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Browsing by Author Klein, Christine
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| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2025 | An Unusual Presentation of a DNMT1 Mutation: Progressive Supranuclear Palsy Look-Alike Disorder | Ječmenica-Lukić, Milica V.  ; Milovanović, Andona ; Mazalica, Nina; Westenberger, Ana; Tomić-Pešić, Aleksandra  ; Petrović, Igor N. ; Marković, Vladana V. ; Kresojević, Nikola D. ; Klein, Christine; Kostić, Vladimir S. ;
Dragašević-Mišković, Nataša T.
; | Article | 22M22 |
| 2024 | ANO10-Related Spinocerebellar Ataxia: MDSGene Systematic Literature Review and a Romani Case Series | Milovanović, Andona ; Westenberger, Ana; Stanković, Iva D. ; Tamaš, Olivera S.; Branković, Marija ; Marjanović, Ana ; ...; Branković, Vesna; Novaković, Ivana V. ; Petrović, Igor N. ;
Svetel, Marina V.
; Klein, Christine; Kostić, Vladimir S. ; Dragašević-Mišković, Nataša T. ; (broj koautora 18); | Article | 21aM21a |
| 2006 | Clinical characteristics of paroxysmal nonkinesigenic dyskinesia in Serbian family with Myofibrillogenesis regulator 1 gene mutation | Stefanova, Elka ; Đarmati, Ana; Momčilović, Dragana; Dragašević-Mišković, Nataša ; Svetel, Marina ; Klein, Christine; Kostić, Vladimir | Article | 21M21 |
| 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;
| Article | 21aM21a |
| 2014 | De novo mutation in the GNAL gene causing seemingly sporadic dystonia in a Serbian patient | Dobričić, Valerija; Kresojević, Nikola ; Westenberger, Ana; Svetel, Marina ; Tomić, Aleksandra ; Ralić, Vesna; Petrović, Igor ; Lukić, Milica Ječmenica ; Lohmann, Katja; Novaković, Ivana ;
Klein, Christine; Kostić, Vladimir
; | Article | 21aM21a |
| 2007 | Delayed-onset dystonia due to perinatal asphyxia - a prospective study | Cerovac, Nataša ; Petrović, Igor ; Klein, Christine; Kostić, Vladimir | Article | 21M21 |
| 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;
| Article | 21aM21a |
| 2009 | Dystonia plus syndromes | Berisavac, Iva I; Svetel, Marina V ; Djuric, Gordana M; Bogosavljevic, Visnja; Klein, Christine; Illarioshkin, SN | Conference Paper | Mp. category will be shown later |
| 2024 | DYT-THAP1: exploring gene expression in fibroblasts for potential biomarker discovery | 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;
| Article | 23M23 |
| 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 ; Garrels, J; Landt, O; Nitschke, M; Pramstaller, Peter P; Reik, W;
Schwinger, E; Sperner, J; Ozelius, LJ; Kostic, Vladimir S; Klein, Christine;
| Article | 21aM21a |
| 2011 | Exclusion of linkage to chromosomes 14q, 2q37 and 8p21.1-q11.23 in a Serbian family with idiopathic basal ganglia calcification | Kostić, Vladimir ; Lukić-Ječmenica, Milica ; Novaković, Ivana ; Dobričić, Valerija; Brajković, Lela; Krajinović, Maja; Klein, Christine; Pavlović, Aleksandra | Article | 21M21 |
| 2006 | Frequency analysis and clinical characterization of different types of spinocerebellar ataxia in Serbian patients | Dragašević-Mišković, Nataša ; Culjković, Biljana; Klein, Christine; Ristić, Aleksandar ; Keckarević-Marković, Milica ; Topisirović, Ivan; Vukosavić, Slobodanka; Svetel, Marina ; Kock, Norman; Stefanova, Elka ;
Romac, Stanka; Kostić, Vladimir
; | Article | 21M21 |
| 2021 | Frequency of Heterozygous Parkin (PRKN) Variants and Penetrance of Parkinson's Disease Risk Markers in the Population-Based CHRIS Cohort | 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;
| Article | 22M22 |
| 2012 | Frequency of the D620N Mutation in VPS35 in Parkinson Disease | Kumar, Kishore R.; Weissbach, Anne; Heldmann, Marcus; Kasten, Meike; Tunc, Sinem; Sue, Carolyn M.; Svetel, Marina ; Kostić, Vladimir ; Segura-Aguilar, Juan; Ramirez, Alfredo;
Simon, David K.; Vieregge, Peter; Münte, Thomas F.; Hagenah, Johann; Klein, Christine; Lohmann, Katja;
| Article | 21aM21a |
| 2017 | GCH1 mutations are common in Serbian patients with dystonia-parkinsonism: Challenging previously reported prevalence rates of DOPA-responsive dystonia | Dobričić, Valerija ; Tomić, Aleksandra ; Branković, Vesna; Kresojević, Nikola ; Janković, Milena ; Westenberger, Ana; Milić Rašić, Vedrana ; Klein, Christine; Novaković, Ivana ; Svetel, Marina ;
Kostić, Vladimir
; | Article | 21M21 |
| 2019 | Gene expression analysis in cortical neurons differentiated from 32 induced pluripotent stem cell (iPSC) lines of THAP1 mutation carriers and controls | Baumann, Hauke; Trilck-Winkler, Michaela; Grosse, M; Munchau, Alexander; Kostic, Vladimir S; Klein, Christine; Kaiser, Frank J; Seibler, Philip; Lohmann, Katja | Conference Paper | Mp. category will be shown later |
| 2019 | Generation and in-depth characterization of 20 induced pluripotent stem cell (iPSC) lines from 10 dystonia patients and healthy carriers of THAP1 mutations | Baumann, H; Trilck, M; Jahn, M; Muenchau, A; Kostic, Vladimir S; Klein, Christine; Seibler, P; Lohmann, Katja | Conference Paper | Mp. category will be shown later |
| 2004 | Genetic heterogeneity in ten families with myoclonus-dystonia | Schule, B; Kock, Norman; Svetel, Marina V ; Dragasevic, Natasa T; Hedrich, Katja; Aguiar, PD; Liu, L; Kabakci, Kemal; Garrels, J; Meyer, EM;
Berisavac, Ivana I
; Schwinger, E; Kramer, PL; Ozelius, LJ; Klein, Christine; Kostic, Vladimir S; | Article | 21aM21a |
| 2013 | Genome-wide association study in musician's dystonia: A risk variant at the arylsulfatase G locus? | Lohmann, Katja; Schmidt, Alexander; Schillert, Arne; Winkler, Susen; Albanese, Alberto; Baas, Frank; Bentivoglio, Anna Rita; Borngräber, Friederike; Brüggemann, Norbert; Defazio, Giovanni;
Del, Sorbo Francesca; Deuschl, Günther; Edwards, Mark J.; Gasser, Thomas; Gómez-Garre, Pilar; Graf, Julia; Groen, Justus L.; Grünewald, Anne; Hagenah, Johann; Hemmelmann, Claudia; Jabusch, Hans-Christian; Kaji, Ryuji; Kasten, Meike; Kawakami, Hideshi; Kostić, Vladimir
; Liguori, Maria; Mir, Pablo; Münchau, Alexander; Ricchiuti, Felicia; Schreiber, Stefan; Siegesmund, Katharina; Svetel, Marina ; Tijssen, Marina A.J.; Valente, Enza Maria; Westenberger, Ana; Zeuner, Kirsten E.; Zittel, Simone; Altenmüller, Eckart; Ziegler, Andreas; Klein, Christine; | Article | 21aM21a |
| 2006 | Heterozygous PINK1 mutations - a susceptibility factor for Parkinson disease? | Đarmati, Ana; Hedrich, Katja; Svetel, Marina ; Lohnau, Thora; Schwinger, Eberhard; Romac, Stanka; Pramstaller, Peter P.; Kostić, Vladimir ; Klein, Christine | Article | 21M21 |