Published in Turk J Pediatr on December 02, 2013
Human and mouse TPIT gene mutations cause early onset pituitary ACTH deficiency. Genes Dev (2003) 1.93
Functional ovarian hyperandrogenism and polycystic ovary syndrome in prepubertal girls with obesity and/or premature pubarche. J Pediatr Endocrinol Metab (2007) 1.43
Pathophysiology of critical illness hyperglycemia in children. J Pediatr Endocrinol Metab (2013) 1.39
Congenital isolated adrenocorticotropin deficiency: an underestimated cause of neonatal death, explained by TPIT gene mutations. J Clin Endocrinol Metab (2004) 1.29
ROHHAD Syndrome: Reasons for Diagnostic Difficulties in Obesity. J Clin Res Pediatr Endocrinol (2014) 1.10
Vitamin D deficiency in Turkish mothers and their neonates and in women of reproductive age. J Clin Res Pediatr Endocrinol (2009) 1.08
Palivizumab prophylaxis during respiratory syncytial virus outbreak in the neonatal intensive care unit. Turk J Pediatr (2013) 1.06
Syndromic disorders with short stature. J Clin Res Pediatr Endocrinol (2014) 0.99
The KBG syndrome: confirmation of autosomal dominant inheritance and further delineation of the phenotype. Am J Med Genet A (2004) 0.95
Acquired bartter-like syndrome associated with colistin use in a preterm infant. Ren Fail (2013) 0.93
Serum IGF-1 and IGFBP-3 levels in healthy children between 0 and 6 years of age. J Clin Res Pediatr Endocrinol (2011) 0.90
Relationships between osteocalcin, glucose metabolism, and adiponectin in obese children: Is there crosstalk between bone tissue and glucose metabolism? J Clin Res Pediatr Endocrinol (2012) 0.87
Distribution of gene mutations associated with familial normosmic idiopathic hypogonadotropic hypogonadism. J Clin Res Pediatr Endocrinol (2012) 0.87
Gonadal malignancy risk and prophylactic gonadectomy in disorders of sexual development. J Pediatr Endocrinol Metab (2015) 0.87
The influence of interferon-alpha and combination interferon-alpha and lamivudine therapy on height and weight in children with chronic hepatitis B infection. J Pediatr Endocrinol Metab (2007) 0.87
Horseshoe lung associated with left-lung hypoplasia, left pulmonary artery sling and bilateral agenesis of upper lobe bronchi. Pediatr Radiol (2009) 0.85
Celiac disease and autoimmune thyroid disease in children with type 1 diabetes mellitus: clinical and HLA-genotyping results. J Clin Res Pediatr Endocrinol (2010) 0.83
Molecular analysis of PROP1, POU1F1, LHX3, and HESX1 in Turkish patients with combined pituitary hormone deficiency: a multicenter study. Endocrine (2014) 0.83
Evaluation of hypercoagulability in obese children with thrombin generation test and microparticle release: effect of metabolic parameters. Clin Appl Thromb Hemost (2011) 0.82
Effects on bone mineral density of gonadotropin releasing hormone analogs used in the treatment of central precocious puberty. J Pediatr Endocrinol Metab (2003) 0.82
The clinical and genetic heterogeneity of mixed gonadal dysgenesis: does "disorders of sexual development (DSD)" classification based on new Chicago consensus cover all sex chromosome DSD? Eur J Pediatr (2012) 0.82
Transient neonatal diabetes with two novel mutations in the KCNJ11 gene and response to sulfonylurea treatment in a preterm infant. J Pediatr Endocrinol Metab (2011) 0.81
Clinical characteristics of recessive and dominant congenital hyperinsulinism due to mutation(s) in the ABCC8/KCNJ11 genes encoding the ATP-sensitive potasium channel in the pancreatic beta cell. J Pediatr Endocrinol Metab (2011) 0.81
Exaggerated TSH responses to TRH in patients with goiter and 'normal' basal TSH levels. Horm Res (2005) 0.81
Management of patent ductus arteriosus in preterm infants. Anadolu Kardiyol Derg (2006) 0.81
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
[Biopsychosocial variables associated with gender of rearing in children with male pseudohermaphroditism]. Turk Psikiyatri Derg (2007) 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
Gastric carcinoid tumor in a 14-year old girl. Scand J Gastroenterol (2014) 0.79
Long-term follow-up of a pseudohypoparathyroidism type 1A patient with missense mutation (Pro115Ser) in exon 5. J Clin Res Pediatr Endocrinol (2010) 0.79
Evaluation of thyroid functions with respect to iodine status and TRH test in chronic autoimmune thyroiditis. J Clin Res Pediatr Endocrinol (2011) 0.79
Does long-term use of valproate cause weight gain in prepubertal epileptic children? Int J Neurosci (2002) 0.79
Gonadotropin-Releasing Hormone Analogue Treatment in Females with Moderately Early Puberty: No Effect on Final Height. J Clin Res Pediatr Endocrinol (2015) 0.79
The effect of colchicine on physical growth in children with familial mediterranean fever. Eur J Pediatr (2009) 0.78
Disorders of gonadal development: a broad clinical, cytogenetic and histopathologic spectrum. Pediatr Endocrinol Rev (2007) 0.78
Report of a case of neonatal chylothorax that responded to long-term octreotide treatment, and review of the literature. Turk J Pediatr (2015) 0.78
Evaluation of glucose homeostasis in transfusion-dependent thalassemic patients. Pediatr Hematol Oncol (2008) 0.78
Serum leptin levels in children receiving long-term carbamazepine. Acta Paediatr Taiwan (2003) 0.77
Two siblings with isolated GH deficiency due to loss-of-function mutation in the GHRHR gene: successful treatment with growth hormone despite late admission and severe growth retardation. J Clin Res Pediatr Endocrinol (2010) 0.77
International Nosocomial Infection Control Consortium (INICC) national report on device-associated infection rates in 19 cities of Turkey, data summary for 2003-2012. Ann Clin Microbiol Antimicrob (2014) 0.77
A Deep Intronic HADH Splicing Mutation (c.636+471G>T) in a Congenital Hyperinsulinemic Hypoglycemia Case: Long Term Clinical Course. J Clin Res Pediatr Endocrinol (2015) 0.77
Relationship between plasma leptin, insulin and tumor necrosis factor alpha in obese children. J Pediatr Endocrinol Metab (2005) 0.77
Hypocalcemic seizure due to congenital rickets in the first day of life. Turk J Pediatr (2007) 0.77
Evaluation of insulin resistance in Turkish girls with premature pubarche using the homeostasis assessment (HOMA) model. Turk J Pediatr (2007) 0.76
Case report: two patients with partial DiGeorge syndrome presenting with attention disorder and learning difficulties. J Clin Res Pediatr Endocrinol (2011) 0.76
Early regular versus late selective poractant treatment in preterm infants born between 25 and 30 gestational weeks: a prospective randomized multicenter study. J Matern Fetal Neonatal Med (2013) 0.76
Combined evaluation of IGF-1 and IGFBP-3 as an index of efficacy and safety in growth hormone treated patients. J Clin Res Pediatr Endocrinol (2009) 0.75
Efficiency of fluid treatments with different sodium concentration in children with type 1 diabetic ketoacidosis. J Clin Res Pediatr Endocrinol (2011) 0.75
Does early diagnosis in cricopharyngeal achalasia affect the success of treatment modality? Turk J Pediatr (2008) 0.75
The Effect of Recombinant Growth Hormone Treatment in Children with Idiopathic Short Stature and Low Insulin-Like Growth Factor-1 Levels. J Clin Res Pediatr Endocrinol (2015) 0.75
Portal Vein Thrombosis of a Newborn with Corrected Total Anomalous Pulmonary Venous Return. Turk J Haematol (2015) 0.75
Transplacental transmission of influenza A (H1N1) virus--is it really possible? Turk J Pediatr (2012) 0.75
Genoa syndrome and central diabetes insipidus: a case report. J Clin Res Pediatr Endocrinol (2010) 0.75
Thrombophilia and neonatal complications in preterm infants. Thromb Haemost (2004) 0.75
Current Status of Childhood Hyperinsulinemic Hypoglycemia in Turkey. J Clin Res Pediatr Endocrinol (2016) 0.75
Synchronous occurrence of papillary carcinoma in the thyroid gland and thyroglossal duct in an adolescent with congenital hypothyroidism. J Clin Res Pediatr Endocrinol (2012) 0.75
Permanent central diabetes insipidus with complete regression of pituitary stalk enlargement after 4 years of follow-up. J Clin Res Pediatr Endocrinol (2008) 0.75
Investigation of SHOX Gene Mutations in Turkish Patients with Idiopathic Short Stature. J Clin Res Pediatr Endocrinol (2015) 0.75
Beneficial effects of Etanercept on experimental necrotizing enterocolitis. Pediatr Surg Int (2013) 0.75
Regulatory T Cells and Vitamin D Status in Children with Chronic Autoimmune Thyroiditis. J Clin Res Pediatr Endocrinol (2016) 0.75
The Growth Characteristics of Patients with Noonan Syndrome: Results of Three Years of Growth Hormone Treatment: A Nationwide Multicenter Study. J Clin Res Pediatr Endocrinol (2016) 0.75
Effect of interferon treatment on glucose metabolism in children with chronic hepatitis B infection. Turk J Gastroenterol (2004) 0.75
Early or later prophylactic INSURE in preterm infants of less than 30 weeks' gestation. Turk J Pediatr (2015) 0.75
Risk factors for non-alcoholic fatty liver disease in obese children. Horm Res (2009) 0.75
Generalized periosteal reaction and tissue swelling secondary to prolonged prostaglandin E1 infusion and venous stasis: a case report. Turk J Pediatr (2014) 0.75
[An Early Neonatal Sepsis Case Due to Streptococcus pneumoniae Serotype 7F]. Mikrobiyol Bul (2013) 0.75
Final height of patients with classical congenital adrenal hyperplasia. Turk J Pediatr (2010) 0.75
The impact of evaluating platelet transfusion need by platelet mass index on reducing the unnecessary transfusions in newborns. J Matern Fetal Neonatal Med (2014) 0.75
Amiodarone-induced thyrotoxicosis in children and adolescents is a possible outcome in patients with low iodine intake. J Pediatr Endocrinol Metab (2010) 0.75
Effect of interferon therapy on glucose metabolism in children with chronic hepatitis B. Turk J Pediatr (2011) 0.75
RESPONSE TO THE ANASTROZOLE TREATMENT IN A CASE WITH PEUTZ-JEGHERS SYNDROME WHO WAS DETECTED TO HAVE LARGE CELL CALCIFYING SERTOLI CELL TUMOR AND DEVELOPED PRE-PUBERTAL GYNECOMASTIA. J Clin Res Pediatr Endocrinol (2016) 0.75
A rare cause of congenital diarrhea in a Turkish newborn: tufting enteropathy. Turk J Pediatr (2015) 0.75
Postnatal oral hydrocortisone in treatment of bronchopulmonary dysplasia: an observational study. Tuberk Toraks (2013) 0.75
Persistently raised thyroid stimulating hormone in adequately treated congenital hypothyroidism on long-term follow-up. J Pediatr Endocrinol Metab (2008) 0.75
A novel TWIST1 gene mutation in a patient with Saethre-Chotzen syndrome. Clin Dysmorphol (2016) 0.75
Chronic recurrent multifocal osteomyelitis as the first presentation of acute lymphoblastic leukemia in a 2-year-old boy. J Pediatr Hematol Oncol (2010) 0.75
The risk of functional ovarian hyperandrogenism and polycystic ovary syndrome in patients with hyperandrogenism. J Pediatr Endocrinol Metab (2003) 0.75
Three cases of Wolfram syndrome with different clinical aspects. J Pediatr Endocrinol Metab (2015) 0.75
Endocrinologic Late Effects of Chemoradiotherapy in Pediatric Acute Leukemia. Turk J Haematol (2002) 0.75
The evaluation of thyroid carcinoma in childhood and concomitance of autoimmune thyroid disorders. J Pediatr Endocrinol Metab (2014) 0.75