Zobrazeno 1 - 10
of 10
pro vyhledávání: '"Jasna Jančić"'
Publikováno v:
Molecules, Vol 27, Iss 15, p 4899 (2022)
In this research, a UHPLC–MS/MS method was developed and validated for the determination of zonisamide in dried plasma spots (DPS) and dried blood spots (DBS). Detection of zonisamide and internal standard, 1-(2,3-dichlorphenyl)piperazine, was carr
Externí odkaz:
https://doaj.org/article/77ca0b0c9017424e979ca5f6362498dc
Autor:
Blažo Nikolić, Nikola Ivančević, Ivan Zaletel, Branislav Rovčanin, Janko Samardžić, Jasna Jančić
Publikováno v:
PLoS ONE, Vol 15, Iss 12, p e0243031 (2020)
ObjectiveThe present study represents one of the largest series of pediatric multiple sclerosis (PedMS) in Western Balkan region. This is the first study aimed to evaluate the characteristics of PedMS in the Serbian population.MethodsThis retrospecti
Externí odkaz:
https://doaj.org/article/7d24ba894d724997bdbb71aa750f8616
Autor:
Janko Samardžić, Jasna Jančić, Janko Zeković, Mila Ćetković, Blažo Nikolić, Nikola Ivančević, Danijela Vučević, Zorica Nešić, Srđan Milovanović, Miroslav Radenković
Publikováno v:
CNSneurological disorders drug targets.
Background: Peripheral facial nerve palsy is a relatively frequent, rather idiopathic, and isolated nonprogressive disorder with a tendency toward spontaneous recovery in children. It is primarily characterized by unilateral paresis or paralysis of t
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:
Michelle M. Adams, Cédric Albinet, Banu Alicioglu, Paolo Amami, Nathalie André, Narin Ilgim Ardic-Avci, Elizabeth Arslanoglou, Guilherme Giannini Artioli, Michel Audiffren, Hande Ozge Aydogan, Francisco Javier Belchí, Marvin H. Berman, Ondrej Bezdicek, Cynthia Bianco, Jasmina Boban, Carlos Roberto Bueno Júnior, Blake E. Butler, Daniele Cartelli, Augusto Pietro Casani, Dilan Celebi-Birand, Zikuan Chen, Zeyuan Chen, Bihong T. Chen, Katie E. Cherry, Christian Chicherio, Jeshya A. Chio, Pere Clavé, Victoria C. Cogger, Márcia Regina Cominetti, Ma Fe P. de Guzman, Maria Clarissa O. del Moral, Eimear Dolan, Jacqueline C. Dominguez, Premchand Dommaraju, Theresa Ebo, Melissa K. Edler, Begun Erbaba, Ghazaleh Eskandari-Sedighi, Delphine Fagot, Fereshteh Farajdokht, Isabel Fariñas, Laís Francielle Francisca Felício, Luiz Felipe da Silva Figueiredo, Karen L. Fortuna, Máximo Ibo Galindo, Ekavi N. Georgousopoulou, Rahul Gokarn, Gabriel Gold, Hayley Groetz, Bruno Gualano, G.M. Halliday, Erin E. Harrington, Claudia Heidenreich, Boris Henčić, Rafael Hernández, Björn Herrmann, Jasna Jančić, R.C. Jeżewski, Hulusi Kafaligonul, Hakki Muammer Karakas, Elif Tugce Karoglu-Eravsar, Dimitris Kiosses, Dusko Kozic, Enikö Kövari, Lewis H. Kuller, Thomas J. LaRocca, David G. Le Couteur, Gary Jek Chong Lee, Unax Lertxundi, Víctor López del Amo, Mariana Luciano de Almeida, Javad Mahmoudi, João O. Malva, Patricia Regina Manzine, Beatriz Martins, Douglas B. Matthews, Derval McCormack, Juan Medrano, Duane D. Mellor, Juan C. Meléndez, Jonas Mengel-From, Jelena Milić, Jody Monkovic, Renato Sobral Monteiro-Junior, Ricardo Moreira, Emily L. Munger, Elena Navari, M. Christopher Newland, João Novo, Reinaldo B. Oriá, Fiadhnait O’Keeffe, Demosthenes B. Panagiotakos, Frederico C. Pereira, Ana Perez-Villalba, Rafaela Peron, Victor R. Preedy, Mary Ann Raghanti, Simona Raimo, Rajkumar Rajendram, Ana López Ramírez, Ramon Raposo, David Raubenheimer, Punam Rawal, Celinda Reese-Melancon, Hannah Reich, Carmen Requena, Carlos Fontes Ribeiro, Ana Carolina de Mello Alves Rodrigues, Luis Miguel Rondón García, Rosa Raquel Ruiz Trascastro, Saeed Sadigh-Eteghad, Farzad Salehpour, Janko Samardžić, Gabriella Santangelo, Encarnación Satorres, Andrew N. Shen, C.E. Shepherd, Stephen J. Simpson, Marina Yazigi Solis, Samantha M. Solon-Biet, Dunja Stankić, Timo E. Strandberg, Astrid M. Suchy-Dicey, Andrea Tapia, Majda M. Thurnher, Paula Álvarez-Merino, Noemí Tomsen, Luigi Trojano, Melek Umay Tuz-Sasik, Henryk F. Urbanski, Rodrigo Portes Ureshino, Ed van Beeck, Candice E. Van Skike, Izabela Pereira Vatanabe, Devin Wahl, David Westaway, Shawn Wong, Long Wu, Túlio Brandão Xavier-Rocha, Janko Zeković, Xin Zhang, Liqin Zhao
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::29030ec9d0d9b573eaa7429179db2306
https://doi.org/10.1016/b978-0-12-818000-6.01002-7
https://doi.org/10.1016/b978-0-12-818000-6.01002-7
Autor:
Tatjana Vrga, Tatjana Šimunić, Jasna Jančić, Katica Boček, Mario Pintar, Igor Vrga, Dubravko Jančić
Publikováno v:
Fizikalna i rehabilitacijska medicina
Volume 31
Issue 1-2
Volume 31
Issue 1-2
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
Publikováno v:
Scandinavian Journal of Child and Adolescent Psychiatry and Psychology, Vol 6, Iss 2 (2018)
Externí odkaz:
https://doaj.org/article/acb2f46cd0de48b1875a0b38de2f5f87