Simultaneous onset and similar course of type 1 diabetes mellitus in monozygotic twins (a 4-year follow-up)

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1. Masthead
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3. Reviews
4. Growth failure in children with cystic fibrosis
5. Approach to the management of slipped capital femoral epiphysis and primary hyperparathyroidism
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7. Thyroid developmental anomalies among first-degree relatives of children with thyroid dysgenesis and congenital hypothyroidism
8. TSHR is the main causative locus in autosomal recessively inherited thyroid dysgenesis
9. When to operate on ovarian cysts in children?
10. Partial anomalous pulmonary venous return is common in Turner syndrome
11. Uterine development in patients with Turner syndrome: Relation to hormone replacement therapy and karyotype
12. Ovarian and uterine ultrasonography and relation to puberty in healthy girls between 6 and 16 years in the Turkish population: a cross-sectional study
13. Assessment of gonadal function in boys and adolescents at the diagnosis of neoplastic disease
14. Environmental and genetic factors influence age at menarche in women with polycystic ovary syndrome
15. Vitamin D status in children with Hashimoto thyroiditis
16. Non-invasive measurement of adrenal response after standardized exercise tests in prepubertal children
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18. Safety and efficacy of a 1-year treatment with zoledronic acid compared with pamidronate in children with osteogenesis imperfecta
19. Evaluation and comparison of safety, convenience and cost of administering intravenous pamidronate infusions to children in the home and ambulatory care settings
20. Clinical profile and etiologies of children with central diabetes insipidus: a single-center experience from Turkey
21. Audiologic evaluation in pediatric patients with type 1 diabetes mellitus
22. An after-school dance and lifestyle education program reduces risk factors for heart disease and diabetes in elementary school children
23. Evaluation of neutrophil gelatinase-associated lipocalin in normoalbuminuric normotensive type 1 diabetic adolescents
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25. Metabolic disorders in vertically HIV-infected children: future adults at risk for cardiovascular disease
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31. Seizure due to somatostatin analog discontinuation in a case diagnosed as congenital hyperinsulinism novel mutation
32. Simultaneous onset and similar course of type 1 diabetes mellitus in monozygotic twins (a 4-year follow-up)
33. 17β-Hydroxysteroid dehydrogenase type 3 deficiency as a result of a homozygous 7 base pair deletion in 17βHSD3 gene
34. Clinical and image-guided chorioretinal findings in long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
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42. Primary familial hypomagnesemia syndrome: a new approach in treatment
43. A case of congenital hypothyroidism in PHACE syndrome
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45. Is vitamin D deficiency a feature of pediatric celiac disease?
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48. Diagnosis of non-alcoholic fatty liver disease in obese children
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