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                             36 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 Aging with CF: Characteristics of people with CF aged 40 and older in the United States Ostrenga, Joshua S.

24 1 p. 183-186
artikel
2 A phase I study assessing the safety and tolerability of SPL84, an inhaled antisense oligonucleotide for treatment of cystic fibrosis patients with the 3849 +10kb C->T Caraco, Yoseph

24 1 p. 66-71
artikel
3 Assessing the impact of elexacaftor/tezacaftor/ivacaftor on anxiety & depression symptom scores in adults with Cystic Fibrosis Nguyen, Minh

24 1 p. 26-29
artikel
4 A W1282X cystic fibrosis mouse allows the study of pharmacological and gene-editing therapeutics to restore CFTR function Michicich, Margaret

24 1 p. 164-174
artikel
5 Bridging the gap: Challenging lung infections and clinical trial development in cystic fibrosis Downey, Damian G.

24 1 p. 79-82
artikel
6 Cardiometabolic risk factors in adults with cystic fibrosis undergoing elexacaftor/tezacaftor/ivacaftor therapy Gramegna, Andrea

24 1 p. 53-56
artikel
7 CF Ferrets exposed to in utero ivacaftor do not develop lens abnormalities Taylor-Cousar, Jennifer L.

24 1 p. 19-20
artikel
8 Changes in factors associated with inhaled antibiotic prescriptions for people with cystic fibrosis over time in the U.S. Muhlebach, Marianne S.

24 1 p. 98-104
artikel
9 Contents
24 1 p. i-iii
artikel
10 Development of metabolic syndrome in people with Cystic Fibrosis one year after exposure to elexacaftor-tezacaftor-ivacaftor Ratti, Gregory A.

24 1 p. 47-52
artikel
11 Differential times of submission and approval of CFTR modulators for the treatment of Cystic Fibrosis in the United States and the European Union Costa, Enrico

24 1 p. 125-132
artikel
12 Efficacy and safety of LAU-7b in a Phase 2 trial in adults with cystic fibrosis Konstan, Michael W.

24 1 p. 83-90
artikel
13 Elevated liver function tests in infants exposed to elexacaftor-tezacaftor-ivacaftor in utero and while breastfeeding – Case reports Kolaczkowski, Theresa Jane

24 1 p. 16-18
artikel
14 Elexacaftor/tezacaftor/ivacaftor efficacy in intestinal organoids with rare CFTR variants in comparison to CFTR-F508del and CFTR-wild type controls Kroes, Suzanne

24 1 p. 175-182
artikel
15 ETD001: A novel inhaled ENaC blocker with an extended duration of action in vivo Danahay, Henry

24 1 p. 72-78
artikel
16 Evidence for secondary ciliary dyskinesia in patients with cystic fibrosis Bonhiver, Romane

24 1 p. 193-200
artikel
17 Exogenous insulin does not reduce protein catabolism in pre-diabetic cystic fibrosis patients: A randomized clinical trial Schiavon, Michele

24 1 p. 57-65
artikel
18 Factors associated with prescription of elexacaftor/tezacaftor/ivacaftor among people with cystic fibrosis aged 12 years or older with at least one F508del allele Hergenroeder, Georgene E

24 1 p. 135-141
artikel
19 Gene expression profile of intestinal organoids from people with cystic fibrosis upon exposure to elexacaftor/tezacaftor/ivacaftor Cinek, Ondrej

24 1 p. 157-163
artikel
20 Glucagon-like-peptide-1 agonist therapy in adults with cystic fibrosis Park, Sanghoon

24 1 p. 40-46
artikel
21 Impact of elexacaftor/tezacaftor/ivacaftor on utilization of routine therapies in cystic fibrosis: Danish nationwide register study Råket, Hans Kristian

24 1 p. 105-111
artikel
22 Insights into epithelial-mesenchymal transition from cystic fibrosis rat models Rout-Pitt, Nathan

24 1 p. 149-156
artikel
23 Learning from the CFTR modulator baby boom Jain, Raksha

24 1 p. 3-4
artikel
24 Lens-related ocular changes in fetal rats following in-utero exposure to elexacaftor-tezacaftor-ivacaftor Zhu, Yimin

24 1 p. 21-25
artikel
25 Linkage of the CF Foundation Patient Registry with the Scientific Registry of Transplant Recipients database Cromwell, Elizabeth A.

24 1 p. 112-117
artikel
26 Metabolic syndrome in the post-ETI era Litvin, Marina

24 1 p. 8-9
artikel
27 News article
24 1 p. 1-2
artikel
28 Next generation triplex-forming PNAs for site-specific genome editing of the F508del CFTR mutation Gupta, Anisha

24 1 p. 142-148
artikel
29 Process and validity of linking cystic fibrosis patient registry with national Medicaid databases Esther Jr, Charles R.

24 1 p. 118-124
artikel
30 Regulatory adverse drug reaction analyses support a temporal increase in psychiatric reactions after initiation of cystic fibrosis combination modulator therapies O'Connor, Jacob

24 1 p. 30-32
artikel
31 Regulatory delays in approval of CFTR modulating agents in Canada Thornton, Christina S.

24 1 p. 133-134
artikel
32 Self-reported chronic therapy use after 24-weeks of follow-up by participants who completed the simplify randomized, controlled trial Gifford, Alex H.

24 1 p. 91-97
artikel
33 Suicidal behaviour and CFTR modulators: A case series and WHO database disproportionality analysis Nidegger, Inès

24 1 p. 33-39
artikel
34 The impact of CFTR modulators on mental health: Moving the field forward Georgiopoulos, AM

24 1 p. 5-7
artikel
35 Theranostics vs theratyping or theranostics plus theratyping? Amaral, Margarida D.

24 1 p. 10-15
artikel
36 What does it mean to be “healthy” when taking elexacaftor/tezacaftor/ivacaftor (ETI)? A qualitative study Everhart, Robin S.

24 1 p. 187-192
artikel
                             36 gevonden resultaten
 
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