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Publications by Seher Polat
Correction: Congenital Adrenal Hyperplasia Due to 11-Beta-Hydroxylase Deficiency: Functional Consequences of Four CYP11B1 Mutations
European Journal of Human Genetics
Genetics
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Congenital Adrenal Hyperplasia Due to 11-Beta-Hydroxylase Deficiency
Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
The Combination of a Novel 2 Bp Deletion Mutation and p.D63H in CYP11B1 Cause Congenital Adrenal Hyperplasia Due to Steroid 11β-Hydroxylase Deficiency
Endocrine Journal
Endocrinology
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Diabetes
Psychological Vulnerability to Stress in Carriers of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
Hormones
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Prevalence of Testicular Adrenal Rest Tumours in Male Children With Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
European Journal of Endocrinology
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Congenital Adrenal Hyperplasia Due to Cytochrome P450 Oxidoreductase Deficiency
Male Gender Identity and Reversible Hypokalemic Hypertension in a 46,XX Child With 11-Beta-Hydroxylase Deficiency Congenital Adrenal Hyperplasia
Cureus
11-Beta-Hydroxylase Deficiency
Long-Term Glucocorticoid Effect on Bone Mineral Density in Patients With Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
European Journal of Endocrinology
Medicine
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