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Distinct association patterns of chemokine profile and cardiometabolic status in children and adolescents with type 1 diabetes and obesity

Frontiers in endocrinology (Lausanne), 2024-07, Vol.15, p.1335371

2024

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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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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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Šećerna bolest u adolescenata

Medicus (Zagreb, Croatia : 1992), 2010-06, Vol.19 (1_Adolescencija_2), p.27

2010

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Glycosyltransferase B4GALNT1 and type 1 diabetes in Croatian population: clinical investigation

Clinical biochemistry, 2009-06, Vol.42 (9), p.819-822

2009

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Experiences with galactosemia in Croatia

Liječnički vjesnik, 2023-03, Vol.145 (1-2), p.1-11

2023

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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, 2019-03, Vol.7 (3), p.213-220

2019

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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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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

Volltextzugriff (PDF)

Glycosyltransferase B4GALNT1 and type 1 diabetes in Croatian population

Clinical biochemistry, 2009-06, Vol.42 (9), p.819-822

2009

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Five patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency (one with associated neuroblastoma) discovered in three generations of one family

Hormone research, 2007-01, Vol.67 (3), p.111-116

2007

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The COVID-19 Pandemic Affects Seasonality, With Increasing Cases of New-Onset Type 1 Diabetes in Children, From the Worldwide SWEET Registry

Diabetes care, 2022-11, Vol.45 (11), p.2594-2601

2022

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Primary pigmented nodular adrenocortical disease as cause of Cushing's syndrome associated with Carney complex

Liječnički vjesnik, 2006-09, Vol.128 (9-10), p.268

2006

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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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Three-year-old boy--a homozygote for familiar hypercholesterolemia

Liječnički vjesnik, 2007-05, Vol.129 (5), p.130

2007

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Distinct association patterns of chemokine profile and cardiometabolic status in children and adolescents with type 1 diabetes and obesity

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

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

Šećerna bolest u adolescenata

Glycosyltransferase B4GALNT1 and type 1 diabetes in Croatian population: clinical investigation

Experiences with galactosemia in Croatia

Natural history, treatment, and long-term follow up of patients with multiple endocrine neoplasia type 2B: an international, multicentre, retrospective study

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

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

Glycosyltransferase B4GALNT1 and type 1 diabetes in Croatian population

Five patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency (one with associated neuroblastoma) discovered in three generations of one family

The COVID-19 Pandemic Affects Seasonality, With Increasing Cases of New-Onset Type 1 Diabetes in Children, From the Worldwide SWEET Registry

Primary pigmented nodular adrenocortical disease as cause of Cushing's syndrome associated with Carney complex

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

Three-year-old boy--a homozygote for familiar hypercholesterolemia

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