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Remde, Hanna; Nölting, Svenja (2021). Phäochromozytom – Modellerkrankung für die personalisierte Medizin. Deutsche Medizinische Wochenschrift, 146(23):1520-1526.
Pheochromocytomas and paragangliomas (PPGL) can be related to a uniquely high rate of underlying germline and somatic mutations. Accordingly, they can be assigned into genetic clusters, which are related to a specific biochemical and clinical phenotype as well as a different long term prognosis. The present article discussed how emerging knowledge on the respective clusters allows individual patient management before, during and after occurrence of a PPGL to improve clinical outcome.
| Other titles: | Pheochromocytoma - Disease Model for Personalized Medicine |
|---|---|
| Item Type: | Journal Article, refereed, original work |
| Communities & Collections: | 04 Faculty of Medicine > University Hospital Zurich > Clinic for Endocrinology and Diabetology |
| Dewey Decimal Classification: | 610 Medicine & health |
| Scopus Subject Areas: | Health Sciences > General Medicine |
| Language: | English |
| Date: | November 2021 |
| Deposited On: | 07 Feb 2022 06:45 |
| Last Modified: | 17 Mar 2025 04:35 |
| Publisher: | Georg Thieme Verlag |
| ISSN: | 0012-0472 |
| OA Status: | Closed |
| Publisher DOI: | https://doi.org/10.1055/a-1240-9835 |
| PubMed ID: | 34826837 |
Remde, Hanna