Familial Micronodular Adrenocortical Disease, Cushing Syndrome, and Mutations of the Gene Encoding Phosphodiesterase 11A4 (PDE11A)

Ítems similars

• Phosphodiesterase 11A (PDE11A) and Genetic Predisposition to Adrenocortical Tumors
  per: Libé, Rossella, et al.
  Publicat: (2008)
• Reversible posterior encephalopathy syndrome associated with micronodular adrenocortical disease and Cushing syndrome
  per: Lodish, Maya, et al.
  Publicat: (2009)
• ACTH-Independent Cushing’s Syndrome with Bilateral Micronodular Adrenal Hyperplasia and Ectopic Adrenocortical Adenoma
  per: Louiset, Estelle, et al.
  Publicat: (2010)
• A phosphodiesterase 11 (Pde11a) knockout mouse expressed functional but reduced Pde11a: phenotype and impact on adrenocortical function
  per: Levy, Isaac, et al.
  Publicat: (2020)
• Germline PRKACA Amplification Leads To Cushing Syndrome Caused By 3 Adrenocortical Pathologic Phenotypes
  per: Carney, J. Aidan, et al.
  Publicat: (2014)