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Browsing by Author Djarmati, Ana
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 |
| 2004 | DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson disease | Hedrich, 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;
| Article | 21a+M21a+ |
| 2004 | Genetics of familial amyotrophic lateral sclerosis in Serbia and Montenegro | Kostic, Svetlana I; Stevic, Zorica D; Keckarevic, Dusan P; Djarmati, Ana; Lavrnic, Dragana V; Rakocevic, Vidosava M; Radunovic, S; Romac, Stanka P; Apostolski, Slobodan A | Conference Paper | Mp. category will be shown later |
| 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 |
| 2010 | Possible Genetic Heterogeneity of Spinocerebellar Ataxia Linked to Chromosome 15 | Weissbach, Anne; Djarmati, Ana; Klein, Christine; Dragasevic, Natasa   ; Zuehlke, Christine; Rakovic, Aleksandar; Gužvić, Miodrag ; Butz, Elisabeth; Toennies, Holger; Siebert, Reiner;
Petrović, Igor
; Svetel, Marina ; Kostic, Vladimir S. ; Lohmann, Katja; | Article | 21aM21a |
| 2007 | Rapid and reliable detection of exon rearrangements in various movement disorders genes by multiplex ligation-dependent probe amplification | Djarmati, Ana; Gužvić, Miodrag ; Gruenewald, Anne; Lang, Anthony E.; Pramstaller, Peter P.; Simon, David K.; Kaindl, Angela M.; Vieregge, Peter; Nygren, Anders O. H.; Beetz, Christian;
Hedrich, Katja; Klein, Christine;
| Article | 21M21 |
| 2003 | SCA2 and SCA3 mutations in young-onset dopa-responsive parkinsonism | Svetel, Marina V ; Djarmati, Ana; Dragasevic, Natasa T; Savic, Dusanka Lj ; Culjkovic, Biljana; Romac, Stanka P; Kostic, Vladimir S | Article | 22M22 |
| 2004 | Spinocerebellar ataxia type 17 in the Yugoslav population | Alendar, A; Culjkovic, Biljana; Savic, Dusanka Lj ; Djarmati, Ana; Keckarevic, Milica; Ristic, Aleksandar J ; Dragasevic, Natasa T; Kostic, Vladimir S; Romac, Stanka P | Article | 22M22 |