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    Results: 1 to 20 of 147

    1.

    Interstitial lung disease in children -- genetic background and associated phenotypes.

    Hartl D, Griese M.

    Respir Res. 2005 Apr 8;6:32. Review.PMID: 15819986 [PubMed - indexed for MEDLINE]Related articlesFree article

    2.

    ABCA3 mutations associated with pediatric interstitial lung disease.

    Bullard JE, Wert SE, Whitsett JA, Dean M, Nogee LM.

    Am J Respir Crit Care Med. 2005 Oct 15;172(8):1026-31. Epub 2005 Jun 23.PMID: 15976379 [PubMed - indexed for MEDLINE]Related articlesFree article

    3.

    Genetics of pediatric interstitial lung disease.

    Nogee LM.

    Curr Opin Pediatr. 2006 Jun;18(3):287-92. Review.PMID: 16721150 [PubMed - indexed for MEDLINE]Related articles

    4.

    Surfactant dysfunction mutations in children's interstitial lung disease and beyond.

    Deterding R, Fan LL.

    Am J Respir Crit Care Med. 2005 Oct 15;172(8):940-1. Review. No abstract available. PMID: 16216835 [PubMed - indexed for MEDLINE]Related articlesFree article

    5.

    Heterozygosity for ABCA3 mutations modifies the severity of lung disease associated with a surfactant protein C gene (SFTPC) mutation.

    Bullard JE, Nogee LM.

    Pediatr Res. 2007 Aug;62(2):176-9.PMID: 17597647 [PubMed - indexed for MEDLINE]Related articles

    6.

    Genetic disorders of surfactant dysfunction.

    Wert SE, Whitsett JA, Nogee LM.

    Pediatr Dev Pathol. 2009 Jul-Aug;12(4):253-74. Review.PMID: 19220077 [PubMed - indexed for MEDLINE]Related articles

    7.

    Ultrastructural and molecular analysis in fatal neonatal interstitial pneumonia caused by a novel ABCA3 mutation.

    Bruder E, Hofmeister J, Aslanidis C, Hammer J, Bubendorf L, Schmitz G, Rufle A, Bührer C.

    Mod Pathol. 2007 Oct;20(10):1009-18. Epub 2007 Jul 27.PMID: 17660803 [PubMed - indexed for MEDLINE]Related articlesFree article

    8.

    Inherited disorders of neonatal lung diseases.

    Yurdakök M.

    Turk J Pediatr. 2004 Apr-Jun;46(2):105-14. Review.PMID: 15214737 [PubMed - indexed for MEDLINE]Related articles

    9.

    Usual interstitial pneumonia in an adolescent with ABCA3 mutations.

    Young LR, Nogee LM, Barnett B, Panos RJ, Colby TV, Deutsch GH.

    Chest. 2008 Jul;134(1):192-5.PMID: 18628224 [PubMed - indexed for MEDLINE]Related articlesFree article

    10.

    Clinical, radiological and pathological features of ABCA3 mutations in children.

    Doan ML, Guillerman RP, Dishop MK, Nogee LM, Langston C, Mallory GB, Sockrider MM, Fan LL.

    Thorax. 2008 Apr;63(4):366-73. Epub 2007 Nov 16.PMID: 18024538 [PubMed - indexed for MEDLINE]Related articles

    11.

    Genetic disorders of surfactant homeostasis.

    Whitsett JA, Wert SE, Xu Y.

    Biol Neonate. 2005;87(4):283-7. Epub 2005 Jun 1. Review.PMID: 15985750 [PubMed - indexed for MEDLINE]Related articles

    12.

    ABCA3 deficiency: neonatal respiratory failure and interstitial lung disease.

    Bullard JE, Wert SE, Nogee LM.

    Semin Perinatol. 2006 Dec;30(6):327-34. Review.PMID: 17142158 [PubMed - indexed for MEDLINE]Related articles

    13.

    Mutation of SFTPC in infantile pulmonary alveolar proteinosis with or without fibrosing lung disease.

    Tredano M, Griese M, Brasch F, Schumacher S, de Blic J, Marque S, Houdayer C, Elion J, Couderc R, Bahuau M.

    Am J Med Genet A. 2004 Apr 1;126A(1):18-26.PMID: 15039969 [PubMed - indexed for MEDLINE]Related articles

    14.

    Population and disease-based prevalence of the common mutations associated with surfactant deficiency.

    Garmany TH, Wambach JA, Heins HB, Watkins-Torry JM, Wegner DJ, Bennet K, An P, Land G, Saugstad OD, Henderson H, Nogee LM, Cole FS, Hamvas A.

    Pediatr Res. 2008 Jun;63(6):645-9.PMID: 18317237 [PubMed - indexed for MEDLINE]Related articlesFree article

    15.

    Surfactant Metabolism Dysfunction and Childhood Interstitial Lung Disease (chILD).

    McFetridge L, McMorrow A, Morrison PJ, Shields MD.

    Ulster Med J. 2009 Jan;78(1):7-9. Review.PMID: 19252722 [PubMed - indexed for MEDLINE]Related articlesFree article

    16.

    Genetic disorders of surfactant proteins.

    Hamvas A, Cole FS, Nogee LM.

    Neonatology. 2007;91(4):311-7. Epub 2007 Jun 7. Review.PMID: 17575475 [PubMed - indexed for MEDLINE]Related articles

    17.

    Genetic mechanisms of surfactant deficiency.

    Nogee LM.

    Biol Neonate. 2004;85(4):314-8. Epub 2004 Jun 8. Review.PMID: 15218289 [PubMed - indexed for MEDLINE]Related articles

    18.

    Inherited surfactant deficiency caused by uniparental disomy of rare mutations in the surfactant protein-B and ATP binding cassette, subfamily a, member 3 genes.

    Hamvas A, Nogee LM, Wegner DJ, Depass K, Christodoulou J, Bennetts B, McQuade LR, Gray PH, Deterding RR, Carroll TR, Kammesheidt A, Kasch LM, Kulkarni S, Cole FS.

    J Pediatr. 2009 Dec;155(6):854-859.e1. Epub 2009 Aug 3.PMID: 19647838 [PubMed - indexed for MEDLINE]Related articlesFree article

    19.

    Aberrant catalytic cycle and impaired lipid transport into intracellular vesicles in ABCA3 mutants associated with nonfatal pediatric interstitial lung disease.

    Matsumura Y, Ban N, Inagaki N.

    Am J Physiol Lung Cell Mol Physiol. 2008 Oct;295(4):L698-707. Epub 2008 Aug 1.PMID: 18676873 [PubMed - indexed for MEDLINE]Related articlesFree article

    20.

    Inherited surfactant protein-B deficiency and surfactant protein-C associated disease: clinical features and evaluation.

    Hamvas A.

    Semin Perinatol. 2006 Dec;30(6):316-26. Review.PMID: 17142157 [PubMed - indexed for MEDLINE]Related articles

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