Astrid Blaschek
Biographic Data
| ID | 8254785 |
|---|---|
| NAME | Astrid Blaschek |
| GIVEN NAMES | Astrid |
| FAMILY NAME | Blaschek |
| SIGNATURE | BLASCHEK A |
| AFFILIATIONS | Ludwig-Maximilians-Universität München |
| ORCID | 0000-0003-2918-0159 |
| VERIFIED | Yes |
| TOTAL WORKS | 2 |
| TOTAL CITATIONS | 0 |
| WORKS AS AUTHOR | 2 |
| WORKS AS EDITOR | 0 |
| FIRST PUBLICATION YEAR | 2022 |
| LATEST PUBLICATION YEAR | 2024 |
| H-INDEX | 0 |
Long-Term Socioeconomic and Neurologic Outcome for Individuals with Childhood-Onset Multiple Sclerosis
This single-centre study has yielded new insights into childhood-onset MS. To enable more accurate comparisons across different centres and countries, it is essential to establish a minimum data set and questionnaire subset for patients with paediatric-onset MS transitioning into adulthood
Parental Burden and Quality of Life in 5q-SMA Diagnosed by Newborn Screening
The aim of this study was to assess the psychosocial burden in parents of children with spinal muscular atrophy (SMA), detected by newborn screening (NBS), for which first pilot projects started in January 2018 in Germany. The survey, performed 1-2 years after children's diagnosis of SMA via NBS, included 3 parent-related questionnaires to evaluate the psychosocial burden, quality of life (QoL)/satisfaction and work productivity and activity impa…
No prominent works on this page.
Parental Burden and Quality of Life in 5q-SMA Diagnosed by Newborn Screening
The aim of this study was to assess the psychosocial burden in parents of children with spinal muscular atrophy (SMA), detected by newborn screening (NBS), for which first pilot projects started in January 2018 in Germany. The survey, performed 1-2 years after children's diagnosis of SMA via NBS, included 3 parent-related questionnaires to evaluate the psychosocial burden, quality of life (QoL)/satisfaction and work productivity and activity impa…
Long-Term Socioeconomic and Neurologic Outcome for Individuals with Childhood-Onset Multiple Sclerosis
This single-centre study has yielded new insights into childhood-onset MS. To enable more accurate comparisons across different centres and countries, it is essential to establish a minimum data set and questionnaire subset for patients with paediatric-onset MS transitioning into adulthood
Anxiety (2 works) · Disease (2 works) · Gerontology (2 works) · Internal Medicine (2 works) · Medicine (2 works) · Pediatrics (2 works) · Psychiatry (2 works) · Quality of life (healthcare (2 works) · Caregiver burden (1 work) · Childhood Cancer Survivors' Quality of Life (1 work)