Autori: Klein Christine
| Naslov | An Unusual Presentation of a DNMT1 Mutation: Progressive Supranuclear Palsy Look-Alike Disorder (Editorial Material; Early Access) |
| Autori | Jecmenica-Lukic Milica V Milovanovic Andona Mazalica Nina Westenberger Ana Tomic-Pesic Aleksandra Petrovic Igor N Markovic Vladana V Kresojevic Nikola D Klein Christine Kostic Vladimir S Dragasevic-Miskovic Natasa T |
| Info | MOVEMENT DISORDERS CLINICAL PRACTICE, (2025), vol. br. , str. - |
| Projekat | German Research Foundation |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: |
| Naslov | DYT-THAP1: exploring gene expression in fibroblasts for potential biomarker discovery (Article) |
| Autori | Diaw Sokhna Haissatou Delcambre Sylvie Much Christoph Ott Fabian Kostic Vladimir S Gajos Agata Muenchau Alexander Zittel Simone Busch Hauke Gruenewald Anne Klein Christine Lohmann Katja |
| Info | NEUROGENETICS, (2024), vol. 25 br. 2, str. 141-147 |
| Projekat | Deutsche Forschungsgemeinschaft [FOR2488, LO1555/9 - 2]; German Research Foundation [INTER/DFG/19/14429377]; Luxembourgish Research Fund |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: |
| Naslov | RFC1 and FGF14 Repeat Expansions in Serbian Patients with Cerebellar Ataxia (Article) |
| Autori | Milovanovic Andona Dragasevic-Miskovic Natasa T Thomsen Mirja Borsche Max Hinrichs Frauke Westenberger Ana Klein Christine Brueggemann Norbert Brankovic Marija Marjanovic Ana Svetel Marina V Kostic Vladimir S Lohmann Katja |
| Info | MOVEMENT DISORDERS CLINICAL PRACTICE, (2024), vol. 11 br. 6, str. 626-633 |
| Projekat | Deutsche Forschungsgemeinschaft; University of Luebeck [FOR 2488]; German Research Foundation |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: |
| Naslov | Frequency of Heterozygous Parkin (PRKN) Variants and Penetrance of Parkinson's Disease Risk Markers in the Population-Based CHRIS Cohort (Article) |
| Autori | Rueda Maria Paulina Castelo Raftopoulou Athina Goegele Martin Borsche Max Emmert David B Fuchsberger Christian Hantikainen Essi M Vukovic Vladimir R Klein Christine Pramstaller Peter P Pichler Irene Hicks Andrew A |
| Info | FRONTIERS IN NEUROLOGY, (2021), vol. 12 br. , str. - |
| Projekat | Deutsche ForschungsgemeinschaftGerman Research Foundation (DFG) [FOR2488]; Department of Educational Assistance, University and Research of the Autonomous Province of Bolzano, Italy |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| Naslov | Linking Penetrance and Transcription in DYT-THAP1: Insights From a Human iPSC-Derived Cortical Model (Article) |
| Autori | Baumann Hauke Ott Fabian Weber Joachim Trilck-Winkler Michaela Munchau Alexander Zittel Simone Kostic Vladimir S Kaiser Frank J Klein Christine Busch Hauke Seibler Philip Lohmann Katja |
| Info | MOVEMENT DISORDERS, (2021), vol. 36 br. 6, str. 1381-1391 |
| Projekat | German Research Foundation (DFG) [FOR2488] |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| Naslov | Gene expression analysis in cortical neurons differentiated from 32 induced pluripotent stem cell (iPSC) lines of THAP1 mutation carriers and controls (Meeting Abstract) |
| Autori | Baumann Hauke Trilck-Winkler Michaela Grosse M Munchau Alexander Kostic Vladimir S Klein Christine Kaiser Frank J Seibler Philip Lohmann Katja |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 2, str. 1430-1430 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science |
| Naslov | Generation and in-depth characterization of 20 induced pluripotent stem cell (iPSC) lines from 10 dystonia patients and healthy carriers of THAP1 mutations (Meeting Abstract) |
| Autori | Baumann H Trilck M Jahn M Muenchau A Kostic Vladimir S Klein Christine Seibler P Lohmann Katja |
| Info | EUROPEAN JOURNAL OF HUMAN GENETICS, (2019), vol. 27 br. , Suppl. 1, str. 314-314 |
| Ispravka | ISI/Web of Science Elečas Rang časopisa Citati: ISI/Web of Science |
| Naslov | WDR45 mutations may cause a MECP2 mutation-negative Rett syndrome phenotype (Editorial Material) |
| Autori | Kulikovskaja Leonora Sarajlija Adrijan Savic-Pavicevic Dusanka Lj Dobricic Valerija S Klein Christine Westenberger Ana |
| Info | NEUROLOGY-GENETICS, (2018), vol. 4 br. 2, str. - |
| Projekat | Hermann and Lilly Schilling Foundation; Land Schleswig-Holstein within the funding programme Open Access Publikationsfonds |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| Naslov | GCH1 mutations are common in Serbian patients with dystonia-parkinsonism: Challenging previously reported prevalence rates of DOPA-responsive dystonia (Article) |
| Autori | Dobricic Valerija S Tomic Aleksandra D Brankovic Vesna Kresojevic Nikola D Jankovic Milena Z Westenberger Ana Milic-Rasic Vedrana M Klein Christine Novakovic Ivana V Svetel Marina V Kostic Vladimir S |
| Info | PARKINSONISM & RELATED DISORDERS, (2017), vol. 45 br. , str. 81-84 |
| Projekat | Ministry of Education and Science, Republic of Serbia [ON175090, ON175091]; Hermann and Lilly Schilling Foundation; German Research Foundation (DFG) Research Unit [FOR2488] |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
| Naslov | Reply Letter to Jinnah "Locus Pocus" and Albanese "Complex Dystonia Is Not a Category in the New 2013 Consensus Classification": Necessary Evolution, No Magic! (Letter) |
| Autori | Klein Christine Lang Anthony E van de Warrenburg Bart P Sue Carolyn M Tabrizi Sarah J Bertram Lars Mercimek-Mahmutoglu Saadet Ebrahimi-Fakhari Darius Warner Thomas T Durr Alexandra Assmann Birgit Kostic Vladimir K Lohmann Katja Marras Connie |
| Info | MOVEMENT DISORDERS, (2016), vol. 31 br. 11, str. 1760-1762 |
| Ispravka | ISI/Web of Science Članak Elečas Rang časopisa Citati: ISI/Web of Science Scopus |
