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Novel CUL7 biallelic mutations alter the skeletal phenotype of 3M syndrome.
Takizaki N, Tsurusaki Y, Katsumata K, Enomoto Y, Murakami H, Muroya K, Ishikawa H, Aida N, Nishimura G, Kurosawa K. Takizaki N, et al. Among authors: katsumata k. Hum Genome Var. 2020 Feb 4;7:1. doi: 10.1038/s41439-020-0090-6. eCollection 2020. Hum Genome Var. 2020. PMID: 32047638 Free PMC article.
Prognosis of conventional vs. high-frequency ventilation for congenital diaphragmatic hernia: a retrospective cohort study.
Fuyuki M, Usui N, Taguchi T, Hayakawa M, Masumoto K, Kanamori Y, Amari S, Yamoto M, Urushihara N, Inamura N, Yokoi A, Okawada M, Okazaki T, Toyoshima K, Furukawa T, Terui K, Ohfuji S, Tazuke Y, Uchida K, Okuyama H; Japanese Congenital Diaphragmatic Hernia Study Group. Fuyuki M, et al. J Perinatol. 2021 Apr;41(4):814-823. doi: 10.1038/s41372-020-00833-6. Epub 2020 Nov 11. J Perinatol. 2021. PMID: 33177680
Death of children with Down syndrome by gestational age and cause.
Shimokaze T, Toyoshima K, Saito T, Katsumata K, Kemmotsu T, Ishikawa H, Kurosawa K. Shimokaze T, et al. Among authors: katsumata k. Pediatr Res. 2024 Apr;95(5):1325-1330. doi: 10.1038/s41390-023-02870-1. Epub 2023 Oct 28. Pediatr Res. 2024. PMID: 37898703
[Significance of Colorectal Cancer Resection for the Elderly].
Kuboyama Y, Kasahara K, Udo R, Tago T, Mazaki J, Hayashi Y, Ishizaki T, Katsumata K, Nagakawa Y. Kuboyama Y, et al. Among authors: katsumata k. Gan To Kagaku Ryoho. 2024 Mar;51(3):314-316. Gan To Kagaku Ryoho. 2024. PMID: 38494816 Japanese.
458 results