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Long-term study of a female hyper-IgM immunodeficiency.
Kaneko H, Fukao T, Inoue R, Kasahara K, Matsui E, Kondo N. Kaneko H, et al. Among authors: kondo n. Exp Clin Immunogenet. 2000;17(4):173-8. doi: 10.1159/000019136. Exp Clin Immunogenet. 2000. PMID: 11096255
Leaky phenotype of X-linked agammaglobulinaemia in a Japanese family.
Kaneko H, Kawamoto N, Asano T, Mabuchi Y, Horikoshi H, Teramoto T, Matsui E, Kondo M, Fukao T, Kasahara K, Kondo N. Kaneko H, et al. Among authors: kondo n, kondo m. Clin Exp Immunol. 2005 Jun;140(3):520-3. doi: 10.1111/j.1365-2249.2005.02784.x. Clin Exp Immunol. 2005. PMID: 15932514 Free PMC article.
The mitochondrial acetoacetyl-CoA thiolase (T2) deficiency in Japanese patients: urinary organic acid and blood acylcarnitine profiles under stable conditions have subtle abnormalities in T2-deficient patients with some residual T2 activity.
Fukao T, Zhang GX, Sakura N, Kubo T, Yamaga H, Hazama A, Kohno Y, Matsuo N, Kondo M, Yamaguchi S, Shigematsu Y, Kondo N. Fukao T, et al. Among authors: kondo n, kondo m. J Inherit Metab Dis. 2003;26(5):423-31. doi: 10.1023/a:1025117226051. J Inherit Metab Dis. 2003. PMID: 14518824
2,227 results