- Association of Neonatal Hospital Length of Stay with Lung Function in Primary Ciliary Dyskinesia. Wee WB, Leigh MW, Davis SD, Rosenfeld M, Sullivan KM, Sawras MG, Ferkol TW, Knowles MR, Milla C, Sagel SD, Zariwala MA, Pullenayegum E, Dell SD.Ann Am Thorac Soc. 2022 Nov;19(11):1865-1870. doi: 10.1513/AnnalsATS.202202-116OC.PMID: 35657736
- Autonomous wearable sweat rate monitoring based on digitized microbubble detection. Lin H, Yu W, Suarez JED, Athavan H, Wang Y, Yeung C, Lin S, Sankararaman S, Milla C, Emaminejad S.Lab Chip. 2022 Nov 8;22(22):4267-4275. doi: 10.1039/d2lc00670g.PMID: 36268642
- Laterality Defects in Primary Ciliary Dyskinesia: Relationship to Ultrastructural Defect or Genotype. Barber AT, Shapiro AJ, Davis SD, Ferkol TW, Atkinson JJ, Sagel SD, Dell SD, Olivier KN, Milla CE, Rosenfeld M, Li L, Lin FC, Sullivan KM, Capps NA, Zariwala MA, Knowles MR, Leigh MW; Genetic Disorders of Mucociliary Clearance Consortium (GDMCC).Ann Am Thorac Soc. 2022 Nov 7. doi: 10.1513/AnnalsATS.202206-487OC. Online ahead of print.PMID: 36342963
- Rate of Lung Function Decline in People with Cystic Fibrosis Having a Residual Function Gene Mutation. Sawicki GS, Konstan MW, McKone EF, Moss RB, Lubarsky B, Suthoff E, Millar SJ, Pasta DJ, Mayer-Hamblett N, Goss CH, Morgan WJ, Duncan ME, Yang Y.Pulm Ther. 2022 Nov 1. doi: 10.1007/s41030-022-00202-y. Online ahead of print.PMID: 36319933