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pro vyhledávání: '"T. Spencer Poore"'
Autor:
T. Spencer Poore, Edith T. Zemanick
Publikováno v:
Microorganisms, Vol 11, Iss 8, p 2013 (2023)
Aspergillus fumigatus (Af) is a mold frequently detected in airway samples from people with cystic fibrosis (pwCF). Abnormal airway mucus may allow Af to germinate, resulting in airway infection or an allergic response. While Af is known to increase
Externí odkaz:
https://doaj.org/article/78aaaf46087845f295c346fb586e4812
Publikováno v:
Pathogens, Vol 10, Iss 5, p 618 (2021)
Fungi are frequently recovered from lower airway samples from people with cystic fibrosis (CF), yet the role of fungi in the progression of lung disease is debated. Recent studies suggest worsening clinical outcomes associated with airway fungal dete
Externí odkaz:
https://doaj.org/article/af343ee5da3d45a68893ac6013067b57
Autor:
John T. Brinton, Maxene Meier, Scott D. Sagel, T Spencer Poore, Emily M. DeBoer, Edith T. Zemanick, Stacey L. Martiniano, Brandie D. Wagner, Elinor Towler
Publikováno v:
Pediatric pulmonology. 57(1)
BACKGROUND: Individuals with cystic fibrosis (CF) and fungal airway infection may present with fungal bronchitis, allergic bronchopulmonary aspergillosis (ABPA) or may appear unaffected despite fungal detection. We sought to characterize people with
Publikováno v:
Pathogens
Pathogens, Vol 10, Iss 618, p 618 (2021)
Pathogens, Vol 10, Iss 618, p 618 (2021)
Fungi are frequently recovered from lower airway samples from people with cystic fibrosis (CF), yet the role of fungi in the progression of lung disease is debated. Recent studies suggest worsening clinical outcomes associated with airway fungal dete
Publikováno v:
International Journal of Pediatric Otorhinolaryngology. 156:111125
Pediatric chronic rhinosinusitis (PCRS) is a unique clinical entity and the underlying source of inflammation is unknown. Certain subgroups, such as children with nasal polyps and cystic fibrosis (CF) sinusitis are often recalcitrant to standard medi
Publikováno v:
Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society. 21(1)
Cystic fibrosis is a genetic disease caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene, leading to dysfunction of the CFTR protein. CFTR dysfunction leads to disease in the respiratory and gastrointestinal sys