Results 141 to 150 of about 975,042 (316)

Is the 1-meter distance enough to prevent cross-infection in cystic fibrosis? Preliminary results of a prospective study

, 2008
Filippo Festini, Valeria Galici, Sabrina Neri, Claudia Mannini, C. Braggion   +4 more
openalex   +1 more source

Infective respiratory exacerbations in young adults with cystic fibrosis: role of viruses and atypical microorganisms. [PDF]

, 1989
Edmund Ong, M E Ellis, A.K. Webb, Keith Neal, M Dodd, E O Caul, Shane C. Burgess   +6 more
openalex   +1 more source

3D Automated Segmentation of Bronchial Abnormalities on Ultrashort Echo Time MRI: A Quantitative MR Outcome in Cystic Fibrosis

Journal of Magnetic Resonance Imaging, EarlyView.
ABSTRACT Background Cystic fibrosis (CF) monitoring relies on computed tomography (CT), but ultra‐short echo time MRI (UTE‐MRI) offers a radiation‐free alternative. However, its clinical adoption is hindered by the laborious and subjective manual analysis, which prevents standardized quantification of bronchial abnormalities.
Amel Imene Hadj Bouzid, Ilyes Benlala, Baudouin Denis de Senneville, Fabien Baldacci, Julie Macey, Wadie Benhassen, Pan Su, Stephanie Bui, Maeva Zysman, Aurelien Bustin, Patrick Berger, Gael Dournes   +11 more
wiley   +1 more source

Antibiotics sensitivity in mucoid and non mucoid Pseudomonas aeruginosa isolates from cystic fibrosis patients

, 2009
Lisa Cariani, G. Defilippi, D. Costantini, Carla Colombo, M.L. Garlaschi, Erminio Torresani, Arianna Biffi   +6 more
openalex   +1 more source

Survey ofPseudomonas aeruginosagenotypes in colonised cystic fibrosis patients [PDF]

, 2006
Sabine Van daele, M. Vaneechoutte, K. De Boeck, C. Knoop, A. Malfroot, P. Lebecque, J. Leclercq-Foucart, L. Van Schil, K. Desager, F. De Baets   +9 more
openalex   +1 more source

Characterization of pediatric eosinophilic gastrointestinal disorders beyond eosinophilic esophagitis in a nationwide cohort

Journal of Pediatric Gastroenterology and Nutrition, EarlyView.
Abstract Objectives Nonesophageal eosinophilic gastrointestinal disorders (non‐EoE EGIDs) are rare, underrecognized inflammatory diseases of the gastrointestinal (GI) tract, especially in children. Their clinical heterogeneity and lack of specific biomarkers contribute to diagnostic delays and therapeutic challenges.
Sara Renzo, Luca Scarallo, Selene Del Vespa, Giulia Angelino, Matteo Bramuzzo, Enrico Felici, Flavio Labriola, Francesca Laganà, Lorenzo Norsa, Salvatore Oliva, Marisa Piccirillo, Elena Pozzi, Francesca Rea, Giusy Russo, Francesco Valitutti, Giovanna Zuin, Paolo Lionetti   +16 more
wiley   +1 more source

Structural studies of Pseudomonas aeruginosa pilY1, a protein central to infections in cystic fibrosis

, 2019
Jillian Orans
openalex   +2 more sources

Quantitative analysis of the IgG and IgG subclass immune responses to chromosomal Pseudomonas aeruginosa beta-lactamase in serum from patients with cystic fibrosis by western blotting and laser scanning densitometry. [PDF]

, 1996
T. D. Petersen, Oana Ciofu, Tacjana Pressler, Birgit Giwercman, Susanne S. Pedersen, Niels Høiby   +5 more
openalex   +1 more source

A medication adherence–enhancing simulation intervention in pediatric cystic fibrosis

, 2021
Guy Van Schandevyl, Georges Casimir, L. Hanssens   +2 more
openalex   +2 more sources

Serum aspartate aminotransferase to platelet ratio index in relation to liver histopathology of biliary atresia

Journal of Pediatric Gastroenterology and Nutrition, EarlyView.
Abstract Objectives To investigate the prognostic significance of aspartate aminotransferase to platelet ratio index (APRI) in relation to histopathological features across the clinical course of biliary atresia (BA). Methods In this observational cohort study, we enroled 135 BA patients with available APRI values at Kasai portoenterostomy (KPE, n ...
Nicholas Nordenheim, Iiris Nyholm, Maria Hukkinen, Nelli Sjöblom, Aino Mutka, Jouko Lohi, Mark Davenport, Mikko P. Pakarinen   +7 more
wiley   +1 more source