Published in Acta Paediatr on November 04, 2011
Acute vitamin D intoxication possibly due to faulty production of a multivitamin preparation. J Clin Res Pediatr Endocrinol (2013) 0.96
Vitamin D and Risk for Vitamin A Intoxication in an 18-Month-Old Boy. Case Rep Pediatr (2016) 0.75
Reference values for serum dehydroepiandrosterone-sulphate in healthy children and adolescents with emphasis on the age of adrenarche and pubarche. Clin Endocrinol (Oxf) (2014) 2.07
Novel associations in disorders of sex development: findings from the I-DSD Registry. J Clin Endocrinol Metab (2013) 1.76
Identification of PENDRIN (SLC26A4) mutations in patients with congenital hypothyroidism and "apparent" thyroid dysgenesis. J Clin Endocrinol Metab (2013) 1.61
Clinically significant neonatal hyperbilirubinemia: an analysis of 646 cases in Istanbul. J Trop Pediatr (2008) 1.47
Cathepsin K analysis in a pycnodysostosis cohort: demographic, genotypic and phenotypic features. Orphanet J Rare Dis (2014) 1.47
Vitamin D deficiency and prevention: Turkish experience. Acta Paediatr (2011) 1.23
Serum alkaline phosphatase levels in healthy children and evaluation of alkaline phosphatase z-scores in different types of rickets. J Clin Res Pediatr Endocrinol (2011) 1.19
Vitamin D intoxication. Turk J Pediatr (2012) 1.15
Rickets in the Middle East: role of environment and genetic predisposition. J Clin Endocrinol Metab (2008) 1.09
Consensus development for the supplementation of vitamin D in childhood and adolescence. Horm Res (2002) 1.02
Addition of orlistat to conventional treatment in adolescents with severe obesity. Eur J Pediatr (2004) 0.99
Puberty and influencing factors in schoolgirls living in Istanbul: end of the secular trend? Pediatrics (2011) 0.99
Free vitamin D supplementation for every infant in Turkey. Arch Dis Child (2007) 0.95
Identification of a novel dentin matrix protein-1 (DMP-1) mutation and dental anomalies in a kindred with autosomal recessive hypophosphatemia. Bone (2009) 0.95
Pitfalls in the diagnosis of thyroid dysgenesis by thyroid ultrasonography and scintigraphy. Eur J Endocrinol (2011) 0.94
Prevalence of type 1 diabetes mellitus in 6-18-yr-old school children living in Istanbul, Turkey. Pediatr Diabetes (2011) 0.94
Relationship between procalcitonin levels and presence of vesicoureteral reflux during first febrile urinary tract infection in children. Urology (2012) 0.91
Significance of acanthosis nigricans in childhood obesity. J Paediatr Child Health (2008) 0.91
Premature pubarche, hyperinsulinemia and hypothyroxinemia: novel manifestations of congenital portosystemic shunts (Abernethy malformation) in children. Horm Res Paediatr (2015) 0.90
Does cord blood bilirubin level help the physician in the decision of early postnatal discharge? J Matern Fetal Neonatal Med (2011) 0.86
Clinical and molecular characterization of Turkish patients with familial hypomagnesaemia: novel mutations in TRPM6 and CLDN16 genes. Nephrol Dial Transplant (2011) 0.86
Hypercalciuria and recurrent urinary tract infections: incidence and symptoms in children over 5 years of age. Pediatr Nephrol (2005) 0.85
Glucose-6-phosphate dehydrogenase deficiency in neonatal indirect hyperbilirubinemia. J Trop Pediatr (2005) 0.85
Effect of zinc supplementation on growth hormone secretion, IGF-I, IGFBP-3, somatomedin generation, alkaline phosphatase, osteocalcin and growth in prepubertal children with idiopathic short stature. J Pediatr Endocrinol Metab (2005) 0.85
Membranous nephropathy in Schimke immuno-osseous dysplasia. Pediatr Nephrol (2006) 0.84
The efficacy of nebulized salbutamol, hypertonic saline and salbutamol/hypertonic saline combination in moderate bronchiolitis. Pulm Pharmacol Ther (2011) 0.84
Comparison of capillary blood ketone measurement by electrochemical method and urinary ketone in treatment of diabetic ketosis and ketoacidosis in children. Acta Diabetol (2008) 0.82
Treatment with insulin detemir or NPH insulin in children aged 2-5 yr with type 1 diabetes mellitus. Pediatr Diabetes (2011) 0.81
Efficacy of salbutamol and ipratropium bromide in the management of acute bronchiolitis--a clinical trial. Respiration (2007) 0.81
A novel homozygous TMEM70 mutation results in congenital cataract and neonatal mitochondrial encephalo-cardiomyopathy. Gene (2012) 0.81
The prevalence and risk factors of premature thelarche and pubarche in 4- to 8-year-old girls. Acta Paediatr (2011) 0.81
Antimicrobial resistance patterns of uropathogens among children in Istanbul, Turkey. Southeast Asian J Trop Med Public Health (2011) 0.81
Four cases of neonatal non-ketotic hyperglycinaemia. Ann Trop Paediatr (2004) 0.80
The role of leptin, soluble leptin receptor, resistin, and insulin secretory dynamics in the pathogenesis of hypothalamic obesity in children. Eur J Pediatr (2008) 0.80
A giant ovarian cyst in a neonate with classical 21-hydroxylase deficiency with very high testosterone levels demonstrating a high-dose hook effect. J Clin Res Pediatr Endocrinol (2012) 0.80
Insulin Receptor and the Kidney: Nephrocalcinosis in Patients with Recessive INSR Mutations. Nephron Physiol (2014) 0.80
Current practice in diagnosis and treatment of growth hormone deficiency in childhood: a survey from Turkey. J Clin Res Pediatr Endocrinol (2015) 0.80
The exon 3-deleted/full-length growth hormone receptor polymorphism and response to growth hormone therapy in growth hormone deficiency and Turner syndrome: a multicenter study. Horm Res Paediatr (2012) 0.80
Content analysis of food advertising in Turkish television. J Paediatr Child Health (2010) 0.80
Detection of Y chromosomal material in patients with a 45,X karyotype by PCR method. Tohoku J Exp Med (2007) 0.80
Upper segment/lower segment ratio and armspan-height difference in healthy Turkish children. Acta Paediatr (2005) 0.80
Alopecia: association with resistance to thyroid hormones. J Pediatr Endocrinol Metab (2009) 0.79
An atypical case of familial glucocorticoid deficiency without pigmentation caused by coexistent homozygous mutations in MC2R (T152K) and MC1R (R160W). J Clin Endocrinol Metab (2012) 0.79
Turner syndrome and associated problems in Turkish children: a multicenter study. J Clin Res Pediatr Endocrinol (2015) 0.79
Maternal thyroid dysfunction and neonatal thyroid problems. Int J Endocrinol (2013) 0.78
T4 plus T3 treatment in children with hypothyroidism and inappropriately elevated thyroid-stimulating hormone despite euthyroidism on T4 treatment. Horm Res Paediatr (2010) 0.78
Hypothalamic obesity in children: pathophysiology to clinical management. J Pediatr Endocrinol Metab (2015) 0.78
Evaluation of glucose intolerance in adolescents relative to adults with type 2 diabetes mellitus. J Pediatr Endocrinol Metab (2006) 0.78
Nanoduct sweat conductivity measurements in 2664 patients: relationship to age, arterial blood gas, serum electrolyte profiles and clinical diagnosis. J Clin Med Res (2013) 0.78
Evaluation of diagnosis and treatment results in children with Graves' disease with emphasis on the pubertal status of patients. J Pediatr Endocrinol Metab (2008) 0.77
Effects of leukemia inhibitory receptor gene mutations on human hypothalamo-pituitary-adrenal function. Pituitary (2015) 0.77
The effect of the mode of delivery on neonatal thyroid function. J Matern Fetal Neonatal Med (2007) 0.77
Alendronate treatment in children with osteogenesis imperfecta. Indian Pediatr (2008) 0.77
Quantitative ultrasound and biochemical parameters for the assessment of osteopenia in preterm infants. J Matern Fetal Neonatal Med (2007) 0.77
Screening of parents and siblings of patients with thyroid dysgenesis by thyroid function tests and ultrasound. Horm Res (2008) 0.76
Puberty in a case with novel 17-hydroxylase mutation and the putative role of estrogen in development of pubic hair. Eur J Endocrinol (2008) 0.76
Growth curves for Turkish Girls with Turner Syndrome: Results of the Turkish Turner Syndrome Study Group. J Clin Res Pediatr Endocrinol (2015) 0.75
Constitutional growth delay pattern of growth in velo-cardio-facial syndrome: longitudinal follow up and final height of two cases. J Clin Res Pediatr Endocrinol (2008) 0.75
Normative Data of Thyroid Volume-Ultrasonographic Evaluation of 422 Subjects Aged 0-55 Years. J Clin Res Pediatr Endocrinol (2015) 0.75
Homozygous loss-of-function mutations in SOHLH1 in patients with nonsyndromic hypergonadotropic hypogonadism. J Clin Endocrinol Metab (2015) 0.75
The relationship between the first episode of wheezing and matrix metalloproteinases-9 and MMP-2 and tissue inhibitors of MMP-1 levels in preterm infants. Ann Thorac Med (2013) 0.75
Severe diabetic ketoacidosis: hyperventilation or relative hypoventilation. Pediatr Crit Care Med (2006) 0.75
Sphingosine-1-phosphate lyase mutations cause primary adrenal insufficiency and steroid-resistant nephrotic syndrome. J Clin Invest (2017) 0.75
Effect of Maternal Factors and Fetomaternal Glucose Homeostasis on Birth Weight and Postnatal Growth. J Clin Res Pediatr Endocrinol (2015) 0.75
9 years follow-up of a patient with pituitary form of resistance to thyroid hormones (PRTH): comparison of two treatment periods of D-thyroxine and triiodothyroacetic acid (TRIAC). J Pediatr Endocrinol Metab (2009) 0.75
THE DISTRIBUTION OF DIFFERENT TYPES OF DIABETES IN CHILDHOOD: A SINGLE CENTER EXPERIENCE. J Clin Res Pediatr Endocrinol (2017) 0.75
VACTERL association: a new case with biotinidase deficiency and annular pancreas. Ren Fail (2011) 0.75
Irisin and Oxytocin as Predictors of Metabolic Parameters in Obese Children. J Clin Res Pediatr Endocrinol (2017) 0.75
Radiologic and hormonal evaluation of pituitary abnormalities in patients with Bardet-Biedl syndrome. Clin Dysmorphol (2011) 0.75
Jacobsen syndrome without thrombocytopenia: a case report and review of the literature. Turk J Pediatr (2013) 0.75
Bone mineral density in children with non-cystic fibrosis bronchiectasis. Respiration (2007) 0.75
Identification of a novel large CYP17A1 deletion by MLPA analysis in a family with classic 17α-hydroxylase deficiency. Sex Dev (2015) 0.75
Cushing's syndrome due to a non-adrenal ectopic adrenocorticotropin-secreting Ewing's sarcoma in a child. J Pediatr Endocrinol Metab (2009) 0.75
H syndrome: a multifaceted histiocytic disorder with hyperpigmentation and hypertrichosis. Acta Derm Venereol (2015) 0.75
Alpha1-acid glycoprotein for the early diagnosis of neonatal sepsis. J Matern Fetal Neonatal Med (2010) 0.75
Effect of breastfeeding on serum zinc levels and growth in healthy infants. Breastfeed Med (2012) 0.75
Infantile loss of teeth: odontohypophosphatasia or childhood hypophosphatasia. Eur J Pediatr (2012) 0.75
Cognitive and psychosocial development in children with familial hypomagnesaemia. Magnes Res (2011) 0.75
A patient with hypopituitarism and isochromosome 18q mosaicism. Horm Res (2005) 0.75
Pediatric hepatotoxicity associated with polygermander (teucrium polium). Clin Toxicol (Phila) (2012) 0.75
Does transient hypothyroxinemia influence metabolic bone disease of prematurity? J Matern Fetal Neonatal Med (2013) 0.75