver perspectives ...... mplications of cystic fibrosis
@en
Family caregiver perspectives ...... plications of cystic fibrosis.
@nl
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Family caregiver perspectives ...... mplications of cystic fibrosis
@en
P2093
Elisabeth P Dellon
Joanne Wolfe
Katherine I Nelson
Laura C Hanson
Mitchell D Shores
Terry L Noah
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P304
P356
10.1016/J.JPAINSYMMAN.2010.03.024
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2010-09-17T00:00:00Z