Faculty of Medicine
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Item type:Publication, THE MESORECTUM AND MESORECTAL FASCIA – A TOPOGRAPHIC-ANATOMICAL OVERVIEW(Serbian Anatomical Society (Српско анатомско друштво – САДС), 2026-09-24); ; ; ; - Some of the metrics are blocked by yourconsent settings
Item type:Publication, VERTEBRAL LEVEL OF ORIGIN OF THE ANTERIOR BRANCHES OF THE ABDOMINAL AORTA IN A CT ANGIOGRAPHIC STUDY(Serbian Anatomical Society (Српско анатомско друштво – САДС), 2026-09-24); ; ; ; - Some of the metrics are blocked by yourconsent settings
Item type:Publication, SEXUAL DIMORPHISM OF DERMATOGLYPHIC PATTERNS IN NORTH MACEDONIA(Comenius University Bratislava, 2026-09-10); ; ; ; - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Evaluation of the C-Reactive Protein to HDL Cholesterol Ratio as a Marker of Cardiovascular and Renal Risk Among Type 2 Diabetic Patients(Galenos Publishing House, 2026-08-27); ; - Some of the metrics are blocked by yourconsent settings
Item type:Publication, ANATOMICAL FEATURES OF THE VERTEBROBASILAR SYSTEM AND CLINICAL SIGNIFICANCE(Serbian Anatomical Society = Српско анатомско друштво – САДС, 2026-09-24) - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Community Engagement and Policy Dialog in Advancing Tobacco Control Legislation in North Macedonia ii.(Society for Research on Nicotine and Tobacco, 2026-09); - Some of the metrics are blocked by yourconsent settings
Item type:Publication, MANAGEMENT OF TWO IVF PREGNANCIES IN A PATIENT WITH A BICORNUATE UTERUS WITH ONE CERVIX AND A TOTAL OCCLUSION OF BOTH TUBES(SHMSHM - AAMD, 2026); ; ; - Some of the metrics are blocked by yourconsent settings
Item type:Publication, ALDOSTERONE SYNTHASE DEFICIENCY FROM HOMOZYGOUS CYP11B2 MUTATION PRESENTING WITH SALT WASTING CRISIS AND FAILURE TO THRIVE IN AN INFANT(Department of Anaesthesia and Reanimation, Faculty of Medicine, Ss. Cyril and Methodius University in Skopje, R.N. Macedonia, 2025-12-17); ; Spasevska, SimonidaAbstract Introduction: Aldosterone synthase deficiency (ASD) is a rare autosomal recessive disorder caused by pathogenic variants in the CYP11B2 gene, leading to impaired aldosterone synthesis and life-threatening salt-wasting. We present a case of an infant with failure to thrive, dehydration, and electrolyte imbalance, diagnosed through next-generation sequencing. Material and Methods: mitted with persistent vomiting, constipation, and a10% weight loss. Laboratory evaluation showed severe hyponatremia (116 mmol/L), hyperkalemia (6.5 mmol/L), hypochloremia (87 mmol/L), and metabolic alkalosis. Differential diagnosis included gastrointestinal loss, renal salt-wasting, cystic fibrosis, celiac disease, and congenital adrenal hyperplasia. Normal 17-hydroxyprogesterone excluded classical CAH. Next-generation sequencing was performed. Results: A homozygous pathogenic variant c.554C>T (p.Thr185Ile) in CYP11B2 confirmed ASD. Treatment with fludrocortisone and sodium supplementation resulted in rapid correction of electrolytes and improved growth. Follow-up at 3.5 years showed normal growth (14.5 kg, 103 cm), stable electrolytes, and normal development, with only mild transient hyponatremia during illness. Conclusion: ASD should be considered in infants with vomiting, dehydration, and combined hyponatremia–hyperkalemia when CAH is excluded. Early diagnosis and mineralocorticoid therapy prevent complications and support normal development. - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Population pharmacokinetics of intravenous moxifloxacin in hospitalized patients with acute exacerbation of COPD(Macedonian Pharmaceutical Association, Ss. Cyril and Methodius University in Skopje, Faculty of Pharmacy, 2026); ; Evgenija Mihajlovska - Some of the metrics are blocked by yourconsent settings
Item type:Publication, COMPARISON OF TWO DIAGNOSTIC IMAGING TECHNIQUES FOR DIAGNOSISNG SYNOVIAL CHONDROMATOSIS OF THE TEMPOROMANDIBULAR JOINT(Macedonian Association of Anatomists and Morphologists, 2025-07-04)