Diagnosis, monitoring, and treatment of primary ciliary dyskinesia: PCD foundation consensus recommendations based on state of the art review-Reference-Cited by-同舟云学术

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

Published:2015-09-29 Issue:2 Volume:51 Page:115-132
ISSN:8755-6863
Container-title:Pediatric Pulmonology
language:en
Short-container-title:Pediatr Pulmonol.

Author:

Shapiro Adam J.¹,Zariwala Maimoona A.²,Ferkol Thomas³,Davis Stephanie D.⁴,Sagel Scott D.⁵,Dell Sharon D.⁶,Rosenfeld Margaret⁷,Olivier Kenneth N.⁸,Milla Carlos⁹,Daniel Sam J.¹⁰,Kimple Adam J.¹¹,Manion Michele¹²,Knowles Michael R.¹³,Leigh Margaret W.¹⁴,

Affiliation:

1. Department of PediatricsMontreal Children's HospitalMcGill UniversityQuebecCanada

2. Department of Pathology and Laboratory Medicine, University of North Carolina School of MedicineMarsico Lung InstituteChapel HillNorth Carolina

3. Department of PediatricsWashington University School of MedicineSt. LouisMissouri

4. Department of Pediatrics, Riley Hospital for ChildrenIndiana UniversityIndianapolisIndiana

5. Department of PediatricsChildren's Hospital Colorado and University of Colorado School of MedicineAuroraColorado

6. Department of PediatricsThe Hospital for Sick Children and University of TorontoTorontoOntarioCanada

7. Department of PediatricsSeattle Children's Hospital and University of WashingtonSeattleWashington

8. National Heart, Lung, and Blood InstituteBethesdaMaryland

9. Department of PediatricsStanford UniversityPalo AltoCalifornia

10. Department of Otolaryngology, Montreal Children's HospitalMcGill UniversityMontrealQuebecCanada

11. Department of Otolaryngology—Head and Neck SurgeryUniversity of North Carolina School of MedicineChapel HillNorth Carolina

12. The PCD Foundation—PresidentMinneapolisMinnesota

13. Department of MedicineUniversity of North Carolina, Marsico Lung InstituteChapel HillNorth Carolina

14. Department of PediatricsUniversity of North Carolina, Marsico Lung InstituteChapel HillNorth Carolina

Funder

National Institutes of Health

The Genetic Disorders of Mucociliary Clearance

Office of Rare Diseases Research (ORDR), NCATS, funded through a collaboration between NCATS and NHLBI

CTSA NIH/NCATS UNC

CTSA NIH/NCATS Colorado

Intramural Research Program of NIH/NIAID

Publisher

Wiley

Subject

Pulmonary and Respiratory Medicine,Pediatrics, Perinatology and Child Health

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/ppul.23304

Reference164 articles.

1. Clinical Features of Childhood Primary Ciliary Dyskinesia by Genotype and Ultrastructural Phenotype

2. Longitudinal lung function and structural changes in children with primary ciliary dyskinesia

3. Lung Function in Patients with Primary Ciliary Dyskinesia

4. Primary Ciliary Dyskinesia. Recent Advances in Diagnostics, Genetics, and Characterization of Clinical Disease

5. The Challenges of Diagnosing Primary Ciliary Dyskinesia

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