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Identification of a homozygous JAK3 V674A mutation caused by acquired uniparental disomy in a relapsed early T-cell precursor ALL patient.
Kawashima-Goto S, Imamura T, Seki M, Kato M, Yoshida K, Sugimoto A, Kaneda D, Fujiki A, Miyachi M, Nakatani T, Osone S, Ishida H, Taki T, Takita J, Shiraishi Y, Chiba K, Tanaka H, Miyano S, Ogawa S, Hosoi H. Kawashima-Goto S, et al. Among authors: osone s. Int J Hematol. 2015 Apr;101(4):411-6. doi: 10.1007/s12185-014-1711-y. Epub 2014 Nov 28. Int J Hematol. 2015. PMID: 25430085
Potential use of procalcitonin concentrations as a diagnostic marker of the PFAPA syndrome.
Yoshihara T, Imamura T, Yokoi K, Shibata M, Kano G, Osone S, Yagi K, Todo S, Murakami Y, Yamada Y, Yamada H, Satomura S, Ishida H. Yoshihara T, et al. Among authors: osone s. Eur J Pediatr. 2007 Jun;166(6):621-2. doi: 10.1007/s00431-006-0281-2. Epub 2006 Sep 30. Eur J Pediatr. 2007. PMID: 17013596 Clinical Trial. No abstract available.
43 results