Maja S. Djordjevic

Belgrade, SE, Serbia

Last Updated: 09/26/2026

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Found 26 publications

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

Current Status of Newborn Screening in Southeastern Europe.

Current Status of Newborn Screening in Southeastern Europe.

Journal: Frontiers in pediatrics

Published: January 02, 2021

Clinical and genetic characteristics of patients with congenital hyperinsulinism in 21 non-consanguineous families from Serbia.

Clinical and genetic characteristics of patients with congenital hyperinsulinism in 21 non-consanguineous families from Serbia.

Journal: European journal of pediatrics

Published: December 14, 2020

The improvement in diagnosis and epilepsy managing in children with progressive myoclonus epilepsy during the last decade - A tertiary center experience in cohort of 51 patients.

The improvement in diagnosis and epilepsy managing in children with progressive myoclonus epilepsy during the last decade - A tertiary center experience in cohort of 51 patients.

Journal: Epilepsy & behavior : E&B

Published: February 15, 2020

Case-control study of primary hyperparathyroidism in juvenile vs. adult patients.

Case-control study of primary hyperparathyroidism in juvenile vs. adult patients.

Journal: International journal of pediatric otorhinolaryngology

Published: October 27, 2019

Untreated PKU Patients without Intellectual Disability: What Do They Teach Us?

Untreated PKU Patients without Intellectual Disability: What Do They Teach Us?

Journal: Nutrients

Published: September 15, 2019

Differences in primary hyperparathyroidism characteristics between children and adolescents.

Differences in primary hyperparathyroidism characteristics between children and adolescents.

Journal: Journal of pediatric surgery

Published: May 22, 2019

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

Case report of parathyroid carcinoma in a pediatric patient.

Case report of parathyroid carcinoma in a pediatric patient.

Journal: International journal of pediatric otorhinolaryngology

Published: February 04, 2019

CRISPR/Cas9 genome editing of SLC37A4 gene elucidates the role of molecular markers of endoplasmic reticulum stress and apoptosis in renal involvement in glycogen storage disease type Ib.

CRISPR/Cas9 genome editing of SLC37A4 gene elucidates the role of molecular markers of endoplasmic reticulum stress and apoptosis in renal involvement in glycogen storage disease type Ib.

Journal: Gene

Published: December 26, 2018

Can untreated PKU patients escape from intellectual disability? A systematic review.

Can untreated PKU patients escape from intellectual disability? A systematic review.

Journal: Orphanet journal of rare diseases

Published: May 04, 2018

Functional Characterization of Novel Phenylalanine Hydroxylase p.Gln226Lys Mutation Revealed Its Non-responsiveness to Tetrahydrobiopterin Treatment in Hepatoma Cellular Model.

Functional Characterization of Novel Phenylalanine Hydroxylase p.Gln226Lys Mutation Revealed Its Non-responsiveness to Tetrahydrobiopterin Treatment in Hepatoma Cellular Model.

Journal: Biochemical genetics

Published: February 06, 2018

Showing 1-12 of 26

Last Updated: 09/26/2026