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Familial episodic limb pain in kindreds with novel Nav1.9 mutations.
Kabata R, Okuda H, Noguchi A, Kondo D, Fujiwara M, Hata K, Kato Y, Ishikawa K, Tanaka M, Sekine Y, Hishikawa N, Mizukami T, Ito J, Akasaka M, Sakurai K, Yoshida T, Minoura H, Hayashi T, Inoshita K, Matsuyama M, Kinjo N, Cao Y, Inoue S, Kobayashi H, Harada KH, Youssefian S, Takahashi T, Koizumi A. Kabata R, et al. Among authors: takahashi t. PLoS One. 2018 Dec 17;13(12):e0208516. doi: 10.1371/journal.pone.0208516. eCollection 2018. PLoS One. 2018. PMID: 30557356 Free PMC article.
Liver fibrosis in an extremely small infant for gestational age.
Arai H, Noguchi A, Goto R, Matsuda T, Nakajima H, Takahashi T. Arai H, et al. Among authors: takahashi t. Tohoku J Exp Med. 2010 Jul;221(3):181-5. doi: 10.1620/tjem.221.181. Tohoku J Exp Med. 2010. PMID: 20513975 Free article.
Congenital hyperinsulinism in an infant with paternal uniparental disomy on chromosome 11p15: few clinical features suggestive of Beckwith-Wiedemann syndrome.
Adachi H, Takahashi I, Higashimoto K, Tsuchida S, Noguchi A, Tamura H, Arai H, Ito T, Masue M, Nishibori H, Takahashi T, Soejima H. Adachi H, et al. Among authors: takahashi i, takahashi t. Endocr J. 2013;60(4):403-8. doi: 10.1507/endocrj.ej12-0242. Epub 2012 Nov 30. Endocr J. 2013. PMID: 23197114 Free article.
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