Rheinische Friedrich-Wilhelms-Universität Bonn

Measurement of amniotic fluid steroids of midgestation via LC-MS/MS (2015) Fahlbusch FB, Heussner K, Schmid M, Schild R, Rübner M, Hübner H, Rascher W, et al. Journal article Palmoplantar Pustular Psoriasis Is Associated with Missense Variants in CARD14, but Not with Loss-of-Function Mutations in IL36RN in European Patients (2015) Moessner R, Frambach Y, Wilsmann-Theis D, Loehr S, Jacobi A, Weyergraf A, Mueller M, et al. Journal article Implementation of the KDIGO guideline on lipid management requires a substantial increase in statin prescription rates (2015) Schneider MP, Hübner S, Titze S, Schmid M, Nadal J, Schlieper G, Busch M, et al. Journal article Cerebrospinal fluid cortisol and clinical disease progression in MCI and dementia of Alzheimer's type (2015) Popp J, Wolfsgruber S, Heuser I, Peters O, Huell M, Schroeder J, Moeller HJ, et al. Journal article A common variant mapping to CACNA1A is associated with susceptibility to exfoliation syndrome (2015) Aung T, Ozaki M, Mizoguchi T, Allingham RR, Li Z, Haripriya A, Nakano S, et al. Journal article De novo mutations in beta-catenin (CTNNB1) appear to be a frequent cause of intellectual disability: expanding the mutational and clinical spectrum (2015) Kuechler A, Willemsen MH, Albrecht B, Bacino CA, Bartholomew DW, Van Bokhoven H, Van Den Boogaard MJH, et al. Journal article Influence of genetic variants in SORL1 gene on the manifestation of Alzheimer's disease (2015) Louwersheimer E, Ramirez A, Cruchaga C, Becker T, Kornhuber J, Peters O, Heilmann S, et al. Journal article Chromatin-Remodeling-Factor ARID1B Represses Wnt/?-Catenin Signaling (2015) Vasileiou G, Ekici AB, Urebe S, Zweier C, Hoyer J, Engels H, Behrens J, et al. Journal article Carbohydrate intake and insulin requirement in children, adolescents and young adults with cystic fibrosis-related diabetes: A multicenter comparison to type 1 diabetes (2015) Scheuing N, Thon A, Konrad K, Bauer M, Karsten C, Meissner T, Seufert J, et al. Journal article Recurrent null mutation in SPG20 leads to Troyer syndrome (2015) Tawamie H, Wohlleber E, Uebe S, Schmael C, Noethen MM, Abou Jamra R Journal article