Lehrstuhl für Kinder- und Jugendmedizin

Variable White Matter Atrophy and Intellectual Development in a Family With X-linked Creatine Transporter Deficiency Despite Genotypic Homogeneity (2017) Heussinger N, Saake M, Mennecke A, Dörr HG, Trollmann R Journal article Evaluation of an Interactive Visualization Tool for the Interpretation of Pediatric Laboratory Test Results (2017) Hirschmann J, Sedlmayr B, Zierk J, Rauh M, Metzler M, Prokosch HU, Toddenroth D Journal article Systematic comparison of donor chimerism in peripheral blood and bone marrow after hematopoietic stem cell transplantation (2017) Bach C, Steffen M, Rösler W, Winkler J, Mackensen A, Stachel D, Metzler M, Spriewald BM Journal article Recurrent Somatic PDGFRB Mutations in Sporadic Infantile/Solitary Adult Myofibromas But Not in Angioleiomyomas and Myopericytomas (2017) Agaimy A, Bieg M, Michal M, Geddert H, Maerkl B, Seitz J, Moskalev E, et al. Journal article Genetic screening confirms heterozygous mutations in ACAN as a major cause of idiopathic short stature (2017) Hauer N, Sticht H, Boppudi S, Büttner C, Kraus C, Trautmann U, Zenker M, et al. Journal article ENGRAFTMENT, DIFFERENTIATION AND BIOLOGICAL EFFECTS OF CORD BLOOD-DERIVED CLONAL CELLS ADMINISTERED INTRAVENOUSLY TO NEWBORN RATS WITH HYPOXIC-ISCHEMIC BRAIN INJURY (2016) Yang X, Griesmaier E, Wegleiter K, Schlager GW, Weisbach VG, Keller M, Park J, Schneider H Conference contribution Blood Pressure in a Large Cohort of Children and Adolescents With Classic Adrenal Hyperplasia (CAH) Due to 21-Hydroxylase Deficiency (2016) Bonfig W, Roehl FW, Riedl S, Dörr HG, Bettendorf M, Braemswig J, Schoenau E, et al. Journal article Pediatric chronic myeloid leukemia is a unique disease that requires a different approach (2016) Hijiya N, Schultz KR, Metzler M, Millot F, Suttorp M Journal article Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements (2016) Wohlfart S, Hammersen J, Schneider H Journal article Reduced Perinatal Leptin Availability May Contribute to Adverse Metabolic Programming in a Rat Model of Uteroplacental Insufficiency (2016) Nuesken E, Wohlfarth M, Lippach G, Rauh M, Schneider H, Doetsch J, Nuesken KD Journal article