Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Christopher J. Nemastil"'
Autor:
Emma L. Guenther, Karen S. McCoy, Mariah Eisner, Shasha Bai, Christopher J. Nemastil, Kimberly J. Novak, Terri Johnson, Emily M. Stephan
Publikováno v:
Journal of Cystic Fibrosis.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa91e5b2e8ea6d131e705753f3a8604b
https://doi.org/10.1016/j.jcf.2023.03.018
https://doi.org/10.1016/j.jcf.2023.03.018
Publikováno v:
Lung. 198:957-964
People with cystic fibrosis (CF) are predisposed to chronic conditions, such as CF-related diabetes (CFRD). Recent attention has been focused on the addition of screening for anxiety and depression in the CF population. Independently, CFRD and mental
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::be126cd49267b78188e4555f5341fde0
https://doi.org/10.1007/s00408-020-00396-5
https://doi.org/10.1007/s00408-020-00396-5
Autor:
Kelly T Sakellaris, Christopher J. Nemastil, Anne Rice, Susan Gemma, Kimberly J. Novak, Ann Salvator, Clarissa J Dilaveris, Emily M Stephan, Karen McCoy
Publikováno v:
J Pediatr Pharmacol Ther
OBJECTIVE Previous trials evaluated the efficacy of lumacaftor/ivacaftor in Phe508del homozygotes. These trials are limited by manufacturer sponsorship and were conducted under strict protocol. Additionally, this therapy is costly and does not allow
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c1f6b7bdf98c54b0e5876caee10630c
https://doi.org/10.5863/1551-6776-25.5.431
https://doi.org/10.5863/1551-6776-25.5.431
Publikováno v:
Journal of Anesthesia. 34:66-71
The gold standard for measuring the partial pressure of carbon dioxide remains arterial blood gas (ABG) analysis. For patients with cystic fibrosis undergoing general anesthesia or polysomnography studies, continuous non-invasive carbon dioxide monit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fbccba1f52e5bbc21b6894eb6a47999a
https://doi.org/10.1007/s00540-019-02706-5
https://doi.org/10.1007/s00540-019-02706-5
Autor:
Katelyn Krivchenia, Christopher J. Nemastil, Michelle L. Gillespie, Mary Lynn Dell, Diana Gilmore, Melissa Moore-Clingenpeel
Publikováno v:
Pediatric pulmonologyREFERENCES. 56(2)
OBJECTIVES Caregivers of infants with cystic fibrosis (CF) carry a heavy treatment burden for their child along with the inherent difficulties of raising an infant. This study investigated the impact of self-reported caregiver mental health diagnoses
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c24bdc7030d41cb114d968dced1eaf49
https://pubmed.ncbi.nlm.nih.gov/33295695
https://pubmed.ncbi.nlm.nih.gov/33295695
Publikováno v:
Lung. 198(6)
People with cystic fibrosis (CF) are predisposed to chronic conditions, such as CF-related diabetes (CFRD). Recent attention has been focused on the addition of screening for anxiety and depression in the CF population. Independently, CFRD and mental
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::dd386ca745a3f79db35339bdac5a83fe
https://pubmed.ncbi.nlm.nih.gov/33231742
https://pubmed.ncbi.nlm.nih.gov/33231742
Publikováno v:
The Journal of asthma : official journal of the Association for the Care of Asthma. 58(6)
Background: Asthma is a common childhood disease with significant morbidity. Severe asthma accounts for just 4–6% of patients, but this group is more difficult to treat and is responsible for up to...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfcc3a96ed3975eb2dec9ff4c5ecf120
https://pubmed.ncbi.nlm.nih.gov/32138568
https://pubmed.ncbi.nlm.nih.gov/32138568
Autor:
Frederick W. Woodley, Christopher J. Nemastil, Emrah Gecili, Benjamin T. Kopp, Don Hayes, Rhonda D. Szczesniak, Chandra L. Shrestha
Publikováno v:
Respir Med
Background People with cystic fibrosis (PWCF) suffer from acute unpredictable reductions in pulmonary function associated with a pulmonary exacerbation (PEx) that may require hospitalization. PEx symptoms vary between PWCF without universal diagnosti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e4ab1760f1a568e673c6ea48964d5c5
https://doi.org/10.1016/j.rmed.2021.106687
https://doi.org/10.1016/j.rmed.2021.106687
Autor:
Frederick W. Woodley, Christopher J. Nemastil, Don Hayes, Benjamin T. Kopp, Chandra L. Shrestha, Emrah Gecili, Rhonda D. Szczesniak
Publikováno v:
Journal of Cystic Fibrosis. 20:S83
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3c3b14d6ab31cfb36ba31f8a79b21ccf
https://doi.org/10.1016/s1569-1993(21)01592-7
https://doi.org/10.1016/s1569-1993(21)01592-7
Autor:
Christopher J. Nemastil, Stella Antonara, Grace R. Paul, Amy Leber, Michael T. Brady, Stephanie Stack-Simone, Alexander L. Greninger, Kimberly J. Novak
Publikováno v:
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society. 19(4)
Background Mycobacterium porcinum is a non-tuberculous mycobacterium (NTM) identified in potable water. The identification and clinical impact of M. porcinum in patients with cystic fibrosis (CF) has not been described. In our institution, M. porcinu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c493b35afa74cb1f8d1230f152befc7
https://pubmed.ncbi.nlm.nih.gov/31982335
https://pubmed.ncbi.nlm.nih.gov/31982335