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Publications by Victoria Kaltzidou

21-Hydroxylase Deficiency Presenting as Bilateral Adrenal Masses in the Sixth Decade of Life in a Phenotypically Male but Genetically Female Patient

Endocrine Abstracts

English

The Diagnostic Value of FNAB for Early Diagnosis of Thyroid Cancer: A Greek Center Experience

Endocrine Abstracts

English

Related publications

Prevalence of Testicular Adrenal Rest Tumours in Male Children With Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

European Journal of Endocrinology

English

111 Cah (21-Hydroxylase Deficiency) Presenting as Central Precocious Puberty

Pediatric Research

English

Late Onset 21-Hydroxylase Deficiency Presenting as Pre-Pubertal Gynaecomastia

Pediatric Research

English

Gender Reversal and Bilateral Giant Adrenal Myelolipomas in a 46,xx Patient With 21-Hydroxylase Deficiency: Case Report and Review of the Literature

AACE Clinical Case Reports

English

Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

English

Adrenal Specific Nuclear Transcription Factor (Tf) Binding Region in 21-Hydroxylase Deficiency

Pediatric Research

English

Steroid 21-Hydroxylase Deficiency in Mice. An Animal Model for Congenital Adrenal Hyperplasia.

Proceedings of The Japanese Association of Animal Models for Human Diseases

English

Psychological Vulnerability to Stress in Carriers of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

English

Bilateral Adrenal Masses: A Single-Centre Experience

Endocrine Connections

Internal Medicine

English