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Lung development is not necessary for diaphragm development in mice.
Arkovitz MS, Hyatt BA, Shannon JM. Arkovitz MS, et al. J Pediatr Surg. 2005 Sep;40(9):1390-4. doi: 10.1016/j.jpedsurg.2005.05.059. J Pediatr Surg. 2005. PMID: 16150338
Mutations in BMPR2 are not present in patients with pulmonary hypertension associated with congenital diaphragmatic hernia.
Chiu JS, Ma L, Wynn J, Krishnan U, Rosenzweig EB, Aspelund G, Arkovitz M, Warner BW, Lim FY, Mychaliska GB, Azarow K, Cusick RA, Chung DH, Chung WK. Chiu JS, et al. J Pediatr Surg. 2017 Nov;52(11):1747-1750. doi: 10.1016/j.jpedsurg.2017.01.007. Epub 2017 Jan 26. J Pediatr Surg. 2017. PMID: 28162765
Increased burden of de novo predicted deleterious variants in complex congenital diaphragmatic hernia.
Yu L, Sawle AD, Wynn J, Aspelund G, Stolar CJ, Arkovitz MS, Potoka D, Azarow KS, Mychaliska GB, Shen Y, Chung WK. Yu L, et al. Among authors: arkovitz ms. Hum Mol Genet. 2015 Aug 15;24(16):4764-73. doi: 10.1093/hmg/ddv196. Epub 2015 Jun 1. Hum Mol Genet. 2015. PMID: 26034137 Free PMC article. Clinical Trial.
Whole exome sequencing identifies de novo mutations in GATA6 associated with congenital diaphragmatic hernia.
Yu L, Bennett JT, Wynn J, Carvill GL, Cheung YH, Shen Y, Mychaliska GB, Azarow KS, Crombleholme TM, Chung DH, Potoka D, Warner BW, Bucher B, Lim FY, Pietsch J, Stolar C, Aspelund G, Arkovitz MS; University of Washington Center for Mendelian Genomics, Mefford H, Chung WK. Yu L, et al. Among authors: arkovitz ms. J Med Genet. 2014 Mar;51(3):197-202. doi: 10.1136/jmedgenet-2013-101989. Epub 2014 Jan 2. J Med Genet. 2014. PMID: 24385578 Free PMC article.
Variants in GATA4 are a rare cause of familial and sporadic congenital diaphragmatic hernia.
Yu L, Wynn J, Cheung YH, Shen Y, Mychaliska GB, Crombleholme TM, Azarow KS, Lim FY, Chung DH, Potoka D, Warner BW, Bucher B, Stolar C, Aspelund G, Arkovitz MS, Chung WK. Yu L, et al. Among authors: arkovitz ms. Hum Genet. 2013 Mar;132(3):285-92. doi: 10.1007/s00439-012-1249-0. Epub 2012 Nov 9. Hum Genet. 2013. PMID: 23138528 Free PMC article.
Timing and expression of the angiopoietin-1-Tie-2 pathway in murine lung development and congenital diaphragmatic hernia.
Grzenda A, Shannon J, Fisher J, Arkovitz MS. Grzenda A, et al. Among authors: arkovitz ms. Dis Model Mech. 2013 Jan;6(1):106-14. doi: 10.1242/dmm.008821. Epub 2012 Aug 23. Dis Model Mech. 2013. PMID: 22917924 Free PMC article.
De novo copy number variants are associated with congenital diaphragmatic hernia.
Yu L, Wynn J, Ma L, Guha S, Mychaliska GB, Crombleholme TM, Azarow KS, Lim FY, Chung DH, Potoka D, Warner BW, Bucher B, LeDuc CA, Costa K, Stolar C, Aspelund G, Arkovitz MS, Chung WK. Yu L, et al. Among authors: arkovitz ms. J Med Genet. 2012 Oct;49(10):650-9. doi: 10.1136/jmedgenet-2012-101135. J Med Genet. 2012. PMID: 23054247 Free PMC article.
Newborns with diaphragmatic hernia: initial chest radiography does not have a role in predicting clinical outcome.
Holt PD, Arkovitz MS, Berdon WE, Stolar CJ. Holt PD, et al. Among authors: arkovitz ms. Pediatr Radiol. 2004 Jun;34(6):462-4. doi: 10.1007/s00247-004-1151-6. Epub 2004 Mar 23. Pediatr Radiol. 2004. PMID: 15042331
Hereditary multiple exostoses of the ribs: an unusual cause of hemothorax and pericardial effusion.
Cowles RA, Rowe DH, Arkovitz MS. Cowles RA, et al. Among authors: arkovitz ms. J Pediatr Surg. 2005 Jul;40(7):1197-200. doi: 10.1016/j.jpedsurg.2005.03.064. J Pediatr Surg. 2005. PMID: 16034772
Outcomes of congenital diaphragmatic hernia in the modern era of management.
Wynn J, Krishnan U, Aspelund G, Zhang Y, Duong J, Stolar CJ, Hahn E, Pietsch J, Chung D, Moore D, Austin E, Mychaliska G, Gajarski R, Foong YL, Michelfelder E, Potolka D, Bucher B, Warner B, Grady M, Azarow K, Fletcher SE, Kutty S, Delaney J, Crombleholme T, Rosenzweig E, Chung W, Arkovitz MS. Wynn J, et al. Among authors: arkovitz ms. J Pediatr. 2013 Jul;163(1):114-9.e1. doi: 10.1016/j.jpeds.2012.12.036. Epub 2013 Jan 30. J Pediatr. 2013. PMID: 23375362 Free PMC article.
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