Universitätsklinikum Aachen (UKA)

Aktuelle MRT-Bildgebung des Knorpels im Kontext der Gonarthrose (Teil 1): Grundlagen und Sequenzen (2024) Lemainque T, Huppertz MS, Yüksel C, Siepmann R, Kuhl C, Roemer F, Truhn D, Nebelung S Journal article, Review article Human organotypic brain slice cultures: a detailed and improved protocol for preparation and long-term maintenance (2024) Bak A, Koch H, van Loo KM, Schmied K, Gittel B, Weber Y, Ort J, et al. Journal article Preserving fairness and diagnostic accuracy in private large-scale AI models for medical imaging (2024) Tayebi Arasteh S, Ziller A, Kuhl C, Makowski MR, Nebelung S, Braren R, Rueckert D, et al. Journal article, Original article Allogeneic Hematopoietic Cell Transplantation in Advanced Systemic Mastocytosis: A retrospective analysis of the DRST and GREM registries (2024) Lübke J, Christen D, Schwaab J, Kaiser A, Naumann N, Shoumariyeh K, Jentzsch M, et al. Journal article Schwangerschaft und Mutterschutz in der Kardiologie und in der Kinder- und Jugendkardiologie (2024) Güder G, Boer J, Busch S, Gaede L, Graf T, Herberg U, Kretschmer A, et al. Journal article Large language models streamline automated machine learning for clinical studies (2024) Tayebi Arasteh S, Han T, Lotfinia M, Kuhl C, Jakob Nikolas K, Truhn D, Nebelung S Journal article, Original article The Impact of Methylphenidate on Pubertal Maturation and Bone Age in ADHD Children and Adolescents: Results from the ADHD Drugs Use Chronic Effects (ADDUCE) Project (2024) Carucci S, Zuddas A, Lampis A, Man KK, Balia C, Buitelaar J, Danckaerts M, et al. Journal article Topographically and Chemically Enhanced Textile Polycaprolactone Scaffolds for Tendon and Ligament Tissue Engineering (2024) Bauer B, Emonts C, Pitts J, Buhl EM, Eschweiler J, Hänsch R, Betsch M, et al. Journal article Inhibition of the renal apical sodium dependent bile acid transporter prevents cholemic nephropathy in mice with obstructive cholestasis (2024) Ghallab A, González D, Strängberg E, Hofmann U, Myllys M, Hassan R, Hobloss Z, et al. Journal article A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3 (2024) Paul MS, Michener SL, Pan H, Chan H, Pfliger JM, Rosenfeld JA, Lerma VC, et al. Journal article