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Autori: Djarmati Ana

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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 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  
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