A5086174671- Neonatal Respiratory Health Research
- Parvovirus B19 Infection Studies
- Neonatal Health and Biochemistry
- Neonatal and fetal brain pathology
- Sexual Differentiation and Disorders
- Herpesvirus Infections and Treatments
- Sepsis Diagnosis and Treatment
- Neonatal and Maternal Infections
- Influenza Virus Research Studies
- Dermatological and COVID-19 studies
- Cytomegalovirus and herpesvirus research
- Streptococcal Infections and Treatments
- Genetic Syndromes and Imprinting
- Metabolism and Genetic Disorders
- Epilepsy research and treatment
- Respiratory viral infections research
- Congenital Diaphragmatic Hernia Studies
- Neuroscience of respiration and sleep
- Urological Disorders and Treatments
- Enterobacteriaceae and Cronobacter Research
- Blood groups and transfusion
- Hormonal and reproductive studies
- Genomic variations and chromosomal abnormalities
- Genetic Neurodegenerative Diseases
- Airway Management and Intubation Techniques
University of Belgrade
2011-2024
Institute of Public Health of Serbia
2007-2023
Institut za Zdravstvenu Zastitu Majke i Deteta
2006-2021
University of Belgrade – Faculty of Medicine
2021
ABSTRACT The syndrome of malignant migrating partial seizures in infancy is a devastating, age‐specific, epileptic encephalopathy, which still presents an aetiological, pathophysiological and therapeutic problem. In this study, we present two patients who were diagnosed with the disease, based on electroclinical symptoms. treated combination sodium bromide, stiripentol levetiracetam. first patient unequivocally responded, following course ineffective conventional drugs, second, was...
Abstract Disseminated neonatal herpes simplex virus (HSV) infection is characterized by progressive multiple organ failure and high mortality rates. It can result from with either HSV-1 or HSV-2. We report a case of disseminated that was caused
The aim of this prospective cohort study was to determine the prevalence gut colonization with multidrug-resistant (MDR) bacteria, risk factors for colonization, infection risk, and outcomes among preterm neonates hospitalized at a tertiary-care center in Serbia. During period from December 2017 April 2018, 103 were screened rectal carriage admission on seventh day life. Characterization MDR strains done by conventional microbiology molecular methods. Out 61 (59.2%) colonized neonates, 12...
We report a case of late onset neonatal invasive group A streptococcal disease characterized with rapidly progressing cellulitis and development sepsis. The infection was acquired from benign mild skin the child's mother. causative agent streptococcus, belonging to emm type 53.2, which usually causes disease.
We describe a female infant who developed transient neonatal diabetes mellitus (TNDM) (MIM 601410). At birth she presented with growth retardation and macroglossia. Diabetes was diagnosed on the fourth day of life it resolved after two months insulin therapy. Genetic testing revealed presence paternal uniparental disomy chromosome 6 (UPD6) including heterodisomy 6q24. This is first documented case for 6.
Introduction/Objective. Air leak syndrome is more frequent in neonatal period than at any other of life. Its timely recognition and treatment a medical emergency. We present results tertiary center air term late preterm neonates. Methods. Neonates born between 34th 0/7 41st 6/7 gestational weeks (g.w.) who were treated for the Neonatal Intensive Care Unit Mother Child Health Institute, from 2005 to 2015 included study. Antropometric data, perinatal history, type respiratory support prior...
Background/Aim. Intravenous immunoglobulin is a blood product made of human polyclonal G. The mode action intravenous very complex. It indicated in treatment neonatal immune thrombocytopenia and haemolytic disease the newborn. aim study was to present our experience use group term neonates. Methods. We analysed all relevant clinical laboratory data 23 neonates who recieved during their hospitalization Neonatal Intensive Care Unit Mother Child Health Institute over five year period, from...
The aim of the present survey was to analyze knowledge and skills in medical paper writing physicians who attended course "how write successfully a scientific paper."A blind used participants' on topic paper." Before starting workshop, participants anonymously filled out input questionnaire containing 12 preliminary data questions. three-hour included lecture steps creating article with examples. At end, all completed exit consisting 18 Differences associations between collected were...
Introduction. Hemophilia is the most frequently diagnosed inborn clotting factor deficiency in newborn. In about half of cases diagnosis made during neonatal period. However, due to different clinical presentation comparing older children, hemophilia newborn could be misdiagnosed, especially setting negative family history. Case report. Clinical features three newborns with history for are described. All were first born children uneventful perinatal history, and they referred investigation...
Disorders of sexual development can present isolated or as a part complex genetic syndromes.A newborn with ambiguous genitalia and prenatally diagnosed brain malformations was referred to our hospital. Prenatal ultrasound examination MRI showed lissencephaly absence the corpus callosum. At admission, physical revealed microphallus, hypospadia complete fusion labioscrotal folds nonpalpable gonads, normal blood pressure serum biochemistry. Cortisol level (201 nmol/L), testosterone elevated...
Fetomaternal hemorrhage (FMH) is a transfu-sion of fetal blood into the maternal circulation. A volume transfused required to cause severe, life-threatening anemia, not clearly defined. Some authors suggest vol-umes 80 mL and 150 as threshold which defines mas-sive FMH. Therefore, rate massive FMH 1 : 1,000 5,000 births, respectively. Fetal neonatal anemia one most serious complications Clinical manifesta-tions are nonspecific, mostly it presented re-duced movements changes in...
Introduction. Non-immune hydrops fetalis is a condition of excessive accumulation extravascular fluid without identifiable circulating antibody to erythrocytes membrane antigens. In newborn infants it characterized by skin oedema and pleural, pericardial or peritoneal effusion. the era routine Rh immunization for prevention foetal erythroblastosis, non-immune pathophysiologic mechanisms are presented in 76-87% all hydropic newborns. can be associated with numerous various disorders. The...
Introduction/Objective. Vitamin K deficiency is common in newborn infants and without prophylaxis there a risk of vitamin bleeding (VKDB). The most frequent prophylactic approach an intramuscular (IM) injection K1 immediately after birth. Its efficiency to prevent late VKDB has been recently questioned by several reports. Based on our experience, we discuss the need for additional supplementation its IM administration at Methods. We present retrospective review 12 infants, 11 with confirmed...
Introduction/aim: Disorders of sex development (DSD) comprise a heterogeneous group congenital conditions with difference between chromosomal, gonadal and the appearance external genitalia. The frequency DSD is 1: 4,500-5,500 newborns per year. Congenital adrenal hyperplasia (CAH) due to deficiency 21-hydroxylase enzyme one most common best-known causes DSD. Other forms CAH, as well other DSD, occur significantly lower individual frequencies are thus more challenging diagnose treat. aim...
With 20-80% mortality, neonatal infection caused by herpes simplex virus (HSV) or is among the most severe of all perinatal infections. The majority HSV infections are acquired during delivery, although in utero and postnatal do occur. Primary maternal associated with a high rate transmission (~50%), compared to <3% infants women reactivated disease. Other factors that influence include type, premature etc. Clinical manifestations have been classified into three forms: skin-eye-mouth...
Introduction: Congenital adrenal hyperplasia (CAH) is a group of autosomal recessive diseases caused by deficiency enzymes responsible for the steroidogenesis. There are three forms CAH due to 21-hydroxylase deficiency: classic form with salt loss, virilizing and non-classic form. The aim paper was analyze changes in diagnosis treatment children during previous 15 years. Material methods: This retrospective cohort study includes patients who were diagnosed period from 2007 2021 endocrinology...
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