Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Valentina Uroić"'
Autor:
Dominika Głąbska, Valentina Uroić, Dominika Guzek, Eva Pavić, Sandra Bival, Kamila Jaworska, Zlatko Giljević, Ewa Lange
Publikováno v:
Nutrients, Vol 10, Iss 9, p 1278 (2018)
Although the role of vitamin D is well known, the possibility of assessing its intake may be constricted in countries with no vitamin D data in food composition tables, as in the case of Croatia. The aim of the presented study was to adjust the VIDEO
Externí odkaz:
https://doaj.org/article/5a8f10c16faf49f38d7c4a6e5c8d0d91
Autor:
Valentina Uroić, Filip Mustač, Zrinka Šmuljić, Eva Pavić, Rea Levicki, Maja Baretić, Sandra Bival, Martina Matovinović
Publikováno v:
Obesity Reviews. 21
Publikováno v:
Acta Clinica Croatica
SUMMARY Gastrointestinal tract is an important connector between food intake and body weight, it senses basic tastes in a similar manner as the tongue. The aim of the study was to find out how gut hormone glucagon-like peptide-1 (GLP-1) influences ta
Autor:
Valentina Uroić
Publikováno v:
Posebna izdanja HAZU. Prilozi za strategiju hrvatskog razvoja. 33:83-92
Publikováno v:
Acta clinica Croatica
Volume 58.
Issue 2.
Volume 58.
Issue 2.
Gastrointestinal tract is an important connector between food intake and body weight, it senses basic tastes in a similar manner as the tongue. The aim of the study was to find out how gut hormone glucagon-like peptide-1 (GLP-1) influences taste pref
Autor:
Valentina Uroić, Ksenija Fumić, Ana Škaričić, Dunja Rogić, Ivo Barić, Tamara Žigman, Danijela Petković Ramadža, Marija Zekušić
Publikováno v:
Clin Mass Spectrom
Tyrosinemia type 1 is an autosomal recessive aminoacidopathy caused by fumarylacetoacetate hydrolase (FAH) deficiency. Consequently, tyrosine and its metabolites accumulate, resulting in liver and kidney toxicity. Symptoms of the disease usually mani
Autor:
Ana Škaričić, Tamara Žigman, Danijela Petković Ramadža, Dunja Rogić, Nenad Vukojević, Valentina Uroić, Véronique Rüfenacht, Ksenija Fumić, Ivo Barić, Marija Zekušić
Publikováno v:
Biochemia Medica
Volume 28
Issue 3
Volume 28
Issue 3
Gyrate atrophy (GA) of the choroid and retina is a rare autosomal recessive disorder that occurs due to deficiency of the mitochondrial enzyme ornithine aminotransferase (OAT). Hyperornithinemia causes degeneration of the retina with symptoms like my
Autor:
Maja Baretić, Ivana Pavlić Renar, Eva Pavić, Martina Matovinovic Osvatic, Nada Rabađija, Nataša Rojnić Putarek, Carolina Koletić, Valentina Uroić
Publikováno v:
Minerva endocrinologica. 43(1)
Background The transition for type 1 diabetes patients from pediatric to adult diabetology care is challenging process for both medical team and patients. Adult diabetology usually insists on stricter goals and focuses on increased empowerment and se