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Plasma Fucosylated Glycans and C-Reactive Protein as Biomarkers of HNF1A-MODY in Young Adult-Onset Nonautoimmune Diabetes

Diabetes care, 2019-01, Vol.42 (1), p.17-26

2019

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Primary hypothyroidism and nipple hypoplasia in a girl with Wolcott–Rallison syndrome

European journal of pediatrics, 2014-04, Vol.173 (4), p.529-531

2014

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Two siblings with triple A syndrome and novel mutation presenting as hereditary polyneuropathy

European journal of pediatrics, 2011-03, Vol.170 (3), p.393-396

2011

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Arterial stiffness as a measure of cardiovascular risk in obese adolescents and adolescents with diabetes type 1

Journal of pediatric endocrinology & metabolism : JPEM, 2018-12, Vol.31 (12), p.1315

2018

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Relative Frequency of Islet Autoimmunity in Children and Adolescents with Autoimmune Thyroid Disease

Journal of clinical research in pediatric endocrinology, 2023-12, Vol.15 (4), p.348-355

2023

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Human Leukocyte Antigen class II polymorphisms among Croatian patients with type 1 diabetes and autoimmune polyglandular syndrome type 3 variant

Gene, 2018-10, Vol.674, p.93-97

2018

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Importance of Immediate Thiamine Therapy in Children with Suspected Thiamine-Responsive Megaloblastic Anemia—Report on Two Patients Carrying a Novel SLC19A2 Gene Mutation

Journal of pediatric genetics (Birmingham, Ala.), 2022-09, Vol.11 (3), p.236-239

2022

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Incidence of type 1 diabetes mellitus in 0 to 14-yr-old children in Croatia - 2004 to 2012 study

Pediatric diabetes, 2015-09, Vol.16 (6), p.448-453

2015

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Role of Parents in Body Mass Reduction in Children with Obesity-Adherence and Success of 1-Year Participation in an Intervention Program

Medicina (Kaunas, Lithuania), 2020-04, Vol.56 (4), p.168

2020

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Jesu li bubrežne malformacije jedno od obilježja sindroma MEN2B? – prikaz bolesnika i pregled literature

Liječnički vjesnik, 2023-01, Vol.145 (5-6), p.212-215

2023

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ACUTE RESPIRATORY DISTRESS SYNDROME IN A FOUR-YEAR-OLD BOY WITH DIABETIC KETOACIDOSIS - CASE REPORT

Acta clinica Croatica (Tisak), 2018-09, Vol.57 (3), p.588-592

2018

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Incidence of type 1 diabetes mellitus in 0 to 14-yr-old children in Croatia - 2004 to 2012 study: Continuous rise in T1DM incidence in Croatia

Pediatric diabetes, 2015-09, Vol.16 (6), p.448-453

2015

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Pretilost u dječjoj dobi

Medicus (Zagreb, Croatia : 1992), 2018-04, Vol.27 (1 Debljina i ...), p.63

Rojnić Putarek, Nataša

2018

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Importance of Immediate Thiamine Therapy in Children with Suspected Thiamine-Responsive Megaloblastic Anemia-Report on Two Patients Carrying a Novel SLC19A2 Gene Mutation

Journal of pediatric genetics, 2022, Vol.11 (3), p.236-239

2022

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Severe virilization in adolescent girl with Sertoli-Leydig cell tumor – case report and review of the literature

Central European journal of paediatrics (Online), 2018-03, Vol.14 (1), p.92-97

Krnic, Nevena

2018

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Low doses of sulphonyluria as a successful replacement for insulin therapy in a patient with neonatal diabetes due to a mutation of KCNJ11 gene encoding Kir6.2

Liječnički vjesnik, 2010-03, Vol.132 (3-4), p.90-93

2010

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Marden-Walker syndrome--a case report

Liječnički vjesnik, 2009-07, Vol.131 (7-8), p.203

2009

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Duplication of the pituitary gland

Liječnički vjesnik, 2009-05, Vol.131 (5-6), p.130

2009

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Epidemiology of congenital heart diseases in Croatia--a multicenter nationwide study, 1995-2000

Liječnički vjesnik, 2003-09, Vol.125 (9-10), p.232

2003

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Diagnostic value of myocardial biopsy in the diagnostic algorithm in cardiomyopathies in children

Liječnički vjesnik, 2004-09, Vol.126 (9-10), p.227

2004

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Sialolithiasis with concurrent sialadenitis in an 18-year-old boy with triple A syndrome

The Journal of otolaryngology, 2007-12, Vol.36 (6), p.E98

2007

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Sindrom akutnog respiracijskog distresa u četvorogodišnjeg dječaka s dijabetičnom ketoacidozom - prikaz slučaja

Acta clinica Croatica, 2018, Vol.57 (3.), p.588

2018

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ACUTE RESPIRATORY DISTRESS SYNDROME IN A FOUR-YEAR-OLD BOY WITH DIABETIC KETOACIDOSIS - CASE REPORT

Acta clinica Croatica, 2018, Vol.57 (3), p.588-592

2018

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Plasma Fucosylated Glycans and C-Reactive Protein as Biomarkers of HNF1A-MODY in Young Adult-Onset Nonautoimmune Diabetes

Trends and cyclical variation in the incidence of childhood type 1 diabetes in 26 European centres in the 25 year period 1989–2013: a multicentre prospective registration study

Primary hypothyroidism and nipple hypoplasia in a girl with Wolcott–Rallison syndrome

Two siblings with triple A syndrome and novel mutation presenting as hereditary polyneuropathy

Arterial stiffness as a measure of cardiovascular risk in obese adolescents and adolescents with diabetes type 1

Relative Frequency of Islet Autoimmunity in Children and Adolescents with Autoimmune Thyroid Disease

Human Leukocyte Antigen class II polymorphisms among Croatian patients with type 1 diabetes and autoimmune polyglandular syndrome type 3 variant

Importance of Immediate Thiamine Therapy in Children with Suspected Thiamine-Responsive Megaloblastic Anemia—Report on Two Patients Carrying a Novel SLC19A2 Gene Mutation

Incidence of type 1 diabetes mellitus in 0 to 14-yr-old children in Croatia - 2004 to 2012 study

Trends and cyclical variation in the incidence of childhood type 1 diabetes in 26 European centres in the 25year period 1989-2013: a multicentre prospective registration study

Role of Parents in Body Mass Reduction in Children with Obesity-Adherence and Success of 1-Year Participation in an Intervention Program

Jesu li bubrežne malformacije jedno od obilježja sindroma MEN2B? – prikaz bolesnika i pregled literature

ACUTE RESPIRATORY DISTRESS SYNDROME IN A FOUR-YEAR-OLD BOY WITH DIABETIC KETOACIDOSIS - CASE REPORT

Incidence of type 1 diabetes mellitus in 0 to 14-yr-old children in Croatia - 2004 to 2012 study: Continuous rise in T1DM incidence in Croatia

Pretilost u dječjoj dobi

Importance of Immediate Thiamine Therapy in Children with Suspected Thiamine-Responsive Megaloblastic Anemia-Report on Two Patients Carrying a Novel SLC19A2 Gene Mutation

Severe virilization in adolescent girl with Sertoli-Leydig cell tumor – case report and review of the literature

Low doses of sulphonyluria as a successful replacement for insulin therapy in a patient with neonatal diabetes due to a mutation of KCNJ11 gene encoding Kir6.2

Marden-Walker syndrome--a case report

Duplication of the pituitary gland

Epidemiology of congenital heart diseases in Croatia--a multicenter nationwide study, 1995-2000

Diagnostic value of myocardial biopsy in the diagnostic algorithm in cardiomyopathies in children

Sialolithiasis with concurrent sialadenitis in an 18-year-old boy with triple A syndrome

Sindrom akutnog respiracijskog distresa u četvorogodišnjeg dječaka s dijabetičnom ketoacidozom - prikaz slučaja

ACUTE RESPIRATORY DISTRESS SYNDROME IN A FOUR-YEAR-OLD BOY WITH DIABETIC KETOACIDOSIS - CASE REPORT

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