Researchers
Sarajlija, Adrijan
Results 1-20 of 60
| Issue Date | Title | Author(s) | Type | Мp-cat. |
|---|---|---|---|---|
| 2026 | Comprehensive Assessment of the Risk of Developing Coronary Artery Aneurysm in Kawasaki Disease: A KawaCOR Score Study![]() | Krasić, Staša; Pašić, Srđan | Article | 21M21 |
| 2026 | Neuromuscular Disorders in Children Through the Lens of Next-Generation Sequencing: A Study of Diagnostic Yield![]() | Ostojić, Slavica; Kovačević, Gordana | Article | 21M21 |
| 2026 | Secretory Breast Carcinoma in a Six-Year-Old Girl: Case Report with Genetic Insights and Therapeutic Implications![]() | Vlahović, Aleksandar M. | Article | 23M23 |
| 2025 | Case Report: A thrombosis of ductus arteriosus aneurysm involving the left pulmonary artery in a full-term newborn with isolated right ventricular hypoplasia![]() | Krasić, Staša D.; Đorović, Nevena; Dizdarević, Ivan D.; Topić, Vesna; Ilić, Nikola; Sarajlija, Adrijan | Article | 21M21 |
| 2025 | Kardiomiopatije sa naslednom osnovom![]() | Vukomanović, Vladislav | Book parts | Mp. category will be shown later |
| 2025 | The Artificial Intelligence-Assisted Diagnosis of Skeletal Dysplasias in Pediatric Patients: A Comparative Benchmark Study of Large Language Models and a Clinical Expert Group![]() | Ilić, Nikola A.; Marić, Nina; Cvetković, Dimitrije; Bogosavljević, Marko; Bukara-Radujković, Gordana; Krstić, Jovana; Paunović, Zoran; Begović, Ninoslav; Panić-Zarić, Sanja; Todorović, Slađana; | Article | 22M22 |
| 2025 | Townes-Brocks Syndrome With Consistent Renal Hypodysplasia and Variable Extrarenal Features Across Three Generations of Serbian Family![]() | Paripović, Aleksandra | Article | 23M23 |
| 2025 | Neuroblastoma Occurring in Nijmegen Breakage Syndrome![]() | Đurišić, Marina; Sarajlija, Adrijan | Article | 22M22 |
| 2025 | Phenotypic Variability of Cowden Syndrome Within a Single Family: Impact on Diagnosis, Management and Genetic Counselling![]() | Ilić, Nikola; Mitrović, Nemanja; Radeta, Ratko N. | Article | 23M23 |
| 2025 | Neuroglial Dysregulation in Autism Spectrum Disorder: Pathogenetic Insights, Genetic Threads, and Therapeutic Horizons![]() | Ilić, Nikola A.; Sarajlija, Adrijan | Reviews | Mp. category will be shown later |
| 2024 | Treatment of RAF1-Related Biventricular Hypertrophy and Double Chamber Right Ventricle by MEK Inhibition Using Trametinib![]() | Krasić, Staša; Đurić, Ivana | Article | 21aM21a |
| 2024 | Reverse Phenotyping after Whole-Exome Sequencing in Children with Developmental Delay/Intellectual Disability-An Exception or a Necessity?![]() | Ilić, Nikola A.; Marić, Nina; Maver, Aleš; Armengol, Lluis; Kravljanac, Ružica M. | Article | 22M22 |
| 2024 | COVID-19 vaccine hesitancy in Serbia![]() | Jeremić-Stojković, Vida | Article | 53M53 |
| 2024 | Noonan Syndrome: Relation of Genotype to Cardiovascular Phenotype-A Multi-Center Retrospective Study![]() | Ilić, Nikola; Krasić, Staša; Marić, Nina; Gašić, Vladimir V. | Article | 22M22 |
| 2024 | Complications of pneumococcal meningitis in a child with proteus syndrome: A case report and literature review![]() | Ostojić, Slavica; Kravljanac, Ružica | Article | 53M53 |
| 2024 | Expanding the Phenotypic Spectrum: Chronic Kidney Disease in a Patient with Combined Oxidative Phosphorylation Defect 21![]() | Paripović, Aleksandra; Maver, Aleš; Stajić, Nataša; Putnik, Jovana; Ostojić, Slavica B.; Alimpić, Biljana; Ilić, Nina; Sarajlija, Adrijan | Article | 23M23 |
| 2024 | Bisphosphonate Therapy in a Pediatric Case Series with Monostotic Form of Fibrous Dysplasia: A Single-Center Retrospective Analysis of Efficacy and Safety![]() | Ilić, Nikola; Cvetković, Dimitrije; Paunović, Zoran; Bogosavljević, Marko; Krstić, Jovana; Todorović, Slađana; Sarajlija, Adrijan | Conference Paper | Mp. category will be shown later |
| 2023 | Age-specific causes of upper gastrointestinal bleeding in children![]() | Kocić, Marija; Rašić, Petar; Marušić, Vuk P. | Article | 21M21 |
| 2023 | Three case reports of patients with rare copy number variations in the recurrent 2q11.1-q11.2 region![]() | Perović, Dijana | Conference Paper | Mp. category will be shown later |
| 2023 | Sensorineural Hearing Loss in a Child with Succinic Semialdehyde Dehydrogenase Deficiency![]() | Parezanović, M.; Ilić, Nina; Ostojić, Slavica; Stevanović, Galina B.; Ječmenica, Jovana R.; Maver, Ales; Sarajlija, Adrijan | Article | 23M23 |
