Alberto M Pereira
Biographic Data
| ID | 3800787 |
|---|---|
| NAME | Alberto M Pereira |
| GIVEN NAMES | Alberto M |
| FAMILY NAME | Pereira |
| SIGNATURE | PEREIRA A M |
| AFFILIATIONS | Leiden University Medical Center, The Netherlands |
| ORCID | 0000-0002-1194-9866 |
| VERIFIED | Yes |
| TOTAL WORKS | 3 |
| TOTAL CITATIONS | 0 |
| WORKS AS AUTHOR | 3 |
| WORKS AS EDITOR | 0 |
| FIRST PUBLICATION YEAR | 2019 |
| LATEST PUBLICATION YEAR | 2026 |
| H-INDEX | 0 |
European Reference Networks as core health structures where referring genetic newborn screening positive infants
Rare diseases (RDs), affecting fewer than 5 people per 10,000, present unique challenges to usual care pathways due to their unique characteristics: rarity and large number of disease entities, heterogeneous clinical manifestations and genetic causes, multisystemic involvement, and high complexity of diagnosis and treatment. This complexity often hampers the setting of appropriate pathways of care, which are not easily identifiable by patients an…
European Reference Networks
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…
No prominent works on this page.
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…
European Reference Networks
European Reference Networks as core health structures where referring genetic newborn screening positive infants
Rare diseases (RDs), affecting fewer than 5 people per 10,000, present unique challenges to usual care pathways due to their unique characteristics: rarity and large number of disease entities, heterogeneous clinical manifestations and genetic causes, multisystemic involvement, and high complexity of diagnosis and treatment. This complexity often hampers the setting of appropriate pathways of care, which are not easily identifiable by patients an…
Genomics and Rare Diseases (2 works) · Acromegaly (1 work) · Biology (1 work) · BRCA gene mutations in cancer (1 work) · Business (1 work) · Cancer Genomics and Diagnostics (1 work) · Childhood Cancer Survivors' Quality of Life (1 work) · Computer Science (1 work) · Constructive (1 work) · Coping (psychology (1 work)