Joint effect of the SMN2 and SERF1A genes on childhood-onset types of spinal muscular atrophy in Serbian patients von Brkušanin, Miloš, Kosać, Ana, Jovanović, Vladimir, Pešović, Jovan, Brajušković, Goran, Dimitrijević, Nikola, Todorović, Slobodanka, Romac, Stanka, Milić Rašić, Vedrana, Savić-Pavićević, Dušanka

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Transcranial brain parenchyma sonography in patients with juvenile myoclonic epilepsy von Djordjević, Ivana, Djordjević, Stefan, Kosać, Ana, Vučinić, Dragana, Ivanović Radović, Nelica, Ždraljević, Mirjana, Mijajlović, Milija

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Tuberous sclerosis complex, Serbian referral center experience von Kosac, Ana, Jovic, Nebojsa

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L-2-Hydroxyglutaric aciduria: a case report von Jović, Nebojsa J, Kosać, Ana, Koprivsek, Katarina

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Terminal remission is possible in some patients with juvenile myoclonic epilepsy without therapy von Jovic, Nebojsa, Kosac, Ana, Babic, Milos

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Phosphorylated neurofilament heavy chain in cerebrospinal fluid and plasma as a Nusinersen treatment response marker in childhood-onset SMA individuals from Serbia von Brkušanin, Miloš, Kosać, Ana, Branković-Srećković, Vesna, Jovanović, Kristina, Perić, Stojan, Karanović, Jelena, Matijašević Joković, Suzana, Garai, Nemanja, Pešović, Jovan, Nikolić, Dimitrije, Stević, Zorica, Brajušković, Goran, Milić-Rašić, Vedrana, Savić-Pavićević, Dušanka

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Glucose and lipid metabolism disorders in children and adolescents with spinal muscular atrophy types 2 and 3 von Djordjevic, Stefan A., Milic-Rasic, Vedrana, Brankovic, Vesna, Kosac, Ana, Dejanovic-Djordjevic, Ivana, Markovic-Denic, Ljiljana, Djuricic, Goran, Milcanovic, Natasa, Kovacevic, Smiljka, Petrovic, Hristina, Djukic, Milan, Zdravkovic, Vera

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The role of gene modifiers on clinical course of Duchenne muscular dystrophy von Kosać, Ana, Milić-Rašić, Vedrana, Savić-Pavićević, Dušanka, Kravljanac, Ružica

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Cardiac findings in pediatric patients with spinal muscular atrophy types 2 and 3 von Djordjevic, Stefan A., Milic‐Rasic, Vedrana, Brankovic, Vesna, Kosac, Ana, Vukomanovic, Goran, Topalovic, Mirko, Marinkovic, Dejan, Mladenovic, Jelena, Pavlovic, Andrija S., Bijelic, Maja, Djukic, Milan, Markovic‐Denic, Ljiljana

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Neurophysiological testing in congenital myasthenic syndromes: A systematic review of published normal data: Issues & Opinions: Testing in CMS von Kosac, Ana, Gavillet, Erika, Whittaker, Roger G.

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Mapping the differences in care for 5,000 Spinal Muscular Atrophy patients, a survey of 24 national registries in North America, Australasia and Europe von Bladen, Catherine L., Thompson, Rachel, Jackson, Jacqueline M., Garland, Connie, Wegel, Claire, Ambrosini, Anna, Pisano, Paolo, Walter, Maggie C., Schreiber, Olivia, Lusakowska, Anna, Jedrzejowska, Maria, Kostera-Pruszczyk, Anna, van der Pol, Ludo, Wadman, Renske I., Gredal, Ole, Karaduman, Ayse, Topaloglu, Haluk, Yilmaz, Oznur, Matyushenko, Vitaliy, Rasic, Vedrana Milic, Kosac, Ana, Karcagi, Veronika, Garami, Marta, Herczegfalvi, Agnes, Monges, Soledad, Moresco, Angelica, Chertkoff, Lilien, Chamova, Teodora, Guergueltcheva, Velina, Butoianu, Niculina, Craiu, Dana, Korngut, Lawrence, Campbell, Craig, Haberlova, Jana, Strenkova, Jana, Alejandro, Moises, Jimenez, Alatorre, Ortiz, Genaro Gabriel, Enriquez, Gracia Viviana Gonzalez, Rodrigues, Miriam, Roxburgh, Richard, Dawkins, Hugh, Youngs, Leanne, Lahdetie, Jaana, Angelkova, Natalija, Saugier-Veber, Pascal, Cuisset, Jean-Marie, Bloetzer, Clemens, Jeannet, Pierre-Yves, Klein, Andrea, Nascimento, Andres, Tizzano, Eduardo, Salgado, David, Mercuri, Eugenio, Sejersen, Thomas, Kirschner, Jan, Rafferty, Karen, Straub, Volker, Bushby, Kate, Verschuuren, Jan, Beroud, Christophe, Lochmüller, Hanns

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Neurophysiological testing in congenital myasthenic syndromes: A systematic review of published normal data von Kosac, Ana, Gavillet, Erika, Whittaker, Roger G.

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ILTBP4/I, ISPP1/I, and ICD40/I Variants: Genetic Modifiers of Duchenne Muscular Dystrophy Analyzed in Serbian Patients von Kosac, Ana, Pesovic, Jovan, Radenkovic, Lana, Brkusanin, Milos, Radovanovic, Nemanja, Djurisic, Marina, Radivojevic, Danijela, Mladenovic, Jelena, Ostojic, Slavica, Kovacevic, Gordana, Kravljanac, Ruzica, Savic Pavicevic, Dusanka, Milic Rasic, Vedrana

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LTBP4 , SPP1 , and CD40 Variants: Genetic Modifiers of Duchenne Muscular Dystrophy Analyzed in Serbian Patients von Kosac, Ana, Pesovic, Jovan, Radenkovic, Lana, Brkusanin, Milos, Radovanovic, Nemanja, Djurisic, Marina, Radivojevic, Danijela, Mladenovic, Jelena, Ostojic, Slavica, Kovacevic, Gordana, Kravljanac, Ruzica, Savic Pavicevic, Dusanka, Milic Rasic, Vedrana

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Nerve Conduction Studies as a Measure of Disease Progression: Objectivity or Illusion? von Lanza, Giuseppe, Kosac, Ana, Trajkovic, Goran, Whittaker, Roger G.

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Phenotypic and genetic spectrum of patients with limb-girdle muscular dystrophy type 2A from Serbia von PERIC, STOJAN, STEVANOVIC, JELENA, JOHNSON, KATHERINE, KOSAC, ANA, PERIC, MARINA, BRANKOVIC, MARIJA, MARJANOVIC, ANA, JANKOVIC, MILENA, BANKO, BOJAN, MILENKOVIC, SANJA, DURDIC, MILICA, BOZOVIC, IVO, GLUMAC, JELENA NIKODINOVIC, LAVRNIC, DRAGANA, MAKSIMOVIC, RUZICA, MILIC-RASIC, VEDRANA, RAKOCEVIC-STOJANOVIC, VIDOSAVA

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Terminal remission is possible in some patients with juvenile myoclonic epilepsy without therapy/Terminalna remisija bez terapije moguca je kod bolesnika sa juvenilnom mioklonicnom... von Jovic, Nebojsa J, Kosac, Ana, Babic, Milos D

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