Atiur RahmanA DEVERNALJournal of Biological ChemistryHoof T, Deer A, Hadam M, Riordan J and Tuler B, Cystic fibrosis-type mutational analysis in the ATP-binding cassette transporter signature of human P-glycoprotein MDR1. J Biol Chem 269: 20575-20583, 1994....
V. Tomati, E. Sondo, A. Armirotti et al., "Genetic inhibition of the ubiquitin ligase Rnf5 attenuates phenotypes associated to F508del cystic fibrosis mutation," Scientific Reports, vol. 5, no. 1, p. 12138, 2015.Tomati V, Sondo E, Armirotti A, Caci E, Pesce E, Marini M, ...
Cystic Fibrosis: End-Stage Lung Disease and TransplantAlexiou, StamatiaGoldfarb, Samuel B.Annals of the American Thoracic Society
Background Cystic fibrosis‐related liver disease (CFLD) is more prevalent in recent decades due to the increasing life expectancy of patients with cystic fibrosis (CF). There is paucity of population‐level data on the impact of CFLD on hospital outcomes. Methods We interrogated nonoverlapping ...
Couples are referred to their local Elder fordoi:10.1016/S1569-1993(12)60493-7P. CatastiniA. MartellacciC. DesiatiS. De MasiC. BraggionElsevier B.V.Journal of Cystic Fibrosis
Cystic fibrosis (CF) is a debilitating and time-consuming disease that can interfere with or impair typical daily life activities and social interactions . This study aims to identify and evaluate behavioral problems and cognitive dysfunction in children with CF.This study was carried out on a ...
Genotype-pheno- type association in infants with cystic fibrosis at the time of diagnosis. Pediatr Res 1998;44(6):920-926.Kraemer R, Birrer P, Liechti-Gallati S : Genotype-Phenotype associa- tion in infants with cystic fibrosis at the time of diagnosis. Pediatr Research 1998 ; 44 : 920-...
Disease severity in cystic fibrosis is modified by variants of the syntaxin 1A genedoi:10.1016/s1569-1993(08)60005-3T. von KanelJ. RacineR. KraemerF. StankeM. SchneiderA. SchallerS. GallatiElsevier
325 Sexuality in cystic fibrosis (CF) patientsdoi:10.1016/s1569-1993(12)60493-7P. CatastiniA. MartellacciC. DesiatiS. De MasiC. BraggionElsevier BVJournal of Cystic Fibrosis
cystic fibrosishigh-resolution computed tomographyHRCTlow-dose CTBackground and Aims: Pulmonary changes in patients with cystic fibrosis (CF) with CFTR I1234V mutation have not been extensively documented. Impact of geographic influence on phenotypical expression is largely unknown. This descriptive ...