about
Mutations of DNAH11 in patients with primary ciliary dyskinesia with normal ciliary ultrastructureCongenital heart disease and other heterotaxic defects in a large cohort of patients with primary ciliary dyskinesiaExome sequencing identifies mutations in CCDC114 as a cause of primary ciliary dyskinesiaZMYND10 is mutated in primary ciliary dyskinesia and interacts with LRRC6Diagnosis, monitoring, and treatment of primary ciliary dyskinesia: PCD foundation consensus recommendations based on state of the art reviewFounder mutation in RSPH4A identified in patients of Hispanic descent with primary ciliary dyskinesiaThe role of molecular genetic analysis in the diagnosis of primary ciliary dyskinesiaVerifying a questionnaire diagnosis of asthma in children using health claims data.Exploring variation and predictors of residential fine particulate matter infiltration.Do questions reflecting indoor air pollutant exposure from a questionnaire predict direct measure of exposure in owner-occupied houses?Laterality defects other than situs inversus totalis in primary ciliary dyskinesia: insights into situs ambiguus and heterotaxy.Primary ciliary dyskinesia and neonatal respiratory distress.Diffuse lung disease in young children: application of a novel classification scheme.Clinical features of childhood primary ciliary dyskinesia by genotype and ultrastructural phenotypeUpdate of respiratory tract disease in children with primary ciliary dyskinesia.Parents and adolescents preferences for asthma control: a best-worst scaling choice experiment using an orthogonal main effects design.COPA mutations impair ER-Golgi transport and cause hereditary autoimmune-mediated lung disease and arthritisWhole-Exome Sequencing and Targeted Copy Number Analysis in Primary Ciliary Dyskinesia.Health risk of air pollution on people living with major chronic diseases: a Canadian population-based studyCase verification of children with asthma in Ontario.A new exposure metric for traffic-related air pollution? An analysis of determinants of hopanes in settled indoor house dust.Mutations in SPAG1 cause primary ciliary dyskinesia associated with defective outer and inner dynein arms.Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia.Diagnostic yield of nasal scrape biopsies in primary ciliary dyskinesia: a multicenter experience.Primary Ciliary Dyskinesia: First Health-related Quality-of-Life Measures for Pediatric Patients.An evaluation of pediatric asthma educational resources.Standardizing nasal nitric oxide measurement as a test for primary ciliary dyskinesia.Mutations in RSPH1 cause primary ciliary dyskinesia with a unique clinical and ciliary phenotype.Evidence-based performance indicators of primary care for asthma: a modified RAND Appropriateness Method.Middle ear ventilation in children with primary ciliary dyskinesia.Treatment recommendations in Primary Ciliary Dyskinesia.Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test.European Respiratory Society guidelines for the diagnosis of primary ciliary dyskinesia.Clinical manifestations in primary ciliary dyskinesia: systematic review and meta-analysis.Asthma deaths in a large provincial health system. A 10-year population-based study.Frequency of health service use in the year prior to asthma death.Predictors of universal influenza vaccination uptake in grades 1 and 2 Toronto school children: effective vaccination strategies should not end with at risk children.Clinical Features and Associated Likelihood of Primary Ciliary Dyskinesia in Children and Adolescents.Can an evidence-based guideline reminder card improve asthma management in the emergency department?The Annual September Peak in Asthma Exacerbation Rates. Still a Reality?
P50
Q24300203-8DB95367-C3EE-4CCE-87A0-C3AF9A0F46E9Q24306479-25717982-473A-4654-8CA8-78106AD082AAQ24306705-781C90B2-E220-4E03-919C-352066DABCEAQ24312017-0FF8BFBA-26F0-4F66-BCC0-A8C0B518BF1AQ28082500-1002221C-D516-4579-A175-83093DADFDB3Q30570040-1DF18265-3991-48AD-832B-CCCAF99DA35DQ33640482-94BFBEEF-841D-486A-BC1D-90439A8D0DA2Q34080380-3F3FA9D7-EFB4-488F-9964-B9CB80A5BD77Q34196912-FCB50BC0-3CA2-4706-B190-E5CA9CFB43FCQ34196938-170CE257-3FF7-4C91-866B-429824D11F4CQ34448317-7C6EEA2C-0075-4710-86B3-DFC305EA2F3DQ34567706-E432D42A-C1CE-4846-9B50-133A13760F91Q34691602-E6A64F49-60AD-48A6-AAAD-F4294EA49E03Q35153440-E2EAEED8-BA6F-47E2-BECB-F338D04DDB54Q35532206-BA6D26CD-E937-4C32-B556-9BB12A8E4669Q35844409-000116E0-FDEC-4FAF-8064-CF80673FEEE3Q35885484-DDCE0DDB-D12B-44AD-A560-B6F8D43FF768Q35926452-E0C6562D-A134-4D5E-8201-72193A77A7C0Q36039115-E4F60E66-F68F-44CC-B178-24DDB484BA23Q36373550-D78346B0-5B84-4BFD-ABA4-AD995D28680EQ37014515-974232C0-5D58-4697-A2CB-8DA9814E9647Q37217004-8ADB0F89-3668-4D6C-B440-BB7D09BF2681Q37217054-12818AE4-E953-48CD-A910-DC8ABBD65ED3Q37419986-B6967DD7-F3E9-459E-981B-DA2B2B8DBDA5Q37437823-AAB69785-CF1D-475E-99E2-844ADC2E3118Q37461057-7C1999C3-15EB-4FF1-B461-B2FF1F56E618Q37651731-BD7B3258-9E74-4B74-820A-76B074C7D7CBQ37698245-2927D952-53C4-469C-BC93-76E9434D35FFQ37803296-D51B68C3-6B5F-42D9-8065-1E178CDB8CF3Q38033809-E5723BAD-F1F7-46B6-A835-4B80AED62CDAQ38639614-B41D7934-549D-473E-8E00-85012756A1D7Q38644619-9ED7ECD1-44B7-433B-BA8A-90170FBB9103Q38796206-0A2981CE-F716-45CE-84FF-17900FC21A83Q38919154-D59B238A-B081-4A32-822D-E3967E6E34D1Q39138475-3BE7E580-FF02-4BEA-BF8D-4CF7BEE9212CQ39788704-4D49F8AD-B593-4A53-956A-A91935047DDAQ39854100-6838F857-2D10-480F-958E-B13D3D38B518Q39857217-DE0904BD-E4A3-490F-BDB7-E1DCDC7956F6Q39877492-B6A6AEEE-8C99-4D2B-BD3E-F851124B7316Q40242755-57A60108-D3BE-4D5E-BE7E-D641218C5FCD
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Sharon D Dell
@nl
Sharon D Dell
@sl
Sharon D. Dell
@en
Sharon D. Dell
@es
type
label
Sharon D Dell
@nl
Sharon D Dell
@sl
Sharon D. Dell
@en
Sharon D. Dell
@es
prefLabel
Sharon D Dell
@nl
Sharon D Dell
@sl
Sharon D. Dell
@en
Sharon D. Dell
@es
P106
P1153
7003653592
P31
P496
0000-0003-2169-9407