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Šmaguc, Ana ; Petković Ramadža, Danijela ; Sarnavka, Vladimir ; Krželj, Vjekoslav ; Lozić, Bernarda ; Pušeljić, Silvija ; Rahelić, Valentina ; Mesarić, Nikola ; Grubić, Marina ; Bogdanić, Ana et al.
Iskustva s galaktozemijom u Hrvatskoj // Liječnički vjesnik : glasilo Hrvatskoga liječničkog zbora, 145 (2023), 1-2; 1-11. doi: 10.26800/LV-145-1-2-1 |
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Tomac, Gordana ; Gojčeta, Koraljka ; Grizelj, Ruža ; Coen Herak, Desiree ; Baršić Ostojić, Sanja ; Golubić Ćepulić, Branka
Severe intracranial haemorrhage in neonatal alloimmune thrombocytopenia due to antibodies against human platelet antigen 1b: Case report and literature review // Transfusion medicine, 32 (2022), 269-275. doi: 10.1111/tme.12892 |
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Petković Ramadža, Danijela ; Žigman, Tamara ; Grizelj, Ruža ; Ninković, Dorotea ; Omerza, Lana ; Aničić, Mirna ; Ćorić, Marijana ; Mayr, Johannes A. ; Feichtinger, René ; Wortmann, Saskia et al.
Early onset liver failure due to mitochondrial DNA depletion: clinical course of four patients // Archives of disease in childhood. 2021. str. A45-A46 doi: 10.1136/archdischild-2021-europaediatrics.107 |
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Katušić, Ana ; Žunić Išasegi, Iris ; Radoš, Milan ; Raguž, Marina ; Grizelj, Ruža ; Ferrari, Fabrizio ; Kostović, Ivica
Transient structural MRI patterns correlate with the motor functions in preterm infants // Brain & development (Tokyo), 43 (2021), 3; 363-371. doi: 10.1016/j.braindev.2020.11.002 |
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Ille, Vanja ; Petković Ramadža, Danijela ; Žigman, Tamara ; Filipović- Grčić, Boris ; Grizelj, Ruža ; Ninković, Dorotea ; Bartoniček, Dorotea ; Škaričić, Ana ; Bilandžija Kuš, Iva ; Mesarić, Nikola et al.
Hypoketotic hypoglycemia and hyperammonemia as presenting features of early onset multiple acyl- CoA dehydrogenase deficiency // Archives of disease in childhood. 2021. str. A44-A44 doi: 10.1136/archdischild-2021-europaediatrics.104 |
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Vukšić, Iva ; Dumić Kubat, Katja ; Ćaleta, Tomislav ; Matić, Toni ; Cigrovski, Nevenka ; Kelečić, Jadranka ; Pasini, Miram ; Luetić, Tomislav ; Vuković, Jurica ; Sindičić Dessardo, Nada et al.
Multiple intestinal atresia with combined immunodeficiendy due to TTC7A gene mutation - case report // Archives of disease in childhood. 2021. str. A51-A52 doi: 10.1136/archdischild-2021-europaediatrics.122 |
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Čičak, Ivana ; Novak, Milivoj ; Cvitković, Miran ; Galić, Slobodan ; Matić, Toni ; Rubić, Filip ; Malčić, Ivan ; Šarić, Dalibor ; Bartoniček, Dorotea ; Dilber, Daniel et al.
Titinopathy - a rare cause of multiorgan failure // Archives of disease in childhood. 2021. str. A142-A142 doi: 10.1136/archdischild-2021-europaediatrics.337 |
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Ćorić, Ana ; Ćaleta, Tomislav ; Vukšić, Iva ; Džepina, Petra ; Ninković, Dorotea ; Dasović Buljević, Andrea ; Benjak, Vesna ; Filipović- Grčić, Boris ; Šarić, Dalibor ; Dilber, Daniel et al.
The association of prenatally diagnosed cardiac rhabdomyoma and tuberous sclerosis complex // Archives of disease in childhood. 2021. str. A76-A77 doi: 10.1136/archdischild-2021-europaediatrics.180 |
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Ćaleta, Tomislav ; Vukšić, Iva ; Živković, Petra ; Benjak, Vesna ; Dasović Buljević, Andrea ; Ninković, Dorotea ; Filipović-Grčić, Boris ; Sabolić, Ivana ; Pasini, Miram ; Ćavar, Stanko et al.
Short-term outcomes for preterm infants with surgical necrotizing enterocolitis // Archives of disease in childhood. 2021. str. A58-A58 doi: 10.1136/archdischild-2021-europaediatrics.136 |
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Braovac, Duje ; Dumić Kubat, Katja ; Matković, Hana ; Ćaleta, Tomislav ; Aničić, Mirna Natalija ; Gotovac Jerčić, Kristina ; Vuković, Jurica ; Sindičić Dessardo, Nada ; Grizelj, Ruža
Novel presentation of neonatal-onset hereditary coproporphyria // Journal of pediatric gastroenterology and nutrition. 2021. str. 895-895 |
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