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Reduced interferon-y production and mutations of the interleukin-12 receptor β₂ chain gene in atopic subjectsKONDO, Naomi; MATSUI, Eiko; KANEKO, Hideo et al.International archives of allergy and immunology. 2001, Vol 124, Num 1-3, pp 117-120, issn 1018-2438Conference Paper

Milder childhood form of very long-chain acyl-CoA dehydrogenase deficiency in a 6-year-old Japanese boyDOI, Toshiaki; ABO, Wataru; TATENO, Masaru et al.European journal of pediatrics. 2000, Vol 159, Num 12, pp 908-911, issn 0340-6199Article

Refractory osteomyelitis caused by bacille Calmette-Guérin vaccination : a case reportFUNATO, Michinori; KANEKO, Hideo; MATSUI, Eiko et al.Diagnostic microbiology and infectious disease. 2007, Vol 59, Num 1, pp 89-91, issn 0732-8893, 3 p.Article

Disruption of the BLM gene in ATM-null DT40 cells does not exacerbate either phenotypeFUKAO, Toshiyuki; CHEN, Philip; LAVIN, Martin F et al.Oncogene (Basingstoke). 2004, Vol 23, Num 8, pp 1498-1506, issn 0950-9232, 9 p.Article

Urinary organic acids in peroxisomal disorders : a simple screening methodYAMAGUCHI, Seiji; IGA, Misako; KIMURA, Masahiko et al.Journal of chromatography. B, Biomedical sciences and applications. 2001, Vol 758, Num 1, pp 81-86, issn 1387-2273Conference Paper

Ketone body metabolism and its defectsFUKAO, Toshiyuki; MITCHELL, Grant; SASS, Jörn Oliver et al.Journal of inherited metabolic disease. 2014, Vol 37, Num 4, pp 541-551, issn 0141-8955, 11 p.Conference Paper

Patients homozygous for the T435N mutation of succinyl-CoA:3-ketoacid CoA transferase (SCOT) do not show permanent ketosisFUKAO, Toshiyuki; SHINTAKU, Haruo; KUSUBAE, Ryou et al.Pediatric research. 2004, Vol 56, Num 6, pp 858-863, issn 0031-3998, 6 p.Article

Pathways and control of ketone body metabolism: on the fringe of lipid biochemistryFUKAO, Toshiyuki; LOPASCHUK, Gary D; MITCHELL, Grant A et al.Prostaglandins, leukotrienes and essential fatty acids. 2004, Vol 70, Num 3, pp 243-251, issn 0952-3278, 9 p.Article

Myopathic form of very-long chain acyl-CoA dehydrogenase deficiency : Evidence for temperature-sensitive mild mutations in both mutant alleles in a Japanese girlFUKAO, Toshiyuki; WATANABE, Hiroh; ORII, Kenji E et al.Pediatric research. 2001, Vol 49, Num 2, pp 227-231, issn 0031-3998Article

A structural mapping of mutations causing succinyl-CoA: 3-ketoacid CoA transferase (SCOT) deficiencySHAFQAT, Naeem; KAVANAGH, Kate L; SASS, Jörn Oliver et al.Journal of inherited metabolic disease. 2013, Vol 36, Num 6, pp 983-987, issn 0141-8955, 5 p.Article

A common variable immunodeficient patient who developed acute disseminated encephalomyelitis followed by the Lennox-Gastaut syndromeKONDO, Masashi; FUKAO, Toshiyuki; TERAMOTO, Takahide et al.Pediatric allergy and immunology. 2005, Vol 16, Num 4, pp 357-360, issn 0905-6157, 4 p.Article

Lysinuric protein intolerance in siblings : complication of systemic lupus erythematosus in the elder sisterAOKI, Minako; FUKAO, Toshiyuki; FUJITA, Yukiko et al.European journal of pediatrics. 2001, Vol 160, Num 8, pp 522-523, issn 0340-6199Article

Succinyl-CoA:3-ketoacid CoA transferase (SCOT) : Cloning of the human SCOT gene, tertiary structural modeling of the human SCOT monomer, and characterization of three pathogenic mutationsFUKAO, Toshiyuki; MITCHELL, Grant A; BERRY, Gerard T et al.Genomics (San Diego, Calif.). 2000, Vol 68, Num 2, pp 144-151, issn 0888-7543Article

Refractory Chronic Pleurisy Caused by Helicobacter equorum-Like Bacterium in a Patient with X-Linked AgammaglobulinemiaFUNATO, Michinori; KANEKO, Hideo; OHKUSU, Kiyofumi et al.Journal of clinical microbiology (Print). 2011, Vol 49, Num 9, pp 3432-3435, issn 0095-1137, 4 p.Article

The response of bovine beta-lactoglobulin-specific T-cell clones to single amino acid substitution of T-cell core epitopeKONDO, Masashi; KANEKO, Hideo; KANDO, Naomi et al.Pediatric allergy and immunology. 2008, Vol 19, Num 7, pp 592-598, issn 0905-6157, 7 p.Article

Age-related changes in intracellular cytokine profiles and Th2 dominance in allergic childrenKAWAMOTO, Norio; KANEKO, Hideo; TAKEMURA, Masao et al.Pediatric allergy and immunology. 2006, Vol 17, Num 2, pp 125-133, issn 0905-6157, 9 p.Article

Mitochondrial acetoacetyl-CoA thiolase (T2) deficiency: T2-deficient patients with mild mutation(s) were previously misinterpreted as normal by the coupled assay with tiglyl-CoAGAI XIU ZHANG; FUKAO, Toshiyuki; ROLLAND, Marie-Odile et al.Pediatric research. 2004, Vol 56, Num 1, pp 60-64, issn 0031-3998, 5 p.Article

Hyper-IgM syndrome with putative dominant negative mutation in activation-induced cytidine deaminaseKASAHARA, Yukiko; KANEKO, Hideo; FUKAO, Toshiyuki et al.Journal of allergy and clinical immunology. 2003, Vol 112, Num 4, pp 755-760, issn 0091-6749, 6 p.Article