Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Čarna Jovanović"'
Autor:
Poornima Jayadev Menon, Sara Sambin, Baptiste Criniere-Boizet, Thomas Courtin, Christelle Tesson, Fanny Casse, Melanie Ferrien, Louise-Laure Mariani, Stephanie Carvalho, Francois-Xavier Lejeune, Sana Rebbah, Gaspard Martet, Marion Houot, Aymeric Lanore, Graziella Mangone, Emmanuel Roze, Marie Vidailhet, Jan Aasly, Ziv Gan Or, Eric Yu, Yves Dauvilliers, Alexander Zimprich, Volker Tomantschger, Walter Pirker, Ignacio Álvarez, Pau Pastor, Alessio Di Fonzo, Kailash P. Bhatia, Francesca Magrinelli, Henry Houlden, Raquel Real, Andrea Quattrone, Patricia Limousin, Prasad Korlipara, Thomas Foltynie, Donald Grosset, Nigel Williams, Derek Narendra, Hsin-Pin Lin, Carna Jovanovic, Marina Svetel, Timothy Lynch, Amy Gallagher, Wim Vandenberghe, Thomas Gasser, Kathrin Brockmann, Huw R. Morris, Max Borsche, Christine Klein, Olga Corti, Alexis Brice, Suzanne Lesage, Jean Christophe Corvol, French Parkinson disease Genetics Study Group (PDG)
Publikováno v:
npj Parkinson's Disease, Vol 10, Iss 1, Pp 1-12 (2024)
Abstract Bi-allelic pathogenic variants in PRKN are the most common cause of autosomal recessive Parkinson’s disease (PD). 647 patients with PRKN-PD were included in this international study. The pathogenic variants present were characterised and i
Externí odkaz:
https://doaj.org/article/70e73e8ef588464cb23a2e9bc5b7be18
Autor:
Ivo Bozovic, Marta Jeremic, Aleksandra Pavlovic, Carna Jovanovic, Nikola Kresojevic, Nikola Vojvodic, Dejana Jovanovic, Dragoslav Sokic, Milija Mijajlovic
Publikováno v:
Brain Sciences, Vol 13, Iss 5, p 747 (2023)
Cerebral amyloid angiopathy-related inflammation (CAA-rI) is a largely reversible, subacute encephalopathy, which is considered as a rare variant of cerebral amyloid angiopathy (CAA). Although the diagnosis of this inflammatory vasculopathy is genera
Externí odkaz:
https://doaj.org/article/6d2c68c3816f4f86acdb2de981b6b4b3
Autor:
Lazar Berbakov, Čarna Jovanović, Marina Svetel, Jelena Vasiljević, Goran Dimić, Nenad Radulović
Publikováno v:
Sensors, Vol 19, Iss 19, p 4246 (2019)
Tremor is most common among the movement disabilities that affect older people, having a prevalence rate of 4.6% in the population older than 65 years. Despite this, distinguishing different types of tremors is clinically challenging, often leading t
Externí odkaz:
https://doaj.org/article/68448b790785402191c753596152dcc9
Autor:
Iva Stanković, Čarna Jovanović, Jelena Vitković, Marina Svetel, Tatjana Pekmezović, Aleksandra Tomić, Nikola Kresojević, Vladana Marković, Milica Ječmenica Lukić, Igor Petrović, Nataša Dragašević-Mišković, Vladimir Kostić
Publikováno v:
Journal of Neurology.
Autor:
Vladimir S. Kostic, Marina Svetel, Jelena Vitković, Čarna Jovanović, Nikola Kresojević, Aleksandra Tomić, Tatjana Pekmezovic, Marija Božić, Marko Svetel, Nataša Dragašević
Publikováno v:
Acta neurologica ScandinavicaREFERENCES. 144(2)
Objectives Wilson disease (WD) is an autosomal recessive disorder that leads to copper accumulation and deposition in different organs, frequently affecting visual pathways. Recent studies have detected morphological changes of the retina in patients
Autor:
Goran Dimic, Jelena Vasiljevic, Lazar Berbakov, Čarna Jovanović, Marina Svetel, Nenad Radulović
Publikováno v:
Sensors
Volume 19
Issue 19
Sensors (Basel, Switzerland)
Sensors, Vol 19, Iss 19, p 4246 (2019)
Volume 19
Issue 19
Sensors (Basel, Switzerland)
Sensors, Vol 19, Iss 19, p 4246 (2019)
Tremor is most common among the movement disabilities that affect older people, having a prevalence rate of 4.6% in the population older than 65 years. Despite this, distinguishing different types of tremors is clinically challenging, often leading t