Akutna ataksija u hitnoj pedijatrijskoj ambulanti – dijagnostički i terapijski pristup von Nina Barišić

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The visibility of the periventricular crossroads of pathways in preterm infants as a predictor of neurological outcome and occurrence of neonatal epileptic seizures von Bunoza, Branka, Nina, Barišić, Grđan Stevanović, Petra, Bogdanić, Ana, Benjak, Vesna, Grizelj, Ruža, Turudić, Daniel, Milošević, Danko, Radoš, Marko

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Vrtoglavice u djece von Čokolić Petrović, Dunja, Markov-Glavaš, Duška, Barišić, Nina

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Total tau in cerebrospinal fluid detects treatment responders among spinal muscular atrophy types 1–3 patients treated with nusinersen von Šimić, Goran, Vukić, Vana, Babić, Marija, Banović, Maria, Berečić, Ivana, Španić, Ena, Zubčić, Klara, Golubić, Anja Tea, Barišić Kutija, Marija, Merkler Šorgić, Ana, Vogrinc, Željka, Lehman, Ivan, Hof, Patrick R., Sertić, Jadranka, Barišić, Nina

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GPi DBS treatment outcome in children with monogenic dystonia: a case series and review of the literature von Chudy, Darko, Raguž, Marina, Vuletić, Vladimira, Rački, Valentino, Papić, Eliša, Nenadić Baranašić, Nataša, Barišić, Nina

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Vaccination in pediatric acquired inflammatory immune-mediated neuromuscular disorders von Barišić, Nina, Turudić, Daniel, Marić, Lorna Stemberger, Tešović, Goran

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Genotype–phenotype correlation in contactin-associated protein-like 2 (CNTNAP-2) developmental disorder von D’Onofrio, Gianluca, Accogli, Andrea, Severino, Mariasavina, Caliskan, Haluk, Kokotović, Tomislav, Blazekovic, Antonela, Jercic, Kristina Gotovac, Markovic, Silvana, Zigman, Tamara, Goran, Krnjak, Barišić, Nina, Duranovic, Vlasta, Ban, Ana, Borovecki, Fran, Ramadža, Danijela Petković, Barić, Ivo, Fazeli, Walid, Herkenrath, Peter, Marini, Carla, Vittorini, Roberta, Gowda, Vykuntaraju, Bouman, Arjan, Rocca, Clarissa, Alkhawaja, Issam Azmi, Murtaza, Bibi Nazia, Rehman, Malik Mujaddad Ur, Al Alam, Chadi, Nader, Gisele, Mancardi, Maria Margherita, Giacomini, Thea, Srivastava, Siddharth, Alvi, Javeria Raza, Tomoum, Hoda, Matricardi, Sara, Iacomino, Michele, Riva, Antonella, Scala, Marcello, Madia, Francesca, Pistorio, Angela, Salpietro, Vincenzo, Minetti, Carlo, Rivière, Jean-Baptiste, Srour, Myriam, Efthymiou, Stephanie, Maroofian, Reza, Houlden, Henry, Vernes, Sonja Catherine, Zara, Federico, Striano, Pasquale, Nagy, Vanja

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De novo variants in RNF213 are associated with a clinical spectrum ranging from Leigh syndrome to early-onset stroke von Brunet, Theresa, Zott, Benedikt, Lieftüchter, Victoria, Lenz, Dominic, Schmidt, Axel, Peters, Philipp, Kopajtich, Robert, Zaddach, Malin, Zimmermann, Hanna, Hüning, Irina, Ballhausen, Diana, Staufner, Christian, Bianzano, Alyssa, Hughes, Joanne, Taylor, Robert W., McFarland, Robert, Devlin, Anita, Mihaljević, Mihaela, Barišić, Nina, Rohlfs, Meino, Wilfling, Sibylle, Sondheimer, Neal, Hewson, Stacy, Marinakis, Nikolaos M., Kosma, Konstantina, Traeger-Synodinos, Joanne, Elbracht, Miriam, Begemann, Matthias, Trepels-Kottek, Sonja, Hasan, Dimah, Scala, Marcello, Capra, Valeria, Zara, Federico, van der Ven, Amelie T., Driemeyer, Joenna, Apitz, Christian, Krämer, Johannes, Strong, Alanna, Hakonarson, Hakon, Watson, Deborah, Mayr, Johannes A., Prokisch, Holger, Meitinger, Thomas, Borggraefe, Ingo, Spiegler, Juliane, Baric, Ivo, Paolini, Marco, Gerstl, Lucia, Wagner, Matias

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Loss-of-function mutations in HINT1 cause axonal neuropathy with neuromyotonia von Zimoń, Magdalena, Baets, Jonathan, Almeida-Souza, Leonardo, De Vriendt, Els, Nikodinovic, Jelena, Parman, Yesim, Battaloǧlu, Esra, Matur, Zeliha, Guergueltcheva, Velina, Tournev, Ivailo, Auer-Grumbach, Michaela, De Rijk, Peter, Petersen, Britt-Sabina, Müller, Thomas, Fransen, Erik, Van Damme, Philip, Löscher, Wolfgang N, Barišić, Nina, Mitrovic, Zoran, Previtali, Stefano C, Topaloǧlu, Haluk, Bernert, Günther, Beleza-Meireles, Ana, Todorovic, Slobodanka, Savic-Pavicevic, Dusanka, Ishpekova, Boryana, Lechner, Silvia, Peeters, Kristien, Ooms, Tinne, Hahn, Angelika F, Züchner, Stephan, Timmerman, Vincent, Van Dijck, Patrick, Rasic, Vedrana Milic, Janecke, Andreas R, De Jonghe, Peter, Jordanova, Albena

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Epileptički status u pedijatriji – dijagnostički i terapijski postupci von Barišić, Nina, Rubić, Filip

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Role of platelet gene polymorphisms in ischemic pediatric stroke subtypes: a case-control study von Čeri, Andrea, Leniček Krleža, Jasna, Coen Herak, Désirée, Miloš, Marija, Pavić, Marina, Barišić, Nina, Đuranović, Vlasta, Zadro, Renata

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Molecular Biomarkers for the Diagnosis, Prognosis, and Pharmacodynamics of Spinal Muscular Atrophy von Babić, Marija, Banović, Maria, Berečić, Ivana, Banić, Tea, Babić Leko, Mirjana, Ulamec, Monika, Junaković, Alisa, Kopić, Janja, Sertić, Jadranka, Barišić, Nina, Šimić, Goran

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The prevalence of muscular dystrophy and spinal muscular atrophy in Croatia: data from national and non-governmental organization registries von Draušnik, Željka, Cerovečki, Ivan, Štefančić, Vesna, Mihel, Sandra, Stevanović, Ranko, Barišić, Nina, Matković, Hana, Melša, Matea, Mirić, Marica, Pjevač, Neda, Benjak, Tomislav

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Izazovi diferencijalne dijagnoze hipotonije u dojenačkoj dobi von Kuzmanić Šamija, Radenka, Barišić, Nina

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Neurotoxicity of cyclosporine A in children with steroid-resistant nephrotic syndrome: is cytotoxic edema really an unfavorable predictor of permanent neurological damage? von Batinić, Danica, Milošević, Danko, Filipović-Grčić, Boris, Topalović-Grković, Marija, Barišić, Nina, Turudić, Daniel

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Long term clinical and electrophysiological assessment of Croatian children with corticospinal tract involvement in Guillain–Barré syndrome (GBS) von Barisic, Nina, Grkovic, Lana

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The TREAT-NMD DMD Global Database: Analysis of More than 7,000 Duchenne Muscular Dystrophy Mutations von Bladen, Catherine L., Salgado, David, Monges, Soledad, Foncuberta, Maria E., Kekou, Kyriaki, Kosma, Konstantina, Dawkins, Hugh, Lamont, Leanne, Roy, Anna J., Chamova, Teodora, Guergueltcheva, Velina, Chan, Sophelia, Korngut, Lawrence, Campbell, Craig, Dai, Yi, Wang, Jen, Barišić, Nina, Brabec, Petr, Lahdetie, Jaana, Walter, Maggie C., Schreiber-Katz, Olivia, Karcagi, Veronika, Garami, Marta, Viswanathan, Venkatarman, Bayat, Farhad, Buccella, Filippo, Kimura, En, Koeks, Zaïda, van den Bergen, Janneke C., Rodrigues, Miriam, Roxburgh, Richard, Lusakowska, Anna, Kostera-Pruszczyk, Anna, Zimowski, Janusz, Santos, Rosário, Neagu, Elena, Artemieva, Svetlana, Rasic, Vedrana Milic, Vojinovic, Dina, Posada, Manuel, Bloetzer, Clemens, Jeannet, Pierre-Yves, Joncourt, Franziska, Díaz-Manera, Jordi, Gallardo, Eduard, Karaduman, A. Ayşe, Topaloğlu, Haluk, El Sherif, Rasha, Stringer, Angela, Shatillo, Andriy V., Martin, Ann S., Peay, Holly L., Bellgard, Matthew I., Kirschner, Jan, Flanigan, Kevin M., Straub, Volker, Bushby, Kate, Verschuuren, Jan, Aartsma-Rus, Annemieke, Béroud, Christophe, Lochmüller, Hanns

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Neurologic complications following lung transplantation von Živković, Saša A, Jumaa, Muhammad, Barišić, Nina, McCurry, Kenneth

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Genetic heterogeneity and pathophysiological mechanisms in congenital myasthenic syndromes von Barišić, Nina, Chaouch, Amina, Müller, Juliane S, Lochmüller, Hanns

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Newborn screening programs for spinal muscular atrophy worldwide: Where we stand and where to go von Dangouloff, Tamara, Vrščaj, Eva, Servais, Laurent, Osredkar, Damjan, Adoukonou, Thierry, Aryani, Omid, Barisic, Nina, Bashiri, Fahad, Bastaki, Laila, Benitto, Afaf, Omran, Tawfeg Ben, Bernert, Guenther, Bertini, Enrico, Borde, Patricia, Born, Peter, Boustani, Rose-Mary, Butoianu, Nina, Castiglioni, Claudia, Catibusic, Feriha, Chan, Sophelia, Chien, Yin Hsiu, Christodoulou, Kyproula, Dejsuphong, Donniphat, Farrar, Michelle, Filip, Duma, Goemans, Nathalie, Guinhouya, Kokou, Haberlova, Jana, Hadzsiev, Kinga, Hovhannesyan, Kristine, Isohanni, Pirjo, Radovic, Nelica Ivanovic, Jacquier, David, Jalloh, Alusine, Jedrzejowska, Maria, Kandawasvika, Gwen, Kaputu, Celestin, Kawatu, Nfwama, Kernohan, Kristin, Kirschner, Jan, Klink, Barbara, Kodsy, Sherry, Kouame-Assouan, Ange-Eric, Kravljanac, Ruzica, Kreile, Madara, Litvinenko, Ivan, McMillan, Hugh, Mesa, Sandra, Mohamed, Inaam, Kanzoska, Liljana Muaremoska, Nevo, Yoram, Nguefack, Seraphin, Nkole, Kafula, O'Grady, Gina, O'Rourke, Declan, Oskoui, Maryam, Piazzon, Flavia, Poddighe, Dimitri, Prasauskiene, Audrone, Prieto, Juan, Rasmussen, Magnhild, Razafindrasata, Santara, Saha, Narayan, Saito, Kayoko, Sakadi, Foksouna, Sangare, Modibo, Schroth, Mary, Shalkevich, Leanid, Shatillo, Andriy, Suthar, Renu, Szabo, Lena, Tatishvili, Nana, Tazir, Meriem, Tizzano, Eduardo, Topaloglu, Haluk, Tulinius, Mar, van der Pol, Ludo, Vazquez, Gabriel, Vlodavets, Dimitry, Wanigasinghe, Jithangi, Wilmshurst, Jo, Xiong, Hui, Zafeiriou, Dimitrios, Zamba, Eleni

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