Published in Pediatr Int on October 23, 2009
Game-based biofeedback for paediatric anxiety and depression. Ment Health Fam Med (2011) 0.86
Mosaic overgrowth with fibroadipose hyperplasia is caused by somatic activating mutations in PIK3CA. Nat Genet (2012) 1.74
Copy-number disorders are a common cause of congenital kidney malformations. Am J Hum Genet (2012) 1.63
Clinical delineation and natural history of the PIK3CA-related overgrowth spectrum. Am J Med Genet A (2014) 1.20
Central precocious puberty that appears to be sporadic caused by paternally inherited mutations in the imprinted gene makorin ring finger 3. J Clin Endocrinol Metab (2014) 1.05
Atypical presentation of distal renal tubular acidosis in two siblings. Pediatr Nephrol (2008) 1.04
The impact of CFNS-causing EFNB1 mutations on ephrin-B1 function. BMC Med Genet (2010) 0.93
Long-acting pegylated human GH in children with GH deficiency: a single-dose, dose-escalation trial investigating safety, tolerability, pharmacokinetics and pharmacodynamics. Eur J Endocrinol (2011) 0.93
Clinical and functional characterization of URAT1 variants. PLoS One (2011) 0.92
Analysis of TSHZ2 and TSHZ3 genes in congenital pelvi-ureteric junction obstruction. Nephrol Dial Transplant (2009) 0.90
Aseptic necrosis of both tali in a child with steroid-dependent nephrotic syndrome. Nephrol Dial Transplant (2006) 0.78
Clinical and laboratory features of Macedonian children with OCRL mutations. Pediatr Nephrol (2011) 0.78
Obesity in childhood and adolescence, genetic factors. Prilozi (2013) 0.78
Nephrotic syndrome occurring during tiopronin treatment for cystinuria. Eur J Pediatr (2010) 0.77
Chronic kidney disease - pediatric risk factors. Pril (Makedon Akad Nauk Umet Odd Med Nauki) (2016) 0.77
Autoimmune thyroiditis and diabetes mellitus type 1 after long-term gonadotropin-releasing hormone agonist treatment for central precocious puberty: evolution or coincidence? J Pediatr Endocrinol Metab (2010) 0.77
QEEG characteristics and spectrum weighted frequency for children diagnosed as autistic spectrum disorder. Nonlinear Biomed Phys (2010) 0.76
Weight, height and puberty in a cohort of Macedonian girls. Med Arh (2009) 0.76
Nephrolithiasis and Nephrocalcinosis in Children - Metabolic and Genetic Factors. Pediatr Endocrinol Rev (2015) 0.75
Compound Galactosylceramidase Gene (GALC) Heterozygosity in a Boy with Infantile Krabbe Disease (KD). Pril (Makedon Akad Nauk Umet Odd Med Nauki) (2015) 0.75
Autoimmune thyroiditis in a child with steroid-dependent nephrotic syndrome. Eur J Pediatr (2008) 0.75
Recurrent urinary tract infections in an infant with antenatal Bartter syndrome. World J Pediatr (2010) 0.75
New insights into septo-optic dysplasia. Prilozi (2014) 0.75
Steroid Resistant Nephrotic Syndrome-Genetic Consideration. Pril (Makedon Akad Nauk Umet Odd Med Nauki) (2015) 0.75
Failure to thrive and nephrolithiasis in a boy with congenital cyanotic heart anomaly. Pediatr Nephrol (2011) 0.75
4th Rare Disease South Eastern Europe (See) Meeting Skopje, Macedonia (November 14th, 2015). Pril (Makedon Akad Nauk Umet Odd Med Nauki) (2015) 0.75
Some Psychological Aspects of T1DM in Children and Adolescents. Pril (Makedon Akad Nauk Umet Odd Med Nauki) (2015) 0.75
Tricho-rhino-phalangeal syndrome in a 13-year-old girl with chronic renal failure and severe growth retardation. Ren Fail (2014) 0.75
LHX4 Gene Alterations: Patient Report and Review of the Literature. Pediatr Endocrinol Rev (2016) 0.75
Where are we now in the investigation of rare diseases in the Republic of Macedonia? Prilozi (2014) 0.75
Kidney diseases in children - early diagnosis and prevention. Pril (Makedon Akad Nauk Umet Odd Med Nauki) (2016) 0.75