Search Results - "Vulin, Katarina"

A case of macrophagic myofasciitis in a girl with developmental delay by 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? by Đaković, Ivana, Kostović, Ivica, Vulin, Katarina, Prvčić, Iva, Tešović, Goran, Krakar, Goran, Gojmerac, Tomislav, Sekelj Fureš, Jadranka, Mejaški Bošnjak, Vlatka

“…Objective Congenital cytomegalovirus infection (cCMV) is a common, frequently unrecognized cause of childhood disability. The aim of the present study was to…”
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Successful antibiotic treatment of liver abscess in an eight-year-old boy after perforated appendix by Marko Bašković, Antun Kljenak, Ante Čizmić, Dora Škrljak Šoša, Katarina Vulin, Ivana Đaković

“…We present the case of an eight-year-old boy who was referred to our Clinic with acute abdomen. After ultrasound, which showed a perforated appendix, an urgent…”
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334 Syncope in pediatric emergency department by Benco, Nikolina, Švigir, Alen, Topalušić, Iva, Vulin, Katarina, Premilovac, Zdenka Pleša

“…The objective of this study was to evaluate the various factors related to the children who presented to the emergency department of Children´s Hospital Zagreb…”
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The first case report of distal 16p12.1p11.2 trisomy and proximal 16p11.2 tetrasomy inherited from both parents by Morožin Pohovski, Leona, Sansović, Ivona, Vulin, Katarina, Odak, Ljubica

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98 Clinical exome sequencing in the diagnosis of autism spectrum disorder by Odak, Ljubica, Meašić, Ana-Marija, Bobinec, Adriana, Kero, Mijana, Sansović, Ivona, Vulin, Katarina, Tomić, Mirko, Barišić, Ingeborg

“…The autism spectrum disorder (ASD) is a complex neurodevelopmental disorder whose etiology is still poorly understood and attributed to genetic and…”
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399 Electrical status epilepticus in sleep (ESES):Clinical and EEG characteristics and response to treatments by Rosko, Sanja Pejic, Lončar, Lana, Fureš, Jadranka Sekelj, Đaković, Ivana, Đuranović, Vlasta, Vulin, Katarina

“…Electrical status epilepticus in sleep (ESES) is defined as an age related, self-limited epileptic encephalopathy. It is characterized by heterogeneous…”
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Neurodevelopmental disorder caused by an inherited novel KMT5B variant: case report by Odak, Ljubica, Vulin, Katarina, Meašić, Ana-Maria, Šamadan, Lara, Batoš, Ana Tripalo

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

“…Infantile colic have been known for the long time and are one of the most common reasons for pediatrician's appointment in early infancy. However, their…”
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Inherited Thrombophilia Associated With Ischemic Pediatric Stroke in Parent-Child Pairs by Krleza, Jasna Lenicek, Coen Herak, Desiree, Đakovic, Ivana, Vulin, Katarina, Roic, Goran, Tripalo Batoš, Ana, Čeri, Andrea, Zadro, Renata, Đuranovic, Vlasta

“…We aimed to examine inherited thrombophilia frequencies by extending genetic profile to previously rarely or not investigated polymorphisms in children with…”
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Spectrum of genetic variants in 306 patients with non-syndromic hearing loss from Croatia by Sansović, Ivona, Meašić, Ana-Maria, Bobinec, Adriana, Morožin Pohovski, Leona, Odak, Ljubica, Vulin, Katarina, Lozić, Bernarda, Kero, Mijana, Huljev Frković, Sanda, Pušeljić, Silvija

“…To determine the spectrum and frequency of disease-causing variants in patients with non-syndromic hearing loss (NSHL) and to investigate the diagnostic yield…”
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Cervicofacial subcutaneous emphysema after facial cosmetic procedure in an 11‐year‐old girl by 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 by Duranovic, Vlasta, Vulin, Katarina, Dakovic, Ivana, Lenicek Krleza, Jasna, Delin, Sanja, Galinovic, Ivana, Marjanovic, Josip, Tripalo Batos, Ana, Plesa Premilovac, Zdenka, Mejaski Bosnjak, Vlatka

“…Purpose Cerebral arteriovenous malformations (AVM) are uncommon lesions. They are most often presented in childhood as intracranial hemorrhage. The aim of this…”
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Clinical and neuroradiological spectrum of biallelic variants in NOTCH3 by 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

“…NOTCH3 encodes a transmembrane receptor critical for vascular smooth muscle cell function. NOTCH3 variants are the leading cause of hereditary cerebral small…”
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Visual impairment in children with cerebral palsy: Croatian population-based study for birth years 2003-2008 by 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

“…To evaluate visual impairment (VI) in children with cerebral palsy (CP). This population-based study included 419 children from the Surveillance of Cerebral…”
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DOJENAČKE KOLIKE – NOVIJI PRISTUP STAROM PROBLEMU by Vulin, Katarina, Hojsak, Iva

“…Dojenačke su kolike od davnina poznate i jedan su od najčešćih razloga posjeta liječniku u ranoj dojenačkoj dobi. Ipak, uzrok njihova pojavljivanja i njihova…”
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Clinical and neuroradiological spectrum of biallelic variants in NOTCH3Research in context by 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

“…Background: NOTCH3 encodes a transmembrane receptor critical for vascular smooth muscle cell function. NOTCH3 variants are the leading cause of hereditary…”
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The first case report of distal 16p12.1p11.2 trisomy and proximal 16p11.2 tetrasomy inherited from both parents by Morožin Pohovski, Leona, Sansović, Ivona, Vulin, Katarina, Odak, Ljubica

“…Recurrent copy number variants in the chromosomal region 16p11.2 are among the most frequent genetic causes of neurodevelopmental disorders. The increasing…”
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Neurodevelopmental disorder caused by an inherited novel KMT5B variant: case report by Odak, Ljubica, Vulin, Katarina, Meašić, Ana-Maria, Šamadan, Lara, Tripalo Batoš, Ana

“…Neurodevelopmental disorders are a large group of disorders that affect ~ 3% of children and represent a serious health problem worldwide. Their etiology is…”
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Cervicofacial subcutaneous emphysema after facial cosmetic procedure in an 11-year-old girl by Vulin, Katarina, Dakovic, Ivana, Grmoja, Tonci, Tripalo Batos, Ana, Resic, Arnes, Baskovic, Marko, Sekelj-Fures, Jadranka

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