Katja K. Dumic

Zagreb, Croatia

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 17 publications

Prevalence of liver disorders in children and adolescents with type 1 diabetes mellitus.

Prevalence of liver disorders in children and adolescents with type 1 diabetes mellitus.

Journal: BMC pediatrics

Published: January 29, 2025

Metabolic Syndrome Spectrum in Children with Classic Congenital Adrenal Hyperplasia-A Comprehensive Review.

Metabolic Syndrome Spectrum in Children with Classic Congenital Adrenal Hyperplasia-A Comprehensive Review.

Journal: Metabolites

Published: December 28, 2024

Managing Children and Adolescents with Type 1 Diabetes and Coexisting Celiac Disease: Real-World Data from a Global Survey.

Managing Children and Adolescents with Type 1 Diabetes and Coexisting Celiac Disease: Real-World Data from a Global Survey.

Journal: Hormone research in paediatrics

Published: March 22, 2024

Fertility and sexual activity in patients with Triple A syndrome.

Fertility and sexual activity in patients with Triple A syndrome.

Journal: Frontiers in endocrinology

Published: December 17, 2023

The prevalence and genotype of 21-hydroxylase deficiency in the Croatian Romani population.

The prevalence and genotype of 21-hydroxylase deficiency in the Croatian Romani population.

Journal: Frontiers in endocrinology

Published: February 20, 2023

Two Single Nucleotide Deletions in the ABCD1 Gene Causing Distinct Phenotypes of X-Linked Adrenoleukodystrophy.

Two Single Nucleotide Deletions in the ABCD1 Gene Causing Distinct Phenotypes of X-Linked Adrenoleukodystrophy.

Journal: International journal of molecular sciences

Published: December 31, 2022

Novel pathogenic variants and quantitative phenotypic analyses of Robinow syndrome: WNT signaling perturbation and phenotypic variability.

Novel pathogenic variants and quantitative phenotypic analyses of Robinow syndrome: WNT signaling perturbation and phenotypic variability.

Journal: HGG advances

Published: July 13, 2021

Genetic Characterization of Short Stature Patients With Overlapping Features of Growth Hormone Insensitivity Syndromes.

Genetic Characterization of Short Stature Patients With Overlapping Features of Growth Hormone Insensitivity Syndromes.

Journal: The Journal of clinical endocrinology and metabolism

Published: January 15, 2021

Insular damage causing transient baroreflex dysfunction in a teenager with Allgrove syndrome.

Insular damage causing transient baroreflex dysfunction in a teenager with Allgrove syndrome.

Journal: Clinical autonomic research : official journal of the Clinical Autonomic Research Society

Published: October 19, 2020

Lowe syndrome - Old and new evidence of secondary mitochondrial dysfunction.

Lowe syndrome - Old and new evidence of secondary mitochondrial dysfunction.

Journal: European journal of medical genetics

Published: January 12, 2020

Warsaw Breakage Syndrome associated DDX11 helicase resolves G-quadruplex structures to support sister chromatid cohesion.

Warsaw Breakage Syndrome associated DDX11 helicase resolves G-quadruplex structures to support sister chromatid cohesion.

Journal: Nature communications

Published: December 20, 2019

Clinical, genetic, and structural basis of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency.

Clinical, genetic, and structural basis of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency.

Journal: Proceedings of the National Academy of Sciences of the United States of America

Published: February 24, 2017

Showing 1-12 of 17

Last Updated: 09/26/2026