Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Martin Ćuk"'
Publikováno v:
International Urology and Nephrology. 53:1529-1534
Purpose To determine the association between urine osmolality (Uosm) in patients with primary monosymptomatic enuresis (PMNE) and response to desmopressin (dDAVP) lyophilisate. Methods This was a prospective cohort study that included 419 children wi
Publikováno v:
Abstracts.
Autor:
Zrinjka Mišak, Mario Mašić, Martin Ćuk, Ivana Trivić, Sanja Kolaček, Tonći Grmoja, Alenka Gagro, Ivančica Škarić, Iva Hojsak, Jurica Vuković, Oleg Jadrešin, Ana Močić Pavić
Publikováno v:
Abstracts.
Autor:
Adela Arapović, Dalibor Šarić, Martin Ćuk, Vesna Herceg-Čavrak, Dejan Balažin, Hrvoje Kniewald, Vesna Jureša, Vera Musil, Ivana Trutin, Nikolina Benco, Bojan Jelaković, Đurðica Košuljandić, Višnja Tokić Pivac, Bernardica Valent Morić
Publikováno v:
Abstracts.
Autor:
Tamara Nikuševa Martić, Slaven Abdović, Matija Horaček, Martin Ćuk, Maja Oroz, Marija Šenjug Perica, Petar Šenjug, Danica Galešić Ljubanović
Publikováno v:
Croatian Medical Journal
Alport syndrome (AS) is a genetically heterogenic, structural disorder of the glomerular basement membrane (GBM) due to the mutation of COL4A3, COL4A4, or COL4A5 genes, which clinically presents as progressive hematuric nephritis with ultrastructural
Autor:
Slaven Abdović, Antonella Geljic, Milan Milošević, Martin Ćuk, N Cekada, M Bastic, S Fusic, Z Bahtijarevic
Publikováno v:
World Journal of Urology. 37:1973-1979
To assess the prediction model for late-presenting posterior urethral valve (PUV) in boys with lower urinary tract symptoms (LUTS) using artificial neural network (ANN). 408 boys aged 3–17 years (median 7.2 years) with LUTS were examined and had bl
Autor:
Boris Keren, Femke Latta, Elise Brimble, Hester Y. Kroes, Maria Szczepańska, Maria I. Tejada, Rutger A.J. Nievelstein, Maria Ruzhnikov, David Germanaud, Dominik N. Müller, Karl-Peter Schlingmann, Martin Konrad, Gijs A C Franken, Anne-Claude Tabet, Cyril Mignot, Martin Ćuk, Joost G. J. Hoenderop, René J. M. Bindels, Luis Alfonso Martínez-Cruz, Jeroen H. F. de Baaij, Jonathan I. Levy, Felix Claverie-Martin
Publikováno v:
Human Mutation, 42, 473-486
Human Mutation
Human Mutation, Wiley, 2021, ⟨10.1002/humu.24182⟩
Human Mutation, 42, 4, pp. 473-486
Human Mutation
Human Mutation, Wiley, 2021, ⟨10.1002/humu.24182⟩
Human Mutation, 42, 4, pp. 473-486
Hypomagnesemia, seizures, and intellectual disability (HSMR) syndrome is a rare disorder caused by mutations in the cyclin M2 (CNNM2) gene. Due to the limited number of cases, extensive phenotype analyses of these patients have not been performed, hi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::badbe08f4c92db6d3bd966157d385104
http://hdl.handle.net/2066/238837
http://hdl.handle.net/2066/238837
Publikováno v:
Pediatric Allergy ISBN: 9783030182816
Adverse drug reactions might rise as a result of reaction to the drug molecule or any of the excipients Allergic reactions caused by corticosteroids have rarely been reported Due to the possible contamination with cow’s milk proteins, lactose used
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d2dd4c26624b664e836152e048489a8
https://doi.org/10.1007/978-3-030-18282-3_51
https://doi.org/10.1007/978-3-030-18282-3_51
Publikováno v:
European Journal of Pediatric Surgery Reports, Vol 07, Iss 01, Pp e79-e82 (2019)
European Journal of Pediatric Surgery Reports
European Journal of Pediatric Surgery Reports
We report the case of a 4-year-old boy who first presented with acute pyelonephritis at the age of 6 months. Diagnostic workup revealed high-grade bilateral vesicourethral reflux (VUR). At the age of 18 months, a bulking agent was used to treat bilat
Autor:
Krešimir Galešić, Ivica Horvatić, Mario Ilić, Martin Ćuk, Matija Crnogorac, Danica Galešić Ljubanović
Publikováno v:
Liječnički vjesnik
Volume 138
Issue 9-10
Volume 138
Issue 9-10
U ovom radu prikazano je 6 bolesnika s hipokaliemijskom metaboličkom alkalozom kod kojih je postavljena dijagnoza Bartterova ili Gitelmanova sindroma. Oba su sindroma posljedica mutacija gena za prijenosnike uključene u reapsorpciju natrija, klorid