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Publications by Ioannis Tzaves
21-Hydroxylase Deficiency Presenting as Bilateral Adrenal Masses in the Sixth Decade of Life in a Phenotypically Male but Genetically Female Patient
Endocrine Abstracts
Primary Thyroid Lymphoma: A Heterogeneous Disease and Presentation of Two Different Cases
Endocrine Abstracts
Related publications
Prevalence of Testicular Adrenal Rest Tumours in Male Children With Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
European Journal of Endocrinology
Medicine
Endocrinology
Metabolism
Diabetes
111 Cah (21-Hydroxylase Deficiency) Presenting as Central Precocious Puberty
Pediatric Research
Child Health
Pediatrics
Perinatology
Late Onset 21-Hydroxylase Deficiency Presenting as Pre-Pubertal Gynaecomastia
Pediatric Research
Child Health
Pediatrics
Perinatology
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
Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
Adrenal Specific Nuclear Transcription Factor (Tf) Binding Region in 21-Hydroxylase Deficiency
Pediatric Research
Child Health
Pediatrics
Perinatology
Steroid 21-Hydroxylase Deficiency in Mice. An Animal Model for Congenital Adrenal Hyperplasia.
Proceedings of The Japanese Association of Animal Models for Human Diseases
Psychological Vulnerability to Stress in Carriers of Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
Hormones
Medicine
Endocrinology
Metabolism
Diabetes
Bilateral Adrenal Masses: A Single-Centre Experience
Endocrine Connections
Internal Medicine
Endocrinology
Metabolism
Diabetes