Central European Group on Genetics of Movement Disorders-Reference-Cited by-同舟云学术

Central European Group on Genetics of Movement Disorders

Published:2023-12-07 Issue: Volume: Page:
ISSN:1351-5101
Container-title:European Journal of Neurology
language:en
Short-container-title:Euro J of Neurology

Author:

Ostrozovicova Miriam¹²³^ORCID,Dusek Petr⁴,Grofik Milan⁵,Han Vladimir¹²,Holly Petr⁴,Jech Robert⁴,Klivenyi Peter⁶,Kovacs Norbert⁷,Kulcsarova Kristina¹²⁸,Kurca Egon⁵,Lackova Alexandra¹²,Magocova Veronika¹²,Necpal Jan⁹,Pinter David⁷^ORCID,Ruzicka Evzen⁴,Serranova Tereza⁴,Smilowska Katarzyna¹⁰^ORCID,Straka Igor¹¹^ORCID,Svorenova Tatiana¹²,Tamas Gertrud¹²^ORCID,Valkovic Peter¹¹¹³^ORCID,Zarubova Katerina¹⁴,Houlden Henry³,Rizig Mie³,Skorvanek Matej¹²

Affiliation:

1. Department of Neurology P.J. Safarik University Kosice Slovak Republic

2. Department of Neurology University Hospital of L. Pasteur Kosice Slovak Republic

3. Department of Neuromuscular Diseases UCL Queen Square Institute of Neurology London UK

4. Department of Neurology and Centre of Clinical Neuroscience, First Faculty of Medicine Charles University and General University Hospital in Prague Prague Czech Republic

5. Department of Neurology Comenius University and University Hospital Martin Martin Slovak Republic

6. Department of Neurology University of Szeged Szeged Hungary

7. Department of Neurology and HUN‐REN–PTE Clinical Neuroscience MR Research Group University of Pecs, Medical School Pécs Hungary

8. Department of Clinical Neurosciences, Scientific Park MEDIPARK P. J. Safarik University Kosice Slovak Republic

9. Department of Neurology Zvolen Hospital Zvolen Slovak Republic

10. Department of Neurology Silesian Centre of Neurology Katowice Katowice Poland

11. Second Department of Neurology, Comenius University in Bratislava Faculty of Medicine University Hospital Bratislava Bratislava Slovak Republic

12. Department of Neurology Semmelweis University Budapest Hungary

13. Institute of Normal and Pathological Physiology, Centre of Experimental Medicine Slovak Academy of Sciences Bratislava Slovak Republic

14. Department of Neurology, Second Faculty of Medicine Charles University and Motol University Hospital Prague Czech Republic

Funder

Agentura Pro Zdravotnický Výzkum České Republiky

Publisher

Wiley

Subject

Neurology (clinical),Neurology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/ene.16165

Reference5 articles.

1. Comparison in detection of prodromal Parkinson's disease patients using original and updated MDS research criteria in two independent cohorts

2. LRRK2 mutations in Parkinson's disease patients from Central Europe: A case control study

3. European Roma groups show complex West Eurasian admixture footprints and a common South Asian genetic origin

4. A Recurrent VPS16 p.Arg187* Nonsense Variant in Early‐Onset Generalized Dystonia

5. WARS2 mutations cause dopa-responsive early-onset parkinsonism and progressive myoclonus ataxia

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