@ARTICLE{
author={Pozun Nika,...,Basa Mihail I,...,Brkusanin Milos,Djordjevic Maja S,...,Kavecan Ivana I,Katanic Jasmina,...,Milenkovic Tatjana,...,Opancina Branka,...,Sovtic Aleksandar D,...,Visekruna Jelena,...,(broj koautora 45)},
year={2026},
title={Current Status of Newborn Screening in Southeastern and Central Europe},
journal={INTERNATIONAL JOURNAL OF NEONATAL SCREENING},
volume={12},
number={1},
pages={-},
document_type={Article},
} 

@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={Tylki-Szymanska Anna,...,Cuturilo Goran,Djordjevic Maja S,...,(broj koautora 18)},
year={2022},
title={The landscape of Mucopolysaccharidosis in Southern and Eastern European countries: a survey from 19 specialistic centers},
journal={ORPHANET JOURNAL OF RARE DISEASES},
volume={17},
number={1},
pages={-},
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={Koracin Vanesa,...,Djordjevic Maja S,...,Milenkovic Tatjana,...,(broj koautora 23)},
year={2021},
title={Current Status of Newborn Screening in Southeastern Europe},
journal={FRONTIERS IN PEDIATRICS},
volume={9},
number={},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Raicevic Maja,Milenkovic Tatjana,Hussain Khalid,Djordjevic Maja S,Martic Jelena M,Todorovic Sladjana,Mitrovic Katarina,Sarajlija Adrijan,Vukovic Rade M},
year={2021},
title={Clinical and genetic characteristics of patients with congenital hyperinsulinism in 21 non-consanguineous families from Serbia},
journal={EUROPEAN JOURNAL OF PEDIATRICS},
volume={180},
number={9},
pages={2815-2821},
document_type={Article},
} 

@ARTICLE{
author={Kravljanac Ruzica M,Vucetic-Tadic Biljana,Djordjevic Maja S,Lalic Tanja,Kravljanac Djordje,Cerovic Ivana B},
year={2020},
title={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},
volume={113},
number={},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Zivaljevic Vladan R,Jovanovic Milan D,Diklic Aleksandar Dj,Zdravkovic Vera M,Djordjevic Maja S,Paunovic Ivan R},
year={2020},
title={Differences in primary hyperparathyroidism characteristics between children and adolescents},
journal={JOURNAL OF PEDIATRIC SURGERY},
volume={55},
number={8},
pages={1660-1662},
document_type={Article},
} 

@ARTICLE{
author={Hillert Alicia,...,Djordjevic Maja S,...,Stojiljkovic Maja M,...,(broj koautora 48)},
year={2020},
title={The Genetic Landscape and Epidemiology of Phenylketonuria},
journal={AMERICAN JOURNAL OF HUMAN GENETICS},
volume={107},
number={2},
pages={234-250},
document_type={Article},
} 

@ARTICLE{
author={Kravljanac Ruzica M,Djordjevic Maja S,Vucetic-Tadic Biljana},
year={2020},
title={The improvement in diagnosis and epilepsy managing in children with progressive myoclonus epilepsy during the last decade - a single tertiary center experience},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={27},
number={},
pages={131-131},
document_type={Meeting Abstract},
} 

@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={Dobric Bojana,Radivojevic Danijela,Lalic Tanja,Miskovic Marijana,Cirkovic Sanja S,Djordjevic Maja S,Djurisic Marina},
year={2019},
title={Incidence of Genetic Causes of Idiopathic Male Infertility in Serbia - Ten Years' Experience of Single Centre},
journal={GENETIKA-BELGRADE},
volume={51},
number={3},
pages={1009-1019},
document_type={Article},
} 

@ARTICLE{
author={Van Vliet Danique,...,Djordjevic Maja S,...,Stojiljkovic Maja M,...,(broj koautora 20)},
year={2019},
title={Untreated PKU Patients without Intellectual Disability: What Do They Teach Us?},
journal={NUTRIENTS},
volume={11},
number={11},
pages={-},
document_type={Article},
} 

@ARTICLE{
author={Molema Femke,...,Djordjevic Maja S,Sarajlija Adrijan,...,(broj koautora 68)},
year={2019},
title={Evaluation of dietary treatment and amino acid supplementation in organic acidurias and urea-cycle disorders: On the basis of information from a European multicenter registry},
journal={JOURNAL OF INHERITED METABOLIC DISEASE},
volume={42},
number={6},
pages={1162-1175},
document_type={Article; Proceedings Paper},
} 

@ARTICLE{
author={Zivaljevic Vladan R,Jovanovic Milan D,Djordjevic Maja S,Diklic Aleksandar Dj,Paunovic Ivan R},
year={2019},
title={Case report of parathyroid carcinoma in a pediatric patient},
journal={INTERNATIONAL JOURNAL OF PEDIATRIC OTORHINOLARYNGOLOGY},
volume={124},
number={},
pages={120-123},
document_type={Article},
} 

@ARTICLE{
author={Molema Femke,...,Djordjevic Maja S,Sarajlija Adrijan,...,(broj koautora 67)},
year={2019},
title={Decreased plasma L-arginine levels in organic acidurias (MMA and PA) and decreased plasma branched-chain amino acid levels in urea cycle disorders as a potential cause of growth retardation: Options for treatment},
journal={MOLECULAR GENETICS AND METABOLISM},
volume={126},
number={4},
pages={397-405},
document_type={Article},
} 

@ARTICLE{
author={Skakic Anita G,Andjelkovic Marina Z,Tosic Natasa M,Klaassen Kristel M,Djordjevic Maja S,Pavlovic Sonja T,Stojiljkovic Maja M},
year={2019},
title={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},
volume={703},
number={},
pages={17-25},
document_type={Article},
} 

@ARTICLE{
author={Klaassen Kristel M,Djordjevic Maja S,Skakic Anita G,Desviat Lourdes R,Pavlovic Sonja T,Perez Belen,Stojiljkovic Maja M},
year={2018},
title={Functional Characterization of Novel Phenylalanine Hydroxylase p.Gln226Lys Mutation Revealed Its Non-responsiveness to Tetrahydrobiopterin Treatment in Hepatoma Cellular Model},
journal={BIOCHEMICAL GENETICS},
volume={56},
number={5},
pages={533-541},
document_type={Article},
} 

@ARTICLE{
author={Van Vliet Danique,...,Djordjevic Maja S,...,Stojiljkovic Maja M,...,(broj koautora 35)},
year={2018},
title={Can untreated PKU patients escape from intellectual disability? A systematic review},
journal={ORPHANET JOURNAL OF RARE DISEASES},
volume={13},
number={},
pages={-},
document_type={Review},
} 

@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={Vukovic Rade M,Milenkovic Tatjana,Djordjevic Maja S,Mitrovic Katarina,Todorovic Sladjana,Sarajlija Adrijan,Hussain Khalid},
year={2017},
title={Postprandial hyperinsulinemic hypoglycemia in a child as a late complication of esophageal reconstruction},
journal={JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM},
volume={30},
number={7},
pages={791-795},
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={Klaassen Kristel M,Stankovic Biljana B,Kotur Nikola M,Djordjevic Maja S,Zukic Branka,Nikcevic Gordana T,Ugrin Milena M,Spasovski Vesna M,Srzentic Sanja V,Pavlovic Sonja T,Stojiljkovic Maja M},
year={2017},
title={New PAH gene promoter KLF1 and 3'-region C/EBPalpha motifs influence transcription in vitro},
journal={JOURNAL OF APPLIED GENETICS},
volume={54},
number={1},
pages={79-85},
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={Tansek Mojca Zerjav,...,Djordjevic Maja S,...,Stojiljkovic Maja M,...,(broj koautora 27)},
year={2015},
title={Phenylketonuria screening and management in southeastern Europe - survey results from 11 countries},
journal={ORPHANET JOURNAL OF RARE DISEASES},
volume={10},
number={},
pages={-},
document_type={Article},
} 

@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={Rodic Predrag,Kraguljac-Kurtovic Nada,Suvajdzic-Vukovic Nada D,Djordjevic Maja S,Mitrovic Mirjana M,Sumarac Zorica R,Janic Dragana M},
year={2014},
title={Flow cytometric assessment of lymphocyte subsets in Gaucher type 1 patients},
journal={BLOOD CELLS MOLECULES AND DISEASES},
volume={53},
number={4},
pages={169-170},
document_type={Letter},
} 

@ARTICLE{
author={Groselj Urh,...,Djordjevic Maja S,...,Stojiljkovic Maja M,...,(broj koautora 30)},
year={2014},
title={Newborn screening in southeastern Europe},
journal={MOLECULAR GENETICS AND METABOLISM},
volume={113},
number={1-2},
pages={42-45},
document_type={Article},
} 

@ARTICLE{
author={Sarajlija Adrijan,Djuric Milena Lj,Kisic-Tepavcevic Darija B,Grkovic Sanja,Djordjevic Maja S},
year={2013},
title={Vitamin D Deficiency in Serbian Patients With Rett Syndrome},
journal={JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM},
volume={98},
number={12},
pages={E1972-E1978},
document_type={Article},
} 

@ARTICLE{
author={Klaassen Kristel M,Djordjevic Maja S,Stojiljkovic-Petrovic Maja M,Pavlovic Sonja T},
year={2013},
title={Association of Mitochondrial Dna Variants and Cognitive Impairment of Phenylketonuria Patients},
journal={JOURNAL OF MEDICAL BIOCHEMISTRY},
volume={32},
number={4},
pages={347-353},
document_type={Article},
} 

@ARTICLE{
author={Kravljanac Ruzica M,Djuric Milena Lj,Jovic Nebojsa J,Djordjevic Maja S,Zamurovic Dragan R,Pekmezovic Tatjana D},
year={2013},
title={Etiology, clinical features and outcome of epilepsia partialis continua in cohort of 51 children},
journal={EPILEPSY RESEARCH},
volume={104},
number={1-2},
pages={112-117},
document_type={Article},
} 

@ARTICLE{
author={Rodic Predrag,Pavlovic Sonja T,Kostic Tatjana M,Suvajdzic-Vukovic Nada D,Djordjevic Maja S,Sumarac Zorica R,Dajak Marijana M,Bonaci-Nikolic Branka M,Janic Dragana M},
year={2013},
title={Gammopathy and B lymphocyte clonality in patients with Gaucher type I disease},
journal={BLOOD CELLS MOLECULES AND DISEASES},
volume={50},
number={3},
pages={222-225},
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={Stojiljkovic Maja M,Djordjevic Maja S,Klaassen Kristel M,Tosic Natasa M,Sarajlija Adrijan,Zukic Branka,Radmilovic Milena M,Spasovski Vesna M,Kotur Nikola M,Pavlovic Sonja T},
year={2012},
title={GENOTYPE-PHENOTYPE ANALYSIS OF SERBIAN P.L48S PKU PATIENTS},
journal={JOURNAL OF INHERITED METABOLIC DISEASE},
volume={35},
number={},
pages={S37-S37},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Elstein Deborah,Foldes Joseph A,Zahrieh David,Cohn Gabriel M,Djordjevic Maja S,Brutaru Costin,Zimran An},
year={2011},
title={Significant, Continuous Improvement in Bone Mineral Density (Bmd) Among Type 1 Gaucher Disease Patients Treated with Velaglucerase Alfa: 69-Month Experience, Including Dose Reduction},
journal={JOURNAL OF INHERITED METABOLIC DISEASE},
volume={34},
number={},
pages={S223-S223},
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,Minic Predrag B,Sarajlija Adrijan,Djuricic Slavisa M,Djokic Dragomir,Markovic Obren},
year={2011},
title={Pulmonary involvement in siblings with Gaucher disease type III},
journal={VOJNOSANITETSKI PREGLED},
volume={68},
number={12},
pages={1071-1074},
document_type={Article},
} 

@ARTICLE{
author={Kravljanac Ruzica M,Djordjevic Maja S,Djuric Milena Lj},
year={2011},
title={Specific Features of Status Epilepticus Caused by Metabolic Diseases in Children},
journal={EPILEPSIA},
volume={52},
number={},
pages={82-82},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Peco-Antic Amira E,Kostic Mirjana K,Bogdanovic Radovan M,Spasojevic Brankica B,Djordjevic Maja S,Paripovic Dusan,Kovacevic Dragana},
year={2011},
title={Infantile Nephropathic Cystinosis},
journal={SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO},
volume={139},
number={7-8},
pages={486-490},
document_type={Article},
} 

@ARTICLE{
author={Sumarac Zorica R,Suvajdzic Nada D,Ignjatovic Svetlana D,Majkic-Singh Nada T,Janic Dragana M,Petakov Milan S,Djordjevic Maja S,Mitrovic Mirjana M,Dajak Marijana M,Golubovic Milka T,Rodic Predrag},
year={2011},
title={Biomarkers in Serbian patients with Gaucher disease},
journal={CLINICAL BIOCHEMISTRY},
volume={44},
number={12},
pages={950-954},
document_type={Article},
} 

@ARTICLE{
author={Elstein Deborah,Foldes Joseph A,Zahrieh David,Cohn Gabriel M,Djordjevic Maja S,Brutaru Costin,Zimran Ari},
year={2011},
title={Significant and continuous improvement in bone mineral density among type 1 Gaucher disease patients treated with velaglucerase alfa: 69-month experience, including dose reduction},
journal={BLOOD CELLS MOLECULES AND DISEASES},
volume={47},
number={1},
pages={56-61},
document_type={Article},
} 

@ARTICLE{
author={Elstein Deborah,Foldes Joseph A,Zahrieh David,Cohn Gabriel M,Djordjevic Maja S,Brutaru Costin,Zimran An},
year={2011},
title={Significant, continuous improvement in Bone Mineral Density (BMD) among type 1 Gaucher disease patients treated with Velaglucerase Alfa: 69-month experience, including dose reduction},
journal={MOLECULAR GENETICS AND METABOLISM},
volume={102},
number={2},
pages={S17-S18},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Elstein Deborah,Cohn Gabriel M,Wang N,Djordjevic Maja S,Brutaru Costin,Zimran An},
year={2011},
title={Early achievement and maintenance of the therapeutic goals using velaglucerase alfa in type 1 Gaucher disease},
journal={BLOOD CELLS MOLECULES AND DISEASES},
volume={46},
number={1},
pages={119-123},
document_type={Article},
} 

@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={Stojiljkovic Maja M,Djordjevic Maja S,Zukic Branka,Tosic Natasa M,Karan-Djurasevic Teodora Z,Radmilovic Milena M,Spasovski Vesna M,Pavlovic Sonja T},
year={2010},
title={PKU MUTATION UPDATE AND ASSESSMENT OF THE POTENTIAL BENEFIT FROM BH4 SUPPLEMENTATION THERAPY IN SERBIA},
journal={JOURNAL OF INHERITED METABOLIC DISEASE},
volume={33},
number={},
pages={S112-S112},
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={Bogdanovic Radovan M,Draaken Markus,Toromanovic Alma,Djordjevic Maja S,Stajic Natasa,Ludwig Michael},
year={2010},
title={A novel CLCN5 mutation in a boy with Bartter-like syndrome and partial growth hormone deficiency},
journal={PEDIATRIC NEPHROLOGY},
volume={25},
number={11},
pages={2363-2368},
document_type={Article},
} 

@ARTICLE{
author={Stajic Natasa,Bogdanovic Radovan M,Putnik Jovana,Paripovic Aleksandra,Jankovic Borisav Z,Djordjevic Maja S,Nikitovic-Martic Jelena},
year={2010},
title={Continuous Renal Replacement Therapy (CRRT) in the Neonatal Intensive Care Unit (NICU): 5-Years Experience},
journal={PEDIATRIC NEPHROLOGY},
volume={25},
number={9},
pages={757-},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Mitrovic Mihajlo,Suvajdzic-Vukovic Nada D,Elezovic Ivo V,Miljic Predrag S,Sumarac Zorica R,Janic Dragana M,Djordjevic Maja S,Petakov Marijana D,Nikolic Tanja,Rodic Predrag,Djunic Irena S},
year={2010},
title={Platelet Function and Coagulation Abnormalities in Type 1 Gaucher Patients: Effects of Enzyme Replacement Therapy},
journal={HAEMATOLOGICA-THE HEMATOLOGY JOURNAL},
volume={95},
number={},
pages={0174-},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Stajic Natasa,Putnik Jovana,Paripovic Aleksandra,Nikolic Ljubica,Martic Jelena M,Ristic Snezana,Djordjevic Maja S,Bogdanovic Radovan M},
year={2010},
title={Indications, Risks, and Outcome of Crrt in Pediatric Intensive Care Unit Over 5 Years},
journal={PEDIATRIC NEPHROLOGY},
volume={25},
number={8},
pages={17-},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Koprivsek Katarina M,Lucic Milos A,Kozic Dusko B,Djordjevic Maja S,Kravljanac Ruzica M},
year={2010},
title={Basal ganglia lesions in the early stage of Menkes disease},
journal={JOURNAL OF INHERITED METABOLIC DISEASE},
volume={33},
number={3},
pages={301-302},
document_type={Editorial Material},
} 

@ARTICLE{
author={Mitrovic-Vasiljevic Mirjana,Suvajdzic Nada D,Elezovic Ivo V,Miljic Predrag S,Sumarac Zorica R,Janic Dragana M,Djordjevic Maja S,Petakov Marijana D,Rodic Predrag,Djunic Irena S,Nikolic Tanja},
year={2009},
title={Haemostatic abnormalities in treatment-naive type 1 Gaucher patients},
journal={HAEMATOLOGICA-THE HEMATOLOGY JOURNAL},
volume={94},
number={},
pages={1790-},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Svetel Marina V,Pekmezovic Tatjana D,Petrovic Igor N,Tomic Aleksandra D,Kresojevic Nikola D,Jesic Rada S,Kazic Slobodan,Raicevic Ranko,Stefanovic Dragana,Delibasic Nenad,Zivanovic D,Djordjevic Maja S,Kostic Vladimir S},
year={2009},
title={Long-term outcome in Serbian patients with Wilson disease},
journal={EUROPEAN JOURNAL OF NEUROLOGY},
volume={16},
number={7},
pages={852-857},
document_type={Article},
} 

@ARTICLE{
author={Grkovic Sanja,Nikolic Rajko R,Djordjevic Maja S,Puzigaca Zarko,Vujic D,Ilic Predrag N},
year={2008},
title={A Novel Mutation of the Abcd1 Gene in Serbian X-Adrenoleukodystrophy},
journal={BALKAN JOURNAL OF MEDICAL GENETICS},
volume={11},
number={1},
pages={65-67},
document_type={Article},
} 

@ARTICLE{
author={Stojiljkovic Maja M,Stevanovic Ana Z,Djordjevic Maja S,Petrucev Branka,Tosic Natasa M,Karan-Djurasevic Teodora Z,Aveic Sanja,Radmilovic Milena M,Pavlovic Sonja T},
year={2007},
title={Mutations in the pah gene: a tool for population genetics study},
journal={ARCHIVES OF BIOLOGICAL SCIENCES},
volume={59},
number={3},
pages={161-167},
document_type={Article},
} 

@ARTICLE{
author={Stojiljkovic Maja M,Jovanovic J,Djordjevic Maja S,Grkovic Sanja,Cvorkov-Drazic Milica,Petrucev Branka,Tosic Natasa M},
year={2007},
title={Molecular and phenotypic characteristics of patients with phenylketonuria in Serbia and Montenegro},
journal={FEBS JOURNAL},
volume={274},
number={},
pages={287-287},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Djordjevic Maja S,Minic Predrag B,Djuricic Slavisa M,Djokic Dragan,Sarajlija Adrijan},
year={2007},
title={Pulmonary involvement in patient with Gaucher disease type III after 4 years of enzyme replacement therapy},
journal={JOURNAL OF INHERITED METABOLIC DISEASE},
volume={30},
number={},
pages={119-119},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Stojiljkovic Maja M,Stevanovic Ana Z,Djordjevic Maja S,Petrucev Branka,Tosic Natasa M,Karan-Djurasevic Teodora Z,Aveic Sanja,Radmilovic Milena M,Pavlovic Sonja T},
year={2007},
title={Elucidation of the origin of L48S PAH mutation in Serbian population},
journal={JOURNAL OF INHERITED METABOLIC DISEASE},
volume={30},
number={},
pages={9-9},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Kravljanac Ruzica M,Djordjevic Maja S,Jovic Nebojsa J,Djuric Milena Lj,Pekmezovic Tatjana D},
year={2006},
title={Status epilepticus in children with progressive myoclonus epilepsies},
journal={EPILEPSIA},
volume={47},
number={},
pages={7-7},
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},
} 

@ARTICLE{
author={Stojiljkovic Maja M,Jovanovic J,Djordjevic Maja S,Grkovic Sanja,Cvorkov-Drazic Milica,Petrucev Branka,Tosic Natasa M,Karan-Djurasevic Teodora Z,Stojanov L,Pavlovic Sonja T},
year={2006},
title={Phenylketonuria in Serbia and Montenegro},
journal={JOURNAL OF INHERITED METABOLIC DISEASE},
volume={29},
number={},
pages={82-82},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Stojiljkovic Maja M,Jovanovic J,Djordjevic Maja S,Grkovic Sanja,Cvorkov-Drazic Milica,Petrucev Branka,Tosic Natasa M,Karan-Djurasevic Teodora Z,Stojanov L,Pavlovic Sonja T},
year={2006},
title={Molecular and phenotypic characteristics of patients with phenylketonuria in Serbia and Montenegro},
journal={CLINICAL GENETICS},
volume={70},
number={2},
pages={151-155},
document_type={Article},
} 

@ARTICLE{
author={Jovasevic L,Djordjevic Maja S},
year={2003},
title={Significance of a complex balneal-physiatric-medical treatment of female patients suffering involutive osteoporosis},
journal={OSTEOPOROSIS INTERNATIONAL},
volume={14},
number={},
pages={S85-S85},
document_type={Meeting Abstract},
} 

@ARTICLE{
author={Marjanovic Borivoj D,Stojanov LM,Zdravkovic Dragan S,Kravljanac Ruzica M,Djordjevic Maja S},
year={2003},
title={Rasmussen syndrome and long-term response to thalidomide},
journal={PEDIATRIC NEUROLOGY},
volume={29},
number={2},
pages={151-156},
document_type={Article},
} 

@ARTICLE{
author={Marjanovic Borivoj D,Stojanov LM,Zamurovic Dragan R,Pasic Srdjan S,Kravljanac Ruzica M,Djordjevic Maja S},
year={2003},
title={Fulminant subacute sclerosing panencephalitis: Two cases with atypical presentation},
journal={PEDIATRIC NEUROLOGY},
volume={29},
number={1},
pages={63-65},
document_type={Article},
} 

@ARTICLE{
author={Guc-Scekic Marija P,Milasin Jelena M,Stevanovic M,Stojanov LJ,Djordjevic Maja S},
year={2002},
title={Tetraploidy in a 26-month-old girl (cytogenetic and molecular studies)},
journal={CLINICAL GENETICS},
volume={61},
number={1},
pages={62-65},
document_type={Article},
}