Frontiers | 21-Hydroxylase-Specific CD8+ T Cells in Autoimmune Addison's Disease Are Restricted by HLA-A2 and HLA-C7 Molecules
French Endocrine Society Guidance on endocrine side effects of immunotherapy in: Endocrine-Related Cancer Volume 26 Issue 2 (2019)
Frontiers | Latent Adrenal Insufficiency: From Concept to Diagnosis
Anticorpi anti-21 hidroxilaza - analiza medicala Synevo
21-Hydroxylase - an overview | ScienceDirect Topics
Clinical advances in the pharmacotherapy of congenital adrenal hyperplasia in: European Journal of Endocrinology Volume 186 Issue 1 (2022)
Sindrom adrenogenital (deficit de 21-hidroxilaza)-mutatii CYP21A2 - Synevo
PDF) Congenital Adrenal Hyperplasia Due to Steroid 21-Hydroxylase Deficiency: An Endocrine Society* Clinical Practice Guideline
Frontiers | 21-Hydroxylase-Specific CD8+ T Cells in Autoimmune Addison's Disease Are Restricted by HLA-A2 and HLA-C7 Molecules
Adrenal steroidogenesis and congenital adrenal hyperplasia. - Abstract - Europe PMC
Congenital Adrenal Hyperplasias - The Medical Biochemistry Page
Two novel <i>CYP21A2</i> missense mutations in Italian patients with 21â•' hydroxylase deficiency: Identificatio
PDF) Congenital Adrenal Hyperplasia (CAH) due to 21-Hydroxylase Deficiency: A Comprehensive Focus on 233 Pathogenic Variants of CYP21A2 Gene
Insuffisance surrénalienne CHRONIQUE
CYP17A1 inhibitor abiraterone, an anti-prostate cancer drug, also inhibits the 21-hydroxylase activity of CYP21A2 - ScienceDirect
Clinically relevant genetic advances in endocrinology | RCP Journals
JCM | Free Full-Text | Pregnancy and Prenatal Management of Congenital Adrenal Hyperplasia | HTML
21-hydroxylase deficiency: MedlinePlus Genetics
NAA Services for Anti-Steroid-21-Hydroxylase (CYP21A2 or P450c21) - Creative Biolabs
Frontiers | Management of the Female With Non-classical Congenital Adrenal Hyperplasia (NCCAH): A Patient-Oriented Approach
Hyperplasie congénitale des surrénales provoquée par un déficit en 21- hydroxylase - Pédiatrie - Édition professionnelle du Manuel MSD
Steroid 17-hydroxylase and 17,20-lyase deficiencies, genetic and pharmacologic - ScienceDirect
Clinical advances in the pharmacotherapy of congenital adrenal hyperplasia in: European Journal of Endocrinology Volume 186 Issue 1 (2022)
21-Hydroxylase - Wikipedia
21-hydroxylase deficiency: MedlinePlus Genetics
Immune Checkpoint Inhibitor-Induced Adrenalitis and Primary Adrenal Insufficiency: Systematic Review and Optimal Management - Endocrine Practice
