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Goran Krnjak
Goran Krnjak
Medicine
Pediatrics
Humanities
Phenotype
Missense mutation
5
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1
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0
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Expanding the known phenotype of Mullegama-Klein-Martinez syndrome in male patients.
2021
Human genome variation
Fiona Freyberger
Tomislav Kokotović
Goran Krnjak
Sanda Huljev Frković
Vanja Nagy
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104 Hypoketotic hypoglycemia and hyperammonemia as presenting features of early onset multiple acyl-CoA dehydrogenase deficiency
2021
Archives of Disease in Childhood
Vanja Ille
Danijela Petković Ramadža
Tamara Žigman
Boris Filipović-Grčić
Ruža Grizelj
Dorotea Ninković
Dorotea Bartoniček
Ana Škaričić
Iva Bilandžija Kuš
Nikola Mesarić
Goran Krnjak
Ksenija Fumić
Ivo Barić
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101 Inherited autoinflammatory encephalopathy in the differential diagnosis of conatal viral infections- newborn with Aicardi-Goutières syndrome
2021
Archives of Disease in Childhood
Dora Bulić
Tea Škorić
Tamara Žigman
Goran Krnjak
Goran Tešović
Nina Barišić
Ivo Barić
Danijela Petković Ramadža
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Prikaz djevojčice s usporenim psihomotornim razvojem i makrofagnim miofasciitisom
2018
Goran Krnjak
Vlasta Đuranović
Ingeborg Barišić
Leo Pažanin
Katarina Vulin
Ivana Đaković
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Urolitijaza - potencijalna komplikacija terapije ceftriaksonom
2014
Paediatria Croatica
Daniel Turudić
Danica Batinić
Branko Miše
Ivan Habuš
Marija Spajić
Goran Krnjak
Danko Milošević
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