@ARTICLE{
author={Sigatullina-Bondarenko Mariya,...,Badnjarevic Ivana,...,Stevanovic Galina B,...,(broj koautora 19)},
year={2025},
title={Consensus Guideline for the Diagnosis and Treatment of Tyrosine Hydroxylase (TH) Deficiency},
journal={JOURNAL OF INHERITED METABOLIC DISEASE},
volume={48},
number={6},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Julia-Palacios Natalia Alexandra,...,Stevanovic Galina B,...,(broj koautora 22)},
year={2024},
title={The continuously evolving phenotype of succinic semialdehyde dehydrogenase deficiency},
journal={JOURNAL OF INHERITED METABOLIC DISEASE},
volume={47},
number={3},
pages={447-462},
document_type={Article},
} 

@ARTICLE{
author={Parezanovic M,Ilic Nina,Ostojic Slavica B,Stevanovic Galina B,Jecmenica Jovana R,Maver Ales,Sarajlija Adrijan},
year={2023},
title={Sensorineural Hearing Loss in a Child with Succinic Semialdehyde Dehydrogenase Deficiency},
journal={BALKAN JOURNAL OF MEDICAL GENETICS},
volume={26},
number={1},
pages={63-67},
document_type={Article},
} 

@ARTICLE{
author={Atanasoska Maya,Vazharova Radoslava,Stevanovic Galina B,Bradinova Irena,Staykova Slavyana Yaneva,Balabanski Lubomir,Mircheva Daniela,Avdjieva-Tzavella Daniela,Toncheva Draga},
year={2023},
title={Dopa-responsive dystonia in Bulgarian patients: report of three cases},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={},
number={},
pages={-},
document_type={Editorial Material; Early Access},
} 

@ARTICLE{
author={Keller Mareike,...,Kavecan Ivana I,...,Stevanovic Galina B,(broj koautora 39)},
year={2021},
title={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},
volume={44},
number={6},
pages={1489-1502},
document_type={Article},
} 

@ARTICLE{
author={Stevanovic Galina B,Jovic Nebojsa J,Kecmanovic Miljana},
year={2020},
title={Is adjunctive perampanel beneficial for Lafora disease?},
journal={VOJNOSANITETSKI PREGLED},
volume={77},
number={5},
pages={539-544},
document_type={Article},
} 

@ARTICLE{
author={Jovic Nebojsa J,Stevanovic Galina B,Borkovic Milan P,Ignjatovic PM},
year={2018},
title={Efficacy and Safety of Intravenous Methylprednisolone Pulse Therapy in Epileptic Encephalopathy with Electrical Status Epilepticus During Sleep},
journal={EPILEPSIA},
volume={59},
number={},
pages={S111-S111},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Kecmanovic Miljana,Jovic ND,Keckarevic-Markovic Milica,Keckarevic Dusan P,Stevanovic Galina B,Ignjatovic PM,Romac Stanka P},
year={2016},
title={Clinical and genetic data on Lafora disease patients of Serbian/Montenegrin origin},
journal={CLINICAL GENETICS},
volume={89},
number={1},
pages={104-108},
document_type={Article},
} 

@ARTICLE{
author={Kostic Nadja M,Dotsikas Yannis,Jovic Nebojsa J,Stevanovic Galina B,Malenovic Andjelija M,Medenica Mirjana B},
year={2015},
title={Quantitation of pregabalin in dried blood spots and dried plasma spots by validated LC-MS/MS methods},
journal={JOURNAL OF PHARMACEUTICAL AND BIOMEDICAL ANALYSIS},
volume={109},
number={},
pages={79-84},
document_type={Article},
} 

@ARTICLE{
author={Kostic Nadja M,Dotsikas Yannis,Jovic Nebojsa J,Stevanovic Galina B,Malenovic Andjelija M,Medenica Mirjana B},
year={2014},
title={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},
volume={962},
number={},
pages={102-108},
document_type={Article},
} 

@ARTICLE{
author={Kecmanovic Miljana,Jovic Nebojsa J,Cukic Mirjana,Keckarevic-Markovic Milica,Keckarevic Dusan P,Stevanovic Galina B,Romac Stanka P},
year={2013},
title={Lafora disease: Severe phenotype associated with homozygous deletion of the NHLRC1 gene},
journal={JOURNAL OF THE NEUROLOGICAL SCIENCES},
volume={325},
number={1-2},
pages={170-173},
document_type={Article},
} 

@ARTICLE{
author={Kecmanovic Miljana,Jovic ND,Keckarevic-Markovic Milica,Keckarevic Dusan P,Stevanovic Galina B,Romac Stanka P},
year={2012},
title={Founder c. 1048-1049delGA mutation in NHLRC1 gene in Lafora's disease patients from Serbia},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={19},
number={},
pages={236-236},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Stevanovic Galina B,Ignjatovic PM},
year={2011},
title={Electrical Status Epilepticus During Slow Sleep in Various Disorders},
journal={EPILEPSIA},
volume={52},
number={},
pages={129-129},
document_type={Meeting Abstract},
} 

