scholarly article | Q13442814 |
P2093 | author name string | Barbara Habermann | |
Ju Young Shin | |||
P2860 | cites work | Parkinsonism: onset, progression, and mortality | Q28259134 |
Does age make a difference in caregiver strain? Comparison of young versus older caregivers in early-stage Parkinson's disease | Q30227267 | ||
Adapters, strugglers, and case managers: a typology of spouse caregivers | Q35150405 | ||
Caring for parents with neurodegenerative disease: a qualitative description. | Q36929300 | ||
The nature and scope of stressful spousal caregiving relationships. | Q37339756 | ||
Correlates of care relationship mutuality among carers of people with Alzheimer's and Parkinson's disease | Q37339765 | ||
Living and coping with Parkinson's disease: perceptions of informal carers. | Q37800758 | ||
Updated research priorities for neuroscience nursing | Q37907038 | ||
Development and initial validation of a Parkinson's disease caregiver strain risk screen | Q40927947 | ||
Challenges and strategies of medication adherence in Parkinson's disease: A qualitative study | Q41330032 | ||
'Being in it together': living with a partner receiving deep brain stimulation for advanced Parkinson's disease--a hermeneutic phenomenological study | Q44618130 | ||
Palliative care and support for people with neurodegenerative conditions and their carers | Q45303040 | ||
Health-related quality of life in early Parkinson's disease: the impact of nonmotor symptoms | Q45749080 | ||
Family caregivers' decision process to institutionalize persons with Parkinson's disease: a grounded theory study. | Q45910755 | ||
Experiences of caregivers of people with Parkinson's disease in Singapore: a qualitative analysis | Q47392450 | ||
Influencing effect of non-motor symptom clusters on quality of life in Parkinson's disease | Q47778000 | ||
Feasibility and impact of a function focused care intervention for Parkinson's disease in the community | Q48128611 | ||
From miracle to reconciliation: a hermeneutic phenomenological study exploring the experience of living with Parkinson's disease following deep brain stimulation | Q48241375 | ||
The impact of non-motor symptoms on health-related quality of life of patients with Parkinson's disease | Q48319936 | ||
Quality of life in Parkinson's disease patients: validation of the Short-Form Eight-item Parkinson's Disease Questionnaire (PDQ-8) in Taiwan | Q48334993 | ||
Health-related quality of life among community-dwelling patients with intractable neurological diseases and their caregivers in Japan | Q48747132 | ||
Factors supporting self-management in Parkinson's disease: implications for nursing practice. | Q51887007 | ||
Would people with Parkinson's disease benefit from palliative care? | Q54056754 | ||
Palliative stage Parkinson’s disease: patient and family experiences of health-care services | Q57083750 | ||
P433 | issue | 2 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Parkinson's disease | Q11085 |
P304 | page(s) | 142-156 | |
P577 | publication date | 2016-02-26 | |
P1433 | published in | Clinical Nursing Research | Q5133780 |
P1476 | title | Nursing Research in Parkinson's Disease From 2006 to 2015. | |
P478 | volume | 26 |
Q38643763 | A Guideline for Parkinson's Disease Nurse Specialists, with Recommendations for Clinical Practice |
Q89849118 | Nursing research priorities based on CINAHL database: A scoping review |
Q47697922 | Patient-centered integrated healthcare improves quality of life in Parkinson's disease patients: a randomized controlled trial |
Q38826867 | Preferences and concerns for care needs in advanced Parkinson's disease: a qualitative study of couples |
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