Zobrazeno 1 - 10
of 71
pro vyhledávání: '"Jasna, Jancic"'
Autor:
Jasna Jancic, Nikola Zarkovic, Blazo Nikolic, Nikola Ivancevic, Branislav Rovcanin, Dejan Nesic
Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
IntroductionNeurofibromatosis type 1 (NF type 1) is an autosomal dominant disease with typical clinical manifestations, such as skin lesions, Lisch nodules, optic pathway gliomas, and neurofibromas, caused by the mutation of the NF1 gene. Visual evok
Externí odkaz:
https://doaj.org/article/4f471dc8701243298c092f4dcbfcfbf0
Autor:
Ljiljana Markovic-Denic, Dusan Popadic, Tanja Jovanovic, Branka Bonaci-Nikolic, Janko Samardzic, Vesna Tomic Spiric, Miljan Rancic, Siddhartha Sankar Datta, Liudmila Mosina, Jasna Jancic, Goran Vukomanovic, Verica Jovanovic, Vladislav Vukomanovic, Darko Antic, Marko Veljkovic, Vladan Saponjic, Lisa Jacques-Carroll
Publikováno v:
Frontiers in Public Health, Vol 10 (2022)
A National Immunization Technical Advisory Group (NITAG) is a multi-disciplinary body of national experts that provide evidence-based recommendations to policy-makers to assist them in making informed immunization policy and programme decisions. Duri
Externí odkaz:
https://doaj.org/article/404a0648d4b54c3caaba5c710af69d6b
Autor:
Robert Waltereit, Guillaume Beaure d’Augères, Jasna Jancic, John Chris Kingswood, Maya Koleva, Ruben Marques, Vicente Villanueva, Stéphane Auvin
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 16, Iss 1, Pp 1-14 (2021)
Abstract Background Tuberous sclerosis complex (TSC) is a rare, genetic, multisystem disorder characterized by the growth of hamartomas in several organs, including the brain, kidneys, heart, eyes, and lungs. Even though over 90% of patients will hav
Externí odkaz:
https://doaj.org/article/54f55df7ba9c4323bef10d8e08c2ec7d
Autor:
Phepy G. A. Dawod, Jasna Jancic, Ana Marjanovic, Marija Brankovic, Milena Jankovic, Janko Samardzic, Ayman Gamil Anwar Dawod, Ivana Novakovic, Fayda I. Abdel Motaleb, Vladimir Radlovic, Vladimir S. Kostic, Dejan Nikolic
Publikováno v:
Diagnostics, Vol 11, Iss 11, p 1969 (2021)
Mitochondrial encephalomyopathies (MEMP) are heterogeneous multisystem disorders frequently associated with mitochondrial DNA (mtDNA) mutations. Clinical presentation varies considerably in age of onset, course, and severity up to death in early chil
Externí odkaz:
https://doaj.org/article/efad65c1e5054e169c32f3dbdc13deda
Autor:
Blazo Nikolic, Nikola Ivancevic, Ana Pepic, Marijana Kovacevic, Jelena Mladenovic, Branislav Rovcanin, Janko Samardzic, Jasna Jancic
Publikováno v:
Neurology. 98:896-900
Neuroretinitis due toBartonella henselaeinfection is a rare cause of vision loss in children. Two pediatric cases of acute unilateral vision loss accompanied by edema of the optic nerve on fundoscopic examination are presented. Severe causes of visio
Publikováno v:
Scandinavian Journal of Child and Adolescent Psychiatry and Psychology, Vol 6, Iss 2 (2018)
Externí odkaz:
https://doaj.org/article/acb2f46cd0de48b1875a0b38de2f5f87
Autor:
Axel Petzold, Yaou Liu, Clare Fraser, Mathias Abegg, Raed Alroughani, Daniah Alshowaeir, Regina Alvarenga, Cécile Andris, Nasrin Asgari, Yael Barnett, Roberto Battistella, Raed Behbehani, Thomas Berger, Mukharram M. Bikbov, Damien Biotti, Valerie Biousse, Antonella Boschi, Milan Brazdil, Andrei Brezhnev, Peter Calabresi, Monique Cordonnier, Fiona Costello, Franz Marie Cruz, Leonardo Provetti Cunha, Smail Daoudi, Romain Deschamps, Jerome DeSeze, Ricarda Diem, Masoud Etemadifar, Jose Flores-Rivera, Pedro Fonseca, Jette Frederiksen, Elliot Frohman, Teresa Frohman, Caroline FromentTilikete, Kazuo Fujihara, Alberto Gálvez, Riadh Gouider, Fernando Gracia, Nikolaos Grigoriadis, José Manuel Guajardo, Mario Habek, Marko Hawlina, Elena Hernández-Martínez de Lapiscina, Juzar Hooker, Jyh Yung Hor, William Howlett, Yumin Huang-Link, Zhannat Idrissova, Zsolt Illes, Jasna Jancic, Panitha Jindahra, Dimitrios Karussis, Emilia Kerty, Ho Jin Kim, Wolf Lagrèze, Letizia Leocani, Netta Levin, Petra Liskova, Youssoufa Maiga, Romain Marignier, Chris McGuigan, Dália Meira, Harold Merle, Mário L.R. Monteiro, Anand Moodley, Frederico Moura, Silvia Muñoz, Sharik Mustafa, Ichiro Nakashima, Susana Noval, Carlos Oehninger, Olufunmilola Ogun, Afekhide Omoti, Lekha Pandit, Friedemann Paul, Gema Rebolleda, Stephen Reddel, Konrad Rejdak, Robert Rejdak, Alfonso Rodriguez-Morales, Marie-Bénédicte Rougier, Maria Jose Sa, Bernardo Sanchez-Dalmau, Deanna Saylor, Ismail Shatriah, Aksel Siva, Hadas Stiebel-Kalish, Gabriella Szatmary, Linh Ta, Sylvia Tenembaum, Huy Tran, Yevgen Trufanov, Vincent VanPesch, An-Guor Wang, Mike P. Wattjes, Ernie Willoughby, Magd Zakaria, Jasmin Zvornicanin, Laura Balcer, Gordon T. Plant
Publikováno v:
International Consortium on Optic Neuritis (ICON) 2023, ' Application of diagnostic criteria for optic neuritis – Authors' reply ', The Lancet Neurology, vol. 22, no. 5, pp. 376-377 . https://doi.org/10.1016/S1474-4422(23)00110-2
The Lancet Neurology, 22(5), 376-377. Lancet Publishing Group
The Lancet Neurology, 22(5), 376-377. Lancet Publishing Group
Autor:
Marija Brankovic, Natasa Dragasevic, Valerija Dobricic, Ales Maver, Gaber Bergant, Igor Petrovic, Stojan Peric, Ana Marjanovic, Milena Jankovic, Jasna Jancic, Ivana Novakovic, Borut Peterlin, Marina Svetel, Vladimir Kostic
Publikováno v:
Genetika. 54:395-409
The aim of the study was to analyze the genetic basis of a various range of neurodegenerative disorders manifesting by movement disorders (MD) using next generation sequencing (NGS) clinical exome panel. The study included a total number of 42 cases,
Publikováno v:
Genes. 14:1095
Pharmacotherapy for neuropsychiatric disorders, such as anxiety and depression, has been characterized by significant inter-individual variability in drug response and the development of side effects. Pharmacogenetics, as a key part of personalized m
Autor:
Janko Samardzic, Nemanja Nenezic, Smiljana Kostic, Dubravka Svob Strac, Marija Grunauer, Dragana Nenezic, Milica Radosavljevic, Jasna Jancic
Publikováno v:
Mini reviews in medicinal chemistry.
Abstract: Dehydroepiandrosterone (DHEA) is the most abundant steroid hormone in primates, which is predominantly synthesized in the adrenal cortex. A characteristic curve of growth and decline of its synthesis during life was observed, together with