Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Anita Špehar Uroić"'
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:
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:
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:
Duje Braovac, Maja Vinkovic, Katja Dumić Kubat, Anita Špehar Uroić, Nevena Krnić, Vesna Kušec
Publikováno v:
Abstracts.
Autor:
Nataša Rojnić Putarek, Anita Špehar Uroić, Lucija Kolega Mrkic, Nevena Krnić, Jadranka Sertić
Publikováno v:
Abstracts.
Publikováno v:
Abstracts.
Autor:
Eva Pavić, Ana Bogdanić, Nataša Rojnić Putarek, Valentina Rahelić, Dominika Guzek, Nevena Krnić, Dominika Głąbska, Anita Špehar Uroić, Ivana Rumora Samarin
Publikováno v:
Medicina
Medicina, Vol 56, Iss 168, p 168 (2020)
Volume 56
Issue 4
Medicina; Volume 56; Issue 4; Pages: 168
Medicina, Vol 56, Iss 168, p 168 (2020)
Volume 56
Issue 4
Medicina; Volume 56; Issue 4; Pages: 168
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
Autor:
Anita Špehar Uroić, Nataša Rojnić Putarek, Elisa De Franco, Dragan Milenkovic, Ernest Bilić, Nevena Krnic
Publikováno v:
J Pediatr Genet
Thiamine-responsive megaloblastic anemia (TRMA) is an autosomal recessive disorder characterized by the development of megaloblastic anemia, diabetes mellitus, and sensorineural deafness. We report on the first two Croatian patients with TRMA, compou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e81b92b57e17f0e509dc5ebf76091127
https://doi.org/10.1055/s-0040-1717136
https://doi.org/10.1055/s-0040-1717136
Autor:
Mariola Pęczkowska, Akihiro Sukurai, Anita Špehar Uroić, Andreas Machens, Laura Fugazzola, Tushar Bandgar, Carla Vaz Ferreira Vargas, Hartmut P. H. Neumann, Martin Schlumberger, Delphine Drui, Patricia Fainstein-Day, Francoise Borson Chazot, Amandine Berdelou, Tom R. Kurzawinski, Delphine Mirebeau-Prunier, Olivier Chabre, Dominique Maiter, Philippe Caron, Gabriella Sanso, Tsuneo Imai, Camilo Jimenez, Frederic Sebag, Márta Korbonits, Atila Patocs, Laura Valerio, Sarka Dvorakova, Claudio Letizia, Srivandana Akshintala, Christian Godballe, Regis Cohen, Eric Baudin, Caterina Mian, Jolanta Krajewska, Rossella Elisei, Laurence Leclerc, Tobias Else, Marc Klein, Kornelia Hasse-Lazar, Thierry Brue, Steven G. Waguespack, Petr Vlcek, Nuria Valdes, Thera P. Links, Ana Luisa Maia, Ana O. Hoff, Henning Dralle, Frederic Castinetti, André Lacroix, Xiao Ping Qi, Maria João Bugalho, Maralyn Druce, Nelson Wohllk, Barbara Jarzab, Birke Bausch, Delmar M. Lourenço, John Glod, Shinya Uchino, Caroline Brain, Letizia Canu, Charis Eng, Marta Barontini, Jes Sloth Mathiesen, Antoine Tabarin, Elizabeth G. Grubbs, Lucieli Ceolin, Sandrine Laboureau
Publikováno v:
The Lancet Diabetes and Endocrinology
The Lancet Diabetes and Endocrinology, 2019, 7 (3), pp.213-220. ⟨10.1016/S2213-8587(18)30336-X⟩
Castinetti, F, Waguespack, S G, Machens, A, Uchino, S, Lazaar, K, Sanso, G, Else, T, Dvorakova, S, Qi, X P, Elisei, R, Maia, A L, Glod, J, Lourenço, D M, Valdes, N, Mathiesen, J, Wohllk, N, Bandgar, T R, Drui, D, Korbonits, M, Druce, M R, Brain, C, Kurzawinski, T, Patocs, A, Bugalho, M J, Lacroix, A, Caron, P, Fainstein-Day, P, Borson Chazot, F, Klein, M, Links, T P, Letizia, C, Fugazzola, L, Chabre, O, Canu, L, Cohen, R, Tabarin, A, Spehar Uroic, A, Maiter, D, Laboureau, S, Mian, C, Peczkowska, M, Sebag, F, Brue, T, Mirebeau-Prunier, D, Leclerc, L, Bausch, B, Berdelou, A, Sukurai, A, Vlcek, P, Krajewska, J, Barontini, M, Vaz Ferreira Vargas, C, Valerio, L, Ceolin, L, Akshintala, S, Hoff, A, Godballe, C, Jarzab, B, Jimenez, C, Eng, C, Imai, T, Schlumberger, M, Grubbs, E, Dralle, H, Neumann, H P & Baudin, E 2019, ' Natural history, treatment, and long-term follow up of patients with multiple endocrine neoplasia type 2B : an international, multicentre, retrospective study ', The Lancet Diabetes & Endocrinology, vol. 7, no. 3, pp. 213-220 . https://doi.org/10.1016/S2213-8587(18)30336-X
The Lancet. Diabetes & Endocrinology
The Lancet. Diabetes & Endocrinology, 2019, 7 (3), pp.213-220. ⟨10.1016/S2213-8587(18)30336-X⟩
Lancet Diabetes & Endocrinology, 7(3), 213-220. ELSEVIER SCIENCE INC
The Lancet Diabetes and Endocrinology, 2019, 7 (3), pp.213-220. ⟨10.1016/S2213-8587(18)30336-X⟩
Castinetti, F, Waguespack, S G, Machens, A, Uchino, S, Lazaar, K, Sanso, G, Else, T, Dvorakova, S, Qi, X P, Elisei, R, Maia, A L, Glod, J, Lourenço, D M, Valdes, N, Mathiesen, J, Wohllk, N, Bandgar, T R, Drui, D, Korbonits, M, Druce, M R, Brain, C, Kurzawinski, T, Patocs, A, Bugalho, M J, Lacroix, A, Caron, P, Fainstein-Day, P, Borson Chazot, F, Klein, M, Links, T P, Letizia, C, Fugazzola, L, Chabre, O, Canu, L, Cohen, R, Tabarin, A, Spehar Uroic, A, Maiter, D, Laboureau, S, Mian, C, Peczkowska, M, Sebag, F, Brue, T, Mirebeau-Prunier, D, Leclerc, L, Bausch, B, Berdelou, A, Sukurai, A, Vlcek, P, Krajewska, J, Barontini, M, Vaz Ferreira Vargas, C, Valerio, L, Ceolin, L, Akshintala, S, Hoff, A, Godballe, C, Jarzab, B, Jimenez, C, Eng, C, Imai, T, Schlumberger, M, Grubbs, E, Dralle, H, Neumann, H P & Baudin, E 2019, ' Natural history, treatment, and long-term follow up of patients with multiple endocrine neoplasia type 2B : an international, multicentre, retrospective study ', The Lancet Diabetes & Endocrinology, vol. 7, no. 3, pp. 213-220 . https://doi.org/10.1016/S2213-8587(18)30336-X
The Lancet. Diabetes & Endocrinology
The Lancet. Diabetes & Endocrinology, 2019, 7 (3), pp.213-220. ⟨10.1016/S2213-8587(18)30336-X⟩
Lancet Diabetes & Endocrinology, 7(3), 213-220. ELSEVIER SCIENCE INC
© 2019 Elsevier Ltd. All rights reserved.
Background: Multiple endocrine neoplasia type 2B is a rare syndrome caused mainly by Met918Thr germline RET mutation, and characterised by medullary thyroid carcinoma, phaeochromocytoma, and extra-endoc
Background: Multiple endocrine neoplasia type 2B is a rare syndrome caused mainly by Met918Thr germline RET mutation, and characterised by medullary thyroid carcinoma, phaeochromocytoma, and extra-endoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb4c67f529d8d0b7cbd0f6301632ecc3
https://hdl.handle.net/10451/54220
https://hdl.handle.net/10451/54220