Aggressive middle turbinate osteoblastoma with intracranial extension: a case report

Por Cikojević, Draško, Čolović, Zaviša, Lozić, Bernarda, Klančnik, Marisa
Publicado em 2014

Full trisomy 5 in a sample of spontaneous abortion and arias stella reaction

Por Čulić, Vida, Lozić, Bernarda, Kuzmić-Prusac, Ivana, Mijaljica, Goran, Pavelić, Jasminka
Publicado em 2011

Influence of the Inherited Glucose-6-phosphate Dehydrogenase Deficiency on the Appearance of Neonatal Hyperbilirubinemia in Southern Croatia

Por Cherepnalkovski, Anet Papazovska, Marusic, Eugenija, Piperkova, Katica, Lozic, Bernarda, Skelin, Ana, Gruev, Todor, Krzelj, Vjekoslav
Publicado no Acta Inform Med (2015)

The OSR1 rs12329305 Polymorphism Contributes to the Development of Congenital Malformations in Cases of Stillborn/Neonatal Death

Por Lozić, Bernarda, Krželj, Vjekoslav, Kuzmić-Prusac, Ivana, Kuzmanić-Šamija, Radenka, Čapkun, Vesna, Lasan, Ružica, Zemunik, Tatijana
Publicado em 2014

Novel NALCN variant: altered respiratory and circadian rhythm, anesthetic sensitivity

Por Lozic, Bernarda, Johansson, Stefan, Lovric Kojundzic, Sanja, Markic, Josko, Knappskog, Per Morten, Hahn, Angelika F., Boman, Helge
Publicado no Ann Clin Transl Neurol (2016)

Limited survivability of unbalanced progeny of carriers of a unique t(4;19)(p15.32;p13.3): a study in multiple generations

Por Šumanović-Glamuzina, Darinka, Lozić, Bernarda, Iwanowski, Piotr S., Zemunik, Tatijana, Bilinovac, Zeljka, Stasiewicz-Jarocka, Beata, Panasiuk, Barbara, Midro, Alina T.
Publicado no Mol Cytogenet (2017)

Correlation of serial MRI findings and clinical outcome in the first Croatian patient with acute necrotizing encephalopathy

Por Kuzmanić Šamija, Radenka, Kolić, Krešimir, Markić, Joško, Polić, Branka, Kalebić Jakupčević, Katija, Lozić, Bernarda, Lazibat, Ines, Unić, Ivana, Zemunik, Tatijana
Publicado em 2014

Dietary Factors Associated with Plasma Thyroid Peroxidase and Thyroglobulin Antibodies

Por Matana, Antonela, Torlak, Vesela, Brdar, Dubravka, Popović, Marijana, Lozić, Bernarda, Barbalić, Maja, Boraska Perica, Vesna, Punda, Ante, Polašek, Ozren, Hayward, Caroline, Zemunik, Tatijana
Publicado no Nutrients (2017)

Association of NOS3 tag polymorphisms with hypoxic-ischemic encephalopathy

Por Kuzmanić Šamija, Radenka, Primorac, Dragan, Rešić, Biserka, Lozić, Bernarda, Krželj, Vjekoslav, Tomasović, Maja, Stoini, Eugenio, Šamanović, Ljubo, Benzon, Benjamin, Pehlić, Marina, Boraska, Vesna, Zemunik, Tatijana
Publicado em 2011

A cohort of 17 patients with kyphoscoliotic Ehlers–Danlos syndrome caused by biallelic mutations in FKBP14: expansion of the clinical and mutational spectrum and description of the...

Por Giunta, Cecilia, Baumann, Matthias, Fauth, Christine, Lindert, Uschi, Abdalla, Ebtesam M, Brady, Angela F, Collins, James, Dastgir, Jahannaz, Donkervoort, Sandra, Ghali, Neeti, Johnson, Diana S, Kariminejad, Ariana, Koch, Johannes, Kraenzlin, Marius, Lahiri, Nayana, Lozic, Bernarda, Manzur, Adnan Y, Morton, Jenny E V, Pilch, Jacek, Pollitt, Rebecca C, Schreiber, Gudrun, Shannon, Nora L, Sobey, Glenda, Vandersteen, Anthony, van Dijk, Fleur S, Witsch-Baumgartner, Martina, Zschocke, Johannes, Pope, F Michael, Bönnemann, Carsten G, Rohrbach, Marianne
Publicado no Genet Med (2018)