Bertschy G

ORCID: 0009-0001-4805-5233 · 2 papers in corpus · active 2022
2022
Frontiers in genetics ·doi:10.3389/fgene.2022.995947

Background: Alström syndrome (AS) is an ultrarare multisystemic progressive disease caused by autosomal recessive variations of the ALMS1 gene (2p13). AS is characterized by double sensory impairment, cardiomyopathy, childhood obesity, extr…

2022
Annals of surgical oncology ·doi:10.1245/s10434-022-12353-y

BackgroundThe term uterine smooth muscle tumor of uncertain malignant potential (STUMP) indicates a rare, equivocal entity between benign leiomyomas and leiomyosarcomas. In the present study, we evaluated a comprehensive range of clinical, …