25 results on '"Ağladıoğlu, Sebahat Yılmaz"'
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2. Loss-of-function variants in SEMA3F and PLXNA3 encoding semaphorin-3F and its receptor plexin-A3 respectively cause idiopathic hypogonadotropic hypogonadism
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3. Density of the crystalline lens in obese and nonobese children
4. Prevalence of hyperthyrotropinemia in obese children before and after weight loss
5. Pediatricians’ COVID-19 experiences and views on the willingness to receive COVID-19 vaccines: a cross-sectional survey in Turkey
6. Letter to the Editor Regarding "Effect of Propolis on Precocious Puberty in Female Rats" - Does Propolis Induce Thelarche and Gynecomastia in Prepubertal Children?
7. Rare causes of primary adrenal insufficiency: Genetic and clinical characterization of a large nationwide cohort
8. Hipotalamik hamartom: Manyetik rezonans görüntüleme bulguları
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10. Maturity onset diabetes of youth (MODY) in Turkish children: sequence analysis of 11 causative genes by next generation sequencing
11. Effects of GnRH analogue treatment on anterior pituitary hormones in children with central precocious puberty
12. Evaluating the Efficacy of Treatment with a GnRH Analogue in Patients with Central Precocious Puberty
13. Evaluation of Asymmetric Dimethylarginine (ADMA) Levels in Children with Growth Hormone Deficiency
14. A common thyroid peroxidase gene mutation (G319R) in Turkish patients with congenital hypothyroidism could be due to a founder effect
15. Long-Term Follow-Up of Cushing’s Disease: A Case Report
16. Hyperinsulinemic Hypoglycemia: Experience in A Series of 17 Cases
17. Report of the first case of precocious puberty in Rett syndrome
18. Does Pseudohypoaldosteronism Mask the Diagnosis of Congenital Adrenal Hyperplasia?
19. Hypothyroidism Due to Hepatic Hemangioendothelioma: A Case Report
20. Effects of GnRH analogue treatment on anterior pituitary hormones in children with central precocious puberty.
21. Long-Term Follow-Up of Cushing's Disease: A Case Report.
22. Sporadic Nonautoimmune Neonatal Hyperthyroidism Due to A623V Germline Mutation in the Thyrotropin Receptor Gene.
23. Insulin Oedema in Newly Diagnosed Type 1 Diabetes Mellitus.
24. Assessment of the knowledge of diabetes mellitus among school teachers within the scope of the managing diabetes at school program.
25. A rare combination: congenital adrenal hyperplasia due to 21 hydroxylase deficiency and Turner syndrome.
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