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Items: 1 to 50 of 79

1.

Evaluation of the pulmonary radioaerosol mucociliary clearance scan as an adjunctive test for the diagnosis of primary ciliary dyskinesia in children.

Vali R, Ghandourah H, Charron M, Nezhad KV, Omarkhail Y, Khazaee A, Shammas A, Dell SD.

Pediatr Pulmonol. 2019 Sep 12. doi: 10.1002/ppul.24509. [Epub ahead of print]

PMID:
31512814
2.

Validation of pediatric health-related quality of life instruments for primary ciliary dyskinesia (QOL-PCD).

Behan L, Leigh MW, Dell SD, Quittner AL, Hogg C, Lucas JS.

Pediatr Pulmonol. 2019 Sep 1. doi: 10.1002/ppul.24507. [Epub ahead of print]

PMID:
31475479
3.

Neighborhood Material Deprivation Is Associated with Childhood Asthma Development: Analysis of Prospective Administrative Data.

Simons E, Dell SD, Moineddin R, To T.

Can Respir J. 2019 May 19;2019:6808206. doi: 10.1155/2019/6808206. eCollection 2019.

4.

Quantitative High-Speed Video Profiling Discriminates between DNAH11 and HYDIN Variants of Primary Ciliary Dyskinesia.

Chioccioli M, Feriani L, Nguyen Q, Kotar J, Dell SD, Mennella V, Amirav I, Cicuta P.

Am J Respir Crit Care Med. 2019 Jun 1;199(11):1436-1438. doi: 10.1164/rccm.201812-2256LE. No abstract available.

PMID:
31116566
5.

Understanding parent perceptions of healthy physical activity for their child with a chronic medical condition: A cross-sectional study.

McMullen JA, McCrindle BW, Dell SD, Feldman BM, Longmuir PE.

Paediatr Child Health. 2019 Jun;24(3):e135-e141. doi: 10.1093/pch/pxy122. Epub 2018 Oct 4.

PMID:
31110464
6.

AnnalsATS: New Developments and Advice for Authors.

Lederer DJ, Au DH, Cooke CR, Dell SD, Gould MK, Redline S, Kotloff RM.

Ann Am Thorac Soc. 2019 May;16(5):540-542. doi: 10.1513/AnnalsATS.201902-143ED. No abstract available.

PMID:
31042094
7.

Prolidase deficiency diagnosed by whole exome sequencing in a child with pulmonary capillaritis.

Rayment JH, Jobling R, Bowdin S, Cutz E, Dell SD.

ERJ Open Res. 2019 Apr 26;5(2). pii: 00205-2018. doi: 10.1183/23120541.00205-2018. eCollection 2019 Apr.

8.

Full-Term Neonatal Respiratory Distress and Chronic Lung Disease.

Chowdhury N, Giles BL, Dell SD.

Pediatr Ann. 2019 Apr 1;48(4):e175-e181. doi: 10.3928/19382359-20190328-01. Review.

PMID:
30986319
9.

Treatment of rituximab-associated chronic CNS enterovirus using IVIg and fluoxetine.

Sham L, Bitnun A, Branson H, Hazrati LN, Dell SD, Yeung RSM, Johnstone J, Yeh EA.

Neurology. 2019 May 7;92(19):916-918. doi: 10.1212/WNL.0000000000007468. Epub 2019 Apr 3. No abstract available.

PMID:
30944242
10.

Pediatric asthma: An unmet need for more effective, focused treatments.

Papadopoulos NG, Čustović A, Cabana MD, Dell SD, Deschildre A, Hedlin G, Hossny E, Le Souëf P, Matricardi PM, Nieto A, Phipatanakul W, Pitrez PM, Pohunek P, Gavornikova M, Jaumont X, Price DB.

Pediatr Allergy Immunol. 2019 Feb;30(1):7-16. doi: 10.1111/pai.12990. Epub 2018 Nov 15. Review.

11.

Severe disease due to CCDC40 gene variants and the perils of late diagnosis in primary ciliary dyskinesia.

Ghandourah H, Dell SD.

BMJ Case Rep. 2018 Sep 12;2018. pii: bcr-2018-224964. doi: 10.1136/bcr-2018-224964.

PMID:
30209139
12.

Primary Ciliary Dyskinesia: Longitudinal Study of Lung Disease by Ultrastructure Defect and Genotype.

Davis SD, Rosenfeld M, Lee HS, Ferkol TW, Sagel SD, Dell SD, Milla C, Pittman JE, Shapiro AJ, Sullivan KM, Nykamp KR, Krischer JP, Zariwala MA, Knowles MR, Leigh MW.

Am J Respir Crit Care Med. 2019 Jan 15;199(2):190-198. doi: 10.1164/rccm.201803-0548OC.

PMID:
30067075
13.

Analysis of pulmonary features and treatment approaches in the COPA syndrome.

Tsui JL, Estrada OA, Deng Z, Wang KM, Law CS, Elicker BM, Jones KD, Dell SD, Gudmundsson G, Hansdottir S, Helfgott SM, Volpi S, Gattorno M, Waterfield MR, Chan AY, Chung SA, Ley B, Shum AK.

ERJ Open Res. 2018 Jun 27;4(2). pii: 00017-2018. doi: 10.1183/23120541.00017-2018. eCollection 2018 Apr.

14.

Diagnosis of Primary Ciliary Dyskinesia. An Official American Thoracic Society Clinical Practice Guideline.

Shapiro AJ, Davis SD, Polineni D, Manion M, Rosenfeld M, Dell SD, Chilvers MA, Ferkol TW, Zariwala MA, Sagel SD, Josephson M, Morgan L, Yilmaz O, Olivier KN, Milla C, Pittman JE, Daniels MLA, Jones MH, Janahi IA, Ware SM, Daniel SJ, Cooper ML, Nogee LM, Anton B, Eastvold T, Ehrne L, Guadagno E, Knowles MR, Leigh MW, Lavergne V; American Thoracic Society Assembly on Pediatrics.

Am J Respir Crit Care Med. 2018 Jun 15;197(12):e24-e39. doi: 10.1164/rccm.201805-0819ST.

15.

Associations between Neighborhood Walkability and Incident and Ongoing Asthma in Children.

Simons E, Dell SD, Moineddin R, To T.

Ann Am Thorac Soc. 2018 Jun;15(6):728-734. doi: 10.1513/AnnalsATS.201708-693OC.

PMID:
29664674
16.

Primary ciliary dyskinesia: mechanisms and management.

Damseh N, Quercia N, Rumman N, Dell SD, Kim RH.

Appl Clin Genet. 2017 Sep 19;10:67-74. doi: 10.2147/TACG.S127129. eCollection 2017. Review.

17.

Tracheobronchomalacia in Neonates: The "New Bronchopulmonary Dysplasia" Is Not Just about the Alveoli.

Dell SD.

Ann Am Thorac Soc. 2017 Sep;14(9):1387-1388. doi: 10.1513/AnnalsATS.201706-507ED. No abstract available.

PMID:
28862496
18.

Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test.

Lionel AC, Costain G, Monfared N, Walker S, Reuter MS, Hosseini SM, Thiruvahindrapuram B, Merico D, Jobling R, Nalpathamkalam T, Pellecchia G, Sung WWL, Wang Z, Bikangaga P, Boelman C, Carter MT, Cordeiro D, Cytrynbaum C, Dell SD, Dhir P, Dowling JJ, Heon E, Hewson S, Hiraki L, Inbar-Feigenberg M, Klatt R, Kronick J, Laxer RM, Licht C, MacDonald H, Mercimek-Andrews S, Mendoza-Londono R, Piscione T, Schneider R, Schulze A, Silverman E, Siriwardena K, Snead OC, Sondheimer N, Sutherland J, Vincent A, Wasserman JD, Weksberg R, Shuman C, Carew C, Szego MJ, Hayeems RZ, Basran R, Stavropoulos DJ, Ray PN, Bowdin S, Meyn MS, Cohn RD, Scherer SW, Marshall CR.

Genet Med. 2018 Apr;20(4):435-443. doi: 10.1038/gim.2017.119. Epub 2017 Aug 3.

19.

The PD20 but not the PC20 in a methacholine challenge test is device independent.

Coates AL, Dell SD, Cockcroft DW, Gauvreau GM.

Ann Allergy Asthma Immunol. 2017 Apr;118(4):508-509. doi: 10.1016/j.anai.2017.01.010. Epub 2017 Mar 6. No abstract available.

PMID:
28274734
20.

Concomitant Diffuse Alveolar Hemorrhage and Pulmonary Embolism in a Child with Isolated Pulmonary Capillaritis.

Rayment JH, Cutz E, Levy DM, Dell SD.

Ann Am Thorac Soc. 2017 Mar;14(3):470-473. doi: 10.1513/AnnalsATS.201610-783LE. No abstract available.

PMID:
28248576
21.

Validation of a health-related quality of life instrument for primary ciliary dyskinesia (QOL-PCD).

Behan L, Leigh MW, Dell SD, Dunn Galvin A, Quittner AL, Lucas JS.

Thorax. 2017 Sep;72(9):832-839. doi: 10.1136/thoraxjnl-2016-209356. Epub 2017 Feb 28.

22.

Misdiagnosis of asthma in schoolchildren.

Yang CL, Simons E, Foty RG, Subbarao P, To T, Dell SD.

Pediatr Pulmonol. 2017 Mar;52(3):293-302. doi: 10.1002/ppul.23541. Epub 2016 Aug 9.

PMID:
27505297
23.

Clinical manifestations in primary ciliary dyskinesia: systematic review and meta-analysis.

Goutaki M, Meier AB, Halbeisen FS, Lucas JS, Dell SD, Maurer E, Casaulta C, Jurca M, Spycher BD, Kuehni CE.

Eur Respir J. 2016 Oct;48(4):1081-1095. doi: 10.1183/13993003.00736-2016. Epub 2016 Aug 4. Review.

24.

Primary Ciliary Dyskinesia: First Health-related Quality-of-Life Measures for Pediatric Patients.

Dell SD, Leigh MW, Lucas JS, Ferkol TW, Knowles MR, Alpern A, Behan L, Morris AM, Hogg C, DunnGalvin A, Quittner AL.

Ann Am Thorac Soc. 2016 Oct;13(10):1726-1735.

25.

Clinical Features and Associated Likelihood of Primary Ciliary Dyskinesia in Children and Adolescents.

Leigh MW, Ferkol TW, Davis SD, Lee HS, Rosenfeld M, Dell SD, Sagel SD, Milla C, Olivier KN, Sullivan KM, Zariwala MA, Pittman JE, Shapiro AJ, Carson JL, Krischer J, Hazucha MJ, Knowles MR.

Ann Am Thorac Soc. 2016 Aug;13(8):1305-13. doi: 10.1513/AnnalsATS.201511-748OC.

26.

Treatment recommendations in Primary Ciliary Dyskinesia.

Polineni D, Davis SD, Dell SD.

Paediatr Respir Rev. 2016 Mar;18:39-45. doi: 10.1016/j.prrv.2015.10.002. Epub 2015 Oct 20. Review.

PMID:
26586601
27.

Diagnosis and management of asthma in preschoolers: A Canadian Thoracic Society and Canadian Paediatric Society position paper.

Ducharme FM, Dell SD, Radhakrishnan D, Grad RM, Watson WT, Yang CL, Zelman M.

Paediatr Child Health. 2015 Oct;20(7):353-71. English, French.

28.

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. Epub 2015 Sep 29. Review.

29.

Whole-Exome Sequencing and Targeted Copy Number Analysis in Primary Ciliary Dyskinesia.

Marshall CR, Scherer SW, Zariwala MA, Lau L, Paton TA, Stockley T, Jobling RK, Ray PN, Knowles MR; FORGE Canada Consortium, Hall DA, Dell SD, Kim RH.

G3 (Bethesda). 2015 Jul 2;5(8):1775-81. doi: 10.1534/g3.115.019851.

30.

Spatial analysis of exposure to traffic-related air pollution at birth and childhood atopic asthma in Toronto, Ontario.

Shankardass K, Jerrett M, Dell SD, Foty R, Stieb D.

Health Place. 2015 Jul;34:287-95. doi: 10.1016/j.healthplace.2015.06.001. Epub 2015 Jun 26.

PMID:
26119253
31.

COPA mutations impair ER-Golgi transport and cause hereditary autoimmune-mediated lung disease and arthritis.

Watkin LB, Jessen B, Wiszniewski W, Vece TJ, Jan M, Sha Y, Thamsen M, Santos-Cortez RL, Lee K, Gambin T, Forbes LR, Law CS, Stray-Pedersen A, Cheng MH, Mace EM, Anderson MS, Liu D, Tang LF, Nicholas SK, Nahmod K, Makedonas G, Canter DL, Kwok PY, Hicks J, Jones KD, Penney S, Jhangiani SN, Rosenblum MD, Dell SD, Waterfield MR, Papa FR, Muzny DM, Zaitlen N, Leal SM, Gonzaga-Jauregui C; Baylor-Hopkins Center for Mendelian Genomics, Boerwinkle E, Eissa NT, Gibbs RA, Lupski JR, Orange JS, Shum AK.

Nat Genet. 2015 Jun;47(6):654-60. doi: 10.1038/ng.3279. Epub 2015 Apr 20.

32.

Diagnosis and management of asthma in preschoolers: A Canadian Thoracic Society and Canadian Paediatric Society position paper.

Ducharme FM, Dell SD, Radhakrishnan D, Grad RM, Watson WT, Yang CL, Zelman M.

Can Respir J. 2015 May-Jun;22(3):135-43. Epub 2015 Apr 20. Erratum in: Paediatr Child Health. 2015 Oct;20(7):361. Can Respir J. 2015 Nov-Dec;22(6):348.

33.

Prediction of childhood atopy by questionnaire.

Simons E, Kwon S, Yang C, Dell SD.

Clin Exp Allergy. 2015 Apr;45(4):835-7. doi: 10.1111/cea.12510. No abstract available.

PMID:
25678339
34.

Provocative dose of methacholine causing a 20% drop in FEV1 should be used to interpret methacholine challenge tests with modern nebulizers.

Dell SD, Bola SS, Foty RG, Marshall LC, Nelligan KA, Coates AL.

Ann Am Thorac Soc. 2015 Mar;12(3):357-63. doi: 10.1513/AnnalsATS.201409-433OC.

PMID:
25575246
35.

Clinical features of childhood primary ciliary dyskinesia by genotype and ultrastructural phenotype.

Davis SD, Ferkol TW, Rosenfeld M, Lee HS, Dell SD, Sagel SD, Milla C, Zariwala MA, Pittman JE, Shapiro AJ, Carson JL, Krischer JP, Hazucha MJ, Cooper ML, Knowles MR, Leigh MW.

Am J Respir Crit Care Med. 2015 Feb 1;191(3):316-24. doi: 10.1164/rccm.201409-1672OC.

36.

Asthma deaths in a large provincial health system. A 10-year population-based study.

To T, Simatovic J, Zhu J, Feldman L, Dell SD, Lougheed MD, Licskai C, Gershon A.

Ann Am Thorac Soc. 2014 Oct;11(8):1210-7. doi: 10.1513/AnnalsATS.201404-138OC.

PMID:
25166217
37.

Trends in the age of diagnosis of childhood asthma.

Radhakrishnan DK, Dell SD, Guttmann A, Shariff SZ, Liu K, To T.

J Allergy Clin Immunol. 2014 Nov;134(5):1057-62.e5. doi: 10.1016/j.jaci.2014.05.012. Epub 2014 Jun 27.

PMID:
24985402
38.

Maternal second-hand smoke exposure in pregnancy is associated with childhood asthma development.

Simons E, To T, Moineddin R, Stieb D, Dell SD.

J Allergy Clin Immunol Pract. 2014 Mar-Apr;2(2):201-7. doi: 10.1016/j.jaip.2013.11.014.

PMID:
24607049
39.

Laterality defects other than situs inversus totalis in primary ciliary dyskinesia: insights into situs ambiguus and heterotaxy.

Shapiro AJ, Davis SD, Ferkol T, Dell SD, Rosenfeld M, Olivier KN, Sagel SD, Milla C, Zariwala MA, Wolf W, Carson JL, Hazucha MJ, Burns K, Robinson B, Knowles MR, Leigh MW; Genetic Disorders of Mucociliary Clearance Consortium.

Chest. 2014 Nov;146(5):1176-1186. doi: 10.1378/chest.13-1704.

40.

Mutations in RSPH1 cause primary ciliary dyskinesia with a unique clinical and ciliary phenotype.

Knowles MR, Ostrowski LE, Leigh MW, Sears PR, Davis SD, Wolf WE, Hazucha MJ, Carson JL, Olivier KN, Sagel SD, Rosenfeld M, Ferkol TW, Dell SD, Milla CE, Randell SH, Yin W, Sannuti A, Metjian HM, Noone PG, Noone PJ, Olson CA, Patrone MV, Dang H, Lee HS, Hurd TW, Gee HY, Otto EA, Halbritter J, Kohl S, Kircher M, Krischer J, Bamshad MJ, Nickerson DA, Hildebrandt F, Shendure J, Zariwala MA.

Am J Respir Crit Care Med. 2014 Mar 15;189(6):707-17. doi: 10.1164/rccm.201311-2047OC.

41.

The role of molecular genetic analysis in the diagnosis of primary ciliary dyskinesia.

Kim RH, A Hall D, Cutz E, Knowles MR, Nelligan KA, Nykamp K, Zariwala MA, Dell SD.

Ann Am Thorac Soc. 2014 Mar;11(3):351-9. doi: 10.1513/AnnalsATS.201306-194OC.

42.

Presence of other allergic disease modifies the effect of early childhood traffic-related air pollution exposure on asthma prevalence.

Dell SD, Jerrett M, Beckerman B, Brook JR, Foty RG, Gilbert NL, Marshall L, Miller JD, To T, Walter SD, Stieb DM.

Environ Int. 2014 Apr;65:83-92. doi: 10.1016/j.envint.2014.01.002. Epub 2014 Jan 25.

PMID:
24472824
43.

Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia.

Austin-Tse C, Halbritter J, Zariwala MA, Gilberti RM, Gee HY, Hellman N, Pathak N, Liu Y, Panizzi JR, Patel-King RS, Tritschler D, Bower R, O'Toole E, Porath JD, Hurd TW, Chaki M, Diaz KA, Kohl S, Lovric S, Hwang DY, Braun DA, Schueler M, Airik R, Otto EA, Leigh MW, Noone PG, Carson JL, Davis SD, Pittman JE, Ferkol TW, Atkinson JJ, Olivier KN, Sagel SD, Dell SD, Rosenfeld M, Milla CE, Loges NT, Omran H, Porter ME, King SM, Knowles MR, Drummond IA, Hildebrandt F.

Am J Hum Genet. 2013 Oct 3;93(4):672-86. doi: 10.1016/j.ajhg.2013.08.015.

44.

Mutations in SPAG1 cause primary ciliary dyskinesia associated with defective outer and inner dynein arms.

Knowles MR, Ostrowski LE, Loges NT, Hurd T, Leigh MW, Huang L, Wolf WE, Carson JL, Hazucha MJ, Yin W, Davis SD, Dell SD, Ferkol TW, Sagel SD, Olivier KN, Jahnke C, Olbrich H, Werner C, Raidt J, Wallmeier J, Pennekamp P, Dougherty GW, Hjeij R, Gee HY, Otto EA, Halbritter J, Chaki M, Diaz KA, Braun DA, Porath JD, Schueler M, Baktai G, Griese M, Turner EH, Lewis AP, Bamshad MJ, Nickerson DA, Hildebrandt F, Shendure J, Omran H, Zariwala MA.

Am J Hum Genet. 2013 Oct 3;93(4):711-20. doi: 10.1016/j.ajhg.2013.07.025. Epub 2013 Sep 19.

45.

Standardizing nasal nitric oxide measurement as a test for primary ciliary dyskinesia.

Leigh MW, Hazucha MJ, Chawla KK, Baker BR, Shapiro AJ, Brown DE, Lavange LM, Horton BJ, Qaqish B, Carson JL, Davis SD, Dell SD, Ferkol TW, Atkinson JJ, Olivier KN, Sagel SD, Rosenfeld M, Milla C, Lee HS, Krischer J, Zariwala MA, Knowles MR.

Ann Am Thorac Soc. 2013 Dec;10(6):574-81. doi: 10.1513/AnnalsATS.201305-110OC.

46.

ZMYND10 is mutated in primary ciliary dyskinesia and interacts with LRRC6.

Zariwala MA, Gee HY, Kurkowiak M, Al-Mutairi DA, Leigh MW, Hurd TW, Hjeij R, Dell SD, Chaki M, Dougherty GW, Adan M, Spear PC, Esteve-Rudd J, Loges NT, Rosenfeld M, Diaz KA, Olbrich H, Wolf WE, Sheridan E, Batten TF, Halbritter J, Porath JD, Kohl S, Lovric S, Hwang DY, Pittman JE, Burns KA, Ferkol TW, Sagel SD, Olivier KN, Morgan LC, Werner C, Raidt J, Pennekamp P, Sun Z, Zhou W, Airik R, Natarajan S, Allen SJ, Amirav I, Wieczorek D, Landwehr K, Nielsen K, Schwerk N, Sertic J, Köhler G, Washburn J, Levy S, Fan S, Koerner-Rettberg C, Amselem S, Williams DS, Mitchell BJ, Drummond IA, Otto EA, Omran H, Knowles MR, Hildebrandt F.

Am J Hum Genet. 2013 Aug 8;93(2):336-45. doi: 10.1016/j.ajhg.2013.06.007. Epub 2013 Jul 25.

47.

Variable clinical outcome of ABCA3 deficiency in two siblings.

Thavagnanam S, Cutz E, Manson D, Nogee LM, Dell SD.

Pediatr Pulmonol. 2013 Oct;48(10):1035-8. doi: 10.1002/ppul.22698. Epub 2013 Jul 2. Review.

PMID:
23818309
48.

Founder mutation in RSPH4A identified in patients of Hispanic descent with primary ciliary dyskinesia.

Daniels ML, Leigh MW, Davis SD, Armstrong MC, Carson JL, Hazucha M, Dell SD, Eriksson M, Collins FS, Knowles MR, Zariwala MA.

Hum Mutat. 2013 Oct;34(10):1352-6. doi: 10.1002/humu.22371. Epub 2013 Aug 6.

49.

Developing alternative delivery systems for methacholine challenge tests.

Coates AL, Leung K, Dell SD.

J Aerosol Med Pulm Drug Deliv. 2014 Feb;27(1):66-70. doi: 10.1089/jamp.2013.1036. Epub 2013 Apr 15.

PMID:
23586502
50.

Severe lung injury and lung biopsy in children post-hematopoietic stem cell transplantation: The differences between allogeneic and autologous transplantation.

Gassas A, Craig-Barnes H, Dell SD, Cox P, Schechter T, Doyle J, Sung L, Egeler M, Palaniyar N.

Pediatr Transplant. 2013 May;17(3):278-84. doi: 10.1111/petr.12060. Epub 2013 Mar 6.

PMID:
23461864

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