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Items: 1 to 20 of 119

1.

Unexplained neonatal respiratory distress due to congenital surfactant deficiency.

Somaschini M, Nogee LM, Sassi I, Danhaive O, Presi S, Boldrini R, Montrasio C, Ferrari M, Wert SE, Carrera P.

J Pediatr. 2007 Jun;150(6):649-53, 653.e1.

PMID:
17517255
2.

Genetic mechanisms of surfactant deficiency.

Nogee LM.

Biol Neonate. 2004;85(4):314-8. Epub 2004 Jun 8. Review.

PMID:
15218289
3.

Inherited disorders of neonatal lung diseases.

Yurdakök M.

Turk J Pediatr. 2004 Apr-Jun;46(2):105-14. Review.

PMID:
15214737
4.

Genetic disorders of surfactant homeostasis.

Whitsett JA.

Paediatr Respir Rev. 2006;7 Suppl 1:S240-2. Epub 2006 Jun 5. Review.

PMID:
16798578
5.

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. doi: 10.1203/PDR.0b013e31816fdbeb.

6.

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.

7.

Large ABCA3 and SFTPC deletions resulting in lung disease.

Henderson LB, Melton K, Wert S, Couriel J, Bush A, Ashworth M, Nogee LM.

Ann Am Thorac Soc. 2013 Dec;10(6):602-7. doi: 10.1513/AnnalsATS.201306-170OC.

8.

Genetic disorders of surfactant proteins.

Hamvas A, Cole FS, Nogee LM.

Neonatology. 2007;91(4):311-7. Epub 2007 Jun 7. Review.

PMID:
17575475
9.

Evaluation and management of inherited disorders of surfactant metabolism.

Hamvas A.

Chin Med J (Engl). 2010 Oct;123(20):2943-7. Review.

PMID:
21034611
10.

[Pulmonary surfactant protein adenosine triphosphate-binding-cassette-A3 gene composite mutations in infant congenital interstitial lung disease: report of a case and review of literature].

Xie N, Chen DH, Lin YN, Wu SZ, Gu YY, Zeng QS, Zhai YY, Yang LY, Xu JX.

Zhonghua Er Ke Za Zhi. 2016 Oct 2;54(10):761-766. doi: 10.3760/cma.j.issn.0578-1310.2016.10.010. Chinese.

PMID:
27784479
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
12.

ABCA3, a key player in neonatal respiratory transition and genetic disorders of the surfactant system.

Peca D, Cutrera R, Masotti A, Boldrini R, Danhaive O.

Biochem Soc Trans. 2015 Oct;43(5):913-9. doi: 10.1042/BST20150100. Review.

PMID:
26517903
13.

Alteration of the pulmonary surfactant system in full-term infants with hereditary ABCA3 deficiency.

Brasch F, Schimanski S, Mühlfeld C, Barlage S, Langmann T, Aslanidis C, Boettcher A, Dada A, Schroten H, Mildenberger E, Prueter E, Ballmann M, Ochs M, Johnen G, Griese M, Schmitz G.

Am J Respir Crit Care Med. 2006 Sep 1;174(5):571-80. Epub 2006 May 25.

PMID:
16728712
14.

Lung surfactant, respiratory failure, and genes.

Hallman M.

N Engl J Med. 2004 Mar 25;350(13):1278-80. No abstract available.

PMID:
15044636
15.

Genetic testing in children with surfactant dysfunction.

Turcu S, Ashton E, Jenkins L, Gupta A, Mok Q.

Arch Dis Child. 2013 Jul;98(7):490-5. doi: 10.1136/archdischild-2012-303166. Epub 2013 Apr 26.

PMID:
23625987
16.

Genetic disorders of surfactant dysfunction.

Wert SE, Whitsett JA, Nogee LM.

Pediatr Dev Pathol. 2009 Jul-Aug;12(4):253-74. doi: 10.2350/09-01-0586.1. Review.

17.

Genetic susceptibility to neonatal lung diseases.

Somaschini M, Castiglioni E, Presi S, Volonteri C, Ferrari M, Carrera P.

Acta Biomed. 2012;83 Suppl 1:10-4.

PMID:
23029870
18.

Population-based frequency of surfactant dysfunction mutations in a native Chinese cohort.

Chen YJ, Wambach JA, DePass K, Wegner DJ, Chen SK, Zhang QY, Heins H, Cole FS, Hamvas A.

World J Pediatr. 2016 May;12(2):190-5. doi: 10.1007/s12519-015-0047-x. Epub 2015 Nov 7.

PMID:
26547207
19.

Single ABCA3 mutations increase risk for neonatal respiratory distress syndrome.

Wambach JA, Wegner DJ, Depass K, Heins H, Druley TE, Mitra RD, An P, Zhang Q, Nogee LM, Cole FS, Hamvas A.

Pediatrics. 2012 Dec;130(6):e1575-82. doi: 10.1542/peds.2012-0918. Epub 2012 Nov 19.

20.

Primary alveolar capillary dysplasia (acinar dysplasia) and surfactant protein B deficiency: a clinical, radiological and pathological study.

Hugosson CO, Salama HM, Al-Dayel F, Khoumais N, Kattan AH.

Pediatr Radiol. 2005 Mar;35(3):311-6. Epub 2004 Oct 14.

PMID:
15490144

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