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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

Masanori Adachi

Department of Endocrinology and Metabolism

Kanagawa Children's Medical Center





Name/email consistency: high



  • Department of Endocrinology and Metabolism, Kanagawa Children's Medical Center, Minami-ku, Yokohama, Japan. 2004 - 2010


  1. Increased Na reabsorption via the Na-Cl cotransporter in autosomal recessive pseudohypoaldosteronism. Adachi, M., Asakura, Y., Muroya, K., Tajima, T., Fujieda, K., Kuribayashi, E., Uchida, S. Clin. Exp. Nephrol. (2010) [Pubmed]
  2. Unfavorable lipoprotein profile in childhood cancer survivors with suprasellar brain tumors--a high Apo B level and increased small dense LDL-cholesterol. Adachi, M., Muroya, K., Asakura, Y. Childs. Nerv. Syst (2009) [Pubmed]
  3. POR R457H is a global founder mutation causing Antley-Bixler syndrome with autosomal recessive trait. Adachi, M., Asakura, Y., Matsuo, M., Yamamoto, T., Hanaki, K., Arlt, W. Am. J. Med. Genet. A (2006) [Pubmed]
  4. A novel mutation in the GATA3 gene in a family with HDR syndrome (Hypoparathyroidism, sensorineural Deafness and Renal anomaly syndrome). Adachi, M., Tachibana, K., Asakura, Y., Tsuchiya, T. J. Pediatr. Endocrinol. Metab. (2006) [Pubmed]
  5. Improved neutrophil function in a glycogen storage disease type 1b patient after liver transplantation. Adachi, M., Shinkai, M., Ohhama, Y., Tachibana, K., Kuratsuji, T., Saji, H., Maruya, E. Eur. J. Pediatr. (2004) [Pubmed]
  6. Compound heterozygous mutations of cytochrome P450 oxidoreductase gene (POR) in two patients with Antley-Bixler syndrome. Adachi, M., Tachibana, K., Asakura, Y., Yamamoto, T., Hanaki, K., Oka, A. Am. J. Med. Genet. A (2004) [Pubmed]
  7. Abnormal steroidogenesis in three patients with Antley-Bixler syndrome: apparent decreased activity of 17alpha-hydroxylase, 17,20-lyase and 21-hydroxylase. Adachi, M., Asakura, Y., Tachibana, K., Shackleton, C. Pediatr. Int (2004) [Pubmed]
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