Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Dumić Kubat, Katja"'
Autor:
Kortüm, Fanny, Niceta, Marcello, Magliozzi, Monia, Dumic Kubat, Katja, Robertson, Stephen P., Moresco, Angelica, Dentici, Maria Lisa, Baban, Anwar, Leoni, Chiara, Onesimo, Roberta, Obregon, Maria Gabriela, Digilio, Maria Cristina, Zampino, Giuseppe, Novelli, Antonio, Tartaglia, Marco, Kutsche, Kerstin
Publikováno v:
In European Journal of Medical Genetics September 2020 63(9)
Autor:
Filipović-Grčić, Maja, Stipanović, Jasminka, Duić, Željko, Vidak, Zoran, Juka Kožul, Gorana, Bojanić, Katarina, Vukasović, Marko, Stipančić, Gordana, La Grasta Sabolić, Lavinia, Dumić Kubat, Katja
Neonatalni dijabetes melitus (NDM) čini skupina nasljednih bolesti kojima je zajednička pojava DM- a u prvih 6 mjeseci života. Danas je poznato oko 20 različitih gena odgovornih za nastanak NDM-a, čije mutacije ometaju normalan razvoj i funkciju
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::9ba421a9185fa35d57164bacfe20b8ed
https://www.bib.irb.hr/1276331
https://www.bib.irb.hr/1276331
Autor:
Kos, Ivanka, Dumić Kubat, Katja, Bartoniček, Dorotea, Lehman, Ivan, Ban, Maja, Matković, Hana, Lamot, Lovro, Kristina, Vrljičak
Introduction: The world is facing COVID-19 pandemic with a complex presentation. Moreover, many people are suffering from a variety of postCOVID symptoms. Although it appears that children experience less severe disease, those with underlying conditi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::01cf0e32f799b46af8a85564b40241b6
https://www.bib.irb.hr/1253617
https://www.bib.irb.hr/1253617
Autor:
Dumić Kubat Katja, Vuković Jurica, Špehar Uroić Anita, Braovac Duje, Marjanac Igor, Krnić Nevena
Publikováno v:
Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ebbbec0d9e5fb8a43e61962216b5ba47
https://doi.org/10.1136/archdischild-2021-europaediatrics.208
https://doi.org/10.1136/archdischild-2021-europaediatrics.208
Autor:
Aničić, Mirna Natalija, Todorić, Ivana, Marčinković, Nedo, Kovačić, Matea, Dumić Kubat, Katja, Špehar Uroić, Anita, Krnić, Nevena, Omerza, Lana, Senečić Čala, Irena, Tješić-Drinković, Duška, Vuković, Jurica
Objectives and Study: Liver disorder associated with type 1 diabetes mellitus (DM1) in children might not be as rare as previously thought. We assessed number of simple and potentially reliable tests for its detection. Methods: Clinical examination,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::9253bce85756e47b329c968203278147
https://doi.org/10.1097/mpg.0000000000003177
https://doi.org/10.1097/mpg.0000000000003177
Autor:
Vukšić, Iva, Dumić Kubat, Katja, Ćaleta, Tomislav, Matić, Toni, Cigrovski, Nevenka, Kelečić, Jadranka, Pasini, Miram, Luetić, Tomislav, Vuković, Jurica, Sindičić Dessardo, Nada, Grizelj, Ruža
Multiple intestinal atresia (MIA) is a congenital malformation disorder in which atresia occurs at multiple levels throughout the gastrointestinal tract, most commonly small bowel. Frequently it presents as an isolated anomaly, but also as a part of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::e61ee6eb27a9ea1342b32074987176a0
https://doi.org/10.1136/archdischild-2021-europaediatrics.122
https://doi.org/10.1136/archdischild-2021-europaediatrics.122
Autor:
Braovac, Duje, Krnić, Nevena, Dumić Kubat, Katja, Špehar Uroić, Anita, Marjanac, Igor, Vuković, Jurica
Introducton Prader-Willi syndrome (PWS) is a rare genetic disease caused by deletions or imprinting defects in the region 15q11-q13 leading to hypothalamic-pituitary dysfunction, hyperphagia with excessive weight gain and behavioral disorders. Obesit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::919594d86565cc18005047168b95c64d
https://www.bib.irb.hr/1199242
https://www.bib.irb.hr/1199242
Autor:
Braovac, Duje, Dumić Kubat, Katja, Matković, Hana, Ćaleta, Tomislav, Aničić, Mirna Natalija, Gotovac Jerčić, Kristina, Vuković, Jurica, Sindičić Dessardo, Nada, Grizelj, Ruža
Hereditary coproporphyria (HCP) is an autosomal dominant disorder of haem synthesis caused by mutation in CPOX gene. Majority of heterozygotes remain asymptomatic throughout life and disease onset before puberty is exceedingly rare. Only two patients
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::860081f183909735adff56dd3e0d9a5e
https://www.bib.irb.hr/1196186
https://www.bib.irb.hr/1196186
Autor:
Krnić, Nevena, Špehar Uroić, Anita, Bogdanić, Ana, Dumić Kubat, Katja, Pavić, Eva, Rojnić Putarek, Nataša
Background: Increasing prevalence of obesity requires improvement in current therapeutic approaches. Multidisciplinary lifestyle intervention programs involving both children and their parents are showing promising results. Aim: To compare the effica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::b5a21569ae9530e9bea194761801e3e1
https://www.bib.irb.hr/965461
https://www.bib.irb.hr/965461
Autor:
Rojnić Putarek, Nataša, Novak, Milivoj, Špehar Uroić, Anita, Krnić, Nevena, Dumić Kubat, Katja
Background: Mild increase in serum lipid concentrations is a common feature of diabetic ketoacidosis (DKA) while severe hyperlipidemia (HL) with milky plasma is rare. HL is an uncommon cause of acute pancreatitis (AP), especially in children. The ris
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::e16bca1aa281029cdc85db5cd62e70fe
https://www.bib.irb.hr/965488
https://www.bib.irb.hr/965488