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Mutation spectrum of the PCCA and PCCB genes in Japanese patients with propionic acidemia.
Yang X, Sakamoto O, Matsubara Y, Kure S, Suzuki Y, Aoki Y, Yamaguchi S, Takahashi Y, Nishikubo T, Kawaguchi C, Yoshioka A, Kimura T, Hayasaka K, Kohno Y, Iinuma K, Ohura T. Yang X, et al. Among authors: nishikubo t. Mol Genet Metab. 2004 Apr;81(4):335-42. doi: 10.1016/j.ymgme.2004.01.003. Mol Genet Metab. 2004. PMID: 15059621
Investigation of type IIC von Willebrand disease.
Uno H, Nishida N, Ishizaki J, Suzuki M, Nishikubo T, Miyata S, Takahashi Y, Yoshioka A, Tsuda K. Uno H, et al. Among authors: nishikubo t. Int J Hematol. 1994 Apr;59(3):219-25. Int J Hematol. 1994. PMID: 8011991
Normal values for KL-6 in cord venous plasma of neonates.
Uchida Y, Minowa H, Ebisu R, Nishikubo T, Takahashi Y, Yoshioka A. Uchida Y, et al. Among authors: nishikubo t. Pediatr Int. 2007 Apr;49(2):167-71. doi: 10.1111/j.1442-200X.2007.02345.x. Pediatr Int. 2007. PMID: 17445033
Children with Down's syndrome display high rates of hyperuricaemia.
Kashima A, Higashiyama Y, Kubota M, Kawaguchi C, Takahashi Y, Nishikubo T. Kashima A, et al. Among authors: nishikubo t. Acta Paediatr. 2014 Aug;103(8):e359-64. doi: 10.1111/apa.12664. Epub 2014 May 21. Acta Paediatr. 2014. PMID: 24766390
Neonatal erythema infectiosum.
Minowa H, Nishikubo T, Uchida Y, Nogami K, Yamashita C, Kamitsuji H, Takahashi Y, Yoshioka A. Minowa H, et al. Among authors: nishikubo t. Acta Paediatr Jpn. 1998 Feb;40(1):88-90. doi: 10.1111/j.1442-200x.1998.tb01411.x. Acta Paediatr Jpn. 1998. PMID: 9583210
77 results