Autori: Djarmati Ana
Naslov | Possible Genetic Heterogeneity of Spinocerebellar Ataxia Linked to Chromosome 15 (Article) |
Autori | Weissbach Anne Djarmati Ana Klein Christine Dragasevic Natasa T Zuehlke Christine Rakovic Aleksandar Guzvic Miodrag Butz Elisabeth Toennies Holger Siebert Reiner Petrovic Igor N Svetel Marina V Kostic Vladimir S Lohmann Katja |
Info | MOVEMENT DISORDERS, (2010), vol. 25 br. 11, str. 1577-1582 |
Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science |
Naslov | ATP13A2 Variants in Early-Onset Parkinson's Disease Patients and Controls (Article) |
Autori | Djarmati Ana Hagenah Johann M Reetz Kathrin Winkler Susen Behrens Maria Isabel Pawlack Heike Lohmann Katja Ramirez Alfredo Tadic Vera Brueggemann Norbert Berg Daniela Siebner Hartwig R Lang Anthony E Pramstaller Peter P Binkofski Ferdinand Kostic Vladimir S Volkmann Jens Gasser Thomas Klein Christine |
Info | MOVEMENT DISORDERS, (2009), vol. 24 br. 14, str. 2104-2111 |
Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
Naslov | Mutations in THAP1 (DYT6) and generalised dystonia with prominent spasmodic dysphonia: a genetic screening study (Article) |
Autori | Djarmati Ana ... Rakovic Aleksandar ... Kostic Vladimir S ... (broj koautora 19) |
Info | LANCET NEUROLOGY, (2009), vol. 8 br. 5, str. 447-452 |
Projekat | Deutsche Forschungsgerneinschaft [DJ 65/3-1]; Volkswagen Foundation ; Dystonia Medical Research Foundation ; University of Lubeck [E48.2009]; Hermann and Lilly Schilling Foundation |
Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
Naslov | Genetic Association Study of the P-Type ATPase ATP13A2 in Late-Onset Parkinson's Disease (Article) |
Autori | Rakovic Aleksandar Stiller Barbara Djarmati Ana Flaquer Antonia Freudenberg Jan Toliat Mohammad-Reza Linnebank Michael Kostic Vladimir S Lohmann Katja Paus Sebastian Nuernberg Peter Kubisch Christian Klein Christine Wuellner Ullrich Ramirez Alfredo |
Info | MOVEMENT DISORDERS, (2009), vol. 24 br. 3, str. 429-433 |
Projekat | Deutsche Forschungsgemeinschaft (DFG) [KU 1344/4-1]; Federal Ministry of Education and Research, German Competence Network on Parkinson's disease [01G19901, 01GI0201, 01GI0401]; Volkswagen Foundation to Christine Klein |
Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
Naslov | MECP2 mutations in Serbian Rett syndrome patients (Editorial Material) |
Autori | Djarmati Ana Dobricic Valerija S Kecmanovic Miljana Marsh P Jancic-Stefanovic Jasna B Klein Christine Djuric Milena Lj Romac Stanka P |
Info | ACTA NEUROLOGICA SCANDINAVICA, (2007), vol. 116 br. 6 , Suppl. , str. 413 -419 |
Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
Naslov | Rapid and reliable detection of exon rearrangements in various movement disorders genes by multiplex ligation-dependent probe amplification (Article) |
Autori | Djarmati Ana Guzvic Miodrag Gruenewald Anne Lang Anthony E Pramstaller Peter P Simon David K Kaindl Angela M Vieregge Peter Nygren Anders OH Beetz Christian Hedrich Katja Klein Christine |
Info | MOVEMENT DISORDERS, (2007), vol. 22 br. 12 , Suppl. , str. 1708 -1714 |
Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
Naslov | Intrafamilial phenotypic and genetic heterogeneity of dystonia (Article) |
Autori | Kostic Vladimir S Svetel Marina V Kabakci Kemal Ristic Aleksandar J Petrovic Igor N Schule B Kock Norman Djarmati Ana Romac Stanka P Klein Christine |
Info | JOURNAL OF THE NEUROLOGICAL SCIENCES, (2006), vol. 250 br. 1-2, str. 92-96 |
Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
Naslov | Clinical characteristics of paroxysmal nonkinesigenic dyskinesia in Serbian family with Myofibrillogenesis regulator 1 gene mutation (Article) |
Autori | Stefanova Elka D Djarmati Ana Momcilovic Dragana R Dragasevic Natasa T Svetel Marina V Klein Christine Kostic Vladimir S |
Info | MOVEMENT DISORDERS, (2006), vol. 21 br. 11, str. 2010-2015 |
Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
Naslov | Heterozygous PINK1 mutations: A susceptibility factor for Parkinson disease? (Article) |
Autori | Djarmati Ana Hedrich Katja Svetel Marina V Lohnau T Schwinger E Romac Stanka P Pramstaller Peter P Kostic Vladimir S Klein Christine |
Info | MOVEMENT DISORDERS, (2006), vol. 21 br. 9, str. 1526-1530 |
Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
Naslov | Clinical spectrum of homozygous and heterozygous PINK1 mutations in a large German family with Parkinson disease Role of a single hit? (Article) |
Autori | 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 |
Info | ARCHIVES OF NEUROLOGY, (2006), vol. 63 br. 6, str. 833-838 |
Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |