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Volumn 98, Issue 7, 2013, Pages 490-496

Genetic testing in children with surfactant dysfunction

Author keywords

[No Author keywords available]

Indexed keywords

ABC TRANSPORTER; ABC TRANSPORTER A3; AZATHIOPRINE; DEXAMETHASONE; HYDROXYCHLOROQUINE; METHYLPREDNISOLONE; PREDNISOLONE; SURFACTANT; SURFACTANT PROTEIN B; SURFACTANT PROTEIN C; UNCLASSIFIED DRUG;

EID: 84879692302     PISSN: 00039888     EISSN: 14682044     Source Type: Journal    
DOI: 10.1136/archdischild-2012-303166     Document Type: Article
Times cited : (58)

References (10)
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    • Wert, S.1    Whitsett, J.2    Nogee, L.3
  • 3
    • 33744800817 scopus 로고    scopus 로고
    • Genetics of pediatric interstitial lung disease
    • Nogee LM, Genetics of pediatric interstitial lung disease. Curr Opin Pediatr 2006;18:287 -92.
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    • Nogee, L.M.1
  • 4
    • 70049096702 scopus 로고    scopus 로고
    • Lung transplantation for inherited disorders of surfactant metabolism
    • Faro A, Hamvas A, Lung transplantation for inherited disorders of surfactant metabolism. Neo Reviews 2008;9:e468-76.
    • (2008) Neo Reviews , vol.9
    • Faro, A.1    Hamvas, A.2
  • 5
    • 41849086990 scopus 로고    scopus 로고
    • Clinical, radiological and pathological features of ABCA3 mutations in children
    • Doan Ml, Guillerman RP, Dishop MK, et al. Clinical, radiological and pathological features of ABCA3 mutations in children. Thorax 2008;63:366-73.
    • (2008) Thorax , vol.63 , pp. 366-373
    • Ml, D.1    Guillerman, R.P.2    Dishop, M.K.3
  • 6
    • 75149175193 scopus 로고    scopus 로고
    • NKX2-1 mutations leading to surfactant protein promoter dysregulation cause interstitial lung disease in "Brain-Lung-Thyroid Syndrome"
    • Guillot L, Carre A, Szinnai G, et al. NKX2-1 mutations leading to surfactant protein promoter dysregulation cause interstitial lung disease in "Brain-Lung-Thyroid Syndrome". Hum Mutat 2010;31:e1146-62.
    • (2010) Hum Mutat , vol.31
    • Guillot, L.1    Carre, A.2    Szinnai, G.3
  • 7
    • 68049091001 scopus 로고    scopus 로고
    • Serum KL-6 differentiates neuroendocrine cell hyperplasia of infancy from the inborn errors of surfactant metabolism
    • Doan ML, Elidemir O, Dishop MK, et al. Serum KL-6 differentiates neuroendocrine cell hyperplasia of infancy from the inborn errors of surfactant metabolism. Thorax 2009;64:677 -81.
    • (2009) Thorax , vol.64 , pp. 677-681
    • Doan, M.L.1    Elidemir, O.2    Dishop, M.K.3
  • 8
    • 77953698896 scopus 로고    scopus 로고
    • Characteristics of disorders associated with genetic mutations of surfactant protein C
    • Thouvenin G, Taam R, Flamein F, et al. Characteristics of disorders associated with genetic mutations of surfactant protein C. Arch Dis Child 2010;95:449-54.
    • (2010) Arch Dis Child , vol.95 , pp. 449-454
    • Thouvenin, G.1    Taam, R.2    Flamein, F.3
  • 9
    • 77953478729 scopus 로고    scopus 로고
    • Fatal familial lung disease caused by ABCA3 deficiency without identified ABCA3 mutations
    • Gower WA, Wert SE, Ginsberg JS, et al. Fatal familial lung disease caused by ABCA3 deficiency without identified ABCA3 mutations. J Pediatr 2010;157:62-8.
    • (2010) J Pediatr , vol.157 , pp. 62-68
    • Gower, W.A.1    Wert, S.E.2    Ginsberg, J.S.3
  • 10
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    • Altered surfactant homeostasis and recurrent respiratory failure secondary to TTF-1 nuclear targeting defect
    • Peca D, Petrini S, Tzialla C, et al. Altered surfactant homeostasis and recurrent respiratory failure secondary to TTF-1 nuclear targeting defect. Respir Res 2011;12:115.
    • (2011) Respir Res , vol.12 , pp. 115
    • Peca, D.1    Petrini, S.2    Tzialla, C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.