Sublingual Immunotherapy with House Dust-Extract for House Dust-Mite Allergic Rhinitis in Children
スポンサーリンク
概要
- 論文の詳細を見る
- 2010-12-01
著者
-
Matsubara Yoichi
東北大学 医学系研究科遺伝病学分野
-
Shimojo Naoki
Department Of Pediatrics Graduate School Of Medicine Chiba University
-
Kohno Yoichi
Department Of Pediatrics Graduate School Of Medicine Chiba University
-
Yonekura Shuji
Dept. Of Otolarygology Chiba University
-
Okamoto Yuko
Department Of Otolaryngology Head And Neck Surgery Graduate School Of Medicine Chiba University
-
Kohno Yoichi
Department Of Pediatrics Chiba University Graduate School Of Medicine
-
Kohno Yoichi
Pediatrics Graduate School Of Medicine Chiba University
-
Hoshioka Akira
Department Of Public Health Graduate School Of Medicine Chiba University
-
Okamoto Yoshitaka
Department Of Otolaryngology Graduate School Of Medicine Chiba University
-
Okamoto Yoshitaka
Dept. Of Otolarygology Chiba University
-
Honda Kohei
Department Of Clinical And Laboratory Medicine Akita University School Of Medicine
-
Nakamaru Yuji
Department Of Pathology Hokkaido University School Of Medicine
-
Matsubara Y
Department Of Medical Genetics Tohoku University School Of Medicine
-
Sakurai Daiju
Department Of Otorhinolaryngology/head And Neck Surgery Graduate School Of Medicine Chiba University
-
Yonekura Syuji
Department Of Otolaryngology Head And Neck Surgery Graduate School Of Medicine Chiba University
-
Horiguchi Shigetoshi
Department Of Otolaryngology Graduate School Of Medicine Chiba University
-
YAMAGUCHI Koichi
Japanese Society of Pediatric Allergy and Clinical Immunology
-
Hanazawa Toyoyuki
Department Of Otolaryngology Head And Neck Surgery Graduate School Of Medicine Chiba University
-
Kohno Yoichi
Division Of Allergy National Center For Children Health And Development
-
NAKANO Atsuko
Division of Otorhinolaryngology, Chiba Children's Hospital
-
KUDOU Fumiyo
Chiba College of Public Health
-
HOSHIOKA Akira
Division of Allergy, Chiba Children's Hospital
-
Sakurai Daiju
Department Of Otolaryngology Head And Neck Surgery Graduate School Of Medicine Chiba University
-
Hoshioka Akira
Division Of Allergy Chiba Children's Hospital
-
Nakano Atsuko
Division Of Otorhinolaryngology Chiba Children's Hospital
-
Yamaguchi Koichi
Division Of Allergy National Center For Children Health And Development
-
Honda Kohei
Department Of Sensory Medicine Division Of Otorhinolaryngology Head And Neck Surgery Akita Universit
-
Nakamaru Yuji
Department Of Otolaryngology-head And Neck Surgery Hokkaido University Graduate School Of Medicine
関連論文
- 日本人小児の Hemophilus influenzae type b 抗芙膜多糖体抗体価に関する検討
- Weekly cisplatin administration concurrent with radiation therapy for locoregionally advanced nasopharyngeal carcinoma
- 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
- A single nucleotide substitution that abolishes the initiator methionine codon of the GLDC gene is prevalent among patients with glycine encephalopathy in Jerusalem
- Functional analysis of PTPN11/SHP-2 mutants identified in Noonan syndrome and childhood leukemia
- Genotyping of Single Nucleotide Polymorphisms (SNPs) Influencing Drug Response by Competitive Allele-specific Short Oligonucleotide Hybridization (CASSOH) with Immunochromatographic Strip
- Novel IRF6 mutations in Japanese patients with Van der Woude Syndrome : two missense mutations (R45Q and P396S) and a 17-kb deletion
- Lack of evidence for a significant association between nonsyndromic cleft lip with or without cleft palate and the retinoic acid receptor alpha gene in the Japanese population
- Chromosomal localization, structure, single-nucleotide polymorphisms, and expression of the human H-protein gene of the glycine cleavage system (GCSH), a candidate gene for nonketotic hyperglycinemia
- Haplotype analysis suggests that the two predominant mutations in Japanese patients with holocarboxylase synthetase deficiency are founder mutations
- A one-base deletion (183delC) and a missense mutation (D276H) in the T-protein gene from a Japanese family with nonketotic hyperglycinemia
- Mutation and polymorphic marker analyses of 65K- and 67K-glutamate decarboxylase genes in two families with pyridoxine-dependent epilepsy
- DINUCLEOTIDE REPEAT POLYMORPHISM IN 65k-GLUTAMATE DECARBOXYLASE GENE
- Reactivity of IgE in fish-allergic patients to fish muscle collagen
- 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
- Mortality From Congenital Cardiovascular Malformations in Japan, 1968 Through 1997
- A case of 6-pyruvoyl-tetrahydropterin synthase deficiency demonstrates a more significant correlation of L-Dopa dosage with serum prolactin levels than CSF homovanillic acid leyels
- Magnetic resonance imaging in late-onset ornithine transcarbamylase deficiency
- Expression analysis of two mutations in carnitine palmitoyltransferase IA deficiency
- Novel mutation of L718X in the ATP7A gene in a Japanese patient with classical Menkes disease, and four novel polymorphisms in the Japanese population
- Identification of two novel mutations of the carnitine/acylcarnitine translocase (CACT) gene in a patient with CACT deficiency
- An Ile/Val polymorphism at codon 1464 of the ATP7A gene
- Identification of three novel mutations in the MNK gene in three unrelated Japanese patients with classical Menkes disease
- Characteristic Height Growth Pattern in Patients with Pseudohypoparathyroidism : Comparison between Type 1a and Type 1b
- Transient Central Hypothyroidisim Due to Pituitary Suppression in a Premature Neonate Born to a Mother with Three-Year-Untreated Graves' Disease
- A Girl with Prolactinoma Presenting Cessation of Pubertal Development and Growth
- The Standard Ratio of Upper Segment Length to Lower Segment Length According to Spina Malleolar Distance in Japanese Children
- A 9-Year-Old Girl Presenting Central Precocious Puberty with Polycystic Ovary Syndrome
- Genital Bleeding in a 2-Month-Old Infant with Congenital Adrenal Hyperplasia
- Estrogen Secreting Adrenal Adenocarcinoma in an 18-Month-old Boy: Aromatase Activity, Protein Expression, mRNA and Utilization of Gonadal Type Promoter
- Characterization of Genes Encoding the Pancreatic β-cell ATP-sensitive K^+ Channel in Persistent Hyperinsulinemic Hypoglycemia of Infancy in Japanese Patients
- Present Situation of Cedar Pollinosis in Japan and its Immune Responses
- Sphingosine 1-Phosphate Inhibits Migration of RBL-2H3 Cells via S1P_2 : Cross-Talk between Platelets and Mast Cells
- Human T_h1 differentiation induced by lipoarabinomannan/lipomannan from Mycobacterium bovis BCG Tokyo-172
- Guidelines for Diagnosis and Management of Pediatric Food Allergy in Japan
- Therapeutic Guidelines for Atopic Dermatitis 2002
- 3P-057 レプリカ交換モンテカルロシミュレーションを用いた膜タンパク質の構造予測シミュレーション(蛋白質-物性(安定性,折れたたみなど),第47回日本生物物理学会年会)
- 3P018 結び目理論を用いた遺伝的交叉による徐冷分子動力学シミュレーション(蛋白質-構造,第48回日本生物物理学会年会)
- A Randomized Double-Blind Comparative Study of Sublingual Immunotherapy for Cedar Pollinosis
- 4 Randomized placebo controlled trial of sublingual iimunotherapy for Japanese cedar pollinosis(Symposium 7 Immunotherapy, Update and Future)
- 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
- 3P075 Pressure dependence of protein conformations studied by generalized simulated tempering molecular dynamics simulations(Protein: Property,The 48th Annual Meeting of the Biophysical Society of Japan)
- A splenial lesion with transiently reduced diffusion in clinically mild encephalitis is not always reversible : A case report
- 3P-054 拡張アンサンブル法を用いた生体分子の温度・圧力依存性の研究(蛋白質-物性(安定性,折れたたみなど),第47回日本生物物理学会年会)
- Mechanisms of Electron Flow through the Q_B Site in Photosystem II. 3.Effects of the Presence of Membrane Structure on the Redox Reactions at the Q_B Site
- Normal Mode Analysis of Polytheonamide B(Cross-disciplinary physics and related areas of science and technology)
- A pediatric patient with acute hepatitis E in Japan
- Combination therapy of in vitro-expanded natural killer T cells and α-galactosylceramide-pulsed antigen-presenting cells in patients with recurrent head and neck carcinoma
- Negative C-reactive protein in children with bacterial infection
- 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
- 2P-172 生体膜のレプリカ交換分子動力学シミュレーション(生体膜・人工膜-構造・物性,第47回日本生物物理学会年会)
- 3P-056 遺伝的交叉を用いた徐冷分子動力学シミュレーション(蛋白質-物性(安定性,折れたたみなど),第47回日本生物物理学会年会)
- Multibaric-Multithermal Molecular Dynamics Simulation of Alanine Dipeptide in Explicit Water
- An Analysis on Protein Folding Problem by Replica-Exchange Method
- Relationship between RANTES polymorphisms and respiratory syncytial virus bronchiolitis in a Japanese infant population
- Serotypes of Haemophilus Influenzae Strains Isolated from Pediatric Patients with Respiratory Tract Infections
- Molecular analysis of methylmalonyl-CoA mutase deficiency : identification of three missense mutations in mut^0 patients
- A posterior fossa lipoma extending into the cervical spine and subcutaneous space via a cranium bifidum
- Secondary-structure design of proteins by a backbone torsion energy
- Comprehensive screening of CREB-binding protein gene mutations among patients with Rubinstein-Taybi syndrome using denaturing high-performance liquid chromatography
- α-Helix Propensities of Amino Acids Studied by Multicanonical Algorithm
- On Existence of Non-Renormalizable Field Theory : Pure SU(2) Lattice Gauge Theory in Five Dimensions : Particles and Fields
- 3 Early intervention for child allergic rhinitis(Symposium 7 Immunotherapy, Update and Future)
- 小児下気道感染症由来インフルエンザ菌の抗菌薬感受性に関する検討
- Value of washed sputum gram stain smear and culture for management of lower respiratory tract infections in children
- A case of persistent Enterobacter cloacae bacteremia
- Impairment of Angiogenic Activity in the Serum From Patients With Coronary Aneurysms Due to Kawasaki Disease
- Incidence of bacterial coinfection with respiratory syncytial virus bronchopulmonary infection in pediatric inpatients
- Increased Production of Vascular Endothelial Growth Factor-D and Lymphangiogenesis in Acute Kawasaki Disease
- Marked pleural and pericardial effusion with elevated Vascular Endothelial Growth Factor production : An uncommon complication of Kawasaki disease
- Efficacy and safety of orally administered pilocarpine hydrochloride for patients with juvenile-onset Sjogren's syndrome
- Genetically modified foods and allergy : assessment of allergenicity (EDUCATIONAL LECTURE) (Proceedings of the 30th Annual Meeting)
- Japanese pediatric guidelines for the treatment and management of bronchial asthma 2008
- Chemoradiotherapy with 5-fluorouracil Inhibits the Expression of Thymidylate Synthase and Dihydropyrimidine Dehydrogenase in Head and Neck Squamous Cell Carcinoma
- Hajdu-Cheney syndrome : Infantile onset of hydrocephalus and serpentine fibulae
- 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
- Antigen-Specific Immunotherapy against Allergic Rhinitis : The State of the Art
- Establishment of diagnosis by bisulfite-treated methylation-specific PCR method and analysis of clinical characteristics of pseudohypoparathyroidism type 1b
- Anti-polyribosylribitol phosphate antibody in pediatric patients with Haemophilus influenzae type b invasive disease
- 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
- Tumor suppressive microRNA-375 regulates oncogene AEG-1/MTDH in head and neck squamous cell carcinoma (HNSCC)
- 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
- Multiple cavitations in posterior reversible leukoencephalopathy syndrome associated with hemolytic-uremic syndrome
- Japanese Guideline for Atopic Dermatitis
- Isoniazid- and Streptomycin-Resistant Miliary Tuberculosis Complicated by Intracranial Tuberculoma in a Japanese Infant
- A case of infantile Takayasu arteritis with a p.D382E NOD2 mutation : an unusual phenotype of Blau syndrome/early-onset sarcoidosis?