Search Results - "Meašić, Ana Maria" :: K.UTB vyhledávací portál

Neurodevelopmental disorder caused by an inherited novel KMT5B variant: case report

by Odak, Ljubica, Vulin, Katarina, Meašić, Ana-Maria, Šamadan, Lara, Batoš, Ana Tripalo
Published in Croatian medical journal (01.10.2023)

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Clinical relevance of the TECTA c.6183G>T variant identified in a family with autosomal dominant hearing loss: a case report

by Sansović, Ivona, Meašić, Ana-Maria, Odak, Ljubica, Kero, Mijana
Published in Croatian medical journal (01.10.2023)

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96 Homozygous ABCG8 mutation in a 14-year-old boy with sitosterolemia

by Meašić, Ana-Maria, Bobinec, Adriana, Sansović, Ivona, Boban, Ljubica, Pavić, Ana Močić, Pušeljić, Silvija, Barišić, Ingeborg
Published in Archives of disease in childhood (11.10.2021)

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84 RARE COPY NUMBER VARIANTS IN CONGENITAL HEART DEFECTS

by Davidović, Maša, Pohovski, Leona Morožin, Rogulj, Nikolina Vidan, Sansovic, Ivona, Bobinec, Adriana, Meašić, Ana-Maria, Kero, Mijana, Boban, Ljubica, Malčić, Ivan, Barišic, Ingeborg
Published in Archives of disease in childhood (11.10.2021)

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Trends in the treatment of undescended testes: a pediatric tertiary care center experience from Croatia

by Bašković, Marko, Zaninović, Luca, Sansović, Ivona, Meašić, Ana Maria, Katušić Bojanac, Ana, Ježek, Davor
Published in World journal of pediatric surgery (01.10.2022)

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Spectrum of genetic variants in 306 patients with non-syndromic hearing loss from Croatia

by Sansović, Ivona, Meašić, Ana-Maria, Bobinec, Adriana, Morožin Pohovski, Leona, Odak, Ljubica, Vulin, Katarina, Lozić, Bernarda, Kero, Mijana, Huljev Frković, Sanda, Pušeljić, Silvija
Published in Croatian medical journal (01.06.2024)

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