29 results on '"Akinci, Aysehan"'
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2. Chronic Disease Management of Children Followed with Type 1 Diabetes Mellitus
3. Presentation, diagnosis and follow-up characteristics of 17α-hydroxylase deficiency cases with exon 1-6 deletion (founder mutation) in the CYP17A1 gene: 20-years single-center experience
4. A girl diagnosed with familial hypocalciuric hypercalcemia with heterozygous p.Cys575Tyr variation in the CaSR gene
5. Change in clinical presentation at admission in children with newly diagnosed type 1 diabetes during the COVID-19 pandemic in the eastern region of Turkey
6. Evaluation of endocrine functions before and after enzyme replacement therapy in children with mucopolysaccharidosis
7. Treatment and follow-up of coronary artery disease in a child with homozygous familial hypercholesterolemia
8. Genomic analysis to screen potential genes and mutations in children with non-syndromic early onset severe obesity: a multicentre study in Turkey
9. The Association Between Anthropometric Findings and Hormonal Values in Obese and Overweight Children
10. The relationship between autoimmunity and HbA1c in type 1 diabetes mellitus patients
11. The relationship between serum FGF-23 concentration and insulin resistance, prediabetes and dyslipidemia in obese children and adolescents
12. Autosomal recessive cutis laxa: a novel mutation in the FBLN5 gene in a family
13. Long-term unidentified complication of IGF-I treatment: Pulmoner hypertension
14. The treatment of severe pain in melorheostosis with daily walking program only: a case report
15. The treatment of severe pain in melorheostosis with daily walking program only: a case report
16. Effect of Type I Diabetes on Cognitive Functions of School-Age Children / Okul Cagindaki Cocuklarda Tip I Diyabetes Mellitusun Bilissel Fonksiyonlari Uzerine Etkisi
17. Rare Causes of Primary Adrenal Insufficiency: Genetic and Clinical Characterization of a Large Nationwide Cohort
18. Bisphosphonate treatment of melorheostosis: A case report
19. Clinical characteristics and phenotype–genotype analysis in Turkish patients with congenital hyperinsulinism; predominance of recessive KATP channel mutations
20. A Novel ERCC6 Splicing Variant Associated with a Mild Cockayne Syndrome Phenotype
21. A Novel ExonicGHRSplicing Mutation(c.784G>C)in a Patient with Classical Growth Hormone Insensitivity Syndrome
22. P-99 THE EFFECT OF IGF-I ON MYOCARDIAL ISCHEMIA AND REPERFUSION INDUCED ARRHYTHMIAS IN RATS
23. The effects of orchiopexy on serum anti-Müllerian hormone levels in unilateral cryptorchid infants
24. Sympathetic skin responses in Type‐1 diabetic children: Relationship to urodynamic findings
25. AChryseobacterium meningosepticumOutbreak in a Neonatal Ward
26. Insulin-like growth factor binding proteins (IGFBPs) in serum and urine and IGFBP-2 protease activity in patients with insulin-dependent diabetes mellitus
27. The signal-averaged electrocardiogram in diabetic children
28. Left Ventricular Dysfunction Due to Hypocalcemia in a Neonate.
29. Dilated Cardiomyopathy with Recurrent Intraventricular Thrombosis.
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