Differences in primary hyperparathyroidism characteristics between children and adolescents von Zivaljevic, Vladan, Jovanovic, Milan, Diklic, Aleksandar, Zdravkovic, Vera, Djordjevic, Maja, Paunovic, Ivan

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Clinical and genetic characteristics of patients with congenital hyperinsulinism in 21 non-consanguineous families from Serbia von Raicevic, Maja, Milenkovic, Tatjana, Hussain, Khalid, Djordjevic, Maja, Martic, Jelena, Todorovic, Sladjana, Mitrovic, Katarina, Sarajlija, Adrijan, Vukovic, Rade

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Case report of parathyroid carcinoma in a pediatric patient von Zivaljevic, Vladan R., Jovanovic, Milan D., Djordjevic, Maja S., Diklic, Aleksandar D., Paunovic, Ivan R.

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Late‐presenting congenital diaphragmatic hernia in a child with TMEM70 deficiency von Sarajlija, Adrijan, Magner, Martin, Djordjevic, Maja, Kecman, Bozica, Grujic, Blagoje, Tesarova, Marketa, Minic, Predrag

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CRISPR/Cas9 genome editing of SLC37A4 gene elucidates the role of molecular markers of endoplasmic reticulum stress and apoptosis in renal involvement in glycogen storage disease t... von Skakic, Anita, Andjelkovic, Marina, Tosic, Natasa, Klaassen, Kristel, Djordjevic, Maja, Pavlovic, Sonja, Stojiljkovic, Maja

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Impact of Diagnosis and Therapy on Cognitive Function in Urea Cycle Disorders von Posset, Roland, Gropman, Andrea L., Nagamani, Sandesh C. S., Burrage, Lindsay C., Bedoyan, Jirair K., Wong, Derek, Berry, Gerard T., Baumgartner, Matthias R., Yudkoff, Marc, Zielonka, Matthias, Hoffmann, Georg F., Burgard, Peter, Schulze, Andreas, McCandless, Shawn E., Garcia‐Cazorla, Angeles, Seminara, Jennifer, Garbade, Sven F., Kölker, Stefan, Lee, Brendan, Harding, Cary O., Coughlin, Curtis R., Le Mons, Cynthia, Dobbelaere, Dries, Leão Teles, Elisa, Cortès‐Saladelafont, Elisenda, Gleich, Florian, Eyskens, Francois, Enns, Gregory, Wilkening, Greta N., Barić, Ivo, Lawrence Merritt, J., Heringer, Jana, Blasco‐Alonso, Javier, Zeman, Jiri, Häberle, Johannes, Sykut‐Cegielska, Jolanta, Djordjevic, Maja, Batshaw, Mark L., Summar, Marshall, Freisinger, Peter, Gallagher, Renata C., Berry, Susan A., Waisbren, Susan, Stricker, Tamar

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The improvement in diagnosis and epilepsy managing in children with progressive myoclonus epilepsy during the last decade — A tertiary center experience in cohort of 51 patients von Kravljanac, Ruzica, Vucetic Tadic, Biljana, Djordjevic, Maja, Lalic, Tanja, Kravljanac, Djordje, Cerovic, Ivana

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Impact of genotype on neutropenia in a large cohort of Serbian patients with glycogen storage disease type Ib von Sarajlija, Adrijan, Djordjevic, Maja, Kecman, Bozica, Skakic, Anita, Pavlovic, Sonja, Pasic, Srdjan, Stojiljkovic, Maja

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Case-control study of primary hyperparathyroidism in juvenile vs. adult patients von Jovanovic, Milan, Paunovic, Ivan, Zdravkovic, Vera, Djordjevic, Maja, Rovcanin, Branislav, Tausanovic, Katarina, Slijepcevic, Nikola, Zivaljevic, Vladan

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Efficacy and safety of empagliflozin in glycogen storage disease type Ib: Data from an international questionnaire von 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.

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Can untreated PKU patients escape from intellectual disability? A systematic review von van Vliet, Danique, van Wegberg, Annemiek M J, Ahring, Kirsten, Bik-Multanowski, Miroslaw, Blau, Nenad, Bulut, Fatma D, Casas, Kari, Didycz, Bozena, Djordjevic, Maja, Federico, Antonio, Feillet, François, Gizewska, Maria, Gramer, Gwendolyn, Hertecant, Jozef L, Hollak, Carla E M, Jørgensen, Jens V, Karall, Daniela, Landau, Yuval, Leuzzi, Vincenzo, Mathisen, Per, Moseley, Kathryn, Mungan, Neslihan Ö, Nardecchia, Francesca, Õunap, Katrin, Powell, Kimberly K, Ramachandran, Radha, Rutsch, Frank, Setoodeh, Aria, Stojiljkovic, Maja, Trefz, Fritz K, Usurelu, Natalia, Wilson, Callum, van Karnebeek, Clara D, Hanley, William B, van Spronsen, Francjan J

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Age at disease onset and peak ammonium level rather than interventional variables predict the neurological outcome in urea cycle disorders von Posset, Roland, Garcia-Cazorla, Angeles, Valayannopoulos, Vassili, Teles, Elisa Leão, Dionisi-Vici, Carlo, Brassier, Anaïs, Burlina, Alberto B., Burgard, Peter, Cortès-Saladelafont, Elisenda, Dobbelaere, Dries, Couce, Maria L., Sykut-Cegielska, Jolanta, Häberle, Johannes, Lund, Allan M., Chakrapani, Anupam, Schiff, Manuel, Walter, John H., Zeman, Jiri, Vara, Roshni, Kölker, Stefan

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Etiology, clinical features and outcome of epilepsia partialis continua in cohort of 51 children von Kravljanac, Ruzica, Djuric, Milena, Jovic, Nebojsa, Djordjevic, Maja, Zamurovic, Dragan, Pekmezovic, Tatjana

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Functional Characterization of Novel Phenylalanine Hydroxylase p.Gln226Lys Mutation Revealed Its Non-responsiveness to Tetrahydrobiopterin Treatment in Hepatoma Cellular Model von Klaassen, Kristel, Djordjevic, Maja, Skakic, Anita, Desviat, Lourdes R., Pavlovic, Sonja, Perez, Belen, Stojiljkovic, Maja

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Phenylketonuria screening and management in southeastern Europe - survey results from 11 countries von Zerjav Tansek, Mojca, Groselj, Urh, Angelkova, Natalija, Anton, Dana, Baric, Ivo, Djordjevic, Maja, Grimci, Lindita, Ivanova, Maria, Kadam, Adil, Kotori, Vjosa, Maksic, Hajrija, Marginean, Oana, Margineanu, Otilia, Miljanovic, Olivera, Moldovanu, Florentina, Muresan, Mariana, Nanu, Michaela, Samardzic, Mira, Sarnavka, Vladimir, Savov, Aleksei, Stojiljkovic, Maja, Suzic, Biljana, Tincheva, Radka, Tahirovic, Husref, Toromanovic, Alma, Usurelu, Natalia, Battelino, Tadej

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Incidence of genetic causes of idiopathic male infertility in Serbia: Ten years’ experience of single centre von Dobric, Bojana, Radivojevic, Danijela, Lalic, Tanja, Miskovic, Marijana, Cirkovic, Sanja, Djordjevic, Maja, Djurisic, Marina

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New PAH gene promoter KLF1 and 3′-region C/EBPalpha motifs influence transcription in vitro von Klaassen, Kristel, Stankovic, Biljana, Kotur, Nikola, Djordjevic, Maja, Zukic, Branka, Nikcevic, Gordana, Ugrin, Milena, Spasovski, Vesna, Srzentic, Sanja, Pavlovic, Sonja, Stojiljkovic, Maja

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Significant and continuous improvement in bone mineral density among type 1 Gaucher disease patients treated with velaglucerase alfa: 69-month experience, including dose reduction von Elstein, Deborah, Foldes, A. Joseph, Zahrieh, David, Cohn, Gabriel M., Djordjevic, Maja, Brutaru, Costin, Zimran, Ari

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Can untreated PKU patients escape from intellectual disability? A systematic review von van Vliet, Danique, van Wegberg, Annemiek M J, Ahring, Kirsten, Bik-Multanowski, Miroslaw, Blau, Nenad, Bulut, Fatma D, Casas, Kari, Didycz, Bozena, Djordjevic, Maja, Federico, Antonio, Feillet, François, Gizewska, Maria, Gramer, Gwendolyn, Hertecant, Jozef L, Hollak, Carla E M, Jørgensen, Jens V, Karall, Daniela, Landau, Yuval, Leuzzi, Vincenzo, Mathisen, Per, Moseley, Kathryn, Mungan, Neslihan Ö, Nardecchia, Francesca, Õunap, Katrin, Powell, Kimberly K, Ramachandran, Radha, Rutsch, Frank, Setoodeh, Aria, Stojiljkovic, Maja, Trefz, Fritz K, Usurelu, Natalia, Wilson, Callum, van Karnebeek, Clara D, Hanley, William B, van Spronsen, Francjan J

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Basal ganglia lesions in the early stage of Menkes disease von Koprivsek, Katarina, Lucic, Milos, Kozic, Dusko, Djordjevic, Maja, Kravljanac, Ruzica

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