Lehrstuhl für Kinder- und Jugendmedizin

Molecular Composition of Genomic TMPRSS2-ERG Rearrangements in Prostate Cancer (2019) Krumbholz M, Agaimy A, Stöhr R, Burger M, Wach S, Taubert H, Wullich B, et al. Journal article Renal Chemerin Expression is Induced in Models of Hypertensive Nephropathy and Glomerulonephritis and Correlates with Markers of Inflammation and Fibrosis (2019) Mocker A, Hilgers KF, Cordasic N, Wachtveitl R, Menendez-Castro C, Wölfle J, Hartner A, Fahlbusch F Journal article A mathematical model of white blood cell dynamics during maintenance therapy of childhood acute lymphoblastic leukemia (2019) Le TT, Jost F, Raupach T, Zierk J, Rauh M, Suttorp M, Stanulla M, et al. Journal article Data mining of reference intervals for coagulation screening tests in adult patients (2019) Zierk J, Ganslandt T, Rauh M, Metzler M, Strasser E Journal article The Influence of the Age of the Bone Marrow Microenvironment on Leukaemia Progression (2019) Zanetti C, Ender J, Hartmann M, Hey J, Godavarthy PS, Weissenberger E, Kumar R, et al. Conference contribution High Platelet Counts, Thrombosis, Bleeding Signs, and Acquired Von Willebrand Syndrome at Diagnosis of Pediatric Chronic Myeloid Leukemia (2019) Suttorp M, Knoefler R, Deutsch H, Paul F, Tiebel O, Metzler M, Millot F Conference contribution Vaccination with Live Attenuated Virus Vaccines in Four Pediatric Patients with CML While on Imatinib Treatment (2019) Da Cunha-Riehm CB, Hildebrand V, Nathrath M, Metzler M, Suttorp M Conference contribution Fatigue and depression predict health-related quality of life in patients with pediatric-onset multiple sclerosis (2019) Gravesande KSV, Blaschek A, Calabrese P, Rostasy K, Huppke P, Kessler JJ, Kalbe E, et al. Journal article Comparative Socioeconomic Study Of Patients In Germany With Dravet Syndrome, Refractory Epilepsy Or Epilepsy In Seizure Remission, And Their Caregivers (2019) Strzelczyk A, Schubert-Bast S, Bast T, Bettendorf U, Hamer H, Herting A, Kalski M, et al. Conference contribution A novel mutation of the StAR gene with congenital adrenal hyperplasia and its association with heterochromia iridis: a case report (2019) Splittstösser V, Schreiner F, Gohlke B, Welzel M, Holterhus PM, Wölfle J Journal article