Items where Department is "Katedra za pedijatriju" and Year is 2018

B

Bojanić, Katarina and Grizelj, Ruža and Vuković, Jurica and Omerza, Lana and Grubić, Marina and Ćaleta, Tomislav and Weingarten, Toby N. and Schroeder, Darrell R. and Sprung, Juraj (2018) Health-related quality of life in children and adolescents with congenital diaphragmatic hernia: a cross-sectional study. Health and Quality of Life Outcomes, 16 (1). ISSN 1477-7525

H

Hojsak, Iva and Niseteo, Tena and Kolaček, Sanja and Despot, Ranka and Jadrešin, Oleg and Jelić, Nevenka and Konjik, Vlatka and Močić-Pavić, Ana and Palčevski, Goran and Senečić-Čala, Irena and Tješić-Drinković, Duška and Vuković, Jurica and Žaja, Orjena and Mišak, Zrinjka (2018) Vegetarijanska i veganska prehrana u dječjoj dobi - smjernice Hrvatskog društva za pedijatrijsku gastroenterologiju, hepatologiju i prehranu Hrvatskog liječničkog zbora [Vegetarian and vegan diet in children - guidelines of the Croatian society for pediatric gastroenterology, hepatology and nutrition of the Croatian Medical Association]. Liječnički vjesnik, 140 (11-12). pp. 279-284. ISSN 0024-3477

K

Katavić, Matej and Dilber, Daniel (2018) Imunizacija djece s kongenitalnim srčanim grješkama – klinički i kritički osvrt [Immunisation of children with congenital heart defects – clinical and critical overview]. Liječnički vjesnik, 140 (1-2). pp. 24-34. ISSN 0024-3477

L

Lamhonwah, Anne-Marie and Barić, Ivo and Lamhonwah, Jessica and Grubić, Marina and Tein, Ingrid (2018) Attention deficit/hyperactivity disorder as an associated feature in OCTN2 deficiency with novel deletion (p.T440-Y449). Clinical Case Reports, 6 (4). pp. 585-591. ISSN 2050-0904

M

Malčić, Ivan and Anić, Darko and Bartoniček, Dorotea and Šarić, Dalibor and Kniewald, Hrvoje and Belina, Dražen and Novak, Milivoj and Galić, Slobodan and Cvitković, Miran and Ivančan, Višnja and Jelašić, Dražen and Stoić Brezak, Jasna (2018) Transplantacija srca u djece u Hrvatskoj – naša prva iskustva [Heart transplantation in children in Croatia – our first experiences]. Liječnički vjesnik, 140 (1-2). pp. 7-18. ISSN 0024-3477

Malčić, Ivan and Tokić Pivac, Višnja and Anić, Darko and Težak, Stanko and Bartoniček, Dorotea and Šarić, Dalibor and Belina, Dražen (2018) Dvostruka (pregrađena) desna klijetka - prikriveni pratitelj ventrikularnoga septalnog defekta [Double chambered right ventricle – concealed companion of ventricular septal defect]. Liječnički vjesnik, 140 (11-12). pp. 307-313. ISSN 0024-3477

Matić, Toni and Šalek, Zrinko and Vrhovac, Radovan and Duraković, Nadira and Lasan-Trčić, Ružica and Bašić-Kinda, Sandra and Dujmović, Dino and Bilić, Ernest (2018) Transplantacija krvotvornih matičnih stanica u djeteta s Fanconijevom anemijom – prikaz bolesnika [Hematopoietic stem cell transplantation in a child with Fanconi anemia – case report]. Liječnički vjesnik, 140 (3-4). pp. 126-128. ISSN 0024-3477

N

Nenadić-Baranašić, Nataša and Gjergja-Juraski, Romana and Lehman, Ivan and Turkalj, Mirjana and Nogalo, Boro and Barišić, Nina (2018) Overnight video-polysomnographic studies in children with Intractable epileptic encephalopathies. Medical Science Monitor, 24. pp. 5405-5411. ISSN 1643-3750

O

O'Byrne, James J. and Tarailo-Graovac, Maja and Ghani, Aisha and Champion, Michael and Deshpande, Charu and Dursun, Ali and Ozgul, Riza K. and Freisinger, Peter and Garber, Ian and Haack, Tobias B. and Horvath, Rita and Barić, Ivo and Husain, Ralf A. and Kluijtmans, Leo A.J. and Kotzaeridou, Urania and Morris, Andrew A. and Ross, Colin J. and Santra, Saikat and Smeitink, Jan and Tarnopolsky, Mark and Wortmann, Saskia B. and Mayr, Johannes A. and Brunner-Krainz, Michaela and Prokisch, Holger and Wasserman, Wyeth W. and Wevers, Ron A. and Engelke, Udo F. and Rodenburg, Richard J. and Ting, Teck Wah and McFarland, Robert and Taylor, Robert W. and Salvarinova, Ramona and van Karnebeek, Clara D.M. (2018) The genotypic and phenotypic spectrum of MTO1 deficiency. Molecular Genetics and Metabolism, 123 (1). pp. 28-42. ISSN 1096-7192

S

Sakaguchi, Tomohiro and Žigman, Tamara and Petković Ramadža, Danijela and Omerza, Lana and Pušeljić, Silvija and Ereš Hrvaćanin, Zrinka and Miyake, Noriko and Matsumoto, Naomichi and Barić, Ivo (2018) A novel PGAP3 mutation in a Croatian boy with brachytelephalangy and a thin corpus callosum. Human Genome Variation, 5. ISSN 2054-345X