List of works - Scott D Sagel

Assessment of airway microbiota and inflammation in cystic fibrosis using multiple sampling methods

scientific article

Changes in Airway Microbiome and Inflammation with Ivacaftor Treatment in Patients with Cystic Fibrosis and the G551D Mutation

scientific article published on 01 February 2020

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

scientific article published on 12 April 2016

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

scientific article

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

scientific article

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

scientific article published on 31 January 2011

Effect of VX-770 in persons with cystic fibrosis and the G551D-CFTR mutation

scientific article

Effects of an Antioxidant-enriched Multivitamin in Cystic Fibrosis: Randomized, Controlled, Multicenter Trial.

scientific article published on 24 April 2018

Exome sequencing identifies mutations in CCDC114 as a cause of primary ciliary dyskinesia

scientific article

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

scientific article

Mutations in CCDC39 and CCDC40 are the major cause of primary ciliary dyskinesia with axonemal disorganization and absent inner dynein arms

scientific article

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

scientific article published on March 2014

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

scientific article published on 19 September 2013

Population Genomics of <i>Mycobacterium abscessus</i> from U.S. Cystic Fibrosis Care Centers

scientific article published on 01 December 2021

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

scientific article published on 01 January 2019

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

scientific article published on December 2013

ZMYND10 is mutated in primary ciliary dyskinesia and interacts with LRRC6

scientific article

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

scientific article published on October 2013

List of works by Scott D Sagel

Assessment of airway microbiota and inflammation in cystic fibrosis using multiple sampling methods

Changes in Airway Microbiome and Inflammation with Ivacaftor Treatment in Patients with Cystic Fibrosis and the G551D Mutation

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

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

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

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

Effect of VX-770 in persons with cystic fibrosis and the G551D-CFTR mutation

Effects of an Antioxidant-enriched Multivitamin in Cystic Fibrosis: Randomized, Controlled, Multicenter Trial.

Exome sequencing identifies mutations in CCDC114 as a cause of primary ciliary dyskinesia

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

Mutations in CCDC39 and CCDC40 are the major cause of primary ciliary dyskinesia with axonemal disorganization and absent inner dynein arms

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

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

Population Genomics of <i>Mycobacterium abscessus</i> from U.S. Cystic Fibrosis Care Centers

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

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

ZMYND10 is mutated in primary ciliary dyskinesia and interacts with LRRC6

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