繰り返す中耳炎から何を考えますか
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Published in | 小児耳鼻咽喉科 Vol. 34; no. 3; pp. 283 - 288 |
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Main Author | |
Format | Journal Article |
Language | Japanese |
Published |
日本小児耳鼻咽喉科学会
2013
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Subjects | |
Online Access | Get full text |
ISSN | 0919-5858 2186-5957 |
DOI | 10.11374/shonijibi.34.283 |
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Author | 金兼, 弘和 |
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References | 11) Roesch K, Curran SP, Tranebjaerg L, et al.: Human deafness dystonia syndrome is caused by a defect in assembly of the DDP1/TIMM8a-TIMM13 complex. Hum Mol Genet 2002; 11(5):477–486. 4) Yarmohammadi H, Estrella L, Doucette J, et al.: Recognizing primary immune deficiency in clinical practice. Clin Vaccine Immunol 2006; 13(3): 329–332. 1) Al-Herz W, Bousfiha A, Casanova JL, et al.: Primary immunodeficiency diseases: an update on the classification from the international union of immunological societies expert committee for primary immunodeficiency. Front Immunol. 2011; 2: 54. 7) Wiertsema SP, Sanders EA, Veenhoven RH, et al.: Antibody levels after regular childhood vaccinations in the immunological screening of children with recurrent otitis media. J Clin Immunol 2004; 24(4): 354–356. 3) Wilson NW, Hogan MB: Otitis media as a presenting complaint in childhood immunodeficiency diseases. Curr Allergy Asthma Rep 2008; 8(6): 519–524. 9) 関根基樹,高橋正紘,浜野巨秀,他:反復性中耳炎に対する術前検査から発見された X 連鎖無 γ グロブリン血症例.耳鼻臨床 2006; 99: 95–100. 6) Veenhoven R, Rijkers G, Schilder A, et al.: Immunoglobulins in otitis-prone children. Pediatr Res 2004; 55(1): 159–162. 10) Arai T, Zhao M, Kanegane H, et al.: Genetic analysis of contiguous X-chromosome deletion syndrome encompassing the BTK and TIMM8A genes. J Hum Genet. 2011; 56(8): 577–582. 5) Haddad J, Brager R, Bluestone CD: Infections of the ears, nose and throat in children with primary immunodeficiencies. Arch Otolaryngol Head Neck Surg 1992; 118(2): 138–141. 8) Prellner K, Kalm O, Harsten G, et al.: Pneumococcal serum antibody concentrations during the first three years of life: a study of otitis-prone and non-otitis-prone children. Int J Pediatr Otorhinolaryngol 1989; 17(3): 267–279. 2) Yilmaz-Demirdag Y: Should newborns be screened for immunodeficiency? lessons learned from infants with recurrent otitis media. Curr Allergy Asthma Rep 2011; 11(6): 491–498. |
References_xml | – reference: 4) Yarmohammadi H, Estrella L, Doucette J, et al.: Recognizing primary immune deficiency in clinical practice. Clin Vaccine Immunol 2006; 13(3): 329–332. – reference: 2) Yilmaz-Demirdag Y: Should newborns be screened for immunodeficiency? lessons learned from infants with recurrent otitis media. Curr Allergy Asthma Rep 2011; 11(6): 491–498. – reference: 5) Haddad J, Brager R, Bluestone CD: Infections of the ears, nose and throat in children with primary immunodeficiencies. Arch Otolaryngol Head Neck Surg 1992; 118(2): 138–141. – reference: 10) Arai T, Zhao M, Kanegane H, et al.: Genetic analysis of contiguous X-chromosome deletion syndrome encompassing the BTK and TIMM8A genes. J Hum Genet. 2011; 56(8): 577–582. – reference: 11) Roesch K, Curran SP, Tranebjaerg L, et al.: Human deafness dystonia syndrome is caused by a defect in assembly of the DDP1/TIMM8a-TIMM13 complex. Hum Mol Genet 2002; 11(5):477–486. – reference: 7) Wiertsema SP, Sanders EA, Veenhoven RH, et al.: Antibody levels after regular childhood vaccinations in the immunological screening of children with recurrent otitis media. J Clin Immunol 2004; 24(4): 354–356. – reference: 8) Prellner K, Kalm O, Harsten G, et al.: Pneumococcal serum antibody concentrations during the first three years of life: a study of otitis-prone and non-otitis-prone children. Int J Pediatr Otorhinolaryngol 1989; 17(3): 267–279. – reference: 6) Veenhoven R, Rijkers G, Schilder A, et al.: Immunoglobulins in otitis-prone children. Pediatr Res 2004; 55(1): 159–162. – reference: 1) Al-Herz W, Bousfiha A, Casanova JL, et al.: Primary immunodeficiency diseases: an update on the classification from the international union of immunological societies expert committee for primary immunodeficiency. Front Immunol. 2011; 2: 54. – reference: 3) Wilson NW, Hogan MB: Otitis media as a presenting complaint in childhood immunodeficiency diseases. Curr Allergy Asthma Rep 2008; 8(6): 519–524. – reference: 9) 関根基樹,高橋正紘,浜野巨秀,他:反復性中耳炎に対する術前検査から発見された X 連鎖無 γ グロブリン血症例.耳鼻臨床 2006; 99: 95–100. |
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SubjectTerms | Primary Immunodeficiency Database in Japan : PIDJ X 連鎖無ガンマグロブリン血症 中耳炎 免疫不全症 |
Title | 繰り返す中耳炎から何を考えますか |
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