Bozica Kecman

Belgrade, SE, Serbia

Last Updated: 09/26/2026

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Found 15 publications

First Reported Use of Recombinant Parathyroid Hormone in Kenny-Caffey Syndrome Type 2: A Case Report and Literature Review.

First Reported Use of Recombinant Parathyroid Hormone in Kenny-Caffey Syndrome Type 2: A Case Report and Literature Review.

Journal: Diseases (Basel, Switzerland)

Published: January 09, 2026

Clinical and Genetic Profile of 35 Patients with Glycogen Storage Disease Type 1b: A Comparative Analysis Before and During SGLT2 Inhibitor Therapy.

Clinical and Genetic Profile of 35 Patients with Glycogen Storage Disease Type 1b: A Comparative Analysis Before and During SGLT2 Inhibitor Therapy.

Journal: Molecular diagnosis & therapy

Published: May 29, 2025

Genomic profiling, implications for genotype-based treatment of 131 patients with phenylketonuria and characterization of novel p.Pro416Leu PAH variant.

Genomic profiling, implications for genotype-based treatment of 131 patients with phenylketonuria and characterization of novel p.Pro416Leu PAH variant.

Journal: Scientific reports

Published: February 17, 2025

Characterization of 13 Novel Genetic Variants in Genes Associated with Epilepsy: Implications for Targeted Therapeutic Strategies.

Characterization of 13 Novel Genetic Variants in Genes Associated with Epilepsy: Implications for Targeted Therapeutic Strategies.

Journal: Molecular diagnosis & therapy

Published: May 26, 2024

Efficacy and safety of empagliflozin in glycogen storage disease type Ib: Data from an international questionnaire.

Efficacy and safety of empagliflozin in glycogen storage disease type Ib: Data from an international questionnaire.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: January 25, 2022

Untreated PKU patients without intellectual disability: SHANK gene family as a candidate modifier.

Untreated PKU patients without intellectual disability: SHANK gene family as a candidate modifier.

Journal: Molecular genetics and metabolism reports

Published: August 23, 2021

Impact of genotype on neutropenia in a large cohort of Serbian patients with glycogen storage disease type Ib.

Impact of genotype on neutropenia in a large cohort of Serbian patients with glycogen storage disease type Ib.

Journal: European journal of medical genetics

Published: May 18, 2019

Genetic characterization of GSD I in Serbian population revealed unexpectedly high incidence of GSD Ib and 3 novel SLC37A4 variants.

Genetic characterization of GSD I in Serbian population revealed unexpectedly high incidence of GSD Ib and 3 novel SLC37A4 variants.

Journal: Clinical genetics

Published: April 21, 2017

Appendiceal involvement in a patient with Gaucher disease.

Appendiceal involvement in a patient with Gaucher disease.

Journal: Blood cells, molecules & diseases

Published: September 24, 2016

Genotype-phenotype correlation in 44 Czech, Slovak, Croatian and Serbian patients with mucopolysaccharidosis type II.

Genotype-phenotype correlation in 44 Czech, Slovak, Croatian and Serbian patients with mucopolysaccharidosis type II.

Journal: Clinical genetics

Published: September 21, 2016

Late-presenting congenital diaphragmatic hernia in a child with TMEM70 deficiency.

Late-presenting congenital diaphragmatic hernia in a child with TMEM70 deficiency.

Journal: Congenital anomalies

Published: July 28, 2016

Early Presentation of Hyperinsulinism/Hyperammonemia Syndrome in Three Serbian Patients.

Early Presentation of Hyperinsulinism/Hyperammonemia Syndrome in Three Serbian Patients.

Journal: Journal of clinical research in pediatric endocrinology

Published: January 14, 2016

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Last Updated: 09/26/2026