Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Danielle M, Goetz"'
Publikováno v:
Pediatric Pulmonology.
Publikováno v:
Journal of Cystic Fibrosis.
Publikováno v:
Respiratory Medicine Case Reports, Vol 16, Iss C, Pp 125-127 (2015)
Cystic fibrosis (CF) causes airways obstruction and a decline in percent predicted forced expiratory volume in 1 s (FEV1%). FEV1% is an objective measure of a pulmonary exacerbation of CF; improvement in FEV1% is the endpoint used often to determine
Externí odkaz:
https://doaj.org/article/0817ed27273d46f4a577da7645b35485
Autor:
Erin E, Hughes, Colleen F, Stevens, Carlos A, Saavedra-Matiz, Norma P, Tavakoli, Lea M, Krein, April, Parker, Zhen, Zhang, Breanne, Maloney, Beth, Vogel, Joan, DeCelie-Germana, Catherine, Kier, Ran D, Anbar, Maria N, Berdella, Paul G, Comber, Allen J, Dozor, Danielle M, Goetz, Louis, Guida, Meyer, Kattan, Andrew, Ting, Karen Z, Voter, Patrick, van Roey, Michele, Caggana, Denise M, Kay
Publikováno v:
Human mutation. 37(2)
Infants are screened for cystic fibrosis (CF) in New York State (NYS) using an IRT-DNA algorithm. The purpose of this study was to validate and assess clinical validity of the US FDA-cleared Illumina MiSeqDx CF 139-Variant Assay (139-VA) in the diver
Publikováno v:
Pediatric pulmonology. 45(4)
Late presentation of congenital diaphragmatic hernia (CDH) is unusual, especially in patients with cystic fibrosis (CF). To our knowledge, cases of CDH in CF patients and the combined effects on lung function have not been previously described. Here