The Croatian Model of Integrative Prospective Management of Epilepsy and Pregnancy
Miškov, Snježana, Gjergja Juraški, Romana, Mikula, Ivan, Bašić, Silvio, Bošnjak Pašić, Marija, Košec, Vesna, Sabol, Zlatko, Fučić, Aleksandra, Sajko, Tomislav, Bašić Kes, Vanja
Published in Acta clinica Croatica (Tisak) (01.12.2016)
Published in Acta clinica Croatica (Tisak) (01.12.2016)
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Journal Article
Clinical sensitivity and specificity of multiple T2-hyperintensities on brain magnetic resonance imaging in diagnosis of neurofibromatosis type 1 in children: diagnostic accuracy study
Sabol, Zlatko, Resić, Biserka, Gjergja Juraski, Romana, Sabol, Filip, Kovac Sizgorić, Matilda, Orsolić, Kresimir, Ozretić, David, Sepić-Grahovac, Dubravka
Published in Croatian medical journal (01.08.2011)
Published in Croatian medical journal (01.08.2011)
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Journal Article
Genetics of Pediatric Epilepsy: Next-Generation Sequencing in Clinical Practice
Blazekovic, Antonela, Gotovac Jercic, Kristina, Meglaj, Sarah, Duranovic, Vlasta, Prpic, Igor, Lozic, Bernarda, Malenica, Masa, Markovic, Silvana, Lujic, Lucija, Petelin Gadze, Zeljka, Juraski, Romana Gjergja, Barišic, Nina, Baric, Ivo, Borovecki, Fran
Published in Genes (01.08.2022)
Published in Genes (01.08.2022)
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Self-reported perinatal depressive symptoms and postnatal symptom severity after treatment with antidepressants in pregnancy: a cross-sectional study across 12 European countries using the Edinburgh Postnatal Depression Scale
Lupattelli, Angela, Twigg, Michael J, Zagorodnikova, Ksenia, Moretti, Myla E, Drozd, Mariola, Panchaud, Alice, Rieutord, Andre, Juraski, Romana Gjergja, Odalovic, Marina, Kennedy, Debra, Rudolf, Gorazd, Juch, Herbert, Nordeng, Hedvig
Published in Clinical epidemiology (01.01.2018)
Published in Clinical epidemiology (01.01.2018)
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Parasomnije: diferencijalno dijagnostički pristup i značaj polisomnografije
Gjergja Juraški, Romana, Kovač Šižgorić, Matilda, Stipoljev, Feodora
Published in Liječnički vjesnik (17.04.2023)
Published in Liječnički vjesnik (17.04.2023)
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Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated with Craniofacial, Neurological, Cardiovascular, and Skeletal Features
Turnpenny, Peter D., Wright, Michael J., Sloman, Melissa, Caswell, Richard, van Essen, Anthony J., Gerkes, Erica, Pfundt, Rolph, White, Susan M., Shaul-Lotan, Nava, Carpenter, Lori, Schaefer, G. Bradley, Fryer, Alan, Innes, A. Micheil, Forbes, Kirsten P., Chung, Wendy K., McLaughlin, Heather, Henderson, Lindsay B., Roberts, Amy E., Heath, Karen E., Paumard-Hernández, Beatriz, Gener, Blanca, Fawcett, Katherine A., Gjergja-Juraški, Romana, Pilz, Daniela T., Fry, Andrew E.
Published in American journal of human genetics (01.11.2018)
Published in American journal of human genetics (01.11.2018)
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Journal Article
Sleep-disordered breathing in children with Prader-Willi Syndrome cannot be attributed solely to increased body weight
Perica, Marija Šenjug, Juraški, Romana Gjergja, Marušić, Ivana, Lipej, Marcel, Miculinić, Andrija, Banić, Ivana, Mirjana, Turkalj
Published in Global pediatrics (01.12.2023)
Published in Global pediatrics (01.12.2023)
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14 Surveillance of Croatian pregnant women with epilepsy and effects of antiepileptic drugs exposure in their offspring
Miškov, Snježana, Juraški, Romana Gjergja, Fučić, Aleksandra, Bakuli, Tomislav Ivičević, Sojat, Ljerka Cvitanović, Vuković, Vlasta, Kes, Vanja Basic, Demarin, Vida
Published in Acta neuropsychiatrica (01.06.2009)
Published in Acta neuropsychiatrica (01.06.2009)
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Journal Article
Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated with Craniofacial, Neurological, Cardiovascular, and Skeletal Features
Turnpenny, Peter D., Wright, Michael J., Sloman, Melissa, Caswell, Richard, van Essen, Anthony J., Gerkes, Erica, Pfundt, Rolph, White, Susan M., Shaul-Lotan, Nava, Carpenter, Lori, Schaefer, G. Bradley, Fryer, Alan, Innes, A. Micheil, Forbes, Kirsten P., Chung, Wendy K., McLaughlin, Heather, Henderson, Lindsay B., Roberts, Amy E., Heath, Karen E., Paumard-Hernández, Beatriz, Gener, Blanca, Fawcett, Katherine A., Gjergja-Juraški, Romana, Pilz, Daniela T., Fry, Andrew E.
Published in American journal of human genetics (06.12.2018)
Published in American journal of human genetics (06.12.2018)
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Journal Article
Sleep phenotype in children with Down syndrome – altered sleep architecture and sleep-disordered breathing
Gjergja Juraški, Romana, Turkalj, Mirjana, Plavec, Davor, Nogalo, Boro, Marušić, Ivana, Miloš, Marija, Anzić, Srđan Ante, Kovač Šižgorić, Matilda, Stipoljev, Feodora
Published in Paediatria Croatica (20.12.2019)
Published in Paediatria Croatica (20.12.2019)
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PATTERNS AND FACTORS ASSOCIATED WITH LOW ADHERENCE TO PSYCHOTROPIC MEDICATIONS DURING PREGNANCY-A CROSS-SECTIONAL, MULTINATIONAL WEB-BASED STUDY
Lupattelli, Angela, Spigset, Olav, Björnsdóttir, Ingunn, Hämeen-Anttila, Katri, Mårdby, Ann-Charlotte, Panchaud, Alice, Juraski, Romana Gjergja, Rudolf, Gorazd, Odalovic, Marina, Drozd, Mariola, Twigg, Michael J, Juch, Herbert, Moretti, Myla E, Kennedy, Debra, Rieutord, Andre, Zagorodnikova, Ksenia, Passier, Anneke, Nordeng, Hedvig
Published in Depression and anxiety (01.06.2015)
Published in Depression and anxiety (01.06.2015)
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Journal Article
The association between antidepressant treatment in pregnancy and self-report of postnatal depressive symptoms using the Edinburgh Postnatal Depression Scale
Lupattelli, Angela, Twigg, Michael J., Zagorodnikova, Ksenia, Moretti, Myla E., Drozd, Mariola, Panchaud, Alice, Rieutord, Andre, Juraski, Romana Gjergja, Odalovic, Marina, Kennedy, Debra, Rudolf, Gorazd, Juch, Herbert, Nordeng, Hedvig
Published in Reproductive toxicology (Elmsford, N.Y.) (01.09.2018)
Published in Reproductive toxicology (Elmsford, N.Y.) (01.09.2018)
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Journal Article
Prenatal diagnosis of complex phenotype in a 13-week-old fetus with an interstitial multigene deletion 20q13.13.-q13.2 by chromosomal microarray
Stipoljev, Feodora, Miric-Tesanic, Danka, Hafner, Tomislav, Barbalic, Maja, Logara, Monika, Lasan-Trcic, Ruzica, Vicic, Ana, Gjergja-Juraski, Romana
Published in European journal of medical genetics (01.11.2017)
Published in European journal of medical genetics (01.11.2017)
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