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Divergent neurodevelopmental profiles of very-low-birth-weight infants.
Ogata R, Watanabe K, Chong PF, Okamoto J, Sakemi Y, Nakashima T, Ohno T, Nomiyama H, Sonoda Y, Ichimiya Y, Inoue H, Ochiai M, Yamashita H, Sakai Y, Ohga S. Ogata R, et al. Among authors: yamashita h. Pediatr Res. 2024 Jan;95(1):233-240. doi: 10.1038/s41390-023-02778-w. Epub 2023 Aug 25. Pediatr Res. 2024. PMID: 37626120
Girl with a PRRT2 mutation and infantile focal epilepsy with bilateral spikes.
Torisu H, Watanabe K, Shimojima K, Sugawara M, Sanefuji M, Ishizaki Y, Sakai Y, Yamashita H, Yamamoto T, Hara T. Torisu H, et al. Among authors: yamashita h. Brain Dev. 2014 Apr;36(4):342-5. doi: 10.1016/j.braindev.2013.05.009. Epub 2013 Jun 12. Brain Dev. 2014. PMID: 23768507
Clinical Epidemiology and Treatment of Febrile and Afebrile Convulsions With Mild Gastroenteritis: A Multicenter Study.
Higuchi Y, Kubo T, Mitsuhashi T, Nakamura N, Yokota I, Komiyama O, Kamimaki I, Yamamoto S, Uchida Y, Watanabe K, Yamashita H, Tanaka S, Iguchi K, Ichimi R, Miyagawa S, Takayanagi T, Koga H, Shukuya A, Saito A, Horibe K. Higuchi Y, et al. Among authors: yamashita h. Pediatr Neurol. 2017 Feb;67:78-84. doi: 10.1016/j.pediatrneurol.2016.05.011. Epub 2016 Aug 3. Pediatr Neurol. 2017. PMID: 28094168
Clarithromycin Plus Intravenous Immunoglobulin Therapy Can Reduce the Relapse Rate of Kawasaki Disease: A Phase 2, Open-Label, Randomized Control Study.
Nanishi E, Nishio H, Takada H, Yamamura K, Fukazawa M, Furuno K, Mizuno Y, Saigo K, Kadoya R, Ohbuchi N, Onoe Y, Yamashita H, Nakayama H, Hara T, Ohno T, Takahashi Y, Hatae K, Harada T, Shimose T, Kishimoto J, Ohga S, Hara T. Nanishi E, et al. Among authors: yamashita h. J Am Heart Assoc. 2017 Jul 6;6(7):e005370. doi: 10.1161/JAHA.116.005370. J Am Heart Assoc. 2017. PMID: 28684643 Free PMC article. Clinical Trial.
Diagnostic challenge of the newborn patients with heritable protein C deficiency.
Ichiyama M, Inoue H, Ochiai M, Ishimura M, Shiraishi A, Fujiyoshi J, Yamashita H, Sato K, Matsumoto S, Hotta T, Uchiumi T, Kang D, Ohga S. Ichiyama M, et al. Among authors: yamashita h. J Perinatol. 2019 Feb;39(2):212-219. doi: 10.1038/s41372-018-0262-0. Epub 2018 Oct 23. J Perinatol. 2019. PMID: 30353081 Free PMC article.
Loss of imprinting of the human-specific imprinted gene ZNF597 causes prenatal growth retardation and dysmorphic features: implications for phenotypic overlap with Silver-Russell syndrome.
Yamazawa K, Inoue T, Sakemi Y, Nakashima T, Yamashita H, Khono K, Fujita H, Enomoto K, Nakabayashi K, Hata K, Nakashima M, Matsunaga T, Nakamura A, Matsubara K, Ogata T, Kagami M. Yamazawa K, et al. Among authors: yamashita h. J Med Genet. 2021 Jun;58(6):427-432. doi: 10.1136/jmedgenet-2020-107019. Epub 2020 Jun 23. J Med Genet. 2021. PMID: 32576657 Free PMC article.
3,538 results