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Sebahat Yılmaz Ağladıoğlu

Pamukkale University

39

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372

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Rare Causes of Primary Adrenal Insufficiency: Genetic and Clinical Characterization of a Large Nationwide Cohort

2016 The Journal of Clinical Endocrinology and Metabolism
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Neonatal Bartter syndrome with cholelithiasis and hydrocephalus: Rare association

2016 Pediatrics International
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Clinical Characteristics and Molecular Analysis of Turkish Patients with Congenital Hyperinsulinism: a Single-Centre Experience with 15 Cases

2015
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Can ultrasound elastography be used as a new technique in the differentiation of undescended testes and reactive lymph nodes in children

2015 Clinical Radiology
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Vitamin D Status in Children in the Western Part of Turkey

2015
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Effects of Subclinically Hypothyroidism on Haemorheological Parameters in Paediatric Population

2015
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Primary Adrenal Insufficiency in Children without Congenital Adrenal Hyperplasia: Molecular and Clinical Characterisation of a Nationwide Cohort

2015
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Perioral Acanthosis nigricans

2015 The Journal of Pediatrics
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Sequence Analysis of 11 Known Causative Genes in Clinically Diagnosed Children as Maturity Onset Diabetes of Youth by Next Generation Sequencing

2014
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Evaluation of Asymmetric Dimethylarginine (ADMA) Levels in Children with Growth Hormone Deficiency

2014 Journal of Clinical Research in Pediatric Endocrinology
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