| Natural history, treatment, and long-term follow up of patients with multiple endocrine neoplasia type 2B: an international, multicentre, retrospective study F Castinetti, SG Waguespack, A Machens, S Uchino, K Hasse-Lazar, ... The lancet Diabetes & endocrinology 7 (3), 213-220, 2019 | 129 | 2019 |
| Incidence of type 1 diabetes mellitus in 0 to 14‐yr‐old children in Croatia–2004 to 2012 study N Rojnic Putarek, J Ille, A Spehar Uroic, V Skrabic, G Stipancic, N Krnic, ... Pediatric diabetes 16 (6), 448-453, 2015 | 68 | 2015 |
| Pregnancy outcomes in women with classical congenital adrenal hyperplasia due to 21-hydroxylase deficiency M Dumic, N Janjanin, J Ille, R Zunec, A Špehar, G Zlopasa, I Francetic, ... Journal of Pediatric Endocrinology and Metabolism 18 (9), 887-896, 2005 | 43 | 2005 |
| Debelo dijete M Dumić, A Špehar, N Janjanin Paediatria Croatica 48, 3-8, 2004 | 27 | 2004 |
| Arterial stiffness as a measure of cardiovascular risk in obese adolescents and adolescents with diabetes type 1 K Putarek, L Banfic, M Pasalic, N Krnic, A Spehar Uroic, N Rojnic Putarek Journal of Pediatric Endocrinology and Metabolism 31 (12), 1315-1323, 2018 | 18 | 2018 |
| Šećerna bolest u adolescenata M Dumić, A Špehar Uroić Medicus 19 (1_Adolescencija_2), 27-34, 2010 | 15 | 2010 |
| Three-year-old boy--a homozygote for familiar hypercholesterolemia M Dumić, AS Uroic, I Francetić, Z Puretić, D Matisić, P Kes, M Mikecin, ... Lijecnicki vjesnik 129 (5), 130-133, 2007 | 13 | 2007 |
| Nonclassic 21-hydroxylase deficiency in Croatia M Dumic, J Ule, R Zunec, V Plavsic, I Francetic, V Skrabic, N Janjanin, ... Journal of Pediatric Endocrinology and Metabolism 17 (2), 157-164, 2004 | 12 | 2004 |
| Five patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency (one with associated neuroblastoma) discovered in three generations of one family N Janjanin, M Dumic, V Skrabic, V Kusec, Z Grubic, A Spehar Uroic Hormone research 67 (3), 111-116, 2007 | 11 | 2007 |
| Primary hypothyroidism and nipple hypoplasia in a girl with Wolcott–Rallison syndrome A Špehar Uroić, V Mulliqi Kotori, N Rojnić Putarek, V Kušec, M Dumić European journal of pediatrics 173, 529-531, 2014 | 10 | 2014 |
| Human Leukocyte Antigen class II polymorphisms among Croatian patients with type 1 diabetes and autoimmune polyglandular syndrome type 3 variant Z Grubic, NR Putarek, M Maskalan, R Zunec, KS Jankovic, MB Kamenaric, ... Gene 674, 93-97, 2018 | 8 | 2018 |
| Role of parents in body mass reduction in children with obesity—Adherence and success of 1-year participation in an intervention program V Rahelić, D Głąbska, D Guzek, E Pavić, I Rumora Samarin, A Bogdanić, ... Medicina 56 (4), 168, 2020 | 7 | 2020 |
| Importance of immediate thiamine therapy in children with suspected thiamine-responsive megaloblastic anemia—report on two patients carrying a novel SLC19A2 gene mutation AS Uroic, D Milenkovic, E De Franco, E Bilic, NR Putarek, N Krnic Journal of pediatric genetics 11 (03), 236-239, 2022 | 6 | 2022 |
| IL12RB2 Gene Is Associated with the Age of Type 1 Diabetes Onset in Croatian Family Trios M Pehlić, D Vrkić, V Škrabić, A Jerončić, G Stipančić, AŠ Urojić, ... Plos one 7 (11), e49133, 2012 | 6 | 2012 |
| Choanal stenosis, hypothelia, deafness, recurrent dacryocystitis, neck fistulas, short stature, and microcephaly: report of a case M Dumić, M Cvitanović, B Ŝarić, A Ŝpehar, S Batinica American journal of medical genetics 113 (3), 295-297, 2002 | 6 | 2002 |
| Skrb djece sa šećernom bolešću. M Dumić, A Špehar Uroić Dijabetes u žena. U_Đelmiš J, Ivanišević M, Metelko Ţ, i suradnici_Zagreb …, 2009 | 5* | 2009 |
| Pretilost u djece–pogled iz klinike versus pristup u praksi E Pavić, V Uroić, N Rojnić Putarek, A Špehar Uroić, N Krnić, J Ille, ... Paediatr Croat 58 (1), 228-232, 2014 | 4 | 2014 |
| Glycosyltransferase B4GALNT1 and type 1 diabetes in Croatian population: clinical investigation V Boraska, V Torlak, V Škrabić, Z Kačić, J Jakšić, G Stipančić, AŠ Uroić, ... Clinical biochemistry 42 (9), 819-822, 2009 | 4 | 2009 |
| Strategije obrazovanja i aktivno učenje u razrednoj nastavi kod učenika s autizmom na primjeru prirodoslovne teme (studija slučaja) D Kiš-Novak, A Špehar Educatio biologiae, 87-97, 2018 | 3 | 2018 |
| The association of HLA class II, CTLA-4 and PTPN22 genetic polymorphisms and β-cell autoantibodies in development of type I diabetes in patients with autoimmune thyroid disease N Rojnić Putarek, Z Grubić, D Grčević, V Kušec, J Knežević-Ćuća, N Krnić, ... 55th annual ESPE (the European Society for Paediatric Endocrinology) meeting …, 2016 | 3 | 2016 |
