List of works - Margaret Rosenfeld

Age-related heterogeneity in dental caries and associated risk factors in individuals with cystic fibrosis ages 6-20 years: A pilot study

scientific article published on 10 July 2018

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

Cystic fibrosis pulmonary exacerbations

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

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

Multiple-Breath Washout as a Lung Function Test in Cystic Fibrosis. A Cystic Fibrosis Foundation Workshop Report

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

Preschool Multiple-Breath Washout Testing. An Official American Thoracic Society Technical Statement

scientific article published on 01 March 2018

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

scientific article published on 01 January 2019

Prospective evaluation of respiratory exacerbations in children with cystic fibrosis from newborn screening to 5 years of age.

scientific article

Pseudomonas acquisition in young patients with cystic fibrosis: pathophysiology, diagnosis, and management ⬇️

scientific article published on November 1, 2003

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 Margaret Rosenfeld

Age-related heterogeneity in dental caries and associated risk factors in individuals with cystic fibrosis ages 6-20 years: A pilot study

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

Cystic fibrosis pulmonary exacerbations

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.

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.

Multiple-Breath Washout as a Lung Function Test in Cystic Fibrosis. A Cystic Fibrosis Foundation Workshop Report

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

Preschool Multiple-Breath Washout Testing. An Official American Thoracic Society Technical Statement

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

Prospective evaluation of respiratory exacerbations in children with cystic fibrosis from newborn screening to 5 years of age.

Pseudomonas acquisition in young patients with cystic fibrosis: pathophysiology, diagnosis, and management ⬇️

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