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New-onset diabetes after renal transplantation in a patient with a novel HNF1B mutation.
Kanda S, Morisada N, Kaneko N, Yabuuchi T, Nawashiro Y, Tada N, Nishiyama K, Miyai T, Sugawara N, Ishizuka K, Chikamoto H, Akioka Y, Iijima K, Hattori M. Kanda S, et al. Among authors: nishiyama k. Pediatr Transplant. 2016 May;20(3):467-71. doi: 10.1111/petr.12690. Epub 2016 Feb 21. Pediatr Transplant. 2016. PMID: 26899772
A childhood-onset intestinal toxemia botulism during chemotherapy for relapsed acute leukemia.
Ohyama N, Torio M, Nakashima K, Koga Y, Kanno S, Nishio H, Nishiyama K, Sasazuki M, Kato H, Asakura H, Akamine S, Sanefuji M, Ishizaki Y, Sakai Y, Ohga S. Ohyama N, et al. Among authors: nishiyama k. Ann Clin Microbiol Antimicrob. 2017 Sep 18;16(1):61. doi: 10.1186/s12941-017-0240-y. Ann Clin Microbiol Antimicrob. 2017. PMID: 28923072 Free PMC article.
Reappraising newborn screening for cobalamin C disorder.
Tocan V, Ohkubo K, Higashi K, Toda N, Kojima-Ishii K, Nishiyama K, Ishimura M, Takada H, Sakamoto O, Sasaki F, Yoshimura K, Hirose S, Ohga S. Tocan V, et al. Among authors: nishiyama k. Pediatr Neonatol. 2018 Aug;59(4):415-417. doi: 10.1016/j.pedneo.2017.11.002. Epub 2017 Nov 22. Pediatr Neonatol. 2018. PMID: 29198615 Free article. No abstract available.
Complement activation associated with ADAMTS13 deficiency may contribute to the characteristic glomerular manifestations in Upshaw-Schulman syndrome.
Itami H, Hara S, Matsumoto M, Imamura S, Kanai R, Nishiyama K, Ishimura M, Ohga S, Yoshida M, Tanaka R, Ogawa Y, Asada Y, Sekita-Hatakeyama Y, Hatakeyama K, Ohbayashi C. Itami H, et al. Among authors: nishiyama k. Thromb Res. 2018 Oct;170:148-155. doi: 10.1016/j.thromres.2018.08.020. Epub 2018 Sep 1. Thromb Res. 2018. PMID: 30195146
Molecular mechanisms determining severity in patients with Pierson syndrome.
Minamikawa S, Miwa S, Inagaki T, Nishiyama K, Kaito H, Ninchoji T, Yamamura T, Nagano C, Sakakibara N, Ishimori S, Hara S, Yoshikawa N, Hirano D, Harada R, Hamada R, Matsunoshita N, Nagata M, Shima Y, Nakanishi K, Nagase H, Takeda H, Morisada N, Iijima K, Nozu K. Minamikawa S, et al. Among authors: nishiyama k. J Hum Genet. 2020 Apr;65(4):355-362. doi: 10.1038/s10038-019-0715-0. Epub 2020 Jan 21. J Hum Genet. 2020. PMID: 31959872
The expanding phenotype of hypokalemic periodic paralysis in a Japanese family with p.Val876Glu mutation in CACNA1S.
Kurokawa M, Torio M, Ohkubo K, Tocan V, Ohyama N, Toda N, Ishii K, Nishiyama K, Mushimoto Y, Sakamoto R, Nakaza M, Horie R, Kubota T, Takahashi MP, Sakai Y, Nomura M, Ohga S. Kurokawa M, et al. Among authors: nishiyama k. Mol Genet Genomic Med. 2020 Apr;8(4):e1175. doi: 10.1002/mgg3.1175. Epub 2020 Feb 27. Mol Genet Genomic Med. 2020. PMID: 32104981 Free PMC article.
1,650 results