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Page 1
A case of Potter sequence with WT1 mutation.
Yoshino M, Shimabukuro W, Takeichi M, Omura J, Yokota C, Yamamoto J, Nakanishi K, Morisada N, Nozu K, Iijima K, Takahashi Y. Yoshino M, et al. CEN Case Rep. 2023 May;12(2):184-188. doi: 10.1007/s13730-022-00742-x. Epub 2022 Oct 13. CEN Case Rep. 2023. PMID: 36227513 Free PMC article.
Common risk variants in NPHS1 and TNFSF15 are associated with childhood steroid-sensitive nephrotic syndrome.
Jia X, Yamamura T, Gbadegesin R, McNulty MT, Song K, Nagano C, Hitomi Y, Lee D, Aiba Y, Khor SS, Ueno K, Kawai Y, Nagasaki M, Noiri E, Horinouchi T, Kaito H, Hamada R, Okamoto T, Kamei K, Kaku Y, Fujimaru R, Tanaka R, Shima Y; Research Consortium on Genetics of Childhood Idiopathic Nephrotic Syndrome in Japan; Baek J, Kang HG, Ha IS, Han KH, Yang EM; Korean Consortium of Hereditary Renal Diseases in Children; Abeyagunawardena A, Lane B, Chryst-Stangl M, Esezobor C, Solarin A; Midwest Pediatric Nephrology Consortium (Genetics of Nephrotic Syndrome Study Group); Dossier C, Deschênes G; NEPHROVIR; Vivarelli M, Debiec H, Ishikura K, Matsuo M, Nozu K, Ronco P, Cheong HI, Sampson MG, Tokunaga K, Iijima K. Jia X, et al. Kidney Int. 2020 Nov;98(5):1308-1322. doi: 10.1016/j.kint.2020.05.029. Epub 2020 Jun 14. Kidney Int. 2020. PMID: 32554042 Free PMC article.
Home High-Flow Nasal Cannula Therapy in Children with Congenital Heart Disease.
Hanaki Y, Muneuchi J, Yamamoto J, Yokota C, Ohmura J, Ezaki H, Yoshino M, Nakamura R, Takeichi M, Sugitani Y, Matsuoka R, Doi H, Watanabe M, Takahashi Y. Hanaki Y, et al. Among authors: yoshino m. Pediatr Cardiol. 2022 Jun;43(5):1131-1135. doi: 10.1007/s00246-022-02834-y. Epub 2022 Jan 31. Pediatr Cardiol. 2022. PMID: 35099569
Trends in endemic of respiratory syncytial virus infection during COVID-19 pandemic and difficulty in obtaining optimal timing of palivizumab prophylaxis.
Taku K, Ichikawa S, Ogawa M, Kokubo T, Manabe T, Takano K, Murakawa S, Takahashi H, Hirakawa J, Sakemi Y, Yoshino M, Nakamura R, Yamamoto J, Hoshina T. Taku K, et al. Among authors: yoshino m. J Infect Chemother. 2024 Dec 10;31(3):102585. doi: 10.1016/j.jiac.2024.12.014. Online ahead of print. J Infect Chemother. 2024. PMID: 39667557
Phenotypic and genetic spectra of galactose mutarotase deficiency: A nationwide survey conducted in Japan.
Mikami-Saito Y, Wada Y, Arai-Ichinoi N, Nakajima Y, Suzuki-Ajihara S, Murayama K, Tanaka T, Numakura C, Hamazaki T, Igarashi N, Esaki H, Kagawa R, Kono T, Sawada T, Sawada T, Nyuzuki H, Hirai H, Fumoto S, Matsuda J, Matsunaga A, Maruyama S, Yamaguchi K, Yoshino M, Totsune E, Kikuchi A, Ohura T, Kure S. Mikami-Saito Y, et al. Among authors: yoshino m. Genet Med. 2024 Aug;26(8):101165. doi: 10.1016/j.gim.2024.101165. Epub 2024 May 16. Genet Med. 2024. PMID: 38762772 Free article.
The importance of early immunotherapy in anti-GluK2 antibody-positive autoimmune cerebellar ataxia: A case report.
Takeishi Y, Yaguchi H, Kudo A, Fujii S, Iwata I, Nomura T, Anada M, Iwami K, Yoshino M, Tanaka D, Mizushima K, Uwatoko H, Shirai S, Matsushima M, Kimura A, Tanaka K, Yabe I. Takeishi Y, et al. Among authors: yoshino m. J Neurol Sci. 2024 Dec 15;467:123306. doi: 10.1016/j.jns.2024.123306. Epub 2024 Nov 14. J Neurol Sci. 2024. PMID: 39626603 No abstract available.
943 results