Department of Paediatrics and Adolescent Medicine

Functional null mutations in the gonosomal homologue gene TBL1Y are associated with non-syndromic coarctation of the aorta (2012) Tagariello A, Breuer C, Birkner Y, Schmidt S, Koch AM, Cesnjevar R, Rueffer A, et al. Journal article Gesundheit, Empathie und Ökonomie Kostbare Werte in der Medizin (2011) Frewer A, Rascher W, Bruns F Edited Volume Fetal programming of gene expression in growth-restricted rats depends on the cause of low birth weight (2011) Nuesken KD, Schneider H, Plank CG, Trollmann R, Nuesken E, Rascher W, Doetsch J Journal article Sweating ability and genotype in individuals with X-linked hypohidrotic ectodermal dysplasia (2011) Schneider H, Hammersen J, Preisler-Adams S, Huttner K, Rascher W, Bohring A Journal article Efficiency of translation termination in humans is highly dependent upon nucleotides in the neighbourhood of a (premature) termination codon (2011) Pacho F, Zambruno G, Calabresi V, Kiritsi D, Schneider H Journal article Systematic evaluation of exertional hyperthermia in children and adolescents with hypohidrotic ectodermal dysplasia: An observational study (2011) Hammersen JE, Neukam V, Nüsken KD, Schneider H Journal article In vivo evaluation of gene transfer into mesenchymal cells (in view of cartilage repair). (2011) Gelse K, Schneider H Journal article Inhibition of tgf-β signaling and decreased apoptosis in iugr-associated lung disease in rats (2011) Alcazar MAA, Morty RE, Lendzian L, Vohlen C, Oestreicher I, Plank CG, Schneider H, Doetsch J Journal article Papilledema and Echographically Detectable Retro-orbital Dilatation of the Sub-arachnoidal Space with open Fontanelle - Six Case Reports (2011) Gusek-Schneider GC, Mardin C, Trollmann R, Eyüpoglu IY, Ganslandt OT Journal article Childhood polyarteritis Nodosa in Autoimmune Lymphoproliferative Syndrome (2010) Naumann-Bartsch N, Stachel D, Morhart P, Staatz G, Jüngert JM, Schwarz K, Holter W Journal article