4 Einträge gefunden

1. Recessively inherited parkinsonism: effect of ATP13A2 mutations on the clinical and neuroimaging phenotype.

   1. Brüggemann, Norbert
   2. Hagenah, Johann
   3. Reetz, Kathrin
   4. Schmidt, Alexander
   5. Kasten, Meike
   6. Buchmann, Inga
   7. Eckerle, Susanne

   2010 - Forschungsinformationssystem des UKE
2. Structural findings in the basal ganglia in genetically determined and idiopathic Parkinson's disease.

   1. Reetz, Kathrin
   2. Gaser, Christian
   3. Klein, Christine
   4. Hagenah, Johannes
   5. Büchel, Christian
   6. Gottschalk, Stefan
   7. Pramstaller, Peter P

   2009 - Forschungsinformationssystem des UKE
3. Limbic and frontal cortical degeneration is associated with psychiatric symptoms in PINK1 mutation carriers.

   1. Reetz, Kathrin
   2. Lencer, Rebekka
   3. Steinlechner, Susanne
   4. Gaser, Christian
   5. Hagenah, Johann
   6. Büchel, Christian
   7. Petersen, Dirk

   2008 - Forschungsinformationssystem des UKE
4. Phenotypic spectrum of PINK1-associated parkinsonism in 15 mutation carriers from 1 family.

   1. Hiller, Anja
   2. Hagenah, Johann M
   3. Djarmati, Ana
   4. Hedrich, Katja
   5. Reetz, Kathrin
   6. Schneider-Gold, Christiane
   7. Kress, Wolfgang

   2007 - Forschungsinformationssystem des UKE