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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2009 | 1 |
2010 | 1 |
2011 | 1 |
2012 | 2 |
2013 | 4 |
2014 | 1 |
2024 | 0 |
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7 results
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Page 1
Picking up speed: advances in the genetics of primary ciliary dyskinesia.
Pediatr Res. 2014 Jan;75(1-2):158-64. doi: 10.1038/pr.2013.200. Epub 2013 Nov 5.
Pediatr Res. 2014.
PMID: 24192704
Free PMC article.
Review.
Ciliopathies: the central role of cilia in a spectrum of pediatric disorders.
Ferkol TW, Leigh MW.
Ferkol TW, et al.
J Pediatr. 2012 Mar;160(3):366-71. doi: 10.1016/j.jpeds.2011.11.024. Epub 2011 Dec 16.
J Pediatr. 2012.
PMID: 22177992
Free PMC article.
Review.
No abstract available.
Item in Clipboard
Primary ciliary dyskinesia-causing mutations in Amish and Mennonite communities.
Ferkol TW, Puffenberger EG, Lie H, Helms C, Strauss KA, Bowcock A, Carson JL, Hazucha M, Morton DH, Patel AC, Leigh MW, Knowles MR, Zariwala MA.
Ferkol TW, et al.
J Pediatr. 2013 Aug;163(2):383-7. doi: 10.1016/j.jpeds.2013.01.061. Epub 2013 Mar 7.
J Pediatr. 2013.
PMID: 23477994
Free PMC article.
Item in Clipboard
LRRC6 mutation causes primary ciliary dyskinesia with dynein arm defects.
Horani A, Ferkol TW, Shoseyov D, Wasserman MG, Oren YS, Kerem B, Amirav I, Cohen-Cymberknoh M, Dutcher SK, Brody SL, Elpeleg O, Kerem E.
Horani A, et al.
PLoS One. 2013;8(3):e59436. doi: 10.1371/journal.pone.0059436. Epub 2013 Mar 19.
PLoS One. 2013.
PMID: 23527195
Free PMC article.
Item in Clipboard
CCDC65 mutation causes primary ciliary dyskinesia with normal ultrastructure and hyperkinetic cilia.
Horani A, Brody SL, Ferkol TW, Shoseyov D, Wasserman MG, Ta-shma A, Wilson KS, Bayly PV, Amirav I, Cohen-Cymberknoh M, Dutcher SK, Elpeleg O, Kerem E.
Horani A, et al.
PLoS One. 2013 Aug 26;8(8):e72299. doi: 10.1371/journal.pone.0072299. eCollection 2013.
PLoS One. 2013.
PMID: 23991085
Free PMC article.
Item in Clipboard
Airway proteins involved in bacterial clearance susceptible to cathepsin G proteolysis.
Farberman MM, Akers KT, Malone JP, Erdman-Gilmore P, Townsend RR, Ferkol T.
Farberman MM, et al.
Eur Respir J. 2010 Feb;35(2):410-7. doi: 10.1183/09031936.00020809. Epub 2009 Aug 13.
Eur Respir J. 2010.
PMID: 19679607
Free PMC article.
Item in Clipboard
Whole-exome capture and sequencing identifies HEATR2 mutation as a cause of primary ciliary dyskinesia.
Horani A, Druley TE, Zariwala MA, Patel AC, Levinson BT, Van Arendonk LG, Thornton KC, Giacalone JC, Albee AJ, Wilson KS, Turner EH, Nickerson DA, Shendure J, Bayly PV, Leigh MW, Knowles MR, Brody SL, Dutcher SK, Ferkol TW.
Horani A, et al.
Am J Hum Genet. 2012 Oct 5;91(4):685-93. doi: 10.1016/j.ajhg.2012.08.022.
Am J Hum Genet. 2012.
PMID: 23040496
Free PMC article.
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