Pronađeno: 1-10 / 16 radova

Autori: Lohmann Katja

>> Prikaži sve rezultate

>> Sve godine

  • 1
  • 2
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 Web of Science   Članak   Elečas   Rang časopisa   Citati:
facebook sharing button
twitter sharing button
linkedin sharing button
gmail sharing button
copy sharing button
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 Web of Science   Članak   Elečas   Rang časopisa   Citati:
facebook sharing button
twitter sharing button
linkedin sharing button
gmail sharing button
copy sharing button
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 Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
facebook sharing button
twitter sharing button
linkedin sharing button
gmail sharing button
copy sharing button
Naslov Novel GNB1 mutations disrupt assembly and function of G protein heterotrimers and cause global developmental delay in humans (Article)
Autori Lohmann Katja ... Dobricic Valerija S ... Savic-Pavicevic Dusanka Lj  ... (broj koautora 18) 
Info HUMAN MOLECULAR GENETICS, (2017), vol. 26 br. 6, str. 1078-1086
Projekat NIH [NS081282, HL105550]; German Ministry of Education and Research (BMBF, DYSTRACT consortium) [01GM1514B]; Ministry of Education, Science and Technological Development, Republic of Serbia [173016, 175090]; Hermann and Lilly Schilling Foundation
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
facebook sharing button
twitter sharing button
linkedin sharing button
gmail sharing button
copy sharing button
Naslov Nomenclature of genetic movement disorders: Recommendations of the international Parkinson and movement disorder society task force (Review)
Autori Marras Connie 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 Lohmann Katja Kostic Vladimir K Klein Christine 
Info MOVEMENT DISORDERS, (2016), vol. 31 br. 4, str. 436-457
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science  
facebook sharing button
twitter sharing button
linkedin sharing button
gmail sharing button
copy sharing button
Naslov The role of mutations in COL6A3 in isolated dystonia (Article)
Autori Lohmann Katja Schlicht Felix Svetel Marina V  ... Kostic Vladimir S ... (broj koautora 23) 
Info JOURNAL OF NEUROLOGY, (2016), vol. 263 br. 4, str. 730-734
Projekat German Research Foundation [LO1555/8-1, KFO247]; University of Luebeck [E36-2014]; Dystonia Coalition (part of the NIH Rare Diseases Clinical Research Network from the NIH Office of Rare Diseases Research and National Institute of Neurological Disorders a
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
facebook sharing button
twitter sharing button
linkedin sharing button
gmail sharing button
copy sharing button
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  
facebook sharing button
twitter sharing button
linkedin sharing button
gmail sharing button
copy sharing button
Naslov Genome-Wide Association Study in Musician's Dystonia: A Risk Variant at the Arylsulfatase G Locus? (Article)
Autori Lohmann Katja ... Kostic Vladimir S ... Svetel Marina V  ... (broj koautora 40) 
Info MOVEMENT DISORDERS, (2014), vol. 29 br. 7, str. 921-927
Projekat German Research Foundation (DFG) [LO1555/4-1, ZI591/18-1]; Volkswagen Foundation; Hermann and Lilly Schilling Foundation
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
facebook sharing button
twitter sharing button
linkedin sharing button
gmail sharing button
copy sharing button
Naslov Whispering dysphonia (DYT4 dystonia) is caused by a mutation in the TUBB4 gene (Article)
Autori Lohmann Katja ... Kostic Vladimir S ... (broj koautora 29) 
Info ANNALS OF NEUROLOGY, (2013), vol. 73 br. 4, str. 537-545
Projekat Bachmann Strauss Dystonia and Parkinson Foundation; University of Lubeck (SPP Genetics); Hermann and Lilly Schilling Foundation; Australian Brain Foundation; National Health and Medical Research Council of Australia; German Research Foundation; Brain Foun
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
facebook sharing button
twitter sharing button
linkedin sharing button
gmail sharing button
copy sharing button
Naslov Glucocerebrosidase mutations in a Serbian Parkinson's disease population (Article)
Autori Kumar Kishore R Ramirez A Goebel A Kresojevic Nikola D  Svetel Marina V  Lohmann Katja Sue Carolyn M Rolfs A Mazzulli JR Alcalay RN Krainc D Klein Christine Kostic Vladimir S Gruenewald Alina 
Info EUROPEAN JOURNAL OF NEUROLOGY, (2013), vol. 20 br. 2, str. 402-405
Projekat Dora Lush National Health and Medical Research Council of Australia; Ministry of Education and Science of the Republic of Serbia [175090]; Australian Brain Foundation; Parkinson's NSW Foundation; Australian Department of Health and Aging; National Health
Ispravka Web of Science   Članak   Elečas   Rang časopisa   Citati: Web of Science   Scopus  
facebook sharing button
twitter sharing button
linkedin sharing button
gmail sharing button
copy sharing button
  • 1
  • 2
>> Sve godine

Ispis zapisa u formatu:TXT | BibTeX