Demir, Korcan

Rare causes of primary adrenal insufficiency: genetic and clinical characterization of a large nationwide cohort

Guran, T., Buonocore, F., Saka, N., Ozbek, M. N., Aycan, Z., Bereket, A., Bas, F., Darcan, S., Bideci, A., Guven, A., et al. (2016) · The Journal of Clinical Endocrinology & Metabolism

Adrenal Hormones and DisordersSexual Differentiation and Disorders

Cited by 207

Diverse Genotypes and Phenotypes of Three Novel Thyroid Hormone Receptor-α Mutations

Demir, K., van Gucht, A. L. M., Büyükinan, M., Çatlı, G., Ayhan, Y., Baş, V. N., Dündar, B., Özkan, B., Meima, M. E., Visser, W. E., et al. (2016) · The Journal of Clinical Endocrinology & Metabolism

Thyroid Disorders and TreatmentsGenomics and Rare Diseases

Cited by 69

Levothyroxine replacement in primary congenital hypothyroidism: the higher the initial dose the higher the rate of overtreatment

Tuhan, H., Abaci, A., Cicek, G., Anik, A., Catli, G., Demir, K., & Bober, E. (2016) · Journal of Pediatric Endocrinology and Metabolism

Thyroid Disorders and TreatmentsThyroid and Parathyroid Surgery

Cited by 21

Anthropometric findings from birth to adulthood and their relation with karyotpye distribution in Turkish girls with Turner syndrome

Sari, E., Bereket, A., Yeşilkaya, E., Baş, F., Bundak, R., Aydın, B. K., Darcan, Ş., Dündar, B., Büyükinan, M., Kara, C., et al. (2016) · American Journal of Medical Genetics Part A

Genetic and Clinical Aspects of Sex Determination and Chromosomal AbnormalitiesSexual Differentiation and Disorders

Cited by 11