Nonoyama Shigeaki | Department Of Human Ontogeny And Childhood Development Tokyo Medical And Dental University School Of

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著作論文

Evans syndrome in a patient with Langerhans cell histiocytosis : possible pathogenesis of autoimmunity in LCH
Mutational Analysis of the WASP Gene in 2 Korean Families with Wiskott-Aldrich Syndrome
Induction of the high-affinity lgE receptor (FcεRI) on human mast cells by IL-4
Type Two Hyper-IgM Syndrome caused by Mutation in Activation-Induced Cytidine Deaminase
Mutations of the WASP Gene in 10 Japanese Patients With Wiskott-Aldrich Syndrome and X-linked Thrombocytopenia
TARC and MDC are produced by CD40 activated human B cells and are elevated in the sera of infantile atopic dermatitis patients
Missense Mutations of the BMPR1B (ALK6) Gene in Childhood Idiopathic Pulmonary Arterial Hypertension
Delayed onset adenosine deaminase deficiency associated with acute disseminated encephalomyelitis
Fetal and Neonatal Development of Ca^ Transients and Functional Sarcoplasmic Reticulum in Beating Mouse Hearts
The SCID mouse, a model for human diseases.
Soluble ST2 and N-terminal pro-Brain Natriuretic Peptide Combination:– Useful Biomarker for Predicting Outcome of Childhood Pulmonary Arterial Hypertension –

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