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Variants of SOS2 are a rare cause of Noonan syndrome with particular predisposition for lymphatic complications
2021 - Forschungsinformationssystem des UKE
Telephone health coaching with exercise monitoring using wearable activity trackers (TeGeCoach) for improving walking impairment in peripheral artery disease:study protocol for a randomised controlled trial and economic evaluation
2020 - Forschungsinformationssystem des UKE
The novel RAF1 mutation p.(Gly361Ala) located outside the kinase domain of the CR3 region in two patients with Noonan syndrome, including one with a rare brain tumor
2018 - Forschungsinformationssystem des UKE