@ARTICLE{
author={Djordjevic-Milosevic Maja,Skakic Anita G,Andjelkovic Marina Z,Delgado-Vega Angelica Maria,Thonberg Hakan,Klaassen Kristel M,Komazec Jovana,Kecman Bozica,Jocic Nikola,Bjorck Erik,Lindstrand Anna,Stojiljkovic Maja M},
year={2026},
title={First Reported Use of Recombinant Parathyroid Hormone in Kenny-Caffey Syndrome Type 2: A Case Report and Literature Review},
journal={DISEASES},
volume={14},
number={3},
pages={-},
document_type={Review},
} 

@ARTICLE{
author={Djordjevic-Milosevic Maja,Skakic Anita G,Kecman Bozica,Stankovic Sara S,Kovacevic Ivona,Pavlovic Sonja T,Stojiljkovic Maja M},
year={2025},
title={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},
volume={},
number={},
pages={-},
document_type={Article; Early Access},
} 

@ARTICLE{
author={Klaassen Kristel M,Kecman Bozica,Stankovic S,Komazec Jovana,Pavlovic Sonja T,Stojiljkovic Maja M,Djordjevic M},
year={2025},
title={Genomic profiling, implications for genotype-based treatment of 131 patients with phenylketonuria and characterization of novel p.Pro416Leu PAH variant},
journal={SCIENTIFIC REPORTS},
volume={15},
number={1},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Maric Nina,Kecman Bozica,Ostojic Slavica B},
year={2024},
title={Novel deep intronic variant in GALC gene in the patient with infantile Krabbe disease},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={32},
number={},
pages={1030-1031},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Maric Nina,Kecman Bozica,Ostojic Slavica B},
year={2024},
title={Novel deep intronic variant in GALC gene in the patient with infantile Krabbe disease},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={32},
number={},
pages={1030-1031},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Andjelkovic Marina Z,Klaassen Kristel M,Skakic Anita G,Marjanovic Irena M,Kravljanac Ruzica M,Djordjevic Maja S,Vucetic-Tadic Biljana,Kecman Bozica,Pavlovic Sonja T,Stojiljkovic Maja M},
year={2024},
title={Characterization of 13 Novel Genetic Variants in Genes Associated with Epilepsy: Implications for Targeted Therapeutic Strategies},
journal={MOLECULAR DIAGNOSIS & THERAPY},
volume={},
number={},
pages={-},
document_type={Article; Early Access},
} 

@ARTICLE{
author={Klaassen Kristel M,Djordjevic Maja S,Skakic Anita G,Kecman Bozica,Parezanovic Marina V,Andjelkovic Marina Z,Stevanovic Nina,Spasovski Vesna M,Ugrin Milena M,Drmanac Radoje,Pavlovic Sonja T,Stojiljkovic Maja M},
year={2023},
title={Untreated PKU patients without intellectual disability: SHANK gene family as a candidate modifier},
journal={EUROPEAN JOURNAL OF HUMAN GENETICS},
volume={31},
number={},
pages={433-433},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Gruenert Sarah C,...,Djordjevic-Milosevic Maja,...,Kecman Bozica,...,(broj koautora 64)},
year={2022},
title={Efficacy and safety of empagliflozin in glycogen storage disease type Ib: Data from an international questionnaire},
journal={GENETICS IN MEDICINE},
volume={24},
number={8},
pages={1781-1788},
document_type={Article},
} 

@ARTICLE{
author={Klaassen Kristel M,Djordjevic Maja S,Skakic Anita G,Kecman Bozica,Drmanac Radoje,Pavlovic Sonja T,Stojiljkovic Maja M},
year={2021},
title={Untreated PKU patients without intellectual disability: SHANK gene family as a candidate modifier},
journal={MOLECULAR GENETICS AND METABOLISM REPORTS},
volume={29},
number={},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Sarajlija Adrijan,Djordjevic Maja S,Kecman Bozica,Skakic Anita G,Pavlovic Sonja T,Pasic Srdjan S,Stojiljkovic Maja M},
year={2020},
title={Impact of genotype on neutropenia in a large cohort of Serbian patients with glycogen storage disease type Ib},
journal={EUROPEAN JOURNAL OF MEDICAL GENETICS},
volume={63},
number={3},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Skakic Anita G,Djordjevic Maja S,Sarajlija Adrijan,Klaassen Kristel M,Tosic Natasa M,Kecman Bozica,Ugrin Milena M,Spasovski Vesna M,Pavlovic Sonja T,Stojiljkovic Maja M},
year={2018},
title={Genetic characterization of GSD I in Serbian population revealed unexpectedly high incidence of GSD Ib and 3 novel SLC37A4 variants},
journal={CLINICAL GENETICS},
volume={93},
number={2},
pages={350-355},
document_type={Article},
} 

@ARTICLE{
author={Kocic Marija,Djuricic Slavisa M,Djordjevic Maja S,Savic Djordje,Kecman Bozica,Sarajlija Adrijan},
year={2018},
title={Appendiceal involvement in a patient with Gaucher disease},
journal={BLOOD CELLS MOLECULES AND DISEASES},
volume={68},
number={},
pages={109-111},
document_type={Article},
} 

@ARTICLE{
author={Sarajlija Adrijan,Magner Martin,Djordjevic Maja S,Kecman Bozica,Grujic Blagoje R,Tesarova Marketa,Minic Predrag B},
year={2017},
title={Late-presenting congenital diaphragmatic hernia in a child with TMEM70 deficiency},
journal={CONGENITAL ANOMALIES},
volume={57},
number={2},
pages={64-65},
document_type={Letter},
} 

@ARTICLE{
author={Dvorakova L,...,Sarajlija Adrijan,...,Kecman Bozica,Djordjevic Maja S,...,(broj koautora 19)},
year={2017},
title={Genotype-phenotype correlation in 44 Czech, Slovak, Croatian and Serbian patients with mucopolysaccharidosis type II},
journal={CLINICAL GENETICS},
volume={91},
number={5},
pages={787-796},
document_type={Article},
} 

@ARTICLE{
author={Stojiljkovic Maja M,Klaassen Kristel M,Djordjevic Maja S,Sarajlija Adrijan,Brasil S,Kecman Bozica,Grkovic Sanja,Kostic Jelena,Rodriguez-Pombo P,Desviat Lourdes R,Pavlovic Sonja T,Perez Belen},
year={2016},
title={Molecular and phenotypic characteristics of seven novel mutations causing branched-chain organic acidurias},
journal={CLINICAL GENETICS},
volume={90},
number={3},
pages={252-257},
document_type={Article},
} 

@ARTICLE{
author={Sarajlija Adrijan,Milenkovic Tatjana,Djordjevic Maja S,Mitrovic Katarina,Todorovic Sladjana,Kecman Bozica,Hussain Khalid},
year={2016},
title={Early Presentation of Hyperinsulinism/Hyperammonemia Syndrome in Three Serbian Patients},
journal={JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY},
volume={8},
number={2},
pages={228-231},
document_type={Article},
} 

@ARTICLE{
author={Stajic Natasa,Putnik Jovana,Paripovic Aleksandra,Djordjevic Maja S,Martic Jelena M,Kecman Bozica,Sarajlija Adrijan,Pejic Katarina,Prokic Dragan,Visekruna Jelena,Bogdanovic Radovan M},
year={2015},
title={Non-Renal Indications for the Continuous Renal Replacement Therapy in the Intensive Care Unit of Terciary Care Center: Eleven Years of Experience},
journal={PEDIATRIC NEPHROLOGY},
volume={30},
number={12},
pages={2248-2248},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Stojiljkovic Maja M,Klaassen Kristel M,Djordjevic Maja S,Sarajlija Adrijan,Kecman Bozica,Ugrin Milena M,Zukic Branka,Desviat Lourdes R,Pavlovic Sonja T,Perez Belen},
year={2015},
title={Tetrahydrobiopterin deficiency among Serbian patients presenting with hyperphenylalaninemia},
journal={JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM},
volume={28},
number={3-4},
pages={477-480},
document_type={Article},
} 

@ARTICLE{
author={Sarajlija Adrijan,Minic Predrag B,Djordjevic Maja S,Rodic Milan,Kecman Bozica,Savic Natasa,Baljosevic Ivan S},
year={2012},
title={EARLY-ONSET RESPIRATORY MANIFESTATIONS IN HUNTER DISEASE: CASE REPORT},
journal={JOURNAL OF INHERITED METABOLIC DISEASE},
volume={35},
number={},
pages={S108-S108},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Sarajlija Adrijan,Djordjevic Maja S,Kecman Bozica},
year={2011},
title={Depression and Health Related Quality of Life in Caregivers of Children with Phenylketonuria},
journal={JOURNAL OF INHERITED METABOLIC DISEASE},
volume={34},
number={},
pages={S98-S98},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Djordjevic Maja S,Sarajlija Adrijan,Kecman Bozica,Stajic Natasa,Bogdanovic Radovan M,Jankovic Borisav Z},
year={2011},
title={Successful Early Treatment of Neonatal Maple Syrup Urine Disease},
journal={JOURNAL OF INHERITED METABOLIC DISEASE},
volume={34},
number={},
pages={S80-S80},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Djordjevic Maja S,Sarajlija Adrijan,Manic-Nikitovic J,Kecman Bozica,Martic Jelena M,Jankovic Borisav Z},
year={2010},
title={INBORN ERRORS OF METABOLISM IN NEONATAL AND PEDIATRIC INTENSIVE CARE UNIT: FIVE YEAR EXPIRIENCE},
journal={JOURNAL OF INHERITED METABOLIC DISEASE},
volume={33},
number={},
pages={S180-S180},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Sarajlija Adrijan,Djordjevic Maja S,Kecman Bozica,Djuricic Slavisa M,Ristic Goran G},
year={2010},
title={ABDOMINAL LYMPHADENOPATHY DURING ENZYME REPLACEMENT THERAPY: AN EMERGING CHALLENGE OF GAUCHER DISEASE?},
journal={JOURNAL OF INHERITED METABOLIC DISEASE},
volume={33},
number={},
pages={S150-S150},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Kecman Bozica,Mayr Johannes A,Djordjevic Maja S,Sarajlija Adrijan,Stajic Natasa},
year={2010},
title={NOVEL MITOCHONDRIAL DNA DELETION IN PATIENT WITH DISTINCT PRESENTATION OF PEARSON SYNDROME},
journal={JOURNAL OF INHERITED METABOLIC DISEASE},
volume={33},
number={},
pages={S91-S91},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Djordjevic Maja S,Grkovic Sanja,Djuric Milena Lj,Jankovic Borisav Z,Sumarac Zorica R,Kecman Bozica,Stojanov L},
year={2006},
title={Diagnosis of inborn errors of metabolism in Serbian children a referral centre experience},
journal={JOURNAL OF INHERITED METABOLIC DISEASE},
volume={29},
number={},
pages={90-90},
document_type={Meeting Abstract},
} 

