Galina B. Stevanovic
Belgrade, SE, Serbia
Last Updated: 09/26/2026
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Found 9 publications
Consensus Guideline for the Diagnosis and Treatment of Tyrosine Hydroxylase (TH) Deficiency.
Journal: Journal of inherited metabolic disease
Published: July 05, 2025
The continuously evolving phenotype of succinic semialdehyde dehydrogenase deficiency.
Journal: Journal of inherited metabolic disease
Published: December 04, 2023
Dopa-responsive dystonia in Bulgarian patients: report of three cases.
Journal: European journal of human genetics : EJHG
Published: March 22, 2023
Assessment of intellectual impairment, health-related quality of life, and behavioral phenotype in patients with neurotransmitter related disorders: Data from the iNTD registry.
Journal: Journal of inherited metabolic disease
Published: May 21, 2021
Genetics of Lafora progressive myoclonic epilepsy: current perspectives.
Journal: The application of clinical genetics
Published: May 20, 2016
Quantitation of pregabalin in dried blood spots and dried plasma spots by validated LC-MS/MS methods.
Journal: Journal of pharmaceutical and biomedical analysis
Published: December 18, 2014
Vigabatrin in dried plasma spots: validation of a novel LC-MS/MS method and application to clinical practice.
Journal: Journal of chromatography. B, Analytical technologies in the biomedical and life sciences
Published: March 05, 2014
Lafora disease: severe phenotype associated with homozygous deletion of the NHLRC1 gene.
Journal: Journal of the neurological sciences
Published: September 27, 2012
Showing 1-9 of 9
Last Updated: 09/26/2026