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Effect of palliative oxygen versus room air in relief of breathlessness in patients with refractory dyspnoea: a double-blind, randomised controlled trial

The Lancet (British edition), 2010-09, Vol.376 (9743), p.784-793

2010

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Dyspnea review for the palliative care professional: treatment goals and therapeutic options

Journal of palliative medicine, 2012-01, Vol.15 (1), p.106

2012

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Feasibility and Acceptability to Patients of a Longitudinal System for Evaluating Cancer-Related Symptoms and Quality of Life: Pilot Study of an e/Tablet Data-Collection System in Academic Oncology

Journal of pain and symptom management, 2009-06, Vol.37 (6), p.1027-1038

2009

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Improving Health Care Efficiency and Quality Using Tablet Personal Computers to Collect Research-Quality, Patient-Reported Data

Health services research, 2008-12, Vol.43 (6), p.1975-1991

2008

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Philanthropy, Medical Research, and the Role of Development

The American journal of medicine, 2014-10, Vol.127 (10), p.903-904

2014

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Validation of the Patient Care Monitor (Version 2.0): A Review of System Assessment Instrument for Cancer Patients

Journal of pain and symptom management, 2010-10, Vol.40 (4), p.545-558

2010

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Development of a Health Information Technology–Based Data System in Community-Based Hospice and Palliative Care

American journal of preventive medicine, 2011-05, Vol.40 (5), p.S217-S224

2011

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A Framework for Generalizability in Palliative Care

Journal of pain and symptom management, 2009-03, Vol.37 (3), p.373-386

2009

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Demonstration of a Sustainable Community-Based Model of Care Across the Palliative Care Continuum

Journal of pain and symptom management, 2012-12, Vol.44 (6), p.797-809

2012

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Key Characteristics of Palliative Care Studies Reported in the Specialized Literature

Journal of pain and symptom management, 2012-06, Vol.43 (6), p.987-992

2012

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Refining a Checklist for Reporting Patient Populations and Service Characteristics in Hospice and Palliative Care Research

Journal of pain and symptom management, 2012-05, Vol.43 (5), p.902-910

2012

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Targeted Investment Improves Access to Hospice and Palliative Care

Journal of pain and symptom management, 2013-11, Vol.46 (5), p.629-639

2013

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Electronic Patient-Reported Data Capture as a Foundation of Rapid Learning Cancer Care

Medical care, 2010-06, Vol.48 (6), p.S32-S38

2010

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Collecting Data on Quality Is Feasible in Community-Based Palliative Care

Journal of pain and symptom management, 2011-11, Vol.42 (5), p.663-667

2011

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Instituting and Teaching Ethical Standards for Grateful Patient Fundraising

Journal of clinical oncology, 2016-04, Vol.34 (12), p.1423-1424

2016

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Cultural differences in truth-telling to cancer patients: Chinese and American approaches to the disclosure of 'bad news'

Progress in palliative care, 2011-05, Vol.19 (3), p.125-131

2011

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Systematic review: reliability of compendia methods for off-label oncology indications

Annals of internal medicine, 2009-03, Vol.150 (5), p.336

2009

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Specialized palliative care services are associated with improved short- and long-term caregiver outcomes

Supportive care in cancer, 2008-06, Vol.16 (6), p.585-597

2008

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A strategy to advance the evidence base in palliative medicine: formation of a palliative care research cooperative group

Journal of palliative medicine, 2010-12, Vol.13 (12), p.1407

2010

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Correlates of quality of life-related outcomes in breast cancer patients participating in the Pathfinders pilot study

Psycho-oncology (Chichester, England), 2011-05, Vol.20 (5), p.559-564

2011

Volltextzugriff (PDF)

Dyspnea review for the palliative care professional: assessment, burdens, and etiologies

Journal of palliative medicine, 2011-10, Vol.14 (10), p.1167

2011

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Total dyspnoea

Current opinion in supportive & palliative care, 2008-06, Vol.2 (2), p.110

2008

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International Perspective: Outcomes of Palliative Oncology

Seminars in oncology, 2011-06, Vol.38 (3), p.343-350

2011

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When a Chance to Cut Is Not a Chance to Cure: A Future for Palliative Surgery?

Annals of surgical oncology, 2011-11, Vol.18 (12), p.3235-3239, Article 3235

2011

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The Value of Data Collection within a Palliative Care Program

Current oncology reports, 2011-08, Vol.13 (4), p.308-315

2011

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Effect of palliative oxygen versus room air in relief of breathlessness in patients with refractory dyspnoea: a double-blind, randomised controlled trial

Dyspnea review for the palliative care professional: treatment goals and therapeutic options

Feasibility and Acceptability to Patients of a Longitudinal System for Evaluating Cancer-Related Symptoms and Quality of Life: Pilot Study of an e/Tablet Data-Collection System in Academic Oncology

Improving Health Care Efficiency and Quality Using Tablet Personal Computers to Collect Research-Quality, Patient-Reported Data

Philanthropy, Medical Research, and the Role of Development

Validation of the Patient Care Monitor (Version 2.0): A Review of System Assessment Instrument for Cancer Patients

Development of a Health Information Technology–Based Data System in Community-Based Hospice and Palliative Care

A Framework for Generalizability in Palliative Care

Demonstration of a Sustainable Community-Based Model of Care Across the Palliative Care Continuum

Key Characteristics of Palliative Care Studies Reported in the Specialized Literature

Refining a Checklist for Reporting Patient Populations and Service Characteristics in Hospice and Palliative Care Research

Targeted Investment Improves Access to Hospice and Palliative Care

Electronic Patient-Reported Data Capture as a Foundation of Rapid Learning Cancer Care

Collecting Data on Quality Is Feasible in Community-Based Palliative Care

Instituting and Teaching Ethical Standards for Grateful Patient Fundraising

Cultural differences in truth-telling to cancer patients: Chinese and American approaches to the disclosure of 'bad news'

Systematic review: reliability of compendia methods for off-label oncology indications

Specialized palliative care services are associated with improved short- and long-term caregiver outcomes

A strategy to advance the evidence base in palliative medicine: formation of a palliative care research cooperative group

Correlates of quality of life-related outcomes in breast cancer patients participating in the Pathfinders pilot study

Dyspnea review for the palliative care professional: assessment, burdens, and etiologies

Total dyspnoea

International Perspective: Outcomes of Palliative Oncology

When a Chance to Cut Is Not a Chance to Cure: A Future for Palliative Surgery?

The Value of Data Collection within a Palliative Care Program

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