메뉴 건너뛰기




Volumn 150, Issue 6, 2007, Pages

Unexplained Neonatal Respiratory Distress Due to Congenital Surfactant Deficiency

Author keywords

[No Author keywords available]

Indexed keywords

ABC TRANSPORTER; ABC TRANSPORTER A3; DNA; LUNG SURFACTANT; SURFACTANT PROTEIN B; UNCLASSIFIED DRUG;

EID: 34248576101     PISSN: 00223476     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jpeds.2007.03.008     Document Type: Article
Times cited : (71)

References (21)
  • 1
    • 3042663294 scopus 로고    scopus 로고
    • Genetic mechanisms of surfactant deficiency
    • Nogee L.M. Genetic mechanisms of surfactant deficiency. Biol Neonate 85 (2004) 314-318
    • (2004) Biol Neonate , vol.85 , pp. 314-318
    • Nogee, L.M.1
  • 2
    • 5444221907 scopus 로고    scopus 로고
    • Genetic disorders influencing lung formation and function at birth
    • Whitsett J.A., Wert S.E., and Trapnell B.C. Genetic disorders influencing lung formation and function at birth. Hum Mol Genet 13 (2004) 207-215
    • (2004) Hum Mol Genet , vol.13 , pp. 207-215
    • Whitsett, J.A.1    Wert, S.E.2    Trapnell, B.C.3
  • 3
    • 0027466161 scopus 로고
    • Deficiency of pulmonary surfactant protein B in congenital alveolar proteinosis
    • Nogee L.M., deMello D.E., Dehner L.P., and Colten H.R. Deficiency of pulmonary surfactant protein B in congenital alveolar proteinosis. N Engl J Med 328 (1993) 406
    • (1993) N Engl J Med , vol.328 , pp. 406
    • Nogee, L.M.1    deMello, D.E.2    Dehner, L.P.3    Colten, H.R.4
  • 5
    • 0035931973 scopus 로고    scopus 로고
    • A mutation in the surfactant protein C gene associated with familial interstitial lung disease
    • Nogee L.M., Dunbar A.E., Wert S.E., Askin F., Hamvas A., and Whitsett J.A. A mutation in the surfactant protein C gene associated with familial interstitial lung disease. N Engl J Med 344 (2001) 573-579
    • (2001) N Engl J Med , vol.344 , pp. 573-579
    • Nogee, L.M.1    Dunbar, A.E.2    Wert, S.E.3    Askin, F.4    Hamvas, A.5    Whitsett, J.A.6
  • 8
    • 28844503843 scopus 로고    scopus 로고
    • Ultrastructure of lamellar bodies in congenital surfactant deficiency
    • Edwards V., Cutz E., Viero S., Moore A.M., and Nogee L.M. Ultrastructure of lamellar bodies in congenital surfactant deficiency. Ultrastruct Pathol 29 (2005) 503-509
    • (2005) Ultrastruct Pathol , vol.29 , pp. 503-509
    • Edwards, V.1    Cutz, E.2    Viero, S.3    Moore, A.M.4    Nogee, L.M.5
  • 10
    • 0031574072 scopus 로고    scopus 로고
    • The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools
    • Thompson J.D., Gibson T.J., Plewniak F., Jeanmougin F., and Higgins D.G. The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools. Nucleic Acid Res 25 (1997) 4876-4882
    • (1997) Nucleic Acid Res , vol.25 , pp. 4876-4882
    • Thompson, J.D.1    Gibson, T.J.2    Plewniak, F.3    Jeanmougin, F.4    Higgins, D.G.5
  • 11
    • 0035094764 scopus 로고    scopus 로고
    • Variation is the spice of life
    • Kruglyak L., and Nickerson D.A. Variation is the spice of life. Nat Genet 27 (2001) 234-236
    • (2001) Nat Genet , vol.27 , pp. 234-236
    • Kruglyak, L.1    Nickerson, D.A.2
  • 12
    • 2342592703 scopus 로고    scopus 로고
    • Alterations in SP-B and SP-C expression in neonatal lung disease
    • Nogee L.M. Alterations in SP-B and SP-C expression in neonatal lung disease. Annu Rev Physiol 66 (2004) 601-623
    • (2004) Annu Rev Physiol , vol.66 , pp. 601-623
    • Nogee, L.M.1
  • 13
    • 10744220727 scopus 로고    scopus 로고
    • Analysis of 40 sporadic or familial neonatal and pediatric cases with severe unexplained respiratory distress: relationship to SFTPB
    • Tredano M., Griese M., de Blic J., Lorant T., Houdayer C., Schumacher S., et al. Analysis of 40 sporadic or familial neonatal and pediatric cases with severe unexplained respiratory distress: relationship to SFTPB. Am J Med Genet 119A (2003) 324-339
    • (2003) Am J Med Genet , vol.119 A , pp. 324-339
    • Tredano, M.1    Griese, M.2    de Blic, J.3    Lorant, T.4    Houdayer, C.5    Schumacher, S.6
  • 15
    • 0034917716 scopus 로고    scopus 로고
    • The human ATP-binding cassette (ABC) transporter superfamily
    • Dean M., Rzhetsky A., and Allikmets R. The human ATP-binding cassette (ABC) transporter superfamily. Genome Res 11 (2001) 1156-1166
    • (2001) Genome Res , vol.11 , pp. 1156-1166
    • Dean, M.1    Rzhetsky, A.2    Allikmets, R.3
  • 16
    • 0035900369 scopus 로고    scopus 로고
    • ABCA3 is a lamellar body membrane protein in human lung alveolar type II cells
    • Yamano G., Funahashi H., Kawanami O., Zhao L.X., Ban N., Uchida Y., et al. ABCA3 is a lamellar body membrane protein in human lung alveolar type II cells. FEBS Lett 508 (2001) 221-225
    • (2001) FEBS Lett , vol.508 , pp. 221-225
    • Yamano, G.1    Funahashi, H.2    Kawanami, O.3    Zhao, L.X.4    Ban, N.5    Uchida, Y.6
  • 17
    • 0030724604 scopus 로고    scopus 로고
    • Lung transplantation for treatment of infants with surfactant protein B deficiency
    • Hamvas A., Nogee L.M., Mallory G.B., Spray T.L., Huddleston C.B., August A., et al. Lung transplantation for treatment of infants with surfactant protein B deficiency. J Pediatr 130 (1997) 231-239
    • (1997) J Pediatr , vol.130 , pp. 231-239
    • Hamvas, A.1    Nogee, L.M.2    Mallory, G.B.3    Spray, T.L.4    Huddleston, C.B.5    August, A.6
  • 18
    • 0031937196 scopus 로고    scopus 로고
    • Transient surfactant protein B deficiency in a term infant with severe respiratory failure
    • Klein J.M., Thompson M.W., Snyder J.M., George T.N., Whitsett J.A., Bell E.F., et al. Transient surfactant protein B deficiency in a term infant with severe respiratory failure. J Pediatr 132 (1998) 244-248
    • (1998) J Pediatr , vol.132 , pp. 244-248
    • Klein, J.M.1    Thompson, M.W.2    Snyder, J.M.3    George, T.N.4    Whitsett, J.A.5    Bell, E.F.6
  • 19
    • 0033883899 scopus 로고    scopus 로고
    • Prolonged survival in hereditary surfactant protein B (SP-B) deficiency associated with a novel splicing mutation
    • Dunbar A.E., Wert S.E., Ikegami M., Whitsett J.A., Hamvas A., White F.V., et al. Prolonged survival in hereditary surfactant protein B (SP-B) deficiency associated with a novel splicing mutation. Pediatr Res 48 (2000) 275-282
    • (2000) Pediatr Res , vol.48 , pp. 275-282
    • Dunbar, A.E.1    Wert, S.E.2    Ikegami, M.3    Whitsett, J.A.4    Hamvas, A.5    White, F.V.6
  • 21
    • 0031757787 scopus 로고    scopus 로고
    • Prenatal diagnosis of congenital alveolar proteinosis (surfactant protein B deficiency)
    • Stuhrmann M., Bohnhorst B., Peters V., Bohle R.M., Poets C.F., and Scmidtke J. Prenatal diagnosis of congenital alveolar proteinosis (surfactant protein B deficiency). Prenat Diagn 18 (1998) 953-955
    • (1998) Prenat Diagn , vol.18 , pp. 953-955
    • Stuhrmann, M.1    Bohnhorst, B.2    Peters, V.3    Bohle, R.M.4    Poets, C.F.5    Scmidtke, J.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.