5 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. Mutations in THAP1 (DYT6) and generalised dystonia with prominent spasmodic dysphonia: a genetic screening study.

   1. Djarmati, Ana
   2. Schneider, Susanne A
   3. Lohmann, Katja
   4. Winkler, Susen
   5. Pawlack, Heike
   6. Hagenah, Johann
   7. Brüggemann, Norbert

   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. Autosomal dominant myoclonus-dystonia and Tourette syndrome in a family without linkage to the SGCE gene.

   1. Orth, Michael
   2. Djarmati, Ana
   3. Bäumer, Tobias
   4. Winkler, Susan
   5. Grünewald, Anne
   6. Lohmann-Hedrich, Katja
   7. Kabakci, Kemal

   2007 - Forschungsinformationssystem des UKE
5. Clinical spectrum of homozygous and heterozygous PINK1 mutations in a large German family with Parkinson disease: role of a single hit?

   1. Hedrich, Katja
   2. Hagenah, Johann
   3. Djarmati, Ana
   4. Hiller, Anja
   5. Lohnau, Thora
   6. Lasek, Kathrin
   7. Grünewald, Anne

   2006 - Forschungsinformationssystem des UKE