YAMAGUCHI Koichi | Japanese Society of Pediatric Allergy and Clinical Immunology

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著作論文

Clinical manifestations in patients with SOS1 mutations range from Noonan syndrome to CFC syndrome
A novel KCNQ4 one-base deletion in a large pedigree with hearing loss : implication for the genotype-phenotype correlation
Association study of the C3 gene with adult and childhood asthma
No Association of Polymorphisms in the 5' Region of the CD14 Gene and Food Allergy in a Japanese Population
Effects of Probiotics on the Immune System and Allergic Diseases
6 Single nucleotide polymorphisms of CD14 and TLR2 is associated with the development of respiratory syncytial virus-induced bronchiolitis in Japanese children(II. Asthma Genetics)
Increased expression of α4β7 integrin on food allergen-stimulated CD4^+ T cells in active food allergic enterocolitis
Guidelines for Diagnosis and Management of Pediatric Food Allergy in Japan
Therapeutic Guidelines for Atopic Dermatitis 2002
Retrocerebellar arachnoid cysts in siblings with mental retardation and undescended testis
Empty sella syndrome in nevoid basal cell carcinoma syndrome
γ-Irradiation Deregulates Cell Cycle Control and Apoptosis in Nevoid Basal Cell Carcinoma Syndrome-derived Cells
A splenial lesion with transiently reduced diffusion in clinically mild encephalitis is not always reversible : A case report
Acute motor axonal neuropathy during intensive immunosuppressive therapy for macrophage activation syndrome
U7 snRNA-mediated correction of aberrant splicing caused by activation of cryptic splice sites
Relationship between RANTES polymorphisms and respiratory syncytial virus bronchiolitis in a Japanese infant population
Comprehensive screening of CREB-binding protein gene mutations among patients with Rubinstein-Taybi syndrome using denaturing high-performance liquid chromatography
Efficacy and safety of orally administered pilocarpine hydrochloride for patients with juvenile-onset Sjogren's syndrome
Japanese pediatric guidelines for the treatment and management of bronchial asthma 2008
我が国における学童・生徒における肥満と喘息症状との関連
Sublingual Immunotherapy with House Dust-Extract for House Dust-Mite Allergic Rhinitis in Children
Clinical application of array-based comparative genomic hybridization by two-stage screening for 536 patients with mental retardation and multiple congenital anomalies
HRAS mutants identified in Costello syndrome patients can induce cellular senescence : possible implications for the pathogenesis of Costello syndrome
A genome-wide association study identifies RNF213 as the first Moyamoya disease gene
Deletion at chromosome 10p11.23-p12.1 defines characteristic phenotypes with marked midface retrusion
Association of the MMP9 gene with childhood cedar pollen sensitization and pollinosis
Replication of genetic association studies in asthma and related phenotypes
Mutation analysis of the SHOC2 gene in Noonan-like syndrome and in hematologic malignancies

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