Olaf Hiort
Biographic Data
| ID | 5224436 |
|---|---|
| NAME | Olaf Hiort |
| GIVEN NAMES | Olaf |
| FAMILY NAME | Hiort |
| SIGNATURE | HIORT O |
| AFFILIATIONS | University of Lübeck |
| ORCID | 0000-0001-7490-4983 |
| VERIFIED | Yes |
| TOTAL WORKS | 3 |
| TOTAL CITATIONS | 1 |
| WORKS AS AUTHOR | 3 |
| WORKS AS EDITOR | 0 |
| FIRST PUBLICATION YEAR | 2006 |
| LATEST PUBLICATION YEAR | 2026 |
| H-INDEX | 1 |
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…
Sex dimorphism of weight and length at birth
The sex dimorphism of weight and length at birth could possibly be influenced by intrauterine androgenic action
Any Decision is Better Than None” Decision-Making About Sex of Rearing for Siblings with 17β-Hydroxysteroid-dehydrogenase-3 Deficiency
Any Decision is Better Than None” Decision-Making About Sex of Rearing for Siblings with 17β-Hydroxysteroid-dehydrogenase-3 Deficiency
Sex dimorphism of weight and length at birth
The sex dimorphism of weight and length at birth could possibly be influenced by intrauterine androgenic action
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…
Biology (2 works) · Sexual Differentiation and Disorders (2 works) · Biochemistry (1 work) · Biochemistry (1 work) · Birth weight (1 work) · BRCA gene mutations in cancer (1 work) · Dehydrogenase (1 work) · Demography (1 work) · Demography (1 work) · Developmental psychology (1 work)