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- Primary Generalized Glucocorticoid Resistance and Hypersensitivity
- Primary Generalized Glucocorticoid Resistance or Chrousos Syndrome: Allostasis Through a Mutated Glucocorticoid Receptor
- Recent advances in the molecular mechanisms causing primary generalized glucocorticoid resistance
- Novel insights into the molecular mechanisms underlying generalized glucocorticoid resistance and hypersensitivity syndromes
- Generalised Glucocorticoid Resistance
- Generalised Glucocorticoid Resistance
- A Novel Point Mutation in the Ligand-Binding Domain (LBD) of the Human Glucocorticoid Receptor (hGR) Causing Generalized Glucocorticoid Resistance: The Importance of the C Terminus of hGR LBD in Conferring Transactivational Activity
- Chrousos syndrome: from molecular pathogenesis to therapeutic management
- Glucocorticoid Resistance Syndrome in 2 Patients With Diverse Genotype
- O-21 FROM ORAL LEVOTHYROXINE RESISTANCE TO INTRAVENOUS LEVOTHYROXINE HYPERSENSITIVITY: A CHALLENGING PRIMARY HYPOTHYROIDISM CASE
- ANIFROLUMAB IN THE MANAGEMENT OF LUPUS HEADACHES: A CASE REPORT
- Alopecia Areata, Primary Sclerosing Cholangitis, and Ulcerative Colitis: Autoimmunity and Apoptosis as Common Links?
- Cutaneous manifestations and considerations in COVID ‐19 pandemic: A systematic review
- The Search for the Causes of Common Hyperandrogenism, 1965 to Circa 2015
- Glucocorticoid Receptor Mutants Demonstrate Increased Motility Inside the Nucleus of Living Cells: Time of Fluorescence Recovery After Photobleaching (FRAP) Is an Integrated Measure of Receptor Function
- Focal and Generalized Alopecia
- Recent advances in the molecular mechanisms determining tissue sensitivity to glucocorticoids: novel mutations, circadian rhythm and ligand-induced repression of the human glucocorticoid receptor
- Unravelling the link between insulin resistance and androgen excess
- Diagnostic approach to low‐renin hypertension
- Skin
- How to diagnose a lipodystrophy syndrome
- The Evaluation and Management of Hirsutism
- Lupus erythematosus: systemic and cutaneous manifestations
- Adrenal causes of endocrine hypertension in childhood or adolescence
- Endocrinopathies and Other Disorders Inducing a Polycystic Ovary Syndrome Phenotype
- Potential role and therapeutic interests of myo-inositol in metabolic diseases
- Nonclassic Congenital Adrenal Hyperplasia
- Endocrine-skin interactions
- Adrenal Disorders and the Paediatric Brain: Pathophysiological Considerations and Clinical Implications
- Clinical-exome sequencing unveils the genetic landscape of polycystic ovarian syndrome (PCOS) focusing on lean and obese phenotypes: implications for cost-effective diagnosis and personalized treatment