Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Ivona Butorac-Ahel"'
Autor:
Ivona Butorac Ahel, Kristina Lah Tomulić, Inge Vlašić Cicvarić, Marta Žuvić, Kristina Baraba Dekanić, Silvije Šegulja, Iva Bilić Čače
Publikováno v:
Medicina, Vol 58, Iss 9, p 1295 (2022)
Background and Objectives: There are limited data regarding the incidence and risk factors for hypoglycemia, hyperglycemia, and unstable glycemia in preterm infants. The aim of the present study was to determine the incidence and risk factors associa
Externí odkaz:
https://doaj.org/article/1006e907b848447cbf74d3f22998959e
Autor:
Kristina Lah Tomulić, Lucija Matko, Arijan Verbić, Ana Milardović, Srećko Severinski, Ivana Kolić, Kristina Baraba Dekanić, Senada Šerifi, Ivona Butorac Ahel
Publikováno v:
Medicina, Vol 58, Iss 5, p 638 (2022)
Background and Objectives: The incidence of severe and moderate forms of DKA as the initial presentation of type 1 diabetes mellitus (T1D) is increasing, especially during the COVID-19 pandemic. This poses a higher risk of developing cerebral edema a
Externí odkaz:
https://doaj.org/article/6f19ec54b7e0425599a3d273947db545
Autor:
Ana Milardović, Ivona Butorac Ahel, Arijan Verbić, Kristina Lah Tomulić, Melita Težak, Iva Bilić Čače
Publikováno v:
Medicina Fluminensis. 58:283-294
Cilj: Cilj istraživanja bio je utvrditi pojavnost, kliničke karakteristike te ishod prijevremeno rođene dojenčadi, liječene na Odjelu intenzivnog liječenja djece Klinike za pedijatriju Kliničkog bolničkog centra Rijeka, u razdoblju 2014. –
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f3fe74d36ae98e7ed5fca7f110169f58
https://doi.org/10.21860/medflum2022_281002
https://doi.org/10.21860/medflum2022_281002
Autor:
Kristina Baraba Dekanić, Ivona Butorac Ahel, Lucija Ružman, Jasmina Dolinšek, Jernej Dolinšek, Goran Palčevski
Publikováno v:
Gastroenterology Research and Practice, Vol 2019 (2019)
Introduction. Celiac disease (CD) is an autoimmune disease triggered by gluten in genetically predisposed individuals. Despite the increasing prevalence of CD, many patients remain undiagnosed. Standard serology tests are expensive and invasive, so s
Externí odkaz:
https://doaj.org/article/7336f7e028fc4490b2a43d87104b5df4
Autor:
Ana Šimunović, Arijan Verbić, Ana Milardović, Aleksandar Ovuka, Ivona Butorac-Ahel, Srđan Banac, Kristina Lah Tomulić
Publikováno v:
Medicina Fluminensis
Volume 57
Issue 2
Medicina Fluminensis : Medicina Fluminensis
Volume 57
Issue 2
Medicina Fluminensis : Medicina Fluminensis
Sažetak. Cilj: Utvrditi metode liječenja bolesnika koji su zaprimljeni na Odjel intenzivnog liječenja djece (OILD) zbog patološkog sadržaja u prsištu. Cilj je također utvrditi indikacije za postavljanje pleuralne drenaže, tehnike postavljanja
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47079804fd429e4389064bded8d611ab
https://doi.org/10.21860/medflum2021_371661
https://doi.org/10.21860/medflum2021_371661
Autor:
Ivona Butorac Ahel, Kristina Baraba Dekanić, Lucija Ružman, Marina Milinović, Goran Palčevski
Publikováno v:
Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9ed4f2f9e8184a66f14af0c803528fd4
https://doi.org/10.1136/archdischild-2021-europaediatrics.274
https://doi.org/10.1136/archdischild-2021-europaediatrics.274
Publikováno v:
Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::74df612db1536e961ecead2b0bd04e93
https://doi.org/10.1136/archdischild-2021-europaediatrics.273
https://doi.org/10.1136/archdischild-2021-europaediatrics.273
Publikováno v:
Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::74a7641da6811a3d5a0be6b445cd969c
https://doi.org/10.1136/archdischild-2021-europaediatrics.217
https://doi.org/10.1136/archdischild-2021-europaediatrics.217
Autor:
Ivona Butorac Ahel, Kristina Lah Tomulić, Jelena Radić Nišević, Silvije Segulja, Kristina Baraba Dekanić, Igor Prpić, Senada Serifi, Inge Vlašić Cicvarić, Aleksandar Ovuka, Ivana Kolić
Publikováno v:
Genes
Genes, Vol 12, Iss 1379, p 1379 (2021)
Volume 12
Issue 9
Genes, Vol 12, Iss 1379, p 1379 (2021)
Volume 12
Issue 9
Glucose transporter type 1 (GLUT1) is the most important energy carrier of the brain across the blood–brain barrier, and a genetic defect of GLUT1 is known as GLUT1 deficiency syndrome (GLUT1DS). It is characterized by early infantile seizures, dev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eec367e3e98c5d650860fadb9bc0b704
https://pubmed.ncbi.nlm.nih.gov/34573360
https://pubmed.ncbi.nlm.nih.gov/34573360
Autor:
Dora Palcevski, Srećko Severinski, Kristina Baraba Dekanić, Ana Milardović, Ivona Butorac Ahel, Kristina Lah Tomulić
Publikováno v:
Journal of Pediatric Endocrinology and Metabolism
Volume 34
Issue 8
Volume 34
Issue 8
Objectives Hyperglycemic hyperosmolar state (HHS) is one of the most severe acute complications of diabetes mellitus (DM) characterized by severe hyperglycemia and hyperosmolality without significant ketosis and acidosis. What is new? Since HHS in th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3fca8409a53b50802293c6aeabc5f5c8
https://repository.medri.uniri.hr/islandora/object/medri:6624/datastream/FILE0
https://repository.medri.uniri.hr/islandora/object/medri:6624/datastream/FILE0
