| Pathogenesis of Thalassemia Major-associated Osteoporosis: A Review with Insights from Clinical Experience |
10 |
| Vitamin D Deficiency in Pregnant Women and Their Infants |
10 |
| High Prenatal Exposure to Bisphenol A Reduces Anogenital Distance in Healthy Male Newborns |
8 |
| Neonatal Screening for Congenital Adrenal Hyperplasia in Turkey: A Pilot Study with 935 Infants |
6 |
| A Meta-Analysis and an Evaluation of Trends in Obesity Prevalence among Children and Adolescents in Turkey: 1990 through 2015 |
6 |
| Efficacy and Safety of Continuous Subcutaneous Insulin Infusion vs. Multiple Daily Injections on Type 1 Diabetes Children: A Meta-Analysis of Randomized Control Trials |
5 |
| Perceived Expressed Emotion, Emotional and Behavioral Problems and Self-Esteem in Obese Adolescents: A Case-Control Study |
5 |
| The Association Between Maternal Subclinical Hypothyroidism and Growth, Development, and Childhood Intelligence: A Meta-analysis |
5 |
| Associations Between Serum Uric Acid Concentrations and Cardiometabolic Risk and Renal Injury in Obese and Overweight Children |
5 |
| Evaluation of Normal Thyroid Tissue and Autoimmune Thyroiditis in Children Using Shear Wave Elastography |
5 |
| A Rare Cause of Congenital Adrenal Hyperplasia: Clinical and Genetic Findings and Follow-up Characteristics of Six Patients with 17-Hydroxylase Deficiency Including Two Novel Mutations |
5 |
| Evaluation of Renal Function in Obese Children and Adolescents Using Serum Cystatin C Levels, Estimated Glomerular Filtration Rate Formulae and Proteinuria: Which is most Useful? |
5 |
| Effect of Telehealth System on Glycemic Control in Children and Adolescents with Type 1 Diabetes |
5 |
| Under-recognized Hypoparathyroidism in Thalassemia |
4 |
| A Novel Mutation of AMHR2 in Two Siblings with Persistent Mullerian Duct Syndrome |
4 |
| The Relationship Between Blood Pressure and Sleep Duration in Turkish Children: A Cross-Sectional Study |
3 |
| XY Disorder of Sex Development due to 17-Beta Hydroxysteroid Dehydrogenase Type 3 Deficiency in an Infant of Greek Origin |
3 |
| A Patient with Proopiomelanocortin Deficiency: An Increasingly Important Diagnosis to Make |
3 |
| The Role of Irisin , Insulin and Leptin in Maternal and Fetal Interaction |
3 |
| Incidence of Type 1 Diabetes in Children Aged Below 18 Years during 2013-2015 in Northwest Turkey |
3 |
| Aromatase Deficiency due to a Novel Mutation in CYP19A1 Gene |
3 |
| Novel Mutations in Obesity-related Genes in Turkish Children with Non-syndromic Early Onset Severe Obesity: A Multicentre Study |
3 |
| A Novel Nonsense Mutation of PHF6 in a Female with Extended Phenotypes of Borjeson-Forssman-Lehmann Syndrome |
3 |
| Sirolimus-Induced Hepatitis in Two Patients with Hyperinsulinemic Hypoglycemia |
3 |
| Investigation of MKRN3 Mutation in Patients with Familial Central Precocious Puberty |
3 |
| Urine Levels of Matrix Metalloproteinases and Tissue Inhibitor of Metalloproteinases in Children with Type 1 Diabetes Mellitus |
3 |
| Abnormal Uterine Bleeding in Adolescents |
3 |
| A Novel KCNJ11 Mutation Associated with Transient Neonatal Diabetes |
3 |
| Neonatal Diabetes: Two Cases with Isolated Pancreas Agenesis due to Homozygous PTF1A Enhancer Mutations and One with Developmental Delay, Epilepsy, and Neonatal Diabetes Syndrome due to KCNJ11 Mutation |
3 |
| Could Alerting Physicians for Low Alkaline Phosphatase Levels Be Helpful in Early Diagnosis of Hypophosphatasia? |
3 |
| Prevalence and Related Factors of Euthyroid Sick Syndrome in Children with Untreated Cancer According to Two Different Criteria |
3 |
| Two Childhood Pheochromocytoma Cases due to von Hippel-Lindau Disease, One Associated with Pancreatic Neuroendocrine Tumor: A Very Rare Manifestation |
3 |
| Remarkable Increase in the Prevalence of Overweight and Obesity Among School Age Children in Antalya, Turkey, Between 2003 and 2015 |
2 |
| Hyperphosphatemic Familial Tumoral Calcinosis in Two Siblings with a Novel Mutation in GALNT3 Gene: Experience from Southern Turkey |
2 |
| Extreme Premature Small for Gestational Age Infants Have Appropriate Catch-up Growth at Term Equivalence Compared with Extreme Premature Appropriate for Gestational Age Infants |
2 |
| A Patient with Berardinelli-Seip Syndrome, Novel AGPAT2 Splicesite Mutation and Concomitant Development of Non-diabetic Polyneuropathy |
2 |
| Klinefelter Syndrome in Childhood: Variability in Clinical and Molecular Findings |
2 |
| Early Menarche is a Risk Factor for Short Stature in Young Korean Females: An Epidemiologic Study |
2 |
| Evaluation of Unfavorable Cardiovascular and Metabolic Risk Factors in Children and Young Adults with Haemophilia |
2 |
| Novel Compound Heterozygous Variants in the LHCGR Gene in a Genetically Male Patient with Female External Genitalia |
2 |
| A Novel Homozygous CYP19A1 Gene Mutation: Aromatase Deficiency Mimicking Congenital Adrenal Hyperplasia in an Infant without Obvious Maternal Virilisation |
2 |
| Neonatal Features of the Prader-Willi Syndrome; The Case for Making the Diagnosis During the First Week of Life |
2 |
| Peripheral Neuropathy as a Complication of Diabetic Ketoacidosis in a Child with Newly Diagnosed Diabetes Type 1: A Case Report |
2 |
| Acute Effects of Blood Transfusion on Insulin Sensitivity and Pancreatic beta-Cell Function in Children with beta-Thalassemia/Hemoglobin E Disease |
2 |
| Use of Vitamin D in Children and Adults: Frequently Asked Questions |
2 |
| SLC34A3 Intronic Deletion in an Iranian Kindred with Hereditary Hypophosphatemic Rickets with Hypercalciuria |
2 |
| Evaluation of the Ovarian Reserve in Adolescents with Hashimoto's Thyroiditis Using Serum Anti-Mfillerian Hormone Levels |
2 |
| Achieving Optimal Short- and Long-term Responses to Paediatric Growth Hormone Therapy |
2 |
| Clinical and Biochemical Phenotype of Adolescent Males with Gynecomastia |
2 |
| A Novel Homozygous Mutation of the Acid-Labile Subunit (IGFALS) Gene in a Male Adolescent |
2 |
