3月の掲載論文・受賞
・内分泌グループ
・Spondyloepiphyseal Dysplasia Congenita Caused by Double Heterozygous Mutations in COL2A1
Osamu Kawano, Akie Nakamura, Shuntaro Morikawa, Kimiaki Uetake, Katsura Ishizu, Toshihiro Tajima
Am J Med Genet A [Epub ahead of print]
・Tumoral calcinosis in a patient with hypoparathyroidism, sensorineural deafness, and renal dysplasia syndrome undergoing hemodialysis.
Hiramatsu R, Ubara Y, Tajima T, Usui T, Namba K, Takeuchi Y, Sawa N, Hasegawa E, Takaichi K.
Clin Case Rep. 2015 Feb;3(2):73-5. doi: 10.1002/ccr3.125. Epub 2015 Jan 22.
・南山堂医学大事典 20版 p.2228
「17-β hydroxysteroid dehydrogenase欠損症」
田島敏広
・Corrigendum to "Gitelman Syndrome in a School Boy Who Presented with Generalized Convulsion and Had a R642H/R642W Mutation in the SLC12A3 Gene".
Makino S, Tajima T, Shinozuka J, Ikumi A, Awaguni H, Tanaka S, Maruyama R, Imashuku S.
Case Rep Pediatr. 2015;2015:853523. doi: 10.1155/2015/853523. Epub 2015 Feb 28.
PMID: 25815233 Free Article
・新生児グループ
Effects of prenatal leydig cell function on the ratio of the second to fourth digit lengths in school-aged children.
Mitsui T, Araki A, Imai A, Sato S, Miyashita C, Ito S, Sasaki S, Kitta T, Moriya K, Cho K, Morioka K, Kishi R, Nonomura K.
PLoS One. 2015 Mar 6;10(3):e0120636. doi: 10.1371/journal.pone.0120636. eCollection 2015.