Margreet Scharloo
Biographic Data
| ID | 2525887 |
|---|---|
| NAME | Margreet Scharloo |
| GIVEN NAMES | Margreet |
| FAMILY NAME | Scharloo |
| SIGNATURE | SCHARLOO M |
| AFFILIATIONS | Leiden University Medical Center, The Netherlands |
| VERIFIED | No |
| TOTAL WORKS | 3 |
| TOTAL CITATIONS | 0 |
| WORKS AS AUTHOR | 3 |
| WORKS AS EDITOR | 0 |
| FIRST PUBLICATION YEAR | 2007 |
| LATEST PUBLICATION YEAR | 2019 |
| H-INDEX | 0 |
The partner's perspective of the impact of pituitary disease
People with pituitary disease report impairments in quality of life. The aim of this study was to elucidate the impact of the pituitary condition on the lives of partners. Four focus groups of partners of people with pituitary disease (Cushing's disease, non-functioning adenoma, acromegaly, prolactinoma) were conducted. Partners mentioned worries related to the pituitary disease and negative beliefs about medication, coping challenges, relationsh…
Perceived Discomfort Levels in Healthy Children Participating in Vaccine Research
When assessing the risks of a research protocol, review boards need to consider not only the possible harms but also the expected discomfort levels caused by the various study procedures. However, data on how children experience various study procedures are scarce. This study assessed perceived discomfort levels in 671 healthy children aged 0-2 years under-going vaccinations, venipunctures, and nasopharyngeal swab taking. In half of the study par…
Quality of life in couples living with Huntington’s disease
Research suggests that chronically ill patients and their partners perceive illness differently, and that these differences have a negative impact on patients' quality of life (QoL). This study assessed whether illness perceptions of patients with Huntington's disease (HD) differ from those of their partners, and examined whether spousal illness perceptions are important for the QoL of the couples (n = 51 couples). Partners reported that their HD…
No prominent works on this page.
Quality of life in couples living with Huntington’s disease
Research suggests that chronically ill patients and their partners perceive illness differently, and that these differences have a negative impact on patients' quality of life (QoL). This study assessed whether illness perceptions of patients with Huntington's disease (HD) differ from those of their partners, and examined whether spousal illness perceptions are important for the QoL of the couples (n = 51 couples). Partners reported that their HD…
Perceived Discomfort Levels in Healthy Children Participating in Vaccine Research
When assessing the risks of a research protocol, review boards need to consider not only the possible harms but also the expected discomfort levels caused by the various study procedures. However, data on how children experience various study procedures are scarce. This study assessed perceived discomfort levels in 671 healthy children aged 0-2 years under-going vaccinations, venipunctures, and nasopharyngeal swab taking. In half of the study par…
The partner's perspective of the impact of pituitary disease
People with pituitary disease report impairments in quality of life. The aim of this study was to elucidate the impact of the pituitary condition on the lives of partners. Four focus groups of partners of people with pituitary disease (Cushing's disease, non-functioning adenoma, acromegaly, prolactinoma) were conducted. Partners mentioned worries related to the pituitary disease and negative beliefs about medication, coping challenges, relationsh…
Medicine (3 works) · Psychiatry (3 works) · Psychology (3 works) · Disease (2 works) · Nursing (2 works) · Quality of life (healthcare (2 works) · Acromegaly (1 work) · Childhood Cancer Survivors' Quality of Life (1 work) · Coping (psychology (1 work) · Developmental psychology (1 work)