Zobrazeno 1 - 10
of 127
pro vyhledávání: '"Peter J, Mogayzel"'
Autor:
Shelby R. Sferra, Melanie K. Nies, Jena L. Miller, Alejandro V. Garcia, Erica I. Hodgman, Annalise B. Penikis, Abigail J. Engwall-Gill, Vera Joanna Burton, Jessica L. Rice, Peter J. Mogayzel, Ahmet A. Baschat, Shaun M. Kunisaki
Publikováno v:
Journal of Pediatric Surgery. 58:14-19
Although fetoscopic endoluminal tracheal occlusion (FETO) was recently shown to improve survival in a multicenter, randomized trial of severe congenital diaphragmatic hernia (CDH), morbidity outcomes remain essentially unknown. The purpose of this st
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::55c8c620d1a17a862e4b5a7821681dd9
https://doi.org/10.1016/j.jpedsurg.2022.09.042
https://doi.org/10.1016/j.jpedsurg.2022.09.042
Publikováno v:
Journal of Cystic Fibrosis. 22:7-8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::86bf1d385da58351b02e090dfd3add80
https://doi.org/10.1016/j.jcf.2023.01.009
https://doi.org/10.1016/j.jcf.2023.01.009
Autor:
Kathryn A. Carson, Garry R. Cutting, Joseph M. Collaco, Peter J. Mogayzel, Pamela L. Zeitlin, Melis A. Aksit, Vanessa L. Richardson, Beth L. Laube, Christopher M. Evans, Gail Sharpless
Publikováno v:
Pediatric Research. 91:612-620
Background This research characterized mucociliary clearance (MCC) in young children with cystic fibrosis (CF). Methods Fourteen children (5-7 years old) with CF underwent: two baseline MCC measurements (Visits 1 and 2); one MCC measurement approxima
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f25f1a0c23cf661cda1d4e697ab12e2
https://doi.org/10.1038/s41390-021-01453-2
https://doi.org/10.1038/s41390-021-01453-2
Autor:
Beryl J. Rosenstein, Lindsay Jablonski, Peter J. Mogayzel, Carlton K. K. Lee, Shruti M. Paranjape, Alice Pan
Publikováno v:
The Journal of Pediatric Pharmacology and Therapeutics. 25:623-628
OBJECTIVES Clinical practice guidelines for eradication of Pseudomonas aeruginosa (PA) in patients with cystic fibrosis (CF) have been established, but current studies have not assessed how these guidelines translate into clinical practice. This stud
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d30e6f00e690dd656a44ed6da94db3b3
https://doi.org/10.5863/1551-6776-25.7.623
https://doi.org/10.5863/1551-6776-25.7.623
Autor:
Kathleen B. Schwarz, Kathryn A. Carson, Alexandra Vasilescu, Paul Wasuwanich, Peter J. Mogayzel, Thammasin Ingviya, Wikrom Karnsakul
Publikováno v:
Journal of Cystic Fibrosis. 19:546-552
Background & Aims A practical, inexpensive, and non-invasive biomarker of liver fibrosis is needed as a reliable screening test for cystic fibrosis-associated liver disease (CFLD). Studies have shown the utility of AST to Platelet Ratio Index (APRI),
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d19eb90f611defb901c3c569f8251288
https://doi.org/10.1016/j.jcf.2020.05.002
https://doi.org/10.1016/j.jcf.2020.05.002
Autor:
Gail Sharpless, Christopher M. Evans, Peter J. Mogayzel, Kathryn A. Carson, Vanessa L. Richardson, Pamela L. Zeitlin, Beth L. Laube
Publikováno v:
Pediatr Pulmonol
Objectives (a) To quantify changes in mucociliary clearance (MCC) over time in children with cystic fibrosis (CF) and the relationship between MCC and rate of infection with Pseudomonas aeruginosa (PA); (b) to determine the impact of MCC on the evolu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ac5725179659f70dcf31e6b7756513c
https://doi.org/10.1002/ppul.24858
https://doi.org/10.1002/ppul.24858
Publikováno v:
J Pediatr Pharmacol Ther
Cystic fibrosis transmembrane conductance regulator (CFTR) modulators have revolutionized care for patients with cystic fibrosis (CF). The triple combination product elexacaftor/tezacaftor/ivacaftor is a highly effective CFTR modulator that is genera
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8abc4c99e4ad1cbcf418e791db4ac521
https://europepmc.org/articles/PMC9268115/
https://europepmc.org/articles/PMC9268115/
Autor:
John P. Clancy, Agathe Ceppe, Jihong Wu, Timothy E. Corcoran, Pradeep Bhambhvani, Peter J. Mogayzel, Beth L. Laube, Scott D. Sagel, Felix Ratjen, Joseph M. Pilewski, Steven M. Rowe, William D. Bennett, Scott H. Donaldson
Publikováno v:
J Cyst Fibros
CFTR function is required for normal mucociliary clearance (MCC) and cough-assisted clearance (CC). Lumacaftor-ivacaftor is approved for use in people with cystic fibrosis (CF) carrying two copies of F508del-CFTR. In this observational study performe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0921b8b1d58af1181fd7ea53dafe02e
https://europepmc.org/articles/PMC8630086/
https://europepmc.org/articles/PMC8630086/
Autor:
Lindsay, Jablonski, Carlton K K, Lee, Beryl J, Rosenstein, Peter J, Mogayzel, Shruti, Paranjape, Alice, Pan
Publikováno v:
J Pediatr Pharmacol Ther
OBJECTIVES: Clinical practice guidelines for eradication of Pseudomonas aeruginosa (PA) in patients with cystic fibrosis (CF) have been established, but current studies have not assessed how these guidelines translate into clinical practice. This stu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b475f0c4a0043626227451fbc5dfce68
https://pubmed.ncbi.nlm.nih.gov/33041717
https://pubmed.ncbi.nlm.nih.gov/33041717
Autor:
Beth L, Laube, Kathryn A, Carson, Christopher M, Evans, Melis A, Aksit, Joseph M, Collaco, Vanessa L, Richardson, Gail, Sharpless, Pamela L, Zeitlin, Garry R, Cutting, Peter J, Mogayzel
Publikováno v:
Pediatric research. 91(3)
This research characterized mucociliary clearance (MCC) in young children with cystic fibrosis (CF).Fourteen children (5-7 years old) with CF underwent: two baseline MCC measurements (Visits 1 and 2); one MCC measurement approximately 1 year later (V
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3b0f4e1ba15efd07d0ee22dc77a7f629
https://pubmed.ncbi.nlm.nih.gov/33753897
https://pubmed.ncbi.nlm.nih.gov/33753897