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journal of clinical research in pediatric endocrinology
سال:2012 - دوره:4 - شماره:4
A rare combination: Congenital adrenal hyperplasia due to 21 hydroxylase deficiency and Turner syndrome
- صفحه:213-215
An infant born to a mother with gestational diabetes presenting with 49,XXXXY syndrome and renal agenesis-A case report
- صفحه:223-225
Assessment of the knowledge of diabetes mellitus among school teachers within the scope of the managing diabetes at school program
- صفحه:199-203
Clinical and laboratory characteristics of children referred for early puberty: Preponderance in 7-8 years of age
- صفحه:208-212
Different aspects of kidney function in well-controlled congenital hypothyroidism
- صفحه:193-198
Growth hormone deficiency and diabetes insipidus as a complication of endoscopic third ventriculostomy
- صفحه:216-219
Hyperinsulinaemic hypoglycaemia: Genetic mechanisms,diagnosis and management
- صفحه:169-181
Hypochondroplasia in a child with 1620C>G (Asn540Lys) mutation in FGFR3
- صفحه:220-222
Prevalence of obesity and associated risk factors among adolescents in Ankara,Turkey
- صفحه:204-207
Relationships between osteocalcin,glucose metabolism,and adiponectin in obese children: Is there crosstalk between bone tissue and glucose metabolism?
- صفحه:182-188
Trends in the frequency of HLA DR-DQ haplotypes among children and adolescents with type 1 diabetes mellitus in the Southeast Region of Turkey
- صفحه:189-192
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