Charité - Universitätsmedizin Berlin

Tumor mutational burden and immune infiltration as independent predictors of response to neoadjuvant immune checkpoint inhibition in early TNBC in GeparNuevo (2020) Karn T, Denkert C, Weber KE, Holtrich U, Hanusch C, Sinn BV, Higgs BW, et al. Journal article Use of CAD-based pre-bent implants reduces theatre time in orbital floor reconstruction: results of a prospective study (2020) von Wilmowsky C, Schwertner M, Nkenke E, Möst T, Adler W, Ebker T Journal article Kutanes Plattenepithelkarzinom (2020) Leiter U, Gutzmer R, Alter M, Ulrich C, Meiwes A, Heppt M, Steeb T, et al. Journal article, Review article Is Laminar Cartilage Composition as Determined by T2 Relaxometry Associated with Incident and Worsening of Cartilage or Bone Marrow Abnormalities? (2020) Roemer F, Eckstein F, Duda G, Guermazi A, Maschek S, Sharma L, Wirth W Journal article Hidradenitis Suppurativa and Concurrent Psoriasis: Comparison of Epidemiology, Comorbidity Profiles, and Risk Factors (2020) Pinter A, Kokolakis G, Rech J, Biermann MH, Häberle BM, Multmeier J, Reinhardt M Journal article Determinants of Successful Use of Sirolimus in Renal Transplant Patients (2020) Naik MG, Jürgensen JS, Arns W, Basic E, Budde K, Eitner F, Fischereder M, et al. Journal article Apps und ihre Anwendungsgebiete in der Rheumatologie (2020) Krusche M, Ruffer N, Grahammer M, Knitza J Journal article The work and training situation for young physicians undergoing specialty training in gynecology and obstetrics in Germany: an assessment of the status quo (2020) Lermann J, Knabl J, Neimann J, Schulte K, Proske K, Schott S, Raspe M Journal article Incidence of SCID in Germany from 2014 to 2015 an ESPED* Survey on Behalf of the API*** Erhebungseinheit für Seltene Pädiatrische Erkrankungen in Deutschland (German Paediatric Surveillance Unit) ** Arbeitsgemeinschaft Pädiatrische Immunologie (2020) Shai S, Perez-Becker R, Andres O, Bakhtiar S, Bauman U, von Bernuth H, Classen CF, et al. Journal article Autosomal dominant polycystic kidney disease in absence of renal cyst formation illustrates genetic interaction between WT1 and PKD1 (2020) Münch J, Kirschner KM, Schlee H, Kraus C, Schönauer R, Jin W, Le Duc GD, et al. Journal article