Masanori Adachi
Department of Endocrinology and Metabolism
Kanagawa Children's Medical Center
Minami-ku
Yokohama
Japan
Name/email consistency: high
- 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)
- 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)
- 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)
- 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)
- 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)
- 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)
- 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)
