eNauka - pregled

Pregled prema Autor Hilker, R

Prikaz rezultata 1 do 2 od 2
GodinaNaslovAutor(i)Tip rezultataMp-kat.
2006Clinical 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;
Naučni članak
21aM21a - Rad u međ. časopisu izuzetnih vrednosti
2004DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson diseaseHedrich, Katja; Djarmati, Ana; Schafer, N; Hering, R; Wellenbrock, C; Weiss, PH; Hilker, R; Vieregge, Peter; Ozelius, LJ; Heutink, P;
Bonifati, V; Schwinger, E; Lang, Anthony E; Noth, J; Bressman, SB; Pramstaller, Peter P; Riess, O; Klein, Christine;
Naučni članak
21aM21a - Rad u međ. časopisu izuzetnih vrednosti