Department of Paediatrics and Adolescent Medicine

Editorial: Gene, Cell and Protein Replacement Therapy for Genetic Muscle, Bone and Skin Disorders (2021) Schneider H, De Luca M Journal article Exome sequencing implicates a novel heterozygous missense variant in DSTYK in autosomal dominant lower urinary tract dysfunction and mild hereditary spastic paraparesis. (2021) Vidic C, Zaniew M, Jurga S, Thiele H, Reutter HM, Hilger AC Journal article A Transmural Path Model Improves the Definition of the Orthotropic Tissue Structure in Heart Simulations (2021) Holz D, Duong MT, Martonová D, Alkassar M, Leyendecker S Journal article, Original article EARLY CHILDHOOD HEIGHT-ADJUSTED TOTAL KIDNEY VOLUME AS A RISK MARKER OF KIDNEY SURVIVAL IN AUTOSOMAL RECESSIVE POLYCYSTIC KIDNEY DISEASE (ARPKD) (2021) Burgmaier K, Kilian S, Arbeiter K, Atmis B, Buescher A, Derichs U, Dursun I, et al. Conference contribution PHENOCOPIESOF CLINICALLY DIAGNOSED ARPKD REVEALED IN CHILDREN (2021) Halawi A, Burgmaier K, Buescher A, Dursun I, Galiano M, Gessner M, Gokce I, et al. Conference contribution Quality of Pediatric Palliative Care Crisis Intervention - A Retrospective Survey (2021) Berkmueller M, Gravou-Apostolatou C, Rascher W Journal article Plasma Metabolome Profiling for the Diagnosis of Catecholamine Producing Tumors (2021) März J, Kurlbaum M, Roche-Lancaster O, Deutschbein T, Peitzsch M, Prehn C, Weismann D, et al. Journal article Assessment of educational and social status of survivors of childhood cancer: Data of a single center late effects clinic (2021) Hahn B, Schuster S, Metzler M, Mackensen A, Meidenbauer N Conference contribution Synergy of simultaneous activation of cell death pathways of unfolded protein response and of protein synthesis inhibition converges at IRE1a-immunotoxins generate a therapeutic window (2021) Gsottberger F, Meier C, Ammon AM, Petkovic S, Mellenthin L, Krumbholz M, Metzler M, et al. Conference contribution Current clinical practice of prenatal dexamethasone treatment in at risk pregnancies for classic 21-hydroxylase deficiency in Europe (2021) Nowotny HF, Neumann U, Tardy-Guidollet V, Ahmed SF, Baronio F, Battelino T, Bertherat J, et al. Conference contribution