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Items: 1 to 20 of 113

1.

The Haplotype TGGAG in the ABCA3 Gene Increases the Risk of Respiratory Distress Syndrome in Preterm Infants in Southern China.

Tian W, Chen X, Qin H, Wei Q, Zhang S, Tang S, Liao L, Zhang Y, Chen Y.

Pediatr Neonatol. 2016 Jun;57(3):188-94. doi: 10.1016/j.pedneo.2015.09.002. Epub 2015 Oct 27.

2.
3.

Haplotype analysis of ABCA3: association with respiratory distress in very premature infants.

Karjalainen MK, Haataja R, Hallman M.

Ann Med. 2008;40(1):56-65. doi: 10.1080/07853890701611094.

PMID:
18246475
4.

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.

5.

Synonymous ABCA3 variants do not increase risk for neonatal respiratory distress syndrome.

Wambach JA, Wegner DJ, Heins HB, Druley TE, Mitra RD, Hamvas A, Cole FS.

J Pediatr. 2014 Jun;164(6):1316-21.e3. doi: 10.1016/j.jpeds.2014.02.021. Epub 2014 Mar 20.

6.

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.

7.

Surfactant protein A associated with respiratory distress syndrome in Korean preterm infants: evidence of ethnic difference.

Jo HS, Cho SI, Chang YH, Kim BI, Choi JH.

Neonatology. 2013;103(1):44-7. doi: 10.1159/000342498. Epub 2012 Oct 3.

PMID:
23038062
8.

Association of polymorphisms in the human surfactant protein-D (SFTPD) gene and postnatal pulmonary adaptation in the preterm infant.

Hilgendorff A, Heidinger K, Bohnert A, Kleinsteiber A, König IR, Ziegler A, Lindner U, Frey G, Merz C, Lettgen B, Chakraborty T, Gortner L, Bein G.

Acta Paediatr. 2009 Jan;98(1):112-7. doi: 10.1111/j.1651-2227.2008.01014.x. Epub 2008 Sep 9.

PMID:
18785967
9.

Surfactant Protein A and B Gene Polymorphisms and Risk of Respiratory Distress Syndrome in Late-Preterm Neonates.

Tsitoura MI, Stavrou EF, Maraziotis IA, Sarafidis K, Athanassiadou A, Dimitriou G.

PLoS One. 2016 Nov 11;11(11):e0166516. doi: 10.1371/journal.pone.0166516. eCollection 2016.

10.

Genetic Polymorphisms of SP-A, SP-B, and SP-D and Risk of Respiratory Distress Syndrome in Preterm Neonates.

Chang HY, Li F, Li FS, Zheng CZ, Lei YZ, Wang J.

Med Sci Monit. 2016 Dec 24;22:5091-5100.

11.

Analysis of nitric oxide synthase gene polymorphisms in neonatal respiratory distress syndrome among the Chinese Han population.

Shen W, Du J, Wang B, Zeng Q.

Ital J Pediatr. 2014 Mar 6;40(1):27. doi: 10.1186/1824-7288-40-27.

12.

Association between the surfactant protein A (SP-A) gene locus and respiratory-distress syndrome in the Finnish population.

Rämet M, Haataja R, Marttila R, Floros J, Hallman M.

Am J Hum Genet. 2000 May;66(5):1569-79. Epub 2000 Apr 4.

13.

G protein-coupled receptor for asthma susceptibility associates with respiratory distress syndrome.

Pulkkinen V, Haataja R, Hannelius U, Helve O, Pitkänen OM, Karikoski R, Rehn M, Marttila R, Lindgren CM, Hästbacka J, Andersson S, Kere J, Hallman M, Laitinen T.

Ann Med. 2006;38(5):357-66.

PMID:
16938805
14.

[Pulmonary surfactant associated gene variants in mixed ethnic population of Han and Zhuang].

Chen YJ, Chen SK, DePass K, Wegner DJ, Hamvas A, Nong GM, Wang YZ, Fan X, Luo JS.

Zhonghua Er Ke Za Zhi. 2012 Nov;50(11):843-6. Chinese.

PMID:
23302616
15.

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
16.

Surfactant protein B deficiency and gene mutations for neonatal respiratory distress syndrome in China Han ethnic population.

Yin X, Meng F, Wang Y, Xie L, Kong X, Feng Z.

Int J Clin Exp Pathol. 2013;6(2):267-72. Epub 2013 Jan 15.

17.

Functional Characterization of ATP-Binding Cassette Transporter A3 Mutations from Infants with Respiratory Distress Syndrome.

Wambach JA, Yang P, Wegner DJ, Heins HB, Kaliberova LN, Kaliberov SA, Curiel DT, White FV, Hamvas A, Hackett BP, Cole FS.

Am J Respir Cell Mol Biol. 2016 Nov;55(5):716-721.

18.

Endothelial NOS gene Glu298Asp polymorphism in preterm neonates with respiratory distress syndrome.

Demirçubuk AG, Coşkun MY, Demiryürek Ş, Dokuyucu R, Öztuzcu S, Taviloğlu ZŞ, Arslan A, Sivaslı E.

Pediatr Pulmonol. 2013 Oct;48(10):976-80. doi: 10.1002/ppul.22759. Epub 2013 Jan 28.

PMID:
23359565
19.

Cytokine gene polymorphisms in Italian preterm infants: association between interleukin-10 -1082 G/A polymorphism and respiratory distress syndrome.

Capasso M, Avvisati RA, Piscopo C, Laforgia N, Raimondi F, de Angelis F, Iolascon A.

Pediatr Res. 2007 Mar;61(3):313-7.

PMID:
17314689
20.

Family-based association tests suggest linkage between surfactant protein B (SP-B) (and flanking region) and respiratory distress syndrome (RDS): SP-B haplotypes and alleles from SP-B-linked loci are risk factors for RDS.

Floros J, Thomas NJ, Liu W, Papagaroufalis C, Xanthou M, Pereira S, Fan R, Guo X, Diangelo S, Pavlovic J.

Pediatr Res. 2006 Apr;59(4 Pt 1):616-21.

PMID:
16549540

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