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2010 1
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2014 3
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2022 1
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Page 1
Perinatal hypophosphatasia caused by uniparental isodisomy.
Watanabe A, Satoh S, Fujita A, Naing BT, Orimo H, Shimada T. Watanabe A, et al. Among authors: naing bt. Bone. 2014 Mar;60:93-7. doi: 10.1016/j.bone.2013.12.009. Epub 2013 Dec 12. Bone. 2014. PMID: 24334170
Identical germline mutations in the TMEM127 gene in two unrelated Japanese patients with bilateral pheochromocytoma.
Takeichi N, Midorikawa S, Watanabe A, Naing BT, Tamura H, Wakakuri-Kano T, Ishizaki A, Sugihara H, Nissato S, Saito Y, Aita Y, Ishii KA, Igarashi T, Kawakami Y, Hara H, Ikeda T, Shimizu K, Suzuki S, Shimano H, Kawamoto M, Shimada T, Watanabe T, Oikawa S, Takekoshi K. Takeichi N, et al. Among authors: naing bt. Clin Endocrinol (Oxf). 2012 Nov;77(5):707-14. doi: 10.1111/j.1365-2265.2012.04421.x. Clin Endocrinol (Oxf). 2012. PMID: 22541004
Ehlers-Danlos syndrome, vascular type: a novel missense mutation in the COL3A1 gene.
Masuno M, Watanabe A, Naing BT, Shimada T, Fujimoto W, Ninomiya S, Ueda Y, Kadota K, Kotaka T, Kondo E, Yamanouchi Y, Inoue M, Ouchi K, Kuroki Y. Masuno M, et al. Among authors: naing bt. Congenit Anom (Kyoto). 2012 Dec;52(4):207-10. doi: 10.1111/j.1741-4520.2011.00353.x. Congenit Anom (Kyoto). 2012. PMID: 23181496
Interaction effect between handedness and CNTNAP2 polymorphism (rs7794745 genotype) on voice-specific frontotemporal activity in healthy individuals: an fMRI study.
Koeda M, Watanabe A, Tsuda K, Matsumoto M, Ikeda Y, Kim W, Tateno A, Naing BT, Karibe H, Shimada T, Suzuki H, Matsuura M, Okubo Y. Koeda M, et al. Among authors: naing bt. Front Behav Neurosci. 2015 Apr 20;9:87. doi: 10.3389/fnbeh.2015.00087. eCollection 2015. Front Behav Neurosci. 2015. PMID: 25941478 Free PMC article.