U54 RR019480/RR/NCRR NIH HHS/United States[Grants and Funding] - Search Results

Year	Number of Results
2005	1
2006	1
2007	2
2008	1
2009	4
2010	1
2011	3
2012	2
2013	6
2015	1
2025	0

1

Primary ciliary dyskinesia: improving the diagnostic approach.

Leigh MW, Zariwala MA, Knowles MR. Leigh MW, et al. Curr Opin Pediatr. 2009 Jun;21(3):320-5. doi: 10.1097/MOP.0b013e328329cddb. Curr Opin Pediatr. 2009. PMID: 19300264 Free PMC article. Review.

2

The challenges of diagnosing primary ciliary dyskinesia.

Leigh MW, O'Callaghan C, Knowles MR. Leigh MW, et al. Proc Am Thorac Soc. 2011 Sep;8(5):434-7. doi: 10.1513/pats.201103-028SD. Proc Am Thorac Soc. 2011. PMID: 21926395 Free PMC article. Review.

3

Genetic defects in ciliary structure and function.

Zariwala MA, Knowles MR, Omran H. Zariwala MA, et al. Annu Rev Physiol. 2007;69:423-50. doi: 10.1146/annurev.physiol.69.040705.141301. Annu Rev Physiol. 2007. PMID: 17059358 Review.

4

Human airway ciliary dynamics.

Sears PR, Thompson K, Knowles MR, Davis CW. Sears PR, et al. Am J Physiol Lung Cell Mol Physiol. 2013 Feb 1;304(3):L170-83. doi: 10.1152/ajplung.00105.2012. Epub 2012 Nov 9. Am J Physiol Lung Cell Mol Physiol. 2013. PMID: 23144323 Free PMC article.

5

Primary ciliary dyskinesia. Recent advances in diagnostics, genetics, and characterization of clinical disease.

Knowles MR, Daniels LA, Davis SD, Zariwala MA, Leigh MW. Knowles MR, et al. Am J Respir Crit Care Med. 2013 Oct 15;188(8):913-22. doi: 10.1164/rccm.201301-0059CI. Am J Respir Crit Care Med. 2013. PMID: 23796196 Free PMC article. Review.

6

Clinical and genetic aspects of primary ciliary dyskinesia/Kartagener syndrome.

Leigh MW, Pittman JE, Carson JL, Ferkol TW, Dell SD, Davis SD, Knowles MR, Zariwala MA. Leigh MW, et al. Genet Med. 2009 Jul;11(7):473-87. doi: 10.1097/GIM.0b013e3181a53562. Genet Med. 2009. PMID: 19606528 Free PMC article. Review.

7

A quality-of-life measure for adults with primary ciliary dyskinesia: QOL-PCD.

Lucas JS, Behan L, Dunn Galvin A, Alpern A, Morris AM, Carroll MP, Knowles MR, Leigh MW, Quittner AL. Lucas JS, et al. Eur Respir J. 2015 Aug;46(2):375-83. doi: 10.1183/09031936.00216214. Epub 2015 May 14. Eur Respir J. 2015. PMID: 25976687 Free PMC article.

8

Primary ciliary dyskinesia in Amish communities.

Lie H, Zariwala MA, Helms C, Bowcock AM, Carson JL, Brown DE 3rd, Hazucha MJ, Forsen J, Molter D, Knowles MR, Leigh MW, Ferkol TW. Lie H, et al. J Pediatr. 2010 Jun;156(6):1023-1025. doi: 10.1016/j.jpeds.2010.01.054. Epub 2010 Mar 29. J Pediatr. 2010. PMID: 20350728 Free PMC article.

9

Deletions and point mutations of LRRC50 cause primary ciliary dyskinesia due to dynein arm defects.

Loges NT, Olbrich H, Becker-Heck A, Häffner K, Heer A, Reinhard C, Schmidts M, Kispert A, Zariwala MA, Leigh MW, Knowles MR, Zentgraf H, Seithe H, Nürnberg G, Nürnberg P, Reinhardt R, Omran H. Loges NT, et al. Am J Hum Genet. 2009 Dec;85(6):883-9. doi: 10.1016/j.ajhg.2009.10.018. Am J Hum Genet. 2009. PMID: 19944400 Free PMC article.

10

Clinical research for rare disease: opportunities, challenges, and solutions.

Griggs RC, Batshaw M, Dunkle M, Gopal-Srivastava R, Kaye E, Krischer J, Nguyen T, Paulus K, Merkel PA; Rare Diseases Clinical Research Network. Griggs RC, et al. Mol Genet Metab. 2009 Jan;96(1):20-6. doi: 10.1016/j.ymgme.2008.10.003. Epub 2008 Nov 13. Mol Genet Metab. 2009. PMID: 19013090 Free PMC article.

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