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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. 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.
Maternal Chronic Disease and Congenital Anomalies of the Kidney and Urinary Tract in Offspring: A Japanese Cohort Study.
Nishiyama K, Sanefuji M, Kurokawa M, Iwaya Y, Hamada N, Sonoda Y, Ogawa M, Shimono M, Suga R, Kusuhara K, Ohga S; Japan Environment and Children’s Study Group. Nishiyama K, et al. Among authors: kurokawa m. Am J Kidney Dis. 2022 Nov;80(5):619-628.e1. doi: 10.1053/j.ajkd.2022.03.003. Epub 2022 Apr 16. Am J Kidney Dis. 2022. PMID: 35439592 Free article.
Plastic bronchitis in a child with nephrotic syndrome.
Maehara K, Kurokawa M, Tezuka J, Lee S, Kaku Y. Maehara K, et al. Among authors: kurokawa m. Pediatr Int. 2022 Jan;64(1):e15015. doi: 10.1111/ped.15015. Pediatr Int. 2022. PMID: 35278244 No abstract available.
1,543 results