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Items: 1 to 20 of 24

1.

High prevalence of respiratory ciliary dysfunction in congenital heart disease patients with heterotaxy.

Nakhleh N, Francis R, Giese RA, Tian X, Li Y, Zariwala MA, Yagi H, Khalifa O, Kureshi S, Chatterjee B, Sabol SL, Swisher M, Connelly PS, Daniels MP, Srinivasan A, Kuehl K, Kravitz N, Burns K, Sami I, Omran H, Barmada M, Olivier K, Chawla KK, Leigh M, Jonas R, Knowles M, Leatherbury L, Lo CW.

Circulation. 2012 May 8;125(18):2232-42. doi: 10.1161/CIRCULATIONAHA.111.079780. Epub 2012 Apr 12.

2.

Primary ciliary dyskinesia: improving the diagnostic approach.

Leigh MW, Zariwala MA, Knowles MR.

Curr Opin Pediatr. 2009 Jun;21(3):320-5. doi: 10.1097/MOP.0b013e328329cddb. Review.

3.

Primary ciliary dyskinesia: recent advances in epidemiology, diagnosis, management and relationship with the expanding spectrum of ciliopathy.

Bush A, Hogg C.

Expert Rev Respir Med. 2012 Dec;6(6):663-82. doi: 10.1586/ers.12.60. Review.

PMID:
23234452
4.

Ciliary defects and genetics of primary ciliary dyskinesia.

Escudier E, Duquesnoy P, Papon JF, Amselem S.

Paediatr Respir Rev. 2009 Jun;10(2):51-4. doi: 10.1016/j.prrv.2009.02.001. Epub 2009 Apr 18. Review.

5.

Genetic causes of bronchiectasis: primary ciliary dyskinesia.

Morillas HN, Zariwala M, Knowles MR.

Respiration. 2007;74(3):252-63. Review.

PMID:
17534128
6.

Genetic defects in ciliary structure and function.

Zariwala MA, Knowles MR, Omran H.

Annu Rev Physiol. 2007;69:423-50. Review.

PMID:
17059358
7.

Primary ciliary dyskinesia: clinical presentation, diagnosis and genetics.

Storm van's Gravesande K, Omran H.

Ann Med. 2005;37(6):439-49. Review.

PMID:
16203616
8.

Congenital Heart Disease and Primary Ciliary Dyskinesia.

Harrison MJ, Shapiro AJ, Kennedy MP.

Paediatr Respir Rev. 2016 Mar;18:25-32. doi: 10.1016/j.prrv.2015.09.003. Epub 2015 Sep 26. Review.

PMID:
26545972
9.

Nasal nitric oxide screening for primary ciliary dyskinesia: systematic review and meta-analysis.

Collins SA, Gove K, Walker W, Lucas JS.

Eur Respir J. 2014 Dec;44(6):1589-99. doi: 10.1183/09031936.00088614. Epub 2014 Oct 16. Review.

10.

The challenges of diagnosing primary ciliary dyskinesia.

Leigh MW, O'Callaghan C, Knowles MR.

Proc Am Thorac Soc. 2011 Sep;8(5):434-7. doi: 10.1513/pats.201103-028SD. Review.

11.

Primary ciliary dyskinesia.

Bush A.

Acta Otorhinolaryngol Belg. 2000;54(3):317-24. Review.

PMID:
11082768
12.

Primary ciliary dyskinesia: diagnosis and standards of care.

Bush A, Cole P, Hariri M, Mackay I, Phillips G, O'Callaghan C, Wilson R, Warner JO.

Eur Respir J. 1998 Oct;12(4):982-8. Review.

13.

[Primary ciliary dyskinesia: a retrospective review of clinical and paraclinical data].

Beucher J, Chambellan A, Segalen J, Deneuville E.

Rev Mal Respir. 2011 Sep;28(7):856-63. doi: 10.1016/j.rmr.2011.02.014. Epub 2011 Sep 3. Review. French.

PMID:
21943530
14.

Primary Ciliary Dyskinesia.

Zariwala MA, Knowles MR, Leigh MW.

In: Pagon RA, Adam MP, Ardinger HH, Wallace SE, Amemiya A, Bean LJH, Bird TD, Ledbetter N, Mefford HC, Smith RJH, Stephens K, editors. GeneReviews® [Internet]. Seattle (WA): University of Washington, Seattle; 1993-2017.
2007 Jan 24 [updated 2015 Sep 3].

15.

Gene mutations in primary ciliary dyskinesia related to otitis media.

Mata M, Milian L, Armengot M, Carda C.

Curr Allergy Asthma Rep. 2014 Mar;14(3):420. doi: 10.1007/s11882-014-0420-1. Review.

PMID:
24459089
16.

Primary Ciliary Dyskinesia.

Knowles MR, Zariwala M, Leigh M.

Clin Chest Med. 2016 Sep;37(3):449-61. doi: 10.1016/j.ccm.2016.04.008. Epub 2016 Jun 30. Review.

PMID:
27514592
17.

[Congenital ciliary dyskinesia. Focus].

Tamalet A, Blanchon S.

Rev Pneumol Clin. 2013 Aug;69(4):217-24. doi: 10.1016/j.pneumo.2013.05.007. Epub 2013 Jul 17. Review. French.

PMID:
23871404
18.

[Nasal ciliary investigations for the diagnosis of primary ciliary dyskinesia in children].

Escudier E, Roger G, Coste A.

Arch Pediatr. 2004 Apr;11(4):390-3. Review. French.

PMID:
15051102
19.

How insights from cardiovascular developmental biology have impacted the care of infants and children with congenital heart disease.

Chin AJ, Saint-Jeannet JP, Lo CW.

Mech Dev. 2012 Jul;129(5-8):75-97. doi: 10.1016/j.mod.2012.05.005. Epub 2012 May 26. Review.

20.

Xenopus as a model organism for birth defects-Congenital heart disease and heterotaxy.

Duncan AR, Khokha MK.

Semin Cell Dev Biol. 2016 Mar;51:73-9. doi: 10.1016/j.semcdb.2016.02.022. Epub 2016 Feb 22. Review.

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