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Browsing by Author Kock, Norman
Showing results 1 to 8 of 8
| 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 |
| 2002 | Evidence that paternal expression of the epsilon-Sarcoglycan gene accounts for reduced penetrance in myoclonus-dystonia | Muller, B; Hedrich, Katja; Kock, Norman; Dragasevic, Natasa T; Svetel, Marina V  ; Garrels, J; Landt, O; Nitschke, M; Pramstaller, Peter P; Reik, W;
Schwinger, E; Sperner, J; Ozelius, LJ; Kostic, Vladimir S; Klein, Christine;
| Article | 21aM21a |
| 2006 | Frequency analysis and clinical characterization of different types of spinocerebellar ataxia in Serbian patients | Dragašević-Mišković, Nataša  ; Culjković, Biljana; Klein, Christine; Ristić, Aleksandar ; Keckarević-Marković, Milica ; Topisirović, Ivan; Vukosavić, Slobodanka; Svetel, Marina ; Kock, Norman; Stefanova, Elka ;
Romac, Stanka; Kostić, Vladimir
; | Article | 21M21 |
| 2004 | Genetic heterogeneity in ten families with myoclonus-dystonia | Schule, B; Kock, Norman; Svetel, Marina V ; Dragasevic, Natasa T; Hedrich, Katja; Aguiar, PD; Liu, L; Kabakci, Kemal; Garrels, J; Meyer, EM;
Berisavac, Ivana I
; Schwinger, E; Kramer, PL; Ozelius, LJ; Klein, Christine; Kostic, Vladimir S; | Article | 21aM21a |
| 2006 | Intrafamilial phenotypic and genetic heterogeneity of dystonia | Kostić, Vladimir ; Svetel, Marina ; Kabakci, Kemal; Ristić, Aleksandar ; Petrović, Igor ; Schüle, Birgitt; Kock, Norman; Đarmati, Ana; Romac, Stanka; Klein, Christine | Article | 21M21 |
| 2002 | Mode of inheritance and susceptibility locus for restless legs syndrome, on chromosome 12q | Kock, Norman; Culjkovic, Biljana; Maniak, S; Schilling, Klaus; Muller, B; Zuhlke, C; Ozelius, L; Klein, Christine; Pramstaller, Peter P; Kramer, PL | Contribution to periodical | 21aM21a |
| 2005 | PINK1, Parkin, and DJ-1 mutations in Italian patients with early-onset parkinsonism | Klein, Christine; Djarmati, Ana; Hedrich, Katja; Schafer, N; Scaglione, C; Marchese, R; Kock, Norman; Schule, B; Hiller, A; Lohnau, T;
Winkler, Susan; Wiegers, K; Hering, R; Bauer, P; Riess, O; Abbruzzese, G; Martinelli, P; Pramstaller, Peter P;
| Article | 21M21 |
| 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+ |