Browsing eNauka
Browsing by Author Hagenah, Johann M
Showing results 1 to 4 of 4
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2006 | Clinical spectrum of homozygous and heterozygous PINK1 mutations in a large German family with Parkinson disease Role of a single hit? | Hedrich, Katja; Hagenah, Johann M; Djarmati, Ana; Hiller, A; Lohnau, T; Lasek, K; Grunewald, RA; Hilker, R; Steinlechner, S; Boston, H;
Kock, Norman; Schneider-Gold, C; Kress, W; Siebner, Hartwig R; Binkofski, Ferdinand; Lencer, R; Munchau, A; Klein, Christine;
| Article | 21aM21a |
| 2004 | Mutations in DYT1 - Extension of the phenotypic and mutational spectrum | Kabakci, Kemal; Hedrich, Katja; Leung, JC; Mitterer, M; Vieregge, Peter; Lencer, R; Hagenah, Johann M; Garrels, J; Witt, K; Klostermann, F;
Svetel, Marina V
 ; Friedman, J; Kostic, Vladimir S; Bressman, SB; Breakefield, XO; Ozelius, LJ; Pramstaller, Peter P; Klein, Christine; | Article | 21a+M21a+ |
| 2002 | Role of SC42 mutations in early- and late-onset dopa-responsive parkinsonism | Kock, Norman; Muller, B; Vieregge, Peter; Pramstaller, Peter P; Marder, K; Abbruzzese, G; Martinelli, P; Lang, Anthony E; Jacobs, H; Hagenah, Johann M;
Harris, J; Meija-Santana, H; Fahn, S; Hedrich, Katja; Kann, M; Gehlken, U; Culjkovic, Biljana; Schwinger, E; Wszolek, ZK; Zuhlke, C; Klein, Christine;
| Contribution to periodical | 21a+M21a+ |
| 2004 | The R98Q variation in DJ-1 represents a rare polymorphism | Hedrich, Katja; Schafer, N; Hering, R; Hagenah, Johann M; Lanthaler, AJ; Schwinger, E; Kramer, PL; Ozelius, LJ; Bressman, SB; Abbruzzese, G;
Martinelli, P; Kostic, Vladimir S; Pramstaller, Peter P; Vieregge, Peter; Riess, O; Klein, Christine;
| Contribution to periodical | 21a+M21a+ |