Zobrazeno 1 - 10
of 82
pro vyhledávání: '"Ninković Dorotea"'
Autor:
Ninković, Dorotea
Niti jedna prirođena srčana greška, neovisno o složenosti, nije poseban entitet, već je rezultat složene interakcije više ili manje poznatih embrioloških i genskih čimbenika, čimbenika okoline u perikoncepcijskom razdoblju te majčinih živ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______4137::2197de62e16b5d7280bcfb57300f3afd
https://urn.nsk.hr/urn:nbn:hr:105:026068
https://urn.nsk.hr/urn:nbn:hr:105:026068
Publikováno v:
Liječnički vjesnik
Volume 145
Issue Supp 2
Volume 145
Issue Supp 2
Urea cycle disorders are a group of metabolic disorders, caused by deficiency of one of the enzymes in the urea cycle, presenting with hyperammonemia triggered by catabolism or protein overload. Newborns with severe mutations in the urea cycle, unles
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______951::b0f3e0874a91a39882ad8c8e80819832
https://hrcak.srce.hr/file/438164
https://hrcak.srce.hr/file/438164
Autor:
Dilber, Daniel, Šarić, Dalibor, Bartoniček, Dorotea, Mihalec, Marina, Bakoš, Matija, Anić, Darko, Belina, Dražen, Đurić, Željko, Planinc, Mislav, Rubić, Filip, Matić, Toni, Cvitković, Miran, Dessardo, Sandro, Galić, Slobodan, Zvonar, Vanja, Ille-Matić, Vanja, Grizelj, Ruža, Dessardo, Nada Sindičić, Ninković, Dorotea, Čolak, Željko
Publikováno v:
Lijecnicki Vjesnik; 2023 Supplement, Vol. 145, p62-66, 5p
Autor:
Sindičić Dessardo Nada, Vuković Jurica, Živković Petra, Antabak Anko, Grizelj Ruža, Benjak Vesna, Pasini Miram, Vukšić Iva, Ćaleta Tomislav, Sabolić Ivana, Ninković Dorotea, Filipović-Grčić Boris, Luetić Tomislav, Ćavar Stanko, Dasović Buljević Andrea
Publikováno v:
Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee7767714b44a47d75e6fbe723616f64
https://doi.org/10.1136/archdischild-2021-europaediatrics.136
https://doi.org/10.1136/archdischild-2021-europaediatrics.136
Autor:
Čičak Ana Marija, Ćaleta Tomislav, Sindičić Dessardo Nada, Perkov Dražen, Ninković Dorotea, Filipović-Grčić Boris, Dasović Buljević Andrea, Radoš Marko, Grizelj Ruža, Vukšić Iva, Benjak Vesna
Publikováno v:
Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::10a09e29073aabc2888a55b8a8e42616
https://doi.org/10.1136/archdischild-2021-europaediatrics.124
https://doi.org/10.1136/archdischild-2021-europaediatrics.124
Autor:
Vukšić Iva, Grizelj Ruža, Ninković Dorotea, Bunoza Branka, Benjak Vesna, Radoš Milan, Grðan Petra, Dasović Buljević Andrea, Ćaleta Tomislav
Publikováno v:
Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d4a1c5f84f2ffaae7726b4e6eb3f170a
https://doi.org/10.1136/archdischild-2021-europaediatrics.125
https://doi.org/10.1136/archdischild-2021-europaediatrics.125
Autor:
Sindičić Dessardo, Nada, Čičak, Ana Marija, Grizelj, Ruža, Vukšić, Iva, Benjak, Vesna, Dasović Buljević, Andrea, Ninković, Dorotea, Ćaleta, Tomislav, Filipović-Grčić, Boris, Perkov, Dražen, Radoš, Marko
Vein of Galen aneurysmal malformation (VGAM) is a complex congenital cerebro-vascular malformation. Despite some controversy, the overall prognosis of VGAM has improved over time. We present a series of VGAM patients with hyperdynamic heart failure d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::ab34e81cf516961a318bf695d1ef09af
https://doi.org/10.1136/archdischild-2021-europaediatrics.124
https://doi.org/10.1136/archdischild-2021-europaediatrics.124
Autor:
Čičak, Ivana, Novak, Milivoj, Cvitković, Miran, Galić, Slobodan, Matić, Toni, Rubić, Filip, Malčić, Ivan, Šarić, Dalibor, Bartoniček, Dorotea, Dilber, Daniel, Belina, Dražen, Benjak, Vesna, Dasović Buljević, Andrea, Grizelj, Ruža, Filipović-Grčić, Boris, Ninković, Dorotea, Vuković, Jurica, Omerza, Lana, Aničić, Mirna, Antabak, Anko, Ćuk, Mario
We report the case of a full term male child with multiple organ dysfunctions caused by mutations of the TTN gene
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::43213b1ec0342be6971faa9f9338231e
https://www.bib.irb.hr/1196992
https://www.bib.irb.hr/1196992
Autor:
Ille, Vanja, Petković Ramadža, Danijela, Žigman, Tamara, Filipović- Grčić, Boris, Grizelj, Ruža, Ninković, Dorotea, Bartoniček, Dorotea, Škaričić, Ana, Bilandžija Kuš, Iva, Mesarić, Nikola, Krnjak, Goran, Fumić, Ksenija, Barić, Ivo
Multiple acyl-coenzyme A dehydrogenase deficiency (MADD) or glutaric aciduria type II is a rare, autosomal recessive disorder of fatty acid and amino acid oxidation. Disease is caused by pathogenic mutations in ETFA or ETFB genes, which encode two su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::41c353cac376de9f2c8df93dcdd56037
https://www.bib.irb.hr/1196189
https://www.bib.irb.hr/1196189
Autor:
Petković Ramadža, Danijela, Žigman, Tamara, Grizelj, Ruža, Ninković, Dorotea, Omerza, Lana, Aničić, Mirna, Ćorić, Marijana, Mayr, Johannes A., Feichtinger, René, Wortmann, Saskia, Prokisch, Holger, Fumić, Ksenija, Vuković, Jurica, Barić, Ivo
Mitochondrial DNA depletion syndromes (MDS) are a group of autosomal recessive disorders caused by disruption of mtDNA maintenance that results in reduced mtDNA content and disturbed energy production. MDS are genetically and phenotypically heterogen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::e103df71a79da7588dd3f6ef7ee451ed
https://doi.org/10.1136/archdischild-2021-europaediatrics.107
https://doi.org/10.1136/archdischild-2021-europaediatrics.107