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Clinical advances in the pharmacotherapy of congenital adrenal hyperplasia  in: European Journal of Endocrinology Volume 186 Issue 1 (2022)
Clinical advances in the pharmacotherapy of congenital adrenal hyperplasia in: European Journal of Endocrinology Volume 186 Issue 1 (2022)

Genetic disruption of 21-hydroxylase in zebrafish causes interrenal  hyperplasia
Genetic disruption of 21-hydroxylase in zebrafish causes interrenal hyperplasia

Adrenal steroidogenesis and congenital adrenal hyperplasia. - Abstract -  Europe PMC
Adrenal steroidogenesis and congenital adrenal hyperplasia. - Abstract - Europe PMC

Frontiers | 21-Hydroxylase-Specific CD8+ T Cells in Autoimmune Addison's  Disease Are Restricted by HLA-A2 and HLA-C7 Molecules
Frontiers | 21-Hydroxylase-Specific CD8+ T Cells in Autoimmune Addison's Disease Are Restricted by HLA-A2 and HLA-C7 Molecules

21-Hydroxylase - Wikipedia
21-Hydroxylase - Wikipedia

Insuffisance surrénalienne CHRONIQUE
Insuffisance surrénalienne CHRONIQUE

Hyperplasie congénitale des surrénales provoquée par un déficit en 21- hydroxylase - Pédiatrie - Édition professionnelle du Manuel MSD
Hyperplasie congénitale des surrénales provoquée par un déficit en 21- hydroxylase - Pédiatrie - Édition professionnelle du Manuel MSD

21-hydroxylase deficiency: MedlinePlus Genetics
21-hydroxylase deficiency: MedlinePlus Genetics

Frontiers | Long-Term Health Outcomes of Korean Adults With Classic  Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
Frontiers | Long-Term Health Outcomes of Korean Adults With Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency

Management of endocrine immune-related adverse events of immune checkpoint  inhibitors: an updated review in: Endocrine Connections Volume 9 Issue 10  (2020)
Management of endocrine immune-related adverse events of immune checkpoint inhibitors: an updated review in: Endocrine Connections Volume 9 Issue 10 (2020)

21-Hydroxylase - Wikipedia
21-Hydroxylase - Wikipedia

MANAGEMENT OF ENDOCRINE DISEASE: Congenital adrenal hyperplasia due to 21- hydroxylase deficiency: update on the management of adult patients and  prenatal treatment in: European Journal of Endocrinology Volume 176 Issue 4  (2017)
MANAGEMENT OF ENDOCRINE DISEASE: Congenital adrenal hyperplasia due to 21- hydroxylase deficiency: update on the management of adult patients and prenatal treatment in: European Journal of Endocrinology Volume 176 Issue 4 (2017)

Congenital Adrenal Hyperplasias - The Medical Biochemistry Page
Congenital Adrenal Hyperplasias - The Medical Biochemistry Page

21-Hydroxylase - an overview | ScienceDirect Topics
21-Hydroxylase - an overview | ScienceDirect Topics

French Endocrine Society Guidance on endocrine side effects of  immunotherapy in: Endocrine-Related Cancer Volume 26 Issue 2 (2019)
French Endocrine Society Guidance on endocrine side effects of immunotherapy in: Endocrine-Related Cancer Volume 26 Issue 2 (2019)

21-Hydroxylase Deficiency - Pediatrics - Medbullets Step 2/3
21-Hydroxylase Deficiency - Pediatrics - Medbullets Step 2/3

Frontiers | Latent Adrenal Insufficiency: From Concept to Diagnosis
Frontiers | Latent Adrenal Insufficiency: From Concept to Diagnosis

Pôle Biologie Pathologie Génétique > Ac anti-21 Hydroxylase
Pôle Biologie Pathologie Génétique > Ac anti-21 Hydroxylase

Immune Checkpoint Inhibitor-Induced Adrenalitis and Primary Adrenal  Insufficiency: Systematic Review and Optimal Management - Endocrine Practice
Immune Checkpoint Inhibitor-Induced Adrenalitis and Primary Adrenal Insufficiency: Systematic Review and Optimal Management - Endocrine Practice

Frontiers | Management of the Female With Non-classical Congenital Adrenal  Hyperplasia (NCCAH): A Patient-Oriented Approach
Frontiers | Management of the Female With Non-classical Congenital Adrenal Hyperplasia (NCCAH): A Patient-Oriented Approach

Frontiers | 21-Hydroxylase-Specific CD8+ T Cells in Autoimmune Addison's  Disease Are Restricted by HLA-A2 and HLA-C7 Molecules
Frontiers | 21-Hydroxylase-Specific CD8+ T Cells in Autoimmune Addison's Disease Are Restricted by HLA-A2 and HLA-C7 Molecules

Two novel <i>CYP21A2</i> missense mutations in Italian patients with 21â•' hydroxylase deficiency: Identificatio
Two novel <i>CYP21A2</i> missense mutations in Italian patients with 21â•' hydroxylase deficiency: Identificatio

Clinical advances in the pharmacotherapy of congenital adrenal hyperplasia  in: European Journal of Endocrinology Volume 186 Issue 1 (2022)
Clinical advances in the pharmacotherapy of congenital adrenal hyperplasia in: European Journal of Endocrinology Volume 186 Issue 1 (2022)

21-hydroxylase deficiency: MedlinePlus Genetics
21-hydroxylase deficiency: MedlinePlus Genetics