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Natural Evolution of Morquio A Syndrome Caused by Two Heterozygous Mutations of the GALNS Gene

Balkan medical journal, 2022-05, Vol.39 (3), p.220-221

2022

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Characteristics and quality of life of substance users and their caregivers

Medicine (Baltimore), 2022-08, Vol.101 (31), p.e29699

2022

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Autism and Hypoplastic Corpus Callosum in a Case of Monocentric Marker Chromosome 15

Pediatric neurology, 2009-07, Vol.41 (1), p.65-67

2009

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Accessory Scrotum Attached to a Peduncular Perineal Lipoma

Pediatric dermatology, 2012-07, Vol.29 (4), p.522-524

2012

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Complete androgen insensitivity syndrome: Review of four cases

Central European journal of medicine, 2012-12, Vol.7 (6), p.729-732

2012

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Oral contraceptive use, coffee consumption, and other risk factors of type 2 diabetes in women: a case-control study

Journal of substance use, 2024-05, Vol.ahead-of-print (ahead-of-print), p.1-9

2024

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Factors associated with smoking habits among undergraduate medical students: a cross-sectional study

Journal of substance use, 2023-03, Vol.28 (2), p.206-210

2023

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LATE INFANTILE TYPE OF METACHROMATIC LEUKODYSTROPHY CAUSED BY NOVEL COMBINATION OF HETEROZYGOUS ARSA MUTATIONS

Acta endocrinologica (Bucharest, Romania : 2005), 2018-01, Vol.14 (1), p.131-131

2018

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Glycogen Storage Disease Type 1B Associated with A Unilateral Hypoplastic Temporal Lobe

Acta endocrinologica (Bucharest, Romania : 2005), 2014, Vol.10 (3), p.530-531

Kavecan, I

2014

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Unilateral Type of Macrodystrophia Lipomatosa of the Thumb, Index Finger, and Thenar

Balkan medical journal, 2019-01, Vol.36 (1), p.60-61

2019

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Monitoring of pregnancies with successful deliveries in a Niemann-Pick disease type B patient - case report and literature review

Srpski arhiv za celokupno lekarstvo, 2023-05, Vol.151 (5-6), p.363-366

2023

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FEBRILE AND AFEBRILE SEIZURES ASSOCIATED WITH MILD ACUTE GASTROENTERITIS IN CHILDHOOD/FEBRILNI I AFEBRILNI NAPADI UDRUZENI SA BLAGIM AKUTNIM GASTROENTERITISOM U DETINJSTVU

Medicinski pregled, 2022-05, Vol.75 (5-6), p.166

2022

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Febrile and afebrile seizures associated with mild acute gastroenteritis in childhood

Medicinski pregled, 2022, Vol.75 (5-6), p.166-170

2022

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Parasitic Twin Presenting Rudimentary Upper Limbs Causes a Unique Spectrum of Anomalies of Autosite

Balkan medical journal, 2018-01, Vol.35 (6), p.445-446

2018

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Birth of a healthy child fathered by a man with Klinefelter`s syndrome after preimplantation genetic testing

Vojnosanitetski pregled, 2021-01, Vol.78 (8), p.896-900

2021

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Evolution of Partially Involuting Congenital Hemangiomas of the Face

Journal of cutaneous medicine and surgery, 2019-03, Vol.23 (2), p.225-225

2019

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Clinical manifestation of Johanson-Blizzard syndrome in patient with nucleotide variants in UBR1 gene

Vojnosanitetski pregled, 2023, Vol.80 (10), p.885-889

2023

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Pachydermodactyly: A Rare Type of Macrodactyly as a Dermatological Sign of Compulsive Behavior and Repetitive Minor Trauma; a Case Report and Review of the Literature

Iranian red crescent medical journal, 2018-09, Vol.20 (9)

2018

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Pediatric acute disseminated encephalomyelitis associated with myelin oligodendrocyte glycoprotein antibodies

Srpski arhiv za celokupno lekarstvo, 2022-03, Vol.150 (3-4), p.212-215

2022

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A case of infant hot water epilepsy: A clinical commentary with video sequences

Seizure (London, England), 2015-09, Vol.31, p.5-6

2015

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Assessment of intellectual impairment, health‐related quality of life, and behavioral phenotype in patients with neurotransmitter related disorders: Data from the iNTD registry

Journal of inherited metabolic disease, 2021-11, Vol.44 (6), p.1489-1502

2021

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Genetic Counseling and Prenatal Diagnosis of Triploidy During the Second Trimester of Pregnancy

Medicinski arhiv, 2017-04, Vol.71 (2), p.144-147

2017

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FOURTEEN YEARS OF NEWBORN SCREENING FOR PHENYLKETONURIA IN VOJVODINA/CETRNAEST GODINA NOVORODENACKOG SKRININGA FENILKETONURIJE U VOJVODINI

Medicinski pregled, 2017-11, Vol.70 (11-12), p.411

2017

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Natural Evolution of Morquio A Syndrome Caused by Two Heterozygous Mutations of the GALNS Gene

Characteristics and quality of life of substance users and their caregivers

Autism and Hypoplastic Corpus Callosum in a Case of Monocentric Marker Chromosome 15

Accessory Scrotum Attached to a Peduncular Perineal Lipoma

Complete androgen insensitivity syndrome: Review of four cases

Oral contraceptive use, coffee consumption, and other risk factors of type 2 diabetes in women: a case-control study

Factors associated with smoking habits among undergraduate medical students: a cross-sectional study

LATE INFANTILE TYPE OF METACHROMATIC LEUKODYSTROPHY CAUSED BY NOVEL COMBINATION OF HETEROZYGOUS ARSA MUTATIONS

Glycogen Storage Disease Type 1B Associated with A Unilateral Hypoplastic Temporal Lobe

Unilateral Type of Macrodystrophia Lipomatosa of the Thumb, Index Finger, and Thenar

Monitoring of pregnancies with successful deliveries in a Niemann-Pick disease type B patient - case report and literature review

FEBRILE AND AFEBRILE SEIZURES ASSOCIATED WITH MILD ACUTE GASTROENTERITIS IN CHILDHOOD/FEBRILNI I AFEBRILNI NAPADI UDRUZENI SA BLAGIM AKUTNIM GASTROENTERITISOM U DETINJSTVU

Febrile and afebrile seizures associated with mild acute gastroenteritis in childhood

Parasitic Twin Presenting Rudimentary Upper Limbs Causes a Unique Spectrum of Anomalies of Autosite

Insights into the expanding phenotypic spectrum of inherited disorders of biogenic amines

Birth of a healthy child fathered by a man with Klinefelter`s syndrome after preimplantation genetic testing

Evolution of Partially Involuting Congenital Hemangiomas of the Face

Clinical manifestation of Johanson-Blizzard syndrome in patient with nucleotide variants in UBR1 gene

Pachydermodactyly: A Rare Type of Macrodactyly as a Dermatological Sign of Compulsive Behavior and Repetitive Minor Trauma; a Case Report and Review of the Literature

Levodopa‐refractory hyperprolactinemia and pituitary findings in inherited disorders of biogenic amine metabolism

Pediatric acute disseminated encephalomyelitis associated with myelin oligodendrocyte glycoprotein antibodies

A case of infant hot water epilepsy: A clinical commentary with video sequences

Assessment of intellectual impairment, health‐related quality of life, and behavioral phenotype in patients with neurotransmitter related disorders: Data from the iNTD registry

Genetic Counseling and Prenatal Diagnosis of Triploidy During the Second Trimester of Pregnancy

FOURTEEN YEARS OF NEWBORN SCREENING FOR PHENYLKETONURIA IN VOJVODINA/CETRNAEST GODINA NOVORODENACKOG SKRININGA FENILKETONURIJE U VOJVODINI

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