eNauka - pregled
Pregled prema Autor Djarmati, Ana
Prikaz rezultata 1 do 8 od 8
| Godina | Naslov | Autor(i) | Tip rezultata | Mp-kat. |
|---|---|---|---|---|
| 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;
| Naučni članak | 21aM21a - Vodeći međunarodni časopis kategorije M21a |
| 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;
| Naučni članak | 21a+M21a+ - Vodeći međunarodni časopis kategorije 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 | Konferencijski rad | Mp kategorija će biti prikazana naknadno. |
| 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;
| Naučni članak | 21M21 - Vodeći međunarodni časopis kategorije M21 |
| 2010 | Possible Genetic Heterogeneity of Spinocerebellar Ataxia Linked to Chromosome 15 | Weissbach, Anne; Djarmati, Ana; Klein, Christine; Dragasevic, Natasa | Naučni članak | 21aM21a - Vodeći međunarodni časopis kategorije M21a |
| 2007 | Rapid and reliable detection of exon rearrangements in various movement disorders genes by multiplex ligation-dependent probe amplification | Djarmati, Ana; Gužvić, Miodrag
Hedrich, Katja; Klein, Christine;
| Naučni članak | 21M21 - Vodeći međunarodni časopis kategorije M21 |
| 2003 | SCA2 and SCA3 mutations in young-onset dopa-responsive parkinsonism | Svetel, Marina V | Naučni članak | 22M22 - Međunarodni časopis kategorije M22 |
| 2004 | Spinocerebellar ataxia type 17 in the Yugoslav population | Alendar, A; Culjkovic, Biljana; Savic, Dusanka Lj | Naučni članak | 22M22 - Međunarodni časopis kategorije M22 |