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Abnormal cystatin C levels in two patients with bardet-biedl syndrome.
Hirano M, Ohishi M, Yamashita T, Ikuno Y, Iwahashi H, Mano T, Ishihara R, Tanaka I, Yanagihara K, Isono C, Sakamoto H, Nakamura Y, Kusunoki S. Hirano M, et al. Among authors: nakamura y. Clin Med Insights Case Rep. 2011;4:17-20. doi: 10.4137/CCRep.S6622. Epub 2011 Mar 10. Clin Med Insights Case Rep. 2011. PMID: 21769262 Free PMC article.
The First Nationwide Survey and Genetic Analyses of Bardet-Biedl Syndrome in Japan.
Hirano M, Satake W, Ihara K, Tsuge I, Kondo S, Saida K, Betsui H, Okubo K, Sakamoto H, Ueno S, Ikuno Y, Ishihara R, Iwahashi H, Ohishi M, Mano T, Yamashita T, Suzuki Y, Nakamura Y, Kusunoki S, Toda T. Hirano M, et al. Among authors: nakamura y. PLoS One. 2015 Sep 1;10(9):e0136317. doi: 10.1371/journal.pone.0136317. eCollection 2015. PLoS One. 2015. PMID: 26325687 Free PMC article.
A case of severe ganciclovir-induced encephalopathy.
Sakamoto H, Hirano M, Nose K, Ueno S, Oki T, Sugimoto K, Nishioka T, Kusunoki S, Nakamura Y. Sakamoto H, et al. Among authors: nakamura y. Case Rep Neurol. 2013 Oct 5;5(3):183-6. doi: 10.1159/000355638. eCollection 2013. Case Rep Neurol. 2013. PMID: 24403897 Free PMC article.
Multiple system involvement in a Japanese patient with a V31A mutation in the SOD1 gene.
Sakamoto H, Akamatsu M, Hirano M, Saigoh K, Ueno S, Isono C, Kusunoki S, Nakamura Y. Sakamoto H, et al. Among authors: nakamura y. Amyotroph Lateral Scler Frontotemporal Degener. 2014 Jun;15(3-4):312-4. doi: 10.3109/21678421.2013.873051. Epub 2014 Mar 10. Amyotroph Lateral Scler Frontotemporal Degener. 2014. PMID: 24611504
14,634 results
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