Zobrazeno 1 - 10
of 107
pro vyhledávání: '"Kristina Gotovac"'
Autor:
Blazekovic, Antonela1,2 antonela.blazekovic@mef.hr, Jercic, Kristina Gotovac1,3, Devedija, Sabina4, Borovecki, Fran1,3
Publikováno v:
Frontiers in Cognition. 2024, p1-10. 10p.
Publikováno v:
Frontiers in Cognition, Vol 3 (2024)
Parkinson's disease (PD) is a complex disorder that is influenced by multiple genetic risk factors. There is a significant heterogeneity in PD presentation, both pathologically and clinically. Some of the most common and important symptoms affecting
Externí odkaz:
https://doaj.org/article/0b562b92ba0f4019966b2fc57472c186
Autor:
Bučić, Dinea, Bakoš, Matija, Ramadža, Danijela Petković, Bartoniček, Dorotea, Dilber, Daniel, Rubić, Filip, Belina, Dražen, Rako, Ivana, Jerčić, Kristina Gotovac, Borovečki, Fran, Jakovčević, Antonia, Barić, Ivo, Žigman, Tamara
Publikováno v:
In Human Gene February 2024 39
Akademický článek
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Autor:
Katja K. Dumic, Zorana Grubic, Vesna Kusec, Duje Braovac, Kristina Gotovac, Maja Vinkovic, Maja Vucinic, Miroslav Dumic
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
ObjectiveCongenital adrenal hyperplasia (CAH) owing to 21-hydroxylase deficiency (21-OHD) is a rare autosomal recessive disorder caused by pathological variants in the CYP21A2 gene. After a high prevalence of classic 21-OHD CAH in the Romani populati
Externí odkaz:
https://doaj.org/article/e78401ebd2f44716a9af33ec243da054
Publikováno v:
Türk Nöroloji Dergisi, Vol 28, Iss 2, Pp 118-121 (2022)
Neurodegeneration with brain iron accumulation (NBIA) encompasses a number of heritable disorders affecting children and adults characterized by diverse clinical manifestations and brain iron deposition detected on magnetic resonance imaging (MRI). T
Externí odkaz:
https://doaj.org/article/bceab3c0c1fd4d609cc87322286defbf
Autor:
Mario Habek, Antonela Blazekovic, Kristina Gotovac Jercic, Nela Pivac, Tiago Fleming Outero, Fran Borovecki, Vesna Brinar
Publikováno v:
Biomedicines, Vol 11, Iss 8, p 2209 (2023)
The aim of this study was to perform a genome-wide expression analysis of whole-blood samples from people with optic neuritis (ON) and to determine differentially expressed mRNAs compared to healthy control subjects. The study included eight people w
Externí odkaz:
https://doaj.org/article/d747763ba34442cf9c5262da59108d8c
Publikováno v:
World Journal of Surgical Oncology, Vol 19, Iss 1, Pp 1-6 (2021)
Abstract Background Li-Fraumeni is a rare autosomal dominant cancer predisposition syndrome. The basis is a germline mutation of TP53 gene which encodes tumor suppressor protein resulting in early onset of tumors, most often breast cancer, soft tissu
Externí odkaz:
https://doaj.org/article/1b61feec495b4937aa63c5cf2dbb285a
Autor:
Perkovic, Romana1 romana.per@gmail.com, Jercic, Kristina Gotovac2, Francic, Manuela3, Ozretic, David4, Borovecki, Fran2
Publikováno v:
Turkish Journal of Neurology / Turk Noroloji Dergisi. Jun2022, Vol. 28 Issue 2, p118-121. 4p.
Autor:
Jerčić, Kristina Gotovac1 kristina.gotovac@kbc-zagreb.hr, Blažeković, Antonela2, Hančević, Mirea1, Bilić, Ervina1, Borovečki, Fran1,3
Publikováno v:
Croatian Medical Journal. Feb2020, Vol. 61 Issue 1, p62-65. 4p.