Zobrazeno 1 - 10
of 53
pro vyhledávání: '"Maja, Djordjevic"'
Autor:
Ljiljana Markovic-Denic, Marija Zdravkovic, Marko Ercegovac, Vladimir Djukic, Vladimir Nikolic, Danica Cujic, Dusan Micic, Tatjana Pekmezovic, Vuk Marusic, Viseslav Popadic, Bogdan Crnokrak, Borislav Toskovic, Slobodan Klasnj, Andrea Manojlovic, Marija Brankovic, Vesna Mioljevic, Zlatko Perisic, E, Maja Djordjevic, Stevana Vukasinovic, Sladjana Mihajlovic, Olivera Ostojic
Publikováno v:
Journal of Infection and Public Health, Vol 15, Iss 7, Pp 739-745 (2022)
Background: Since the COVID-19 pandemic has started, Serbia has faced problems in implementing proper public health measures in the population, including non-pharmaceutical interventions, as well as protecting health care workers (HCWs) from disease,
Externí odkaz:
https://doaj.org/article/83e4cf04c88346579ff01ca02adfd09d
Autor:
Vanesa Koracin, Matej Mlinaric, Ivo Baric, Ian Brincat, Maja Djordjevic, Ana Drole Torkar, Ksenija Fumic, Mirjana Kocova, Tatjana Milenkovic, Florentina Moldovanu, Vjosa Mulliqi Kotori, Michaela Iuliana Nanu, Ziga Iztok Remec, Barbka Repic Lampret, Dimitrios Platis, Alexey Savov, Mira Samardzic, Biljana Suzic, Ildiko Szatmari, Alma Toromanovic, Mojca Zerjav Tansek, Tadej Battelino, Urh Groselj
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Significant part of Southeastern Europe (with a population of 76 million) has newborn screening (NBS) programs non-harmonized with developed European countries. Initial survey was conducted in 2013/2014 among 11 countries from the region (Albania, Bu
Externí odkaz:
https://doaj.org/article/ec423af9e8d3444db4d23e83a269945c
Autor:
Danique van Vliet, Annemiek M. J. van Wegberg, Kirsten Ahring, Miroslaw Bik-Multanowski, Nenad Blau, Fatma D. Bulut, Kari Casas, Bozena Didycz, Maja Djordjevic, Antonio Federico, François Feillet, Maria Gizewska, Gwendolyn Gramer, Jozef L. Hertecant, Carla E. M. Hollak, Jens V. Jørgensen, Daniela Karall, Yuval Landau, Vincenzo Leuzzi, Per Mathisen, Kathryn Moseley, Neslihan Ö. Mungan, Francesca Nardecchia, Katrin Õunap, Kimberly K. Powell, Radha Ramachandran, Frank Rutsch, Aria Setoodeh, Maja Stojiljkovic, Fritz K. Trefz, Natalia Usurelu, Callum Wilson, Clara D. van Karnebeek, William B. Hanley, Francjan J. van Spronsen
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-6 (2018)
Abstract Background Phenylketonuria (PKU) is often considered as the classical example of a genetic disorder in which severe symptoms can nowadays successfully be prevented by early diagnosis and treatment. In contrast, untreated or late-treated PKU
Externí odkaz:
https://doaj.org/article/fa8d0419b00e4e5aaeec6593e5894762
Akademický článek
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Autor:
Grünert, Sarah C., Derks, Terry G.J., Adrian, Katarina, Al-Thihli, Khalid, Ballhausen, Diana, Bidiuk, Joanna, Bordugo, Andrea, Boyer, Monica, Bratkovic, Drago, Brunner-Krainz, Michaela, Burlina, Alberto, Chakrapani, Anupam, Corpeleijn, Willemijn, Cozens, Alison, Dawson, Charlotte, Dhamko, Helena, Milosevic, Maja Djordjevic, Eiroa, Hernan, Finezilber, Yael, Moura de Souza, Carolina Fischinger, Garcia-Jiménez, Maria Concepción, Gasperini, Serena, Haas, Dorothea, Häberle, Johannes, Halligan, Rebecca, Fung, Law Hiu, Hörbe-Blindt, Alexandra, Horka, Laura Maria, Huemer, Martina, Uçar, Sema Kalkan, Kecman, Bozica, Kilavuz, Sebile, Kriván, Gergely, Lindner, Martin, Lüsebrink, Natalia, Makrilakis, Konstantinos, Mei-Kwun Kwok, Anne, Maier, Esther M., Maiorana, Arianna, McCandless, Shawn E., Mitchell, John James, Mizumoto, Hiroshi, Mundy, Helen, Ochoa, Carlos, Pierce, Kathryn, Fraile, Pilar Quijada, Regier, Debra, Rossi, Alessandro, Santer, René, Schuman, Hester C., Sobieraj, Piotr, Spenger, Johannes, Spiegel, Ronen, Stepien, Karolina M., Tal, Galit, Tanšek, Mojca Zerjav, Torkar, Ana Drole, Tchan, Michel, Thyagu, Santhosh, Schrier Vergano, Samantha A., Vucko, Erika, Weinhold, Natalie, Zsidegh, Petra, Wortmann, Saskia B.
Publikováno v:
In Genetics in Medicine August 2022 24(8):1781-1788
Autor:
Sonja Pavlovic, Maja Stojiljkovic, Maja Djordjevic, R. Drmanac, Kristel Klaassen, Bozica Kecman, Anita Skakic
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 29, Iss, Pp 100822-(2021)
Phenylketonuria (PKU) is an inborn error of metabolism caused by variants in the phenylalanine hydroxylase (PAH) gene and it is characterized by excessively high levels of phenylalanine in body fluids. PKU is a paradigm for a genetic disease that can
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eab72b5607f5a00d5beea8cb538af58f
http://www.sciencedirect.com/science/article/pii/S2214426921001178
http://www.sciencedirect.com/science/article/pii/S2214426921001178
Publikováno v:
International Journal of Pediatric Otorhinolaryngology. 124:120-123
Parathyroid carcinoma is extremely rare in pediatric population. The authors report a case of 15-year-old girl with extremely elevated serum calcium (4.1 mmol/L) and parathyroid hormone (1170 pg/mL), with palpable neck mass. After en bloc resection,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2026e5cd178dbaf29bfdc90a7db0f74
https://doi.org/10.1016/j.ijporl.2019.06.003
https://doi.org/10.1016/j.ijporl.2019.06.003
Autor:
Kristel Klaassen, Natasa Tosic, Sonja Pavlovic, Maja Djordjevic, Maja Stojiljkovic, Anita Skakic, Marina Andjelkovic
Publikováno v:
Gene. 703:17-25
Glycogen storage disease type Ib (GSD Ib) is an autosomal recessive disorder, caused by a deficiency of ubiquitously expressed SLC37A4 protein. Deficiency of SLC37A4 leads to abnormal storage of glycogen in the liver and kidneys, resulting in long-te
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81655c17f208be574e880f01037d3ea1
https://doi.org/10.1016/j.gene.2019.04.002
https://doi.org/10.1016/j.gene.2019.04.002
Autor:
Sanja Cirkovic, Danijela Radivojevic, Marina Djurisic, Tanja Lalic, Marijana Miskovic, Bojana Dobric, Maja Djordjevic
Publikováno v:
Genetika, Vol 51, Iss 3, Pp 1009-1019 (2019)
The aim of the study was to estimate the type and the prevalence of chromosomal abnormalities and Y-chromosome microdeletions, analysed together for the first time in idiopathic infertile men in Serbia. During 10 years period among 823 couples with i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f08444fd53a504e8d37ad66bb286499
https://doi.org/10.2298/gensr1903009d
https://doi.org/10.2298/gensr1903009d
Autor:
Ivo Barić, Ildikó Szatmári, Vjosa Kotori, Urh Groselj, Matej Mlinaric, Mira Samardzic, Maja Djordjevic, Mojca Zerjav Tansek, Vanesa Koracin, Ian Brincat, Biljana Suzic, Alma Toromanovic, Michaela Iuliana Nanu, Tadej Battelino, Dimitrios Platis, Mirjana Kocova, Barbka Repic Lampret, Ksenija Fumić, Ziga Iztok Remec, Florentina Moldovanu, Tatjana Milenkovic, Ana Drole Torkar, Alexey Savov
Publikováno v:
Frontiers in Pediatrics, Vol 9 (2021)
Frontiers in Pediatrics
Frontiers in Pediatrics
Significant part of Southeastern Europe (with a population of 76 million) has newborn screening (NBS) programs non-harmonized with developed European countries. Initial survey was conducted in 2013/2014 among 11 countries from the region (Albania, Bu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::922557920e39686bee9572250bbf004a
https://doi.org/10.3389/fped.2021.648939
https://doi.org/10.3389/fped.2021.648939