Researchers
Svetel, Marina
Results 301-320 of 323
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2004 | Clinical presentation of Hallervorden-Spatz disease: Report of four cases | Svetel, Marina V | Conference Paper | Mp. category will be shown later |
| 2004 | Cardiovascular risk predictors for sudden heart death by patients with Parkinson’s disease![]() | Milovanović, Branislav | Conference Paper | Mp. category will be shown later |
| 2004 | Bilateral chorea-ballism associated with hyperthyroidism | Ristic, Aleksandar J | Article | 21M21 |
| 2004 | Incidence of vascular hemiballism in the population of Belgrade | Pekmezović, Tatjana | Article | 21M21 |
| 2004 | Autosomal dominant cerebellar ataxias in Serbia: A clinical and molecular study | Ristic, Aleksandar J | Conference Paper | Mp. category will be shown later |
| 2004 | Myoclonus dystonia (MD) in Serbian population - clinical and genetic analysis | Berisavac, Iva I; Klein, Christine; Svetel, Marina V | Conference Paper | Mp. category will be shown later |
| 2004 | Urogenital disorders in de novo parkinsonian patients![]() | De Luka, Silvio | Conference Paper | Mp. category will be shown later |
| 2004 | Characteristics of dystonic movements in primary and symptomatic dystonias | Svetel, Marina V | Article | 21aM21a |
| 2004 | Initial and follow-up brain MRI findings and correlation with neurological manifestations in Wilson's disease | Petrovic, Igor N; Svetel, Marina V | Conference Paper | Mp. category will be shown later |
| 2004 | Spinocerebellar ataxia type 1 in Serbia | Dragasevic, Natasa T; Ristic, Aleksandar J | Conference Paper | Mp. category will be shown later |
| 2004 | Mutations in DYT1 - Extension of the phenotypic and mutational spectrum | Kabakci, Kemal; Hedrich, Katja; Leung, JC; Mitterer, M; Vieregge, Peter; Lencer, R; Hagenah, Johann M; Garrels, J; Witt, K; Klostermann, F; | Article | 21a+M21a+ |
| 2003 | Prevalence of primary late-onset focal dystonia in the Belgrade population | Pekmezovic, Tatjana D | Article | 21M21 |
| 2003 | MR imaging of the brain in patients with hepatic form of Wilson's disease | Kozic, Dusko B | Article | 22M22 |
| 2003 | Characterization of the molecular defect in the ATP7B gene in Wilson disease patients from Yugoslavia | Loudianos, Georgios; Kostic, Vladimir S; Solinas, P; Lovicu, Mario; Dessi, Valentina; Svetel, Marina V | Article | 22M22 |
| 2003 | SCA2 and SCA3 mutations in young-onset dopa-responsive parkinsonism | Svetel, Marina V | Article | 22M22 |
| 2002 | The effect of stage of Parkinson's disease at the onset of levodopa therapy on development of motor complications | Kostic, Vladimir S; Marinkovic, Jelena M; Svetel, Marina V | Article | 22M22 |
| 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
Schwinger, E; Sperner, J; Ozelius, LJ; Kostic, Vladimir S; Klein, Christine;
| Article | 21aM21a |
| 2001 | DYT1 mutation in primary torsion dystonia in a Serbian population | Major, Tamara | Article | 21aM21a |
| 2001 | Dystonia in Wilson's disease | Svetel, Marina V | Article | 21aM21a |
| 2001 | Penicillamine-induced lethal status dystonicus in a patient with Wilson's disease | Svetel, Marina V | Article | 21aM21a |
