Corinna Grasemann

18PUBLICATIONS
122CO-AUTHORS
Major global burdens of diseaseOrthodontics and dentofacial orthopaedicsInfant and child healthAdolescent healthEpigenetics (incl. genome methylation and epigenomics)
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Publications (18)

|Apr 10, 2026
Mapping transition of care for rare endocrine conditions: findings from a cross-sectional survey by the Endo-ERN ToC Working Group.

Francesco Carlomagno, Matteo Spaziani, Charlotte M W Gaasterland

|Apr 09, 2026
The use of denosumab in rare bone diseases in adults: a systematic review from the ECTS Rare Bone Disease Action Group.

Oana O Bulaicon, Femke M van Haalen, Gavin P R Clunie

|Oct 19, 2025
Continuity of care in Klinefelter syndrome: age-adapted modules for standardized clinical data collection (I-KS).

Corinna Grasemann, Claus H Gravholt, Lexi Breen

|May 09, 2025
Transition Care for Young Persons with Rare Bone Mineral Conditions: A Consensus Recommendation from the ECTS Rare Bone Disease Action Group.

Corinna Grasemann, Joline Wernsmann, Natasha M Appelman-Dijkstra

|May 02, 2025
Developing a Standardised Dataset for Natural History Studies in Fibrous Dysplasia/McCune-Albright Syndrome.

Ana Luisa Priego Zurita, Oana O Bulaicon, Jillian Bryce

|Apr 17, 2025
X-Linked Hypophosphatemia Management in Adults: An International Working Group Clinical Practice Guideline.

Aliya A Khan, Dalal S Ali, Natasha M Appelman-Dijkstra

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