eNauka - pregled
Pregled prema Autor Westenberger, Ana
Prikaz rezultata 1 do 10 od 10
Godina | Naslov | Autor(i) | Tip rezultata | Mp-kat. |
---|---|---|---|---|
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 ; | Naučni članak | 21aM21a - Rad u međ. časopisu izuzetnih vrednosti |
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 ; | Naučni članak | 21M21 - Rad u vrhunskom međ. časopisu |
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;
| Naučni članak | 21aM21a - Rad u međ. časopisu izuzetnih vrednosti |
2014 | Mutations in GNAL: a novel cause of craniocervical dystonia | Kumar, Kishore R.; Lohmann, Katja; Masuho, Ikuo; Miyamoto, Ryosuke; Ferbert, Andreas; Lohnau, Thora; Kasten, Meike; Hagenah, Johann; Brüggemann, Norbert; Graf, Julia; | Naučni članak | 21aM21a - Rad u međ. časopisu izuzetnih vrednosti |
2013 | Mutations in the gene encoding PDGF-B cause brain calcifications in humans and mice | Keller, Annika; Westenberger, Ana; Sobrido, Maria J; García-Murias, Maria; Domingo, Aloysius; Sears, Renee L; Lemos, Roberta R; Ordoñez-Ugalde, Andres; Nicolas, Gael; da, Cunha José E Gomes;
Rushing, Elisabeth J; Hugelshofer, Michael; Wurnig, Moritz C; Kaech, Andres; Reimann, Regina; Lohmann, Katja; Dobričić, Valerija; Carracedo, Angel; Petrović, Igor ; Miyasaki, Janis M; Abakumova, Irina; Mäe, Maarja Andaloussi; Raschperger, Elisabeth; Zatz, Mayana; Zschiedrich, Katja; Klepper, Jörg; Spiteri, Elizabeth; Prieto, Jose M; Navas, Inmaculada; Preuss, Michael; Dering, Carmen; Janković, Milena; Paucar, Martin; Svenningsson, Per; Saliminejad, Kioomars; Khorshid, Hamid R K; Novaković, Ivana; Aguzzi, Adriano; Boss, Andreas; Le, Ber Isabelle; Defer, Gilles; Hannequin, Didier; Kostić, Vladimir ; Campion, Dominique; Geschwind, Daniel H; Coppola, Giovanni; Betsholtz, Christer; Klein, Christine; Oliveira, Joao R M;
| Naučni članak | 21aM21a - Rad u međ. časopisu izuzetnih vrednosti |
2014 | Novel GNAL Mutations in Two German Patients With Sporadic Dystonia | Ziegan, Julia; Wittstock, Matthias; Westenberger, Ana; Dobricic, Valerija S; Wolters, Alexander; Benecke, Reiner; Klein, Christine; Kamm, Christoph | Informativni prilog | 21aM21a - Rad u međ. časopisu izuzetnih vrednosti |
2017 | Novel GNB1 mutations disrupt assembly and function of G protein heterotrimers and cause global developmental delay in humans | Lohmann, Katja; Masuho, Ikuo; Patil, Dipak N.; Baumann, Hauke; Hebert, Eva; Steinrücke, Sofia; Trujillano, Daniel; Skamangas, Nickolas K.; Dobricic, Valerija; Hüning, Irina; | Naučni članak | 21aM21a - Rad u međ. časopisu izuzetnih vrednosti |
2015 | Phenotype of non-c.907_909delGAG mutations in TOR1A: DYT1 dystonia revisited (✓) | Dobričić, Valerija ; Kresojević, Nikola ; Žarković, Milena; Tomić, Aleksandra ; Marjanović, Ana ; Westenberger, Ana; Cvetković, Dragana ; Svetel, Marina ; Novaković, Ivana ; Kostić, Vladimir | Naučni članak | 21M21 - Rad u vrhunskom međ. časopisu |
2016 | Seemingly dominant inheritance of a recessive ANO10 mutation in romani families with cerebellar ataxia | Mišković, Nataša Dragašević; Domingo, Aloysius; Dobričić, Valerija; Max, Christoph; Braenne, Ingrid; Petrović, Igor ; Grütz, Karen; Pawlack, Heike; Tournev, Ivailo; Kalaydjieva, Luba; | Naučni članak | 21aM21a - Rad u međ. časopisu izuzetnih vrednosti |
2018 | WDR45 mutations may cause a MECP2 mutation-negative Rett syndrome phenotype | Kulikovskaja, Leonora; Sarajlija, Adrijan ; Savić Pavićević, Dušanka ; Dobricic, Valerija; Klein, Christine; Westenberger, Ana | Naučni članak | Mp kategorija će biti prikazana naknadno. |