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Page 1
Evaluation of Suspected Autosomal Alport Syndrome Synonymous Variants.
Rossanti R, Horinouchi T, Yamamura T, Nagano C, Sakakibara N, Ishiko S, Aoto Y, Kondo A, Nagai S, Okada E, Ishimori S, Nagase H, Matsui S, Tamagaki K, Ubara Y, Nagahama M, Shima Y, Nakanishi K, Ninchoji T, Matsuo M, Iijima K, Nozu K. Rossanti R, et al. Among authors: nagase h. Kidney360. 2021 Oct 13;3(3):497-505. doi: 10.34067/KID.0005252021. eCollection 2022 Mar 31. Kidney360. 2021. PMID: 35582193 Free PMC article.
Somatic mosaicism of a CDKL5 mutation identified by next-generation sequencing.
Kato T, Morisada N, Nagase H, Nishiyama M, Toyoshima D, Nakagawa T, Maruyama A, Fu XJ, Nozu K, Wada H, Takada S, Iijima K. Kato T, et al. Among authors: nagase h. Brain Dev. 2015 Oct;37(9):911-5. doi: 10.1016/j.braindev.2015.03.002. Epub 2015 Mar 27. Brain Dev. 2015. PMID: 25819767
Short and long-term outcomes in children with suspected acute encephalopathy.
Nishiyama M, Nagase H, Tanaka T, Fujita K, Kusumoto M, Kajihara S, Yamaguchi Y, Maruyama A, Takeda H, Uetani Y, Tomioka K, Toyoshima D, Taniguchi-Ikeda M, Morioka I, Takada S, Iijima K. Nishiyama M, et al. Among authors: nagase h. Brain Dev. 2016 Sep;38(8):731-7. doi: 10.1016/j.braindev.2016.02.011. Epub 2016 Mar 4. Brain Dev. 2016. PMID: 26952815
Gestational age-dependency of height and body mass index trajectories during the first 3 years in Japanese small-for-gestational age children.
Maeyama K, Morioka I, Iwatani S, Fukushima S, Kurokawa D, Yamana K, Nishida K, Ohyama S, Fujioka K, Awano H, Taniguchi-Ikeda M, Nozu K, Nagase H, Nishimura N, Shirai C, Iijima K. Maeyama K, et al. Among authors: nagase h. Sci Rep. 2016 Dec 9;6:38659. doi: 10.1038/srep38659. Sci Rep. 2016. PMID: 27934914 Free PMC article.
Evaluation of BiliCare™ transcutaneous bilirubin device in Japanese newborns.
Yamana K, Morioka I, Kurokawa D, Fukushima S, Nishida K, Ohyama S, Nishimura N, Nozu K, Taniguchi-Ikeda M, Nagase H, Fujioka K, Iwatani S, Nakamura H, Iijima K. Yamana K, et al. Among authors: nagase h. Pediatr Int. 2017 Oct;59(10):1058-1063. doi: 10.1111/ped.13364. Epub 2017 Aug 31. Pediatr Int. 2017. PMID: 28703875 Clinical Trial.
Changes in the numbers of patients with acute gastroenteritis after voluntary introduction of the rotavirus vaccine in a Japanese children's primary emergency medical center.
Morioka I, Kamiyoshi N, Nishiyama M, Yamamura T, Minamikawa S, Iwatani S, Nagase H, Nozu K, Nishimura N, Taniguchi-Ikeda M, Ishibashi K, Ishida A, Iijima K. Morioka I, et al. Among authors: nagase h. Environ Health Prev Med. 2017 Mar 31;22(1):15. doi: 10.1186/s12199-017-0638-3. Environ Health Prev Med. 2017. PMID: 29165124 Free PMC article.
Congenital Cytomegalovirus Infection in Children with Autism Spectrum Disorder: Systematic Review and Meta-Analysis.
Maeyama K, Tomioka K, Nagase H, Yoshioka M, Takagi Y, Kato T, Mizobuchi M, Kitayama S, Takada S, Nagai M, Sakakibara N, Nishiyama M, Taniguchi-Ikeda M, Morioka I, Iijima K, Nishimura N. Maeyama K, et al. Among authors: nagase h. J Autism Dev Disord. 2018 May;48(5):1483-1491. doi: 10.1007/s10803-017-3412-x. J Autism Dev Disord. 2018. PMID: 29185167
Two patients with PNKP mutations presenting with microcephaly, seizure, and oculomotor apraxia.
Taniguchi-Ikeda M, Morisada N, Inagaki H, Ouchi Y, Takami Y, Tachikawa M, Satake W, Kobayashi K, Tsuneishi S, Takada S, Yamaguchi H, Nagase H, Nozu K, Okamoto N, Nishio H, Toda T, Morioka I, Wada H, Kurahashi H, Iijima K. Taniguchi-Ikeda M, et al. Among authors: nagase h. Clin Genet. 2018 Apr;93(4):931-933. doi: 10.1111/cge.13106. Epub 2017 Dec 15. Clin Genet. 2018. PMID: 29243230 No abstract available.
Development of ultra-deep targeted RNA sequencing for analyzing X-chromosome inactivation in female Dent disease.
Minamikawa S, Nozu K, Nozu Y, Yamamura T, Taniguchi-Ikeda M, Nakanishi K, Fujimura J, Horinouchi T, Shima Y, Nakanishi K, Hattori M, Kanda K, Tanaka R, Morisada N, Nagano C, Sakakibara N, Nagase H, Morioka I, Kaito H, Iijima K. Minamikawa S, et al. Among authors: nagase h. J Hum Genet. 2018 May;63(5):589-595. doi: 10.1038/s10038-018-0415-1. Epub 2018 Feb 19. J Hum Genet. 2018. PMID: 29459630
1,533 results