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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
2004 4
2005 1
2006 1
2007 1
2008 3
2010 3
2011 6
2012 7
2013 4
2014 4
2015 5
2016 9
2017 7
2018 9
2019 11
2020 6
2021 9
2022 5
2023 12
2024 5

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83 results

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Page 1
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: ochiai m. Pediatr Res. 2024 Jan;95(1):233-240. doi: 10.1038/s41390-023-02778-w. Epub 2023 Aug 25. Pediatr Res. 2024. PMID: 37626120
Prenatal metal levels and congenital anomalies of the kidney and urinary tract: The Japan Environment and Children's Study.
Iwaya Y, Sanefuji M, Nishiyama K, Sonoda Y, Hamada N, Suga R, Ochiai M, Shimono M, Kusuhara K, Ohga S; Japan Environment and Children's Study Group. Iwaya Y, et al. Among authors: ochiai m. Sci Total Environ. 2023 Sep 10;890:164356. doi: 10.1016/j.scitotenv.2023.164356. Epub 2023 May 23. Sci Total Environ. 2023. PMID: 37230340 Free article.
Role of glutathione in dimethylarsinic acid-induced apoptosis.
Sakurai T, Ochiai M, Kojima C, Ohta T, Sakurai MH, Takada NO, Qu W, Waalkes MP, Fujiwara K. Sakurai T, et al. Among authors: ochiai m. Toxicol Appl Pharmacol. 2004 Aug 1;198(3):354-65. doi: 10.1016/j.taap.2003.10.015. Toxicol Appl Pharmacol. 2004. PMID: 15276415 Review.
Recurrent de novo MAPK8IP3 variants cause neurological phenotypes.
Iwasawa S, Yanagi K, Kikuchi A, Kobayashi Y, Haginoya K, Matsumoto H, Kurosawa K, Ochiai M, Sakai Y, Fujita A, Miyake N, Niihori T, Shirota M, Funayama R, Nonoyama S, Ohga S, Kawame H, Nakayama K, Aoki Y, Matsumoto N, Kaname T, Matsubara Y, Shoji W, Kure S. Iwasawa S, et al. Among authors: ochiai m. Ann Neurol. 2019 Jun;85(6):927-933. doi: 10.1002/ana.25481. Epub 2019 Apr 25. Ann Neurol. 2019. PMID: 30945334
Progressive myoclonic epilepsy as an expanding phenotype of NGLY1-associated congenital deglycosylation disorder: A case report and review of the literature.
Sonoda Y, Fujita A, Torio M, Mukaino T, Sakata A, Matsukura M, Yonemoto K, Hatae K, Ichimiya Y, Chong PF, Ochiai M, Wada Y, Kadoya M, Okamoto N, Murakami Y, Suzuki T, Isobe N, Shigeto H, Matsumoto N, Sakai Y, Ohga S. Sonoda Y, et al. Among authors: ochiai m. Eur J Med Genet. 2024 Feb;67:104895. doi: 10.1016/j.ejmg.2023.104895. Epub 2023 Dec 7. Eur J Med Genet. 2024. PMID: 38070824 Free article. Review.
Management of apnea in infants with trisomy 18.
Taira R, Inoue H, Sawano T, Fujiyoshi J, Ichimiya Y, Torio M, Sanefuji M, Ochiai M, Sakai Y, Ohga S. Taira R, et al. Among authors: ochiai m. Dev Med Child Neurol. 2020 Jul;62(7):874-878. doi: 10.1111/dmcn.14403. Epub 2019 Nov 25. Dev Med Child Neurol. 2020. PMID: 31763690 Free article.
Stroke in a protein C-deficient infant after stem cell transplant for CHARGE syndrome.
Tanaka A, Sakaguchi Y, Inoue H, Egami N, Sonoda Y, Sonoda M, Ishimura M, Ochiai M, Hotta T, Uchiumi T, Sakai Y, Ohga S. Tanaka A, et al. Among authors: ochiai m. Pediatr Blood Cancer. 2023 Apr;70(4):e30047. doi: 10.1002/pbc.30047. Epub 2022 Nov 4. Pediatr Blood Cancer. 2023. PMID: 36330782 No abstract available.
83 results