Asymptomatic Congenital Hyperinsulinism due to a Glucokinase-Activating Mutation, Treated as Adrenal Insufficiency for Twelve Years

Eitemau Tebyg

• Asymptomatic Congenital Hyperinsulinism due to a Glucokinase-Activating Mutation, Treated as Adrenal Insufficiency for Twelve Years
  gan: Morishita, Kae, et al.
  Cyhoeddwyd: (2017)
• Asymptomatic Congenital Hyperinsulinism due to a Glucokinase-Activating Mutation, Treated as Adrenal Insufficiency for Twelve Years
  gan: Kae Morishita, et al.
  Cyhoeddwyd: (2017-01-01)
• ARMC5 Alterations in Primary Macronodular Adrenal Hyperplasia (PMAH) and the Clinical State of Variant Carriers
  gan: Kyo, Chika, et al.
  Cyhoeddwyd: (2019)
• SAT-232 Pheochromocytoma Presenting Rare Skin Findings: Livedoid Vasculopathy and Raynaud’s Phenomenon
  gan: Kyo, Chika, et al.
  Cyhoeddwyd: (2020)
• Novel germline variant of TMEM127 gene in a patient with familial pheochromocytoma
  gan: Kohei Saitoh, et al.
  Cyhoeddwyd: (2017-04-01)