Ruzica Kravljanac

Belgrade, SE, Serbia

Last Updated: 09/26/2026

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Found 31 publications

RHOBTB2-Associated Neurological Phenotypes and Underlying Mechanisms: Alternating Hemiplegia of Childhood Beyond ATP1A3.

RHOBTB2-Associated Neurological Phenotypes and Underlying Mechanisms: Alternating Hemiplegia of Childhood Beyond ATP1A3.

Journal: Diseases (Basel, Switzerland)

Published: April 27, 2026

Severe adenylosuccinate lyase deficiency with early autonomic dysfunction: functional characterization of a novel ADSL variant and exploratory treatment with disulfiram.

Severe adenylosuccinate lyase deficiency with early autonomic dysfunction: functional characterization of a novel ADSL variant and exploratory treatment with disulfiram.

Journal: Molecular genetics and metabolism

Published: April 21, 2026

Pyridoxine-dependent and other pyridoxine-responsive epilepsies-insights into phenotype overlapping and the long-term outcome in a cohort of 21 children.

Pyridoxine-dependent and other pyridoxine-responsive epilepsies-insights into phenotype overlapping and the long-term outcome in a cohort of 21 children.

Journal: Frontiers in neurology

Published: April 14, 2026

A phase 3, randomized clinical trial of soticlestat as adjunctive therapy for Lennox-Gastaut syndrome.

A phase 3, randomized clinical trial of soticlestat as adjunctive therapy for Lennox-Gastaut syndrome.

Journal: Epilepsia

Published: October 16, 2025

Clinical Characteristics of Seizures and Course of Epilepsy in Children with Neurofibromatosis Type 1-A Tertiary Center Experience in a Cohort of 118 Children.

Clinical Characteristics of Seizures and Course of Epilepsy in Children with Neurofibromatosis Type 1-A Tertiary Center Experience in a Cohort of 118 Children.

Journal: Diagnostics (Basel, Switzerland)

Published: September 05, 2025

Developmental and epileptic encephalopathy with spike-wave activation in sleep (D/EE-SWAS): Clinical and treatment insights from a cohort of 50 children.

Developmental and epileptic encephalopathy with spike-wave activation in sleep (D/EE-SWAS): Clinical and treatment insights from a cohort of 50 children.

Journal: Seizure

Published: April 17, 2025

Insight into Haploinsufficiency of the ERBB4 Gene: Expanding the Spectrum of Associated Phenotypes.

Insight into Haploinsufficiency of the ERBB4 Gene: Expanding the Spectrum of Associated Phenotypes.

Journal: Journal of autism and developmental disorders

Published: March 21, 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

Reverse Phenotyping after Whole-Exome Sequencing in Children with Developmental Delay/Intellectual Disability-An Exception or a Necessity?

Reverse Phenotyping after Whole-Exome Sequencing in Children with Developmental Delay/Intellectual Disability-An Exception or a Necessity?

Journal: Genes

Published: May 02, 2024

Main features and disease outcome of congenital myotonic dystrophy - experience from a single tertiary center.

Main features and disease outcome of congenital myotonic dystrophy - experience from a single tertiary center.

Journal: Neuromuscular disorders : NMD

Published: February 11, 2024

"The Red Flags" in Clinical Approach to Acute Ataxia-the Experience in Cohort of 76 Children.

"The Red Flags" in Clinical Approach to Acute Ataxia-the Experience in Cohort of 76 Children.

Journal: Cerebellum (London, England)

Published: November 18, 2023

LTBP4, SPP1, and CD40 Variants: Genetic Modifiers of Duchenne Muscular Dystrophy Analyzed in Serbian Patients.

LTBP4, SPP1, and CD40 Variants: Genetic Modifiers of Duchenne Muscular Dystrophy Analyzed in Serbian Patients.

Journal: Genes

Published: June 28, 2022

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Last Updated: 09/26/2026