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Naslov RFC1 and FGF14 Repeat Expansions in Serbian Patients with Cerebellar Ataxia (Article; Early Access)
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. br. , str. -
Projekat Deutsche Forschungsgemeinschaft; University of Luebeck [FOR 2488]; German Research Foundation
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati:
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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 Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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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 Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Seemingly Dominant Inheritance of a Recessive ANO10 Mutation in Romani Families With Cerebellar Ataxia (Letter)
Autori Dragasevic-Miskovic Natasa T Domingo Aloysius Dobricic Valerija S Max Christoph Braenne Ingrid Petrovic Igor N Grutz Karen Pawlack Heike Tournev Ivailo Kalaydjieva Luba Svetel Marina V  Lohmann Katja Kostic Vladimir S Westenberger Ana 
Info MOVEMENT DISORDERS, (2016), vol. 31 br. 12, str. 1929-1931
Projekat Ministry of Education and Science, Republic of Serbia [ON175090]; Medical Genetics Priority Program of the University of Lubeck, Germany; National Research Fund of Ministry of Education and Science of Bulgaria
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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Naslov Phenotype of non-c.907_909delGAG mutations in TOR1A: DYT1 dystonia revisited (Article)
Autori Dobricic Valerija S Kresojevic Nikola D  Zarkovic Milena Tomic Aleksandra D Marjanovic Ana  Westenberger Ana Cvetkovic Dragana D Svetel Marina V  Novakovic Ivana V  Kostic Vladimir S 
Info PARKINSONISM & RELATED DISORDERS, (2015), vol. 21 br. 10, str. 1256-1259
Projekat Ministry of Education and Science, Republic of Serbia [ON175090, ON175091]; Fritz Thyssen Foundation [Az. 10.14.1.233]
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science  
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Naslov Novel GNAL Mutations in Two German Patients With Sporadic Dystonia (Letter)
Autori Ziegan Julia Wittstock Matthias Westenberger Ana Dobricic Valerija S Wolters Alexander Benecke Reiner Klein Christine Kamm Christoph 
Info MOVEMENT DISORDERS, (2014), vol. 29 br. 14, str. 1833-1834
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science  
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Naslov De Novo Mutation in the GNAL Gene Causing Seemingly Sporadic Dystonia in a Serbian Patient (Article)
Autori Dobricic Valerija S Kresojevic Nikola D  Westenberger Ana Svetel Marina V  Tomic Aleksandra D Ralic Vesna Petrovic Igor N Jecmenica-Lukic Milica V  Lohmann Katja Novakovic Ivana V  Klein Christine Kostic Vladimir S 
Info MOVEMENT DISORDERS, (2014), vol. 29 br. 9, str. 1190-1193
Projekat Ministry of Education and Science, Republic of Serbia [ON175090, ON175091]; Hermann and Lilly Schilling Foundation
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
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