Rheinische Friedrich-Wilhelms-Universität Bonn

Gaps Between Aims and Achievements in Therapeutic Modification of Neuronal Damage ("Neuroprotection") (2015) Wiendl H, Elger C, Foerstl H, Hartung HP, Oertel W, Reichmann H, Schwab S Journal article A genome-wide association study confirms PNPLA3 and identifies TM6SF2 and MBOAT7 as risk loci for alcohol-related cirrhosis (2015) Buch S, Stickel F, Trepo E, Way M, Herrmann A, Nischalke HD, Brosch M, et al. Journal article Application of surface plasmon resonance imaging technique for the detection of single spherical biological submicrometer particles (2015) Shpacovitch V, Temchura V, Matrosovich M, Hamacher J, Skolnik J, Libuschewski P, Siedhoff D, et al. Journal article A New Sonographic Weight Estimation Formula for Fetuses with Congenital Diaphragmatic Hernia (2015) Faschingbauer F, Mayr A, Geipel A, Gembruch U, Dammer U, Raabe E, Beckmann M, et al. Journal article 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