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Преглед према Аутор Muller, B

Приказ резултата 1 до 3 од 3
ГодинаНасловАутор(и)Тип резултатаМп-кат.
2002Evidence that paternal expression of the epsilon-Sarcoglycan gene accounts for reduced penetrance in myoclonus-dystoniaMuller, 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;
Naučni članak
21aM21a - Vodeći međunarodni časopis kategorije M21a
2002Mode of inheritance and susceptibility locus for restless legs syndrome, on chromosome 12qKock, Norman; Culjkovic, Biljana; Maniak, S; Schilling, Klaus; Muller, B; Zuhlke, C; Ozelius, L; Klein, Christine; Pramstaller, Peter P; Kramer, PLInformativni prilog
21aM21a - Vodeći međunarodni časopis kategorije M21a
2002Role of SC42 mutations in early- and late-onset dopa-responsive parkinsonismKock, 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;
Informativni prilog
21a+M21a+ - Vodeći međunarodni časopis kategorije M21a+