Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Anita Spehar Uroic"'
Autor:
Anita Špehar Uroić, Maša Filipović, Alan Šućur, Tomislav Kelava, Nataša Kovačić, Danka Grčević
Publikováno v:
Frontiers in Endocrinology, Vol 15 (2024)
ObjectiveWe compared peripheral blood (PBL) chemokine ligand/receptor profiles in children and adolescents with type 1 diabetes mellitus (T1D) or obesity (OB) (both involving inflammation and vascular complications) to identify their associations wit
Externí odkaz:
https://doaj.org/article/192c9812037043ca87f44dd3fc862a65
Autor:
Anita Špehar Uroić, Nataša Rojnić Putarek, Lucija Kolega Mrkić, Sanja Kusačić-Kuna, Ana Merkler Šorgić, Jadranka Sertić, Sanja Perić, Nevena Krnić
Publikováno v:
Liječnički vjesnik, Vol 145, Iss 5-6, Pp 212-215 (2023)
Sindrom multiple endokrine neoplazije 2B (MEN2B) rijetka je autosomno dominatno nasljedna bolest uzrokovana mutacijama protoonkogena RET. Karakteriziran je pojavom medularnog karcinoma štitnjače već od rane, nerijetko dojenačke dobi, feokromocito
Externí odkaz:
https://doaj.org/article/0cb29b6e012046b18847b84b8731ac6c
Autor:
Valentina Rahelić, Dominika Głąbska, Dominika Guzek, Eva Pavić, Ivana Rumora Samarin, Ana Bogdanić, Anita Špehar Uroić, Nataša Rojnić Putarek, Nevena Krnić
Publikováno v:
Medicina, Vol 56, Iss 4, p 168 (2020)
Background and Objectives: Obesity in children and adolescents results in a number of serious health-related consequences necessitating early treatment. Support from family members and family-focused lifestyle interventions can improve effectiveness
Externí odkaz:
https://doaj.org/article/3e01ed7dd2694bb2ac8e9fc66ff3f909
Autor:
Nataša Rojnić Putarek, Nevena Krnić, Lana Škrgatić, Mihajlo Strelec, Marija Macan, Anita Spehar Uroic, Vesna Kušec, Katja Dumić Kubat
Objective – The aim was to report a case of a 17-year-old girl with marked virilization and secondary amenorrhea due to androgen producing Sertoli-Leydig cell tumor (SLCT). We also provided a brief review of the literature with insight into clinica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31e45badda2f24358587ef912a0c8aca
https://doi.org/10.5457/p2005-114.205.
https://doi.org/10.5457/p2005-114.205.
Autor:
Jadranka Knezevic-Cuca, Zorana Grubić, Marija Maskalan, Miroslav Dumić, Renata Zunec, Nataša Rojnić Putarek, Anita Spehar Uroic, Marija Burek Kamenaric, Katarina Stingl Jankovic
Publikováno v:
Gene. 674
This study included 161 patients: 92 patients had type 1 diabetes (T1D) while 69 patients had a combination of T1D and autoimmune thyroiditis, the so-called autoimmune polyglandular syndrome type 3 variant (APS3v). Those patients, as well as 93 contr
Autor:
Ana Šmaguc, Danijela Petković Ramadža, Vladimir Sarnavka, Vjekoslav Krželj, Bernarda Lozić, Silvija Pušeljić, Valentina Rahelić, Nikola Mesarić, Marina Grubić, Ana Bogdanić, Anita Špehar Uroić, Tamara Žigman, Ruža Grizelj, Jurica Vuković, Duško Mardešić, Ildiko Szatmari, Isabel Rivera, Ksenija Fumić, Ivo Barić
Publikováno v:
Liječnički vjesnik, Vol 145, Iss 1-2, Pp 1-11 (2023)
The aim of our study was to describe the characteristics of patients with classical galactosemia in Croatia, with the description of patients with galactokinase deficiency and a patient who was a double heterozygote for mutations of the galactose-1-p
Externí odkaz:
https://doaj.org/article/172aeb75c94342c59411f163b00e629a
Autor:
Natasa, Rojnic Putarek, Jasenka, Ille, Anita, Spehar Uroic, Veselin, Skrabic, Gordana, Stipancic, Nevena, Krnic, Ana, Radica, Igor, Marjanac, Srecko, Severinski, Alen, Svigir, Ana, Bogdanic, Miroslav, Dumic
Publikováno v:
Pediatric diabetes. 16(6)
The incidence of type 1 diabetes mellitus (T1DM) among children and adolescents increased during the last 50 yr. The T1DM incidence in Croatia was 8.87/100.000/yr over 1995-2003, with an annual increase of 9%, which placed Croatia among countries wit
Autor:
Miroslav, Dumić, Anita Spehar, Uroic, Igor, Francetić, Zvonimir, Puretić, Danica, Matisić, Petar, Kes, Martina, Mikecin, Zeljko, Reiner
Publikováno v:
Lijecnicki vjesnik. 129(5)
Homozygous familial hypercholesterolemia (FH) is a rare autosomal dominant disorder caused by mutations in the low-density-lipoprotein (LDL) receptor gene. It occurs with a frequency of approximately 1 per million persons world-wide. Clinically, homo