Wert SE - Search Results

1

Novel mutations in the gene encoding ATP binding cassette protein member A3 (ABCA3) resulting in fatal neonatal lung disease.

Saugstad OD, Hansen TW, Rønnestad A, Nakstad B, Tølløfsrud PA, Reinholt F, Hamvas A, Coles FS, Dean M, Wert SE, Whitsett JA, Nogee LM. Saugstad OD, et al. Among authors: wert se. Acta Paediatr. 2007 Feb;96(2):185-90. doi: 10.1111/j.1651-2227.2007.00016.x. Acta Paediatr. 2007. PMID: 17429902

2

ABCA3 gene mutations in newborns with fatal surfactant deficiency.

Shulenin S, Nogee LM, Annilo T, Wert SE, Whitsett JA, Dean M. Shulenin S, et al. Among authors: wert se. N Engl J Med. 2004 Mar 25;350(13):1296-303. doi: 10.1056/NEJMoa032178. N Engl J Med. 2004. PMID: 15044640 Free article.

3

ABCA3 mutations associated with pediatric interstitial lung disease.

Bullard JE, Wert SE, Whitsett JA, Dean M, Nogee LM. Bullard JE, et al. Among authors: wert se. Am J Respir Crit Care Med. 2005 Oct 15;172(8):1026-31. doi: 10.1164/rccm.200503-504OC. Epub 2005 Jun 23. Am J Respir Crit Care Med. 2005. PMID: 15976379 Free PMC article.

4

ABCA3 deficiency: neonatal respiratory failure and interstitial lung disease.

Bullard JE, Wert SE, Nogee LM. Bullard JE, et al. Among authors: wert se. Semin Perinatol. 2006 Dec;30(6):327-34. doi: 10.1053/j.semperi.2005.12.001. Semin Perinatol. 2006. PMID: 17142158 Review.

5

Large ABCA3 and SFTPC deletions resulting in lung disease.

Henderson LB, Melton K, Wert S, Couriel J, Bush A, Ashworth M, Nogee LM. Henderson LB, et al. Ann Am Thorac Soc. 2013 Dec;10(6):602-7. doi: 10.1513/AnnalsATS.201306-170OC. Ann Am Thorac Soc. 2013. PMID: 24024739 Free PMC article.

6

Genetic disorders of surfactant dysfunction.

Wert SE, Whitsett JA, Nogee LM. Wert SE, et al. Pediatr Dev Pathol. 2009 Jul-Aug;12(4):253-74. doi: 10.2350/09-01-0586.1. Pediatr Dev Pathol. 2009. PMID: 19220077 Free PMC article. Review.

7

Fatal familial lung disease caused by ABCA3 deficiency without identified ABCA3 mutations.

Gower WA, Wert SE, Ginsberg JS, Golan A, Whitsett JA, Nogee LM. Gower WA, et al. Among authors: wert se. J Pediatr. 2010 Jul;157(1):62-8. doi: 10.1016/j.jpeds.2010.01.010. Epub 2010 Mar 20. J Pediatr. 2010. PMID: 20304423

8

Pulmonary nodules in a newborn with ATP-binding cassette transporter A3 (ABCA3) mutations.

Uchida DA, Wert SE, Nogee LM, Carroll TR, Chatfield BA. Uchida DA, et al. Among authors: wert se. Pediatrics. 2011 May;127(5):e1347-51. doi: 10.1542/peds.2010-1477. Epub 2011 Apr 4. Pediatrics. 2011. PMID: 21464189

9

Deficiency of lamellar bodies in alveolar type II cells associated with fatal respiratory disease in a full-term infant.

Cutz E, Wert SE, Nogee LM, Moore AM. Cutz E, et al. Among authors: wert se. Am J Respir Crit Care Med. 2000 Feb;161(2 Pt 1):608-14. doi: 10.1164/ajrccm.161.2.9905062. Am J Respir Crit Care Med. 2000. PMID: 10673207

10

Genetic disorders influencing lung formation and function at birth.

Whitsett JA, Wert SE, Trapnell BC. Whitsett JA, et al. Among authors: wert se. Hum Mol Genet. 2004 Oct 1;13 Spec No 2:R207-15. doi: 10.1093/hmg/ddh252. Hum Mol Genet. 2004. PMID: 15358727 Review.

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