A case of macrophagic myofasciitis in a girl with developmental delay von Krnjak, Goran, Vulin, Katarina, Pazanin, Leo, Barisic, Ingeborg, Duranovic, Vlasta

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Are important predictors of adverse outcome in children with symptomatic congenital cytomegalovirus infection overlooked in clinical settings? von Đaković, Ivana, Kostović, Ivica, Vulin, Katarina, Prvčić, Iva, Tešović, Goran, Krakar, Goran, Gojmerac, Tomislav, Sekelj Fureš, Jadranka, Mejaški Bošnjak, Vlatka

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Successful antibiotic treatment of liver abscess in an eight-year-old boy after perforated appendix von Marko Bašković, Antun Kljenak, Ante Čizmić, Dora Škrljak Šoša, Katarina Vulin, Ivana Đaković

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The first case report of distal 16p12.1p11.2 trisomy and proximal 16p11.2 tetrasomy inherited from both parents von Morožin Pohovski, Leona, Sansović, Ivona, Vulin, Katarina, Odak, Ljubica

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Neurodevelopmental disorder caused by an inherited novel KMT5B variant: case report von Odak, Ljubica, Vulin, Katarina, Meašić, Ana-Maria, Šamadan, Lara, Batoš, Ana Tripalo

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INFANTILE COLIC - NEWER APPROACH TO AN OLD PROBLEM von Vulin, Katarina, Hojsak, Iva

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Inherited Thrombophilia Associated With Ischemic Pediatric Stroke in Parent-Child Pairs von Krleza, Jasna Lenicek, Coen Herak, Desiree, Đakovic, Ivana, Vulin, Katarina, Roic, Goran, Tripalo Batoš, Ana, Čeri, Andrea, Zadro, Renata, Đuranovic, Vlasta

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Spectrum of genetic variants in 306 patients with non-syndromic hearing loss from Croatia von Sansović, Ivona, Meašić, Ana-Maria, Bobinec, Adriana, Morožin Pohovski, Leona, Odak, Ljubica, Vulin, Katarina, Lozić, Bernarda, Kero, Mijana, Huljev Frković, Sanda, Pušeljić, Silvija

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Cervicofacial subcutaneous emphysema after facial cosmetic procedure in an 11‐year‐old girl von Vulin, Katarina, Dakovic, Ivana, Grmoja, Tonci, Tripalo Batos, Ana, Resic, Arnes, Baskovic, Marko, Sekelj‐Fures, Jadranka

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The characteristics of transcranial color-coded duplex sonography in children with cerebral arteriovenous malformation presenting with headache von Duranovic, Vlasta, Vulin, Katarina, Dakovic, Ivana, Lenicek Krleza, Jasna, Delin, Sanja, Galinovic, Ivana, Marjanovic, Josip, Tripalo Batos, Ana, Plesa Premilovac, Zdenka, Mejaski Bosnjak, Vlatka

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Clinical and neuroradiological spectrum of biallelic variants in NOTCH3 von Iruzubieta, Pablo, Alves, César Augusto Pinheiro Ferreira, Al Shamsi, Aisha M., ElGhazali, Gehad, Zaki, Maha S., Pinelli, Lorenzo, Lopergolo, Diego, Cho, Bernard P.H., Jolly, Amy A., Al Futaisi, Amna, Al-Amrani, Fatema, Galli, Jessica, Fazzi, Elisa, Vulin, Katarina, Barajas-Olmos, Francisco, Hengel, Holger, Aljamal, Bayan Mohammed, Nasr, Vahideh, Assarzadegan, Farhad, Ragno, Michele, Trojano, Luigi, Ojeda, Naomi Meave, Çakar, Arman, Bianchi, Silvia, Pescini, Francesca, Poggesi, Anna, Al Tenalji, Amal, Aziz, Majid, Mohammad, Rahema, Chedrawi, Aziza, De Stefano, Nicola, Zifarelli, Giovanni, Schöls, Ludger, Haack, Tobias B., Rebelo, Adriana, Zuchner, Stephan, Koc, Filiz, Griffiths, Lyn R., Orozco, Lorena, Helmes, Karla García, Babaei, Meisam, Bauer, Peter, Chan Jeong, Won, Karimiani, Ehsan Ghayoor, Schmidts, Miriam, Gleeson, Joseph G., Chung, Wendy K., Alkuraya, Fowzan Sami, Shalbafan, Bita, Markus, Hugh S., Houlden, Henry, Maroofian, Reza

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Visual impairment in children with cerebral palsy: Croatian population-based study for birth years 2003-2008 von Striber, Neda, Vulin, Katarina, Đaković, Ivana, Prvčić, Iva, Đuranović, Vlasta, Cerovski, Branimir, Pejić Roško, Sanja, Čokolić Petrović, Dunja, Martinec, Sunčica, Dawidowsky, Barbara, Mejaški Bošnjak, Vlatka

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DOJENAČKE KOLIKE – NOVIJI PRISTUP STAROM PROBLEMU von Vulin, Katarina, Hojsak, Iva

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Clinical and neuroradiological spectrum of biallelic variants in NOTCH3Research in context von Pablo Iruzubieta, César Augusto Pinheiro Ferreira Alves, Aisha M. Al Shamsi, Gehad ElGhazali, Maha S. Zaki, Lorenzo Pinelli, Diego Lopergolo, Bernard P.H. Cho, Amy A. Jolly, Amna Al Futaisi, Fatema Al-Amrani, Jessica Galli, Elisa Fazzi, Katarina Vulin, Francisco Barajas-Olmos, Holger Hengel, Bayan Mohammed Aljamal, Vahideh Nasr, Farhad Assarzadegan, Michele Ragno, Luigi Trojano, Naomi Meave Ojeda, Arman Çakar, Silvia Bianchi, Francesca Pescini, Anna Poggesi, Amal Al Tenalji, Majid Aziz, Rahema Mohammad, Aziza Chedrawi, Nicola De Stefano, Giovanni Zifarelli, Ludger Schöls, Tobias B. Haack, Adriana Rebelo, Stephan Zuchner, Filiz Koc, Lyn R. Griffiths, Lorena Orozco, Karla García Helmes, Meisam Babaei, Peter Bauer, Won Chan Jeong, Ehsan Ghayoor Karimiani, Miriam Schmidts, Joseph G. Gleeson, Wendy K. Chung, Fowzan Sami Alkuraya, Bita Shalbafan, Hugh S. Markus, Henry Houlden, Reza Maroofian

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The first case report of distal 16p12.1p11.2 trisomy and proximal 16p11.2 tetrasomy inherited from both parents von Morožin Pohovski, Leona, Sansović, Ivona, Vulin, Katarina, Odak, Ljubica

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Neurodevelopmental disorder caused by an inherited novel KMT5B variant: case report von Odak, Ljubica, Vulin, Katarina, Meašić, Ana-Maria, Šamadan, Lara, Tripalo Batoš, Ana

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Cervicofacial subcutaneous emphysema after facial cosmetic procedure in an 11-year-old girl von Vulin, Katarina, Dakovic, Ivana, Grmoja, Tonci, Tripalo Batos, Ana, Resic, Arnes, Baskovic, Marko, Sekelj-Fures, Jadranka

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