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Effectiveness of evidence-based decision aids for women with pathogenic BRCA1 or BRCA2 variants in the german health care context: results from a randomized controlled trial

2023 . Kautz-Freimuth, Sibylle | Redaèlli, Marcus | Shukri, Arim | Kentenich, Hannah | Simic, Dusan | Mildenberger, Vanessa | Schmutzler, Rita | Rhiem, Kerstin | Stock, Stephanie

Smoking and alcohol, health-related quality of life and psychiatric comorbidities in Leber’s Hereditary Optic Neuropathy mutation carriers: a prospective cohort study

2021 . , Andrea | Catarino, Claudia B. | Rampeltshammer, Verena | Schindler, David | Gallenmüller, Constanze | Priglinger, Claudia | Pogarell, Oliver | Rüther, Tobias | Klopstock, Thomas

Past medical history of tumors other than meningioma is a negative prognostic factor for tumor recurrence in meningiomas WHO grade I

2021 . Biczok, Annamaria | Karschnia, Philipp | Vitalini, Raffaela | Lenski, Markus | Greve, Tobias | Thorsteinsdottir, Jun | Egensperger, Rupert | Dorn, Franziska | Tonn, Jörg-Christian | Schichor, Christian

Impaired in vitro growth response of plasma-treated cardiomyocytes predicts poor outcome in patients with transthyretin amyloidosis

2021 . Hein, Selina | Furkel, Jennifer | Knoll, Maximilian | aus dem Siepen, Fabian | Schönland, Stefan | Hegenbart, Ute | Katus, Hugo A. | Kristen, Arnt V. | Konstandin, Mathias H.

Identification of disease-causing variants by comprehensive genetic testing with exome sequencing in adults with suspicion of hereditary FSGS

Primary mismatch repair deficient IDH-mutant astrocytoma (PMMRDIA) is a distinct type with a poor prognosis