Zobrazeno 1 - 10
of 72
pro vyhledávání: '"Vladimir Kostić"'
Publikováno v:
BizInfo, Vol 13, Iss 2, Pp 29-40 (2022)
The paper investigates the impact of total fertility rate as one of the basic demographic variables on economic growth per capita concerning six selected transition countries (including the five countries of the Western Balkans: Serbia, Bosnia & Herz
Externí odkaz:
https://doaj.org/article/264bf2fc8279472cadc0c5e2cd1bab0f
Sustainable development management seen through the prism of natural capital preservation imperative
Publikováno v:
BizInfo, Vol 13, Iss 1, Pp 41-48 (2022)
After explaining the content coverage and elementary explanation of the basic dimensions of the paradigm of sustainable development, the concept of sustainability is considered in the light of preserving the total amount of capital in the production
Externí odkaz:
https://doaj.org/article/bec723f0359b4c0c93524c69a1cbf347
Publikováno v:
Heliyon, Vol 9, Iss 4, Pp e14824- (2023)
Background: Parkinson's disease (PD) is the second most common neurodegenerative disorder whose prevalence rises with age, yet clinical diagnosis is still a challenging task due to similar manifestations of other neurodegenerative movement disorders.
Externí odkaz:
https://doaj.org/article/4a30748d5c6349dbac4c177dc52c9c18
Autor:
Vladana Marković, Iva Stanković, Saša Radovanović, Igor Petrović, Milica Ječmenica Lukić, Nataša Dragašević Mišković, Marina Svetel, Vladimir Kostić
Publikováno v:
PLoS ONE, Vol 17, Iss 7, p e0269886 (2022)
BackgroundProgressive gait impairment in Parkinson's disease (PD) leads to significant disability. Quantitative gait parameters analysis provides valuable information about fine gait alterations.ObjectivesTo analyse change of gait parameters in patie
Externí odkaz:
https://doaj.org/article/b26c38bd36c44389b21a37ae0d5ce50f
Publikováno v:
Sport Mont, Vol III, Iss 6-7, Pp 95-102 (2005)
Externí odkaz:
https://doaj.org/article/96f7cffca790483c830c60bc1cea13a6
Autor:
Ljiljana Cvetković, Vladimir Kostić
Publikováno v:
Sport Mont, Vol I, Iss 1, Pp 11-19 (2003)
Externí odkaz:
https://doaj.org/article/a68ffdf66271412192ee75591b57e573
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.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::76d655910fa5b0a57e2fcfe7fa3317e1
https://doi.org/10.1007/s00415-023-11681-7
https://doi.org/10.1007/s00415-023-11681-7
Autor:
Joanne Trinh, Andrew A Hicks, Inke R König, Sylvie Delcambre, Theresa Lüth, Susen Schaake, Kobi Wasner, Jenny Ghelfi, Max Borsche, Carles Vilariño-Güell, Faycel Hentati, Elisabeth L Germer, Peter Bauer, Masashi Takanashi, Vladimir Kostić, Anthony E Lang, Norbert Brüggemann, Peter P Pramstaller, Irene Pichler, Alex Rajput, Nobutaka Hattori, Matthew J Farrer, Katja Lohmann, Hansi Weissensteiner, Patrick May, Christine Klein, Anne Grünewald
Publikováno v:
Brain.
Biallelic mutations in PINK1/PRKN cause recessive Parkinson’s disease. Given the established role of PINK1/Parkin in regulating mitochondrial dynamics, we explored mitochondrial DNA integrity and inflammation as disease modifiers in carriers of mut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9cb8c5287f93823b46ee05614fa2715c
https://doi.org/10.1093/brain/awac464
https://doi.org/10.1093/brain/awac464
Autor:
Nikola Kresojević, Vladana Marković, Valerija Dobričić, Iva Stanković, Tanja Stojković, Aleksandra Tomić, MIlica Ječmenica Lukić, Milena Janković, Ana Marjanović, Marija Branković, Ivana Novaković, Igor Petrović, Nataša Dragašević, Marina Svetel, Vladimir Kostić
Publikováno v:
Movement Disorders. 38:712-713
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0ce6c7b2898caa756ae41f3374a9b254
https://doi.org/10.1002/mds.29351
https://doi.org/10.1002/mds.29351
Autor:
Joanne Trinh, Andrew A. Hicks, Inke R. König, Sylvie Delcambre, Theresa Lüth, Susen Schaake, Kobi Wasner, Jenny Ghelfi, Max Borsche, Carles Vilariño-Güell, Faycel Hentati, Elisabeth L. Germer, Peter Bauer, Masashi Takanashi, Vladimir Kostić, Anthony E. Lang, Norbert Brüggemann, Peter P. Pramstaller, Irene Pichler, Alex Rajput, Nobutaka Hattori, Matthew J. Farrer, Katja Lohmann, Hansi Weissensteiner, Patrick May, Christine Klein, Anne Grünewald
Biallelic mutations in PINK1 and PRKN cause recessively inherited Parkinson’s disease (PD). Though some studies suggest that PINK1/PRKN monoallelic mutations may not contribute to risk, deep phenotyping assessment showed that PINK1 or PRKN monoalle
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0836d3f412d7c5a70521c23028039e3f
https://doi.org/10.1101/2022.05.17.22275087
https://doi.org/10.1101/2022.05.17.22275087
