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Metacarpophalangeal pattern profile analysis for a 3-month-old infant with Feingold syndrome 2.
Isobe A, Maeda N, Fujita H, Banno S, Kageyama T, Hatabu N, Sato R, Suzuki E, Miharu M, Komiyama O, Nakashima M, Matsunaga T, Nishimura G, Yamazawa K. Isobe A, et al. Among authors: sato r. Am J Med Genet A. 2021 Mar;185(3):952-954. doi: 10.1002/ajmg.a.62038. Epub 2020 Dec 27. Am J Med Genet A. 2021. PMID: 33369046 Review. No abstract available.
Compound heterozygous variants in the ABCG8 gene in a Japanese girl with sitosterolemia.
Hashimoto N, Dateki S, Suzuki E, Tsuchihashi T, Isobe A, Banno S, Kageyama T, Maeda N, Hatabu N, Sato R, Miharu M, Fujita H, Komiyama O, Shimizu H, Hasegawa T, Yamazawa K. Hashimoto N, et al. Among authors: sato r. Hum Genome Var. 2020 Sep 14;7:25. doi: 10.1038/s41439-020-00112-y. eCollection 2020. Hum Genome Var. 2020. PMID: 33014402 Free PMC article.
[No title available]
[No authors listed] [No authors listed] PMID: 33419975
RNase T2 deficiency promotes TLR13-dependent replenishment of tissue-protective Kupffer cells.
Sato R, Liu K, Shibata T, Hoshino K, Yamaguchi K, Miyazaki T, Hiranuma R, Fukui R, Motoi Y, Fukuda-Ohta Y, Zhang Y, Reuter T, Ishida Y, Kondo T, Chiba T, Asahara H, Taoka M, Yamauchi Y, Isobe T, Kaisho T, Furukawa Y, Latz E, Nakatani K, Izumi Y, Nie Y, Taniguchi H, Miyake K. Sato R, et al. J Exp Med. 2025 Mar 3;222(3):e20230647. doi: 10.1084/jem.20230647. Epub 2025 Jan 24. J Exp Med. 2025. PMID: 39853307
Acute therapeutic effects and pathophysiology of eosinophilic granulomatosis with polyangiitis neuropathy.
Yamanaka N, Takeshita Y, Sato R, Nawata T, Okafuji T, Fujikawa S, Fujisawa M, Matsuo K, Nemoto J, Mizumoto Y, Nishihara H, Honda M, Oishi M, Maeda T, Shimizu F, Koga M, Kanda T, Nakamori M. Yamanaka N, et al. Among authors: sato r. BMJ Neurol Open. 2025 Jan 19;7(1):e000938. doi: 10.1136/bmjno-2024-000938. eCollection 2025. BMJ Neurol Open. 2025. PMID: 39850792 Free PMC article.
2,600 results