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Genetic analysis of isolated persistent hypermethioninemia with dominant inheritance
  • M. Nagao, K. Oyanagi
  • Medicine, Biology
  • Acta paediatrica Japonica : Overseas edition
  • 1 October 1997
We describe a type of mild hypermethioninemia due to a point mutation in the MATA1 gene, which was inherited dominantly in a family. Three patients coming from the same family pedigree were detectedExpand
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Higher allergenicity of high molecular weight hydrolysed wheat protein in cosmetics for percutaneous sensitization
Background Wheat protein derivatives are used in a variety of products worldwide. Gluten is commercially used ‘as is' or with modifications such as hydrolysis, which is carried out to overcome itsExpand
  • 31
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Antigen-induced expression of CD203c on basophils predicts IgE-mediated wheat allergy.
BACKGROUND For in vitro diagnosis of wheat allergy, specific IgE to wheat is known to be a poor predictive marker. Oral food challenge, the gold standard for the diagnosis, is accompanied by a riskExpand
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"Spike" in acute asthma exacerbations during enterovirus D68 epidemic in Japan: A nation-wide survey.
BACKGROUND In September 2015, Japan experienced an unusual increase in acute asthma hospitalizations of children that coincided with an enterovirus D68 (EV-D68) epidemic. The objective of this studyExpand
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  • 1
Recent advances in primary ciliary dyskinesia.
Primary ciliary dyskinesia (PCD) is a genetic disease inherited in an autosomal recessive manner. The prevalence of PCD is estimated to be 1 in 20,000 live births. Congenital abnormality of theExpand
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1,25-Dihydroxyvitamin D3 Upregulates Functional C-X-C Chemokine Receptor Type 4 Expression in Human Eosinophils
Background: Epidemiological studies suggest that vitamin D may be protective against the inception and exacerbation of allergic diseases. However, the direct effect of vitamin D on eosinophils, theExpand
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Frequency of 985A‐to‐G mutation in medium‐chain acyl‐CoA dehydrogenase gene among patients with sudden infant death syndrome, Reye syndrome, severe motor and intellectual disabilities and healthy
  • M. Nagao
  • Medicine
  • Acta paediatrica Japonica : Overseas edition
  • 1 August 1996
The prevalence of the 985A‐to‐G mutation in the medium‐chain acyl‐CoA dehydrogenase (MCAD) gene among Japanese patients with sudden infant death syndrome, Reye syndrome, unknown fatty acid oxidationExpand
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Adverse prognostic impact of KIT mutations in childhood CBF-AML: the results of the Japanese Pediatric Leukemia/Lymphoma Study Group AML-05 trial
Adverse prognostic impact of KIT mutations in childhood CBF-AML: the results of the Japanese Pediatric Leukemia/Lymphoma Study Group AML-05 trial
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Anaphylactic transfusion reaction in homozygous haptoglobin deficiency detected by CD203c expression on basophils
To the Editor: It has been reported that the incidence of anhaptoglobinemia who are homozygous for Hp is very rare in Africans or European-Africans. However, it is relatively high incidence in EastExpand
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Outcomes and Prognostic Features of Patients With Influenza Requiring Hospitalization and Receiving Early Antiviral Therapy: A Prospective Multicenter Cohort Study.
BACKGROUND In Japan, the routine use of early antiviral therapy for patients with influenza is standard. METHODS This multicenter prospective cohort evaluation of hospitalized patients withExpand
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