Published in J Clin Res Pediatr Endocrinol on December 18, 2015
Practice parameter for the assessment and treatment of children and adolescents with attention-deficit/hyperactivity disorder. J Am Acad Child Adolesc Psychiatry (2007) 6.57
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The goiter prevalence and urinary iodine levels among adolescents. Turk J Pediatr (2011) 1.40
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Determining median urinary iodine concentration that indicates adequate iodine intake at population level. Bull World Health Organ (2002) 1.02
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A developmental index using the Wechsler Intelligence Scale for Children: implications for the diagnosis and nature of ADHD. J Learn Disabil (1992) 0.78
Psychosocial status and quality of life in mothers of infants with colic. Turk J Pediatr (2013) 1.41
Report of the first case of precocious puberty in Rett syndrome. J Pediatr Endocrinol Metab (2013) 1.41
A case report of neonatal diabetes due to neonatal hemochromatosis. J Pediatr Endocrinol Metab (2010) 1.39
[Differential diagnosis between Schizotypal Personality Disorder and Autism Spectrum Disorders: a case report]. Turk Psikiyatri Derg (2015) 1.38
Thyroid dyshormonogenesis is mainly caused by TPO mutations in consanguineous community. Clin Endocrinol (Oxf) (2013) 1.05
Insulin oedema in newly diagnosed type 1 diabetes mellitus. J Clin Res Pediatr Endocrinol (2010) 1.04
Testis sparing surgery for steroid unresponsive testicular tumors of the congenital adrenal hyperplasia. Pediatr Surg Int (2005) 1.02
Novel TSHR mutations in consanguineous families with congenital nongoitrous hypothyroidism. Clin Endocrinol (Oxf) (2010) 1.00
A truncating DUOX2 mutation (R434X) causes severe congenital hypothyroidism. J Pediatr Endocrinol Metab (2014) 0.95
The relationship between pediatric nonalcoholic fatty liver disease and cardiovascular risk factors and increased risk of atherosclerosis in obese children. Pediatr Cardiol (2012) 0.92
Diabetes care, glycemic control, complications, and concomitant autoimmune diseases in children with type 1 diabetes in Turkey: a multicenter study. J Clin Res Pediatr Endocrinol (2013) 0.91
Iatrogenic Cushing syndrome due to nasal steroid drops. Eur J Pediatr (2011) 0.90
A common thyroid peroxidase gene mutation (G319R) in Turkish patients with congenital hypothyroidism could be due to a founder effect. J Pediatr Endocrinol Metab (2014) 0.88
TSHR is the main causative locus in autosomal recessively inherited thyroid dysgenesis. J Pediatr Endocrinol Metab (2012) 0.88
Relationship between intraocular pressure and obesity in children. J Glaucoma (2007) 0.88
Early subclinical left-ventricular dysfunction in obese nonhypertensive children: a tissue Doppler imaging study. Pediatr Cardiol (2013) 0.87
A nonsense thyrotropin receptor gene mutation (R609X) is associated with congenital hypothyroidism and heart defects. J Pediatr Endocrinol Metab (2014) 0.85
Vitamin D status and insulin requirements in children and adolescent with type 1 diabetes. J Pediatr Endocrinol Metab (2011) 0.85
Paternal X could relate to arithmetic function; study of cognitive function and parental origin of X chromosome in Turner syndrome. Pediatr Int (2008) 0.85
The treatment of cerebral salt wasting with fludrocortisone in a child with lissencephaly. Turk Neurosurg (2010) 0.84
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
Mild and severe congenital primary hypothyroidism in two patients by thyrotropin receptor (TSHR) gene mutation. J Pediatr Endocrinol Metab (2012) 0.83
An uncommon cause of hypoglycemia: insulin autoimmune syndrome. Horm Res Paediatr (2014) 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
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 use of pamidronate for acute vitamin D intoxication, clinical experience with three cases. J Pediatr Endocrinol Metab (2015) 0.82
Effects of growth hormone on growth, insulin resistance and related hormones (ghrelin, leptin and adiponectin) in Turner syndrome. Horm Res (2007) 0.82
Value of pelvic sonography in the diagnosis of various forms of precocious puberty in girls. J Clin Ultrasound (2012) 0.82
A novel mutation of 5alpha-steroid reductase 2 deficiency (CD 65 ALA-PRO) with severe virilization defect in a Turkish family and difficulty in gender assignment. Eur J Pediatr (2010) 0.81
Exaggerated TSH responses to TRH in patients with goiter and 'normal' basal TSH levels. Horm Res (2005) 0.81
Prevalence of hyperthyrotropinemia in obese children before and after weight loss. Eat Weight Disord (2013) 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
A girl with steroid cell ovarian tumor misdiagnosed as non-classical congenital adrenal hyperplasia. Turk J Pediatr (2013) 0.80
Evaluation of bone mineral density in children with type 1 diabetes mellitus. J Pediatr Endocrinol Metab (2013) 0.79
Central corneal thickness in children with diabetes. J Refract Surg (2009) 0.79
A rare combination: congenital adrenal hyperplasia due to 21 hydroxylase deficiency and Turner syndrome. J Clin Res Pediatr Endocrinol (2012) 0.79
Hypothyroidism due to hepatic hemangioendothelioma: a case report. J Clin Res Pediatr Endocrinol (2010) 0.79
Does pseudohypoaldosteronism mask the diagnosis of congenital adrenal hyperplasia? J Clin Res Pediatr Endocrinol (2011) 0.79
Increased central corneal thickness in patients with Turner syndrome. Eur J Ophthalmol (2013) 0.79
Do the Anti-Müllerian Hormone Levels of Adolescents with Polycystic Ovary Syndrome, Those Who Are at Risk for Developing Polycystic Ovary Syndrome, and Those Who Exhibit Isolated Oligomenorrhea Differ from Those of Adolescents with Normal Menstrual Cycles? Horm Res Paediatr (2016) 0.79
Variables related to behavioral and emotional problems and gender typed behaviors in female patients with congenital adrenal hyperplasia. J Pediatr Endocrinol Metab (2009) 0.78
Hyperinsulinemic hypoglycemia: experience in a series of 17 cases. J Clin Res Pediatr Endocrinol (2013) 0.78
Disorders of gonadal development: a broad clinical, cytogenetic and histopathologic spectrum. Pediatr Endocrinol Rev (2007) 0.78
Management of central diabetes insipidus with oral desmopressin in a patient with ectrodactyly and cleft lip/palate (ECP) syndrome. Turk J Pediatr (2009) 0.78
Audiologic evaluation in pediatric patients with type 1 diabetes mellitus. J Pediatr Endocrinol Metab (2012) 0.77
Decreased retinal nerve fiber layer thickness in patients with congenital isolated growth hormone deficiency. Eur J Ophthalmol (2014) 0.77
Evaluation of insulin resistance in Turkish girls with premature pubarche using the homeostasis assessment (HOMA) model. Turk J Pediatr (2007) 0.76
Donohue syndrome in a neonate with homozygous deletion of exon 3 of the insulin receptor gene. J Pediatr Endocrinol Metab (2009) 0.76
Seizure due to somatostatin analog discontinuation in a case diagnosed as congenital hyperinsulinism novel mutation. J Pediatr Endocrinol Metab (2012) 0.76
The evaluation of transient hypothyroidism in patients diagnosed with congenital hypothyroidism. Turk J Med Sci (2015) 0.76
Diseases accompanying congenital hypothyroidism. J Pediatr Endocrinol Metab (2014) 0.76
A RARE CAUSE OF SHORT STATURE: PATIENT WITH 3M SYNDROME REVEALED A NOVEL MUTATION IN OBSL1 GENE. J Clin Res Pediatr Endocrinol (2016) 0.75
Rett syndrome and precocious puberty association. J Pediatr Endocrinol Metab (2015) 0.75
Diabetes mellitus with Laron syndrome: case report. J Pediatr Endocrinol Metab (2013) 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
Long-term follow-up of Cushing's disease:a case report. J Clin Res Pediatr Endocrinol (2013) 0.75
Evaluation of asymmetric dimethylarginine (ADMA) levels in children with growth hormone deficiency. J Clin Res Pediatr Endocrinol (2014) 0.75
A very rare cause of virilization in childhood: ovarian Leydig cell tumor. J Pediatr Endocrinol Metab (2008) 0.75
Refractive errors and strabismus in children with laurence-moon-biedl syndrome. J Pediatr Ophthalmol Strabismus (2010) 0.75
Urinary C-Peptide/Creatinine Ratio Can Distinguish Maturity-Onset Diabetes of the Young from Type 1 Diabetes in Children and Adolescents: A Single-Center Experience. Horm Res Paediatr (2015) 0.75
Galactorrhea After Selective Serotonin Reuptake Inhibitor Use in an Adolescent Girl: A Case Report. J Clin Psychopharmacol (2017) 0.75
The clinical and radiological assessment of cyclic intravenous pamidronate administration in children with osteogenesis imperfecta. Turk J Pediatr (2005) 0.75
A pediatric Conn syndrome case. J Pediatr Endocrinol Metab (2012) 0.75
Thyroid nodules in children and adolescents: a single institution's experience. J Pediatr Endocrinol Metab (2012) 0.75
Investigation of autoimmune diseases accompanying Hashimoto's thyroiditis in children and adolescents and evaluation of cardiac signs. J Pediatr Endocrinol Metab (2015) 0.75
Treatment experience and long-term follow-up data in two severe neonatal hyperparathyroidism cases. J Pediatr Endocrinol Metab (2016) 0.75
Incidence of iodine deficiency in patients presenting with goitre--discrepancy between clinical and ultrasonographic evaluation of the thyroid: comparison of patients with and without autoimmune thyroiditis--clinical, hormonal and urinary iodine excretion studies. J Pediatr Endocrinol Metab (2006) 0.75
Assessment of the 21-hydroxylase deficiency and the adrenal functions in young females with Turner syndrome. J Pediatr Endocrinol Metab (2012) 0.75
17βHSD-3 enzyme deficiency due to novel mutations in the HSD17B3 gene diagnosed in a neonate. J Pediatr Endocrinol Metab (2015) 0.75
Investigation of androgen receptor gene mutations in a series of 21 patients with 46,XY disorders of sex development. J Pediatr Endocrinol Metab (2015) 0.75
Plasma testosterone response at 1st and 4th day after short- and long-term hCG stimulation test. Turk J Pediatr (2005) 0.75
The description of a new case with proopiomelanocortin (POMC) deficiency: an increasingly important diagnosis to make. J Clin Res Pediatr Endocrinol (2017) 0.75
Co-Existence of Thyroid Nodule and Thyroid Cancer in Children and Adolescents with Hashimoto Thyroiditis: A Single-Center Study. Horm Res Paediatr (2016) 0.75
17α-Hydroylase/17,20-lyase deficiency related to P.Y27*(c.81C>A) mutation in CYP17A1 gene. J Pediatr Endocrinol Metab (2015) 0.75
Risk factors affecting the development of nephrocalcinosis, the most common complication of hypophosphatemic rickets. J Pediatr Endocrinol Metab (2015) 0.75
5 alpha steroid reductase deficiency in Turkey. Pediatr Endocrinol Rev (2006) 0.75
LEOPARD syndrome and hypertrophic obstructive cardiomyopathy: a case report. Turk J Pediatr (2005) 0.75
Effects of GnRH analogue treatment on anterior pituitary hormones in children with central precocious puberty. J Pediatr Endocrinol Metab (2015) 0.75
Testicular adrenal rest tumor in a patient with 11beta-hydroxylase deficient congenital adrenal hyperplasia. J Pediatr Endocrinol Metab (2010) 0.75
Maturity onset diabetes of youth (MODY) in Turkish children: sequence analysis of 11 causative genes by next generation sequencing. J Pediatr Endocrinol Metab (2016) 0.75
Clinical, biochemical and genetic features with nonclassical 21-hydroxylase deficiency and final height. J Pediatr Endocrinol Metab (2017) 0.75
Corneal biomechanical characteristics in children with diabetes mellitus. Int Ophthalmol (2014) 0.75
AMH levels in girls with various pubertal problems. J Pediatr Endocrinol Metab (2017) 0.75
A case of Langerhans cell histiocytosis with thyroid involvement. J Pediatr Endocrinol Metab (2011) 0.75
The evaluation of the adrenal and thyroid axes and glucose metabolism after burn injury in children. J Pediatr Endocrinol Metab (2010) 0.75
Ambulatory blood pressure monitoring for 24 hours in children with type-1 diabetes mellitus. Saudi Med J (2007) 0.75
No seasonality of birth in children with type 1 diabetes mellitus in Ankara, Turkey. J Pediatr Endocrinol Metab (2002) 0.75
Ophthalmic Manifestations in Children With Congenital Hypothyroidism. J Pediatr Ophthalmol Strabismus (2016) 0.75
Approach to thyroid nodules in children and adolescents. Turk J Pediatr (2014) 0.75