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UCSF School of Medicine | Department of Pediatrics UCSF Medical Center

Approach to the patient: transgender youth: endocrine considerations.

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Use of aromatase inhibitors in large cell calcifying sertoli cell tumors: effects on gynecomastia, growth velocity, and bone age.

  • Read more about Use of aromatase inhibitors in large cell calcifying sertoli cell tumors: effects on gynecomastia, growth velocity, and bone age.

Quantitation of CYP24A1 enzymatic activity with a simple two-hybrid system.

  • Read more about Quantitation of CYP24A1 enzymatic activity with a simple two-hybrid system.

Vandetanib successfully controls medullary thyroid cancer-related Cushing syndrome in an adolescent patient.

  • Read more about Vandetanib successfully controls medullary thyroid cancer-related Cushing syndrome in an adolescent patient.

Macronodular adrenal hyperplasia due to mutations in an armadillo repeat containing 5 (ARMC5) gene: a clinical and genetic investigation.

  • Read more about Macronodular adrenal hyperplasia due to mutations in an armadillo repeat containing 5 (ARMC5) gene: a clinical and genetic investigation.

Differences in adiposity in Cushing syndrome caused by PRKAR1A mutations: clues for the role of cyclic AMP signaling in obesity and diagnostic implications.

  • Read more about Differences in adiposity in Cushing syndrome caused by PRKAR1A mutations: clues for the role of cyclic AMP signaling in obesity and diagnostic implications.

Clinical review: kinase inhibitors: adverse effects related to the endocrine system.

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Recovery of the hypothalamic-pituitary-adrenal axis in children and adolescents after surgical cure of Cushing's disease.

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(111)In-octreotide scintigraphy for identification of metastatic medullary thyroid carcinoma in children and adolescents.

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Frequent phosphodiesterase 11A gene (PDE11A) defects in patients with Carney complex (CNC) caused by PRKAR1A mutations: PDE11A may contribute to adrenal and testicular tumors in CNC as a modifier of the phenotype.

  • Read more about Frequent phosphodiesterase 11A gene (PDE11A) defects in patients with Carney complex (CNC) caused by PRKAR1A mutations: PDE11A may contribute to adrenal and testicular tumors in CNC as a modifier of the phenotype.

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