Sharon Dell
Sharon Dell
Full Professor, Department of Pediatrics, The Hospital for Sick Children, University of Toronto
Verified email at - Homepage
Cited by
Cited by
Clinical and genetic aspects of primary ciliary dyskinesia/Kartagener syndrome
MW Leigh, JE Pittman, JL Carson, TW Ferkol, SD Dell, SD Davis, ...
Genetics in Medicine 11 (7), 473-487, 2009
Diffuse lung disease in young children: application of a novel classification scheme
GH Deutsch, LR Young, RR Deterding, LL Fan, SD Dell, JA Bean, ...
American journal of respiratory and critical care medicine 176 (11), 1120-1128, 2007
MP Kennedy, H Omran, MW Leigh, S Dell, L Morgan, PL Molina, ...
Circulation 115 (22), 2814-2821, 2007
Impact of maternal intrapartum antibiotics, method of birth and breastfeeding on gut microbiota during the first year of life: a prospective cohort study
MB Azad, T Konya, RR Persaud, DS Guttman, RS Chari, CJ Field, ...
BJOG: An International Journal of Obstetrics & Gynaecology 123 (6), 983-993, 2016
Canadian Thoracic Society 2012 guideline update: diagnosis and management of asthma in preschoolers, children and adults
MD Lougheed, C Lemiere, FM Ducharme, C Licskai, SD Dell, BH Rowe, ...
Canadian respiratory journal 19, 2012
An official American Thoracic Society clinical practice guideline: classification, evaluation, and management of childhood interstitial lung disease in infancy
G Kurland, RR Deterding, JS Hagood, LR Young, AS Brody, RG Castile, ...
American journal of respiratory and critical care medicine 188 (3), 376-394, 2013
European Respiratory Society guidelines for the diagnosis of primary ciliary dyskinesia
JS Lucas, A Barbato, SA Collins, M Goutaki, L Behan, D Caudri, S Dell, ...
European Respiratory Journal 49 (1), 2017
Canadian Thoracic Society Asthma Management Continuum–2010 Consensus Summary for children six years of age and over, and adults
MD Lougheed, C Lemière, SD Dell, FM Ducharme, JM FitzGerald, ...
Canadian Respiratory Journal 17, 2010
Standardizing nasal nitric oxide measurement as a test for primary ciliary dyskinesia
MW Leigh, MJ Hazucha, KK Chawla, BR Baker, AJ Shapiro, DE Brown, ...
Annals of the American Thoracic Society 10 (6), 574-581, 2013
Diagnosis, monitoring, and treatment of primary ciliary dyskinesia: PCD foundation consensus recommendations based on state of the art review
AJ Shapiro, MA Zariwala, T Ferkol, SD Davis, SD Sagel, SD Dell, ...
Pediatric pulmonology 51 (2), 115-132, 2016
Mutations of DNAH11 in patients with primary ciliary dyskinesia with normal ciliary ultrastructure
MR Knowles, MW Leigh, JL Carson, SD Davis, SD Dell, TW Ferkol, ...
Thorax 67 (5), 433-441, 2012
Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test
AC Lionel, G Costain, N Monfared, S Walker, MS Reuter, SM Hosseini, ...
Genetics in Medicine 20 (4), 435-443, 2018
Zebrafish ciliopathy screen plus human mutational analysis identifies C21orf59 and CCDC65 defects as causing primary ciliary dyskinesia
C Austin-Tse, J Halbritter, MA Zariwala, RM Gilberti, HY Gee, N Hellman, ...
The American Journal of Human Genetics 93 (4), 672-686, 2013
Breastfeeding and asthma in young children: findings from a population-based study
S Dell, T To
Archives of pediatrics & adolescent medicine 155 (11), 1261-1265, 2001
Clinical features of childhood primary ciliary dyskinesia by genotype and ultrastructural phenotype
SD Davis, TW Ferkol, M Rosenfeld, HS Lee, SD Dell, SD Sagel, C Milla, ...
American journal of respiratory and critical care medicine 191 (3), 316-324, 2015
ZMYND10 is mutated in primary ciliary dyskinesia and interacts with LRRC6
MA Zariwala, HY Gee, M Kurkowiak, DA Al-Mutairi, MW Leigh, TW Hurd, ...
The American Journal of Human Genetics 93 (2), 336-345, 2013
Is obesity associated with asthma in young children?
T To, TN Vydykhan, S Dell, M Tassoudji, JK Harris
The Journal of pediatrics 144 (2), 162-168, 2004
Mutations in RSPH1 cause primary ciliary dyskinesia with a unique clinical and ciliary phenotype
MR Knowles, LE Ostrowski, MW Leigh, PR Sears, SD Davis, WE Wolf, ...
American journal of respiratory and critical care medicine 189 (6), 707-717, 2014
COPA mutations impair ER-Golgi transport and cause hereditary autoimmune-mediated lung disease and arthritis
LB Watkin, B Jessen, W Wiszniewski, TJ Vece, M Jan, Y Sha, M Thamsen, ...
Nature genetics 47 (6), 654-660, 2015
Laterality defects other than situs inversus totalis in primary ciliary dyskinesia: insights into situs ambiguus and heterotaxy
AJ Shapiro, SD Davis, T Ferkol, SD Dell, M Rosenfeld, KN Olivier, ...
Chest 146 (5), 1176-1186, 2014
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