A study of the etiology of transient congenital hypothyroidism in Niigata Prefecture, Japan

Eitemau Tebyg

• Re-Evaluation of the Prevalence of Permanent Congenital Hypothyroidism in Niigata, Japan: A Retrospective Study
  gan: Nagasaki, Keisuke, et al.
  Cyhoeddwyd: (2021)
• H62L Mutation of CYP21A2 Identified in the Non-classical Form of 21-Hydroxylase Deficiency
  gan: Nagasaki, Keisuke, et al.
  Cyhoeddwyd: (2009)
• A novel mutation in the human mineralocorticoid receptor gene in a Japanese family with autosomal-dominant pseudohypoaldosteronism type 1
  gan: Nishizaki, Yoshimi, et al.
  Cyhoeddwyd: (2016)
• Longitudinal Growth of the Short Bones of the Hand in a Girl with Pseudohypoparathyroidism Type Ia
  gan: Nagasaki, Keisuke, et al.
  Cyhoeddwyd: (2007)
• The Relationship between Preheparin Lipoprotein Lipase and Metabolic Derangements in Obese Japanese Children
  gan: Abe, Yuki, et al.
  Cyhoeddwyd: (2011)