Danijela Radivojevic
Belgrade, SE, Serbia
Last Updated: 09/26/2026
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Found 12 publications
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
Chronic Kidney Disease in Children with Suspected Genetic Etiology: Diagnostic Yield and Clinical Implications.
Journal: Journal of personalized medicine
Published: March 14, 2026
Reverse Phenotyping after Whole-Exome Sequencing in Children with Developmental Delay/Intellectual Disability-An Exception or a Necessity?
Journal: Genes
Published: May 02, 2024
Neuroblastoma Occurring in Nijmegen Breakage Syndrome.
Journal: Journal of pediatric hematology/oncology
Published: February 26, 2024
Novel intragenic deletions within the UBE3A gene in two unrelated patients with Angelman syndrome: case report and review of the literature.
Journal: BMC medical genetics
Published: February 28, 2017
Ten years of experience in molecular prenatal diagnosis and carrier testing for spinal muscular atrophy among families from Serbia.
Journal: International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics
Published: April 17, 2013
Potential influence of tubular dysfunction on the difference between estimated and measured glomerular filtration rate after kidney transplantation.
Journal: Transplantation proceedings
Published: December 13, 2012
Newborn screening for cystic fibrosis in Serbia: a pilot study.
Journal: Pediatrics international : official journal of the Japan Pediatric Society
Published: August 07, 2012
Molecular analysis of ring y chromosome in a 10-year-old boy with mixed gonadal dysgenesis and growth hormone deficiency.
Journal: Balkan journal of medical genetics : BJMG
Published: December 01, 2011
Lower incidence of deletions in the survival of motor neuron gene and the neuronal apoptosis inhibitory protein gene in children with spinal muscular atrophy from Serbia.
Journal: The Tohoku journal of experimental medicine
Published: October 06, 2011
Showing 1-12 of 12
Last Updated: 09/26/2026