Adrijan Sarajlija
Belgrade, SE, Serbia
Last Updated: 09/26/2026
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Found 40 publications
Secretory Breast Carcinoma in A Six-Year-Old Girl: Case Report With Genetic Insights and Therapeutic Implications.
Journal: Balkan journal of medical genetics : BJMG
Published: May 18, 2026
The Diagnostic Journey from Rhabdomyolysis to Myopathy with Tubular Aggregates: A Family-Based Case Report and Review of the Literature.
Journal: Pediatric reports
Published: May 18, 2026
Townes-Brocks Syndrome With Consistent Renal Hypodysplasia and Variable Extrarenal Features Across Three Generations of Serbian Family.
Journal: Balkan journal of medical genetics : BJMG
Published: May 18, 2026
From Suspected Congenital Cytomegalovirus Infection to Malan Syndrome: Delayed Genetic Diagnosis Due to Diagnostic Anchoring.
Journal: Diseases (Basel, Switzerland)
Published: April 26, 2026
Neuromuscular Disorders in Children Through the Lens of Next-Generation Sequencing: A Study of Diagnostic Yield.
Journal: International journal of molecular sciences
Published: March 23, 2026
Chronic Kidney Disease in Children with Suspected Genetic Etiology: Diagnostic Yield and Clinical Implications.
Journal: Journal of personalized medicine
Published: March 14, 2026
Comprehensive Assessment of the Risk of Developing Coronary Artery Aneurysm in Kawasaki Disease: A KawaCOR Score Study.
Journal: Life (Basel, Switzerland)
Published: February 15, 2026
Severe Familial Hypertriglyceridemia in a Child with Compound Heterozygous Pathogenic APOA5 Variants: A Case Report and Therapeutic Challenge.
Journal: Journal of clinical research in pediatric endocrinology
Published: October 30, 2025
Artificial Intelligence in the Diagnosis of Pediatric Rare Diseases: From Real-World Data Toward a Personalized Medicine Approach.
Journal: Journal of personalized medicine
Published: July 15, 2025
Case Report: A thrombosis of ductus arteriosus aneurysm involving the left pulmonary artery in a full-term newborn with isolated right ventricular hypoplasia.
Journal: Frontiers in pediatrics
Published: May 06, 2025
Phenotypic Variability of Cowden Syndrome Within a Single Family: Impact on Diagnosis, Management and Genetic Counselling.
Journal: Balkan journal of medical genetics : BJMG
Published: March 12, 2025
Last Updated: 09/26/2026