	The role of sweat chloride in determining CFTR protein restoration in people with cystic fibrosis. Lancet Respir Med Zemanick ET, Graeber SY, Castellani C, Cutting GR, Fajac I, Konstan MW, Linnemann RW, McKone EF, Metcalf A, Solomon GM, Taylor-Cousar JL, Mayer-Hamblett N, Mall MA. PMID: 42442377 [PubMed - as supplied by publisher]
	Reproductive health guidance for the cystic fibrosis community: a Cystic Fibrosis Foundation Position Paper. Lancet Respir Med Jain R, Taylor JL, Kazmerski TM, Lonabaugh K, Trimble A, Velez Leitner D, Foil K, Hong G, Johns WB, Kolarova T, Meier E, Perry A, Singh KE, Stahl C, Szentpetery S, Weiss MS, West NE, Wilson A, Wright B, Brown AW, Hempstead SE, Lomas P, Middleton PG, Shteinberg M, Felton I, Roe AH. PMID: 42442376 [PubMed - as supplied by publisher]
	Delayed Diagnosis of Cystic Fibrosis and Nontuberculous Mycobacterial Infection in Refractory CRSwNP. Respirol Case Rep Greig R, Suter P, Chan R, Connell D, Lipworth B. PMID: 42427916 [PubMed]
	Online peer support and shared care experiences: A netnographic study of parents of children with cystic fibrosis. J Pediatr Nurs Gümü, Karakul A, Düzkaya DS. PMID: 42425015 [PubMed - as supplied by publisher]
	Diet composition and quality in children with cystic fibrosis in the modulator era: A scoping review. Clin Nutr Schembri LK, Carr SB, Davies JC, Collins SA. PMID: 42424717 [PubMed - as supplied by publisher]
	From Awareness to Action: Developing A Cystic Fibrosis-Tailored Screening for Disordered Eating Behaviors. Pediatr Pulmonol McCoy J, Behrman M, Robichaud J, Bruce AS, Powers KE. PMID: 42419735 [PubMed - indexed for MEDLINE]
	Participants' experiences of living with cystic fibrosis related diabetes and using a hybrid closed-loop system to support self-management: qualitative study. BMC Endocr Disord Lawton J, Adler AI, Brennan A, Holt RIG, Hovorka R, Kadiyala N, Lau D, Peacock M, Boughton CK, Rankin D. PMID: 42414998 [PubMed - as supplied by publisher]
	Regulation of CFTR stability at the plasma membrane-Mechanisms and therapeutic opportunities inÂ cystic fibrosis. FEBS Lett Farinha CM, Oliveira J. PMID: 42403151 [PubMed - as supplied by publisher]
	Perspective of the European Cystic Fibrosis Society on Improving Global Cystic Fibrosis Care. Pediatr Pulmonol Davies JC, Bakkeheim E, Chansard A, Drevinek P, Dubois C, Matthews J, Sheremet M, Smith C. PMID: 42400501 [PubMed - indexed for MEDLINE]
	Impact of Elexacaftor/Tezacaftor/Ivacaftor (ETI) on Airway and Aystemic Inflammation in Cystic Fibrosis: A Systematic Review. Ann Am Thorac Soc AlMunefi F, Dyce JP, Zhao JY, Quon BS. PMID: 42397988 [PubMed - as supplied by publisher]
	Unlocking growth potential: Ivacaftor therapy and developmental gains in lung and height in a cohort study of children and young adults with cystic fibrosis. Eur Respir J Guimbellot JS, Baker E, Chalamalla A, Rose NR, Edwards LJ, Jain M. PMID: 42392826 [PubMed - as supplied by publisher]
	Real-time prediction of rapid weight change in children with cystic fibrosis who have initiated modulator therapy. Clin Nutr ESPEN Garter A, Gecili E, Hossain MM, Nakamura A, Wackler M, Boat T, Szczesniak RD. PMID: 42392543 [PubMed - as supplied by publisher]
	Real-time breath metabolomics to assess early response to CFTR modulators in adults with cystic fibrosis: An open-label proof-of-concept study. J Cyst Fibros Bardin E, Salvator H, Roquencourt C, Lamy E, Hunzinger N, Sermet-Gaudelus I, De Miranda S, Grenet D, Devillier P, Grassin-Delyle S. PMID: 42386422 [PubMed - as supplied by publisher]
	Cystic fibrosis nutrition: Addressing emerging trends following the 2024 ESPEN-ESPGHAN-ECFS guidelines. Expert opinion recommendations. J Cyst Fibros Smith C, Collins S, Colombo C, Declercq D, Katz T, Kalnins D, Scheers I, Peckham D, Snowball J, Wilschanski M. PMID: 42386421 [PubMed - as supplied by publisher]
	CT-derived vascular parameters and bone mineral density in adults with cystic fibrosis. Respir Med Ç, Alev E, Mercanc, Kan, Kan, Karakurt S. PMID: 42386011 [PubMed - as supplied by publisher]
	Prevalence of Cystic Fibrosis and Pattern of Lung Function Impairment in Adults Presenting With Bronchiectasis at a Tertiary Care Hospital in Resource Poor Country Bangladesh: A Cross-Sectional Study. Health Sci Rep Majumder S, Biswas P, Rahman MM, Islam MS, Rahman MM, Paul SK, Hamza M, Kabir MH, Islam S, Chowdhury FR, Chakrabortty R, Ahmed S, Rahman MA. PMID: 42382502 [PubMed]
	Male reproductive phenotype in cystic fibrosis: comparison of existing animal models. Lab Anim (NY) Boursier A, Cottart CH, Balde-Camara A, Vialard F, Barbotin AL. PMID: 42380629 [PubMed - as supplied by publisher]
	Maternal, Infant, Reproductive and Child Health in Cystic Fibrosis (MATRIARCH_CF): a prospective, observational study to evaluate pregnancy and parenthood in females with cystic fibrosis and health of the offspring in the CFTR-modulator era. BMJ Open Respir Res Downes A, Bokobza I, Weitnauer L, Scott R, Dobra R, Short C, Semple T, Beaumont O, Williamson C, Davies JC, Felton I. PMID: 42379640 [PubMed - indexed for MEDLINE]
	Transformations within cystic fibrosis model of care in the era of CFTR modulators: a Scoping Review. Respir Med Gautiez R, Reix P, Poupon-Bourdy S, Reynaud Q, Fayolle R, Cornec S, Durieu I, Haesebaert J. PMID: 42379530 [PubMed - as supplied by publisher]
	Suboptimal vaccine coverage for preventable respiratory infections in children with cystic fibrosis in the Cystic Fibrosis Regional Reference Centre of Tuscany: Need for improving preventive strategies. Hum Vaccin Immunother Forgione F, Canessa C, Taccetti G, Fevola C, Azzari C, Ricci S, Terlizzi V. PMID: 42373575 [PubMed - indexed for MEDLINE]

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