Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Bilić Čače Iva"'
Publikováno v:
Medicina Fluminensis
Volume 59
Issue 1
Volume 59
Issue 1
Cilj: Prikazati klinički tijek dviju djevojčica s kongenitalnom crijevnom opstrukcijom uzrokovanom duodenalnom membranom, liječenih od ove rijetke anomalije u Kliničkom bolničkom centru Rijeka u razmaku od pet mjeseci. Prikaz slučaja: Kod prve
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::b0c0c21a80cdc59e37a841fa84a26b73
https://repository.medri.uniri.hr/islandora/object/medri:7411/datastream/FILE0
https://repository.medri.uniri.hr/islandora/object/medri:7411/datastream/FILE0
Autor:
Milardović, Ana, Bilić Čače, Iva, Težak, Melita, Lah Tomulić, Kristina, Verbić, Arijan, Butorac Ahel, Ivona
Publikováno v:
Medicina Fluminensis : Medicina Fluminensis
Volume 58
Issue 3
Medicina Fluminensis
Volume 58
Issue 3
Medicina Fluminensis
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=dedup_wf_001::b506587d46c4b1e7189538885d729d40
https://urn.nsk.hr/urn:nbn:hr:184:261830
https://urn.nsk.hr/urn:nbn:hr:184:261830
The DNMT3B gene codes for DNA methyltransferase 3b (DNMT3b), a protein required for genome-wide de novo methylation during the early stage of embryonic development. Evidence suggested that impaired DNA methylation could be a risk factor for congenita
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::a627325b679da87388179c1c5f376266
https://www.bib.irb.hr/1191454
https://www.bib.irb.hr/1191454
Autor:
Vraneković, Jadranka, Barišić, Anita, Majstorović, Dijana, Babić Božović, Ivana, Bilić Čače, Iva Brajenović Milić, Bojana
Background: Approximately 50% of people with Down syndrome (DS) have congenital heart defect (CHD), mostly septal defect. Better understanding of the etiology of CHD is fundamental to improve diagnosis, clinical management and counselling. The DNA me
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::1c0699af499e90f3c509d28eb16d7a85
https://www.bib.irb.hr/1191634
https://www.bib.irb.hr/1191634
Akademický článek
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Publikováno v:
Archives of Obstetrics and Gynecology
Volume 1
Issue 4
Volume 1
Issue 4
Spontaneous skull fractures are particularly interesting due to the vague circumstances of their occurrence. Apart from scientific and professional significance, fetal fractures may have medico-legal implications for obstetricians and midwives becaus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::813c14343765b6e61e799a5f9677cca1
https://doi.org/10.36879/aog.20.000120
https://doi.org/10.36879/aog.20.000120
Autor:
Vraneković, Jadranka, Babić Božović, Ivana, Slivšek, Goran, Bilić Čače, Iva, Brajenović, Bojana
Congenital heart defects (CHD) are among the most common abnormalities in 40%–60% of Down Syndrome (DS) cases. Most commonly, these are septal defects, including atrial septal defect, ventricular septal defect, and complete atrioventricular canal.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::7d4ba860da68dff5d89c8468562b8de9
https://www.bib.irb.hr/1260410
https://www.bib.irb.hr/1260410
Publikováno v:
In European Journal of Medical Genetics April 2017 60(4):217-219
Publikováno v:
Medicina Fluminensis : Medicina Fluminensis
Volume 52.
Issue 4.
Volume 52.
Issue 4.
CILJ: Intraventrikularno krvarenje (IVH) jedno je od najznačajnijih uzroka oštećenja središnjeg živčanog sustava u prijevremeno rođene novorođenčadi. Niz je istraženih čimbenika rizika za nastanak IVH u prematurusa: genetski, prenatalni, f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::861c33406c83c85d00d309711b641c53
https://urn.nsk.hr/urn:nbn:hr:184:649311
https://urn.nsk.hr/urn:nbn:hr:184:649311
Publikováno v:
Human Heredity; 2020, Vol. 85 Issue 2, p61-65, 5p