Items where Author is "Jung, Hans H."

2015

Petersen, Jens A. and Kuntzer, Thierry and Fischer, Dirk and von der Hagen, Maja and Huebner, Angela and Kana, Veronika and Lobrinus, Johannes A. and Kress, Wolfram and Rushing, Elisabeth J. and Sinnreich, Michael and Jung, Hans H.. (2015) Dysferlinopathy in Switzerland: clinical phenotypes and potential founder effects. BMC Neurology, 15. p. 182.

2011

Polymenidou, Magdalini and Prokop, Stefan and Jung, Hans H. and Hewer, Ekkehard and Peretz, David and Moos, Rita and Tolnay, Markus and Aguzzi, Adriano. (2011) Atypical Prion Protein Conformation in Familial Prion Disease with PRNP P105T Mutation. Brain pathology, Vol. 21, no. 2. pp. 209-214.

2003

Wollmer, M. Axel and Streffer, Johannes R. and Lütjohann, Dieter and Tsolaki, Magdalini and Iakovidou, Vassiliki and Hegi, Thomas and Pasch, Thomas and Jung, Hans H. and Bergmann, Klaus von and Nitsch, Roger M. and Hock, Christoph and Papassotiropoulos, Andreas. (2003) ABCA1 modulates CSF cholesterol levels and influences the age at onset of Alzheimer's disease. Neurobiology of aging, Vol. 24, H. 3. pp. 421-426.

Maddalena, Alessia and Papassotiropoulos, Andreas and Müller-Tillmanns, Britta and Jung, Hans H. and Hegi, Thomas and Nitsch, Roger M. and Hock, Christoph. (2003) Biochemical diagnosis of Alzheimer disease by measuring the cerebrospinal fluid ratio of phosphorylated tau protein to beta-amyloid peptide42. Archives of neurology, Vol. 60, H. 9. pp. 1202-1206.

2002

Wollmer, M. Axel and Papassotiropoulos, Andreas and Streffer, Johannes R. and Grimaldi, Luigi M. E. and Kapaki, Elisabeth and Salani, Giuliana and Paraskevas, George P. and Maddalena, Alessia and de Quervain, Dominique and Bieber, Claudia and Umbricht, Daniel and Lemke, Ulrike and Bosshardt, Simone and Degonda, Nadia and Henke, Katharina and Hegi, Thomas and Jung, Hans H. and Pasch, Thomas and Hock, Christoph and Nitsch, Roger M.. (2002) Genetic polymorphisms and cerebrospinal fluid levels of tissue inhibitor of metalloproteinases 1 in sporadic Alzheimer's disease. Psychiatric Genetics, Vol. 12, H. 3. pp. 155-160.