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Items: 19

1.

Diagnostic yield of nasal scrape biopsies in primary ciliary dyskinesia: a multicenter experience.

Olin JT, Burns K, Carson JL, Metjian H, Atkinson JJ, Davis SD, Dell SD, Ferkol TW, Milla CE, Olivier KN, Rosenfeld M, Baker B, Leigh MW, Knowles MR, Sagel SD; Genetic Disorders of Mucociliary Clearance Consortium..

Pediatr Pulmonol. 2011 May;46(5):483-8. doi: 10.1002/ppul.21402.

2.

[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
3.

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.

4.

[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. Review. French.

PMID:
21943530
5.

[Primary ciliary dyskinesia in highlights of consensus statement. Presentation of pediatric cases].

Cichocka-Jarosz E, Jedynak-Wasowicz U, Głodzik I, Lis G, Pietrzyk JJ.

Przegl Lek. 2010;67(2):135-40. Polish.

PMID:
20557016
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.

Genet Med. 2009 Jul;11(7):473-87. doi: 10.1097/GIM.0b013e3181a53562. Review.

7.

Up to date on primary ciliary dyskinesia in children.

Pifferi M, Di Cicco M, Piras M, Cangiotti AM, Saggese G.

Early Hum Dev. 2013 Oct;89 Suppl 3:S45-8. doi: 10.1016/j.earlhumdev.2013.07.022. Review.

PMID:
23973004
8.

[How useful is the ultrastructural study of the cilia of the respiratory tract in the diagnosis of an immotile cilia syndrome?].

Fischer L, Burri PH, Bauer W, Kraemer R, Sauter K.

Schweiz Med Wochenschr. 1984 May 5;114(18):610-9. Review. German.

PMID:
6374886
9.

Recent advances in primary ciliary dyskinesia genetics.

Kurkowiak M, Ziętkiewicz E, Witt M.

J Med Genet. 2015 Jan;52(1):1-9. doi: 10.1136/jmedgenet-2014-102755. Review.

10.

Transmission electron microscopy in the diagnosis of primary ciliary dyskinesia.

Roomans GM, Ivanovs A, Shebani EB, Johannesson M.

Ups J Med Sci. 2006;111(1):155-68. Review.

PMID:
16553254
11.

Nasal versus tracheobronchial biopsies to diagnose primary ciliary dyskinesia: A meta-analysis.

Adil EA, Kawai K, Dombrowski N, Irace AL, Cunningham MJ.

Laryngoscope. 2017 Jan;127(1):6-13. doi: 10.1002/lary.26070. Review.

PMID:
27312809
12.

[Primary ciliary dyskinesia, immotile cilia syndrome, and Kartagener syndrome: diagnostic criteria].

Dombi VH, Walt H.

Schweiz Med Wochenschr. 1996 Mar 16;126(11):421-33. Review. German.

PMID:
8643941
13.

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.

14.

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

Knowles MR, Daniels LA, Davis SD, Zariwala MA, Leigh MW.

Am J Respir Crit Care Med. 2013 Oct 15;188(8):913-22. doi: 10.1164/rccm.201301-0059CI. Review.

15.

The emerging genetics of primary ciliary dyskinesia.

Zariwala MA, Omran H, Ferkol TW.

Proc Am Thorac Soc. 2011 Sep;8(5):430-3. doi: 10.1513/pats.201103-023SD. Review.

16.

Diagnosis and management of primary ciliary dyskinesia.

Lucas JS, Burgess A, Mitchison HM, Moya E, Williamson M, Hogg C; National PCD Service, UK..

Arch Dis Child. 2014 Sep;99(9):850-6. doi: 10.1136/archdischild-2013-304831. Review.

17.

Primary ciliary dyskinesia: a review.

Carlén B, Stenram U.

Ultrastruct Pathol. 2005 May-Aug;29(3-4):217-20. Review.

PMID:
16036877
18.

Primary ciliary dyskinesia.

Lobo J, Zariwala MA, Noone PG.

Semin Respir Crit Care Med. 2015 Apr;36(2):169-79. doi: 10.1055/s-0035-1546748. Review.

19.

Diagnosis, monitoring, and treatment of primary ciliary dyskinesia: PCD foundation consensus recommendations based on state of the art review.

Shapiro AJ, Zariwala MA, Ferkol T, Davis SD, Sagel SD, Dell SD, Rosenfeld M, Olivier KN, Milla C, Daniel SJ, Kimple AJ, Manion M, Knowles MR, Leigh MW; Genetic Disorders of Mucociliary Clearance Consortium..

Pediatr Pulmonol. 2016 Feb;51(2):115-32. doi: 10.1002/ppul.23304. Review.

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