Effect of Outdoor Cycling, Virtual and Enhanced Reality Indoor Cycling on Heart Rate, Motivation, Enjoyment and Intention to Perform Green Exercise in Healthy Adults.

Autor: Poli L; Department of Translational Biomedicine and Neuroscience (DiBraiN), University of Study of Bari, 70124 Bari, Italy., Greco G; Department of Translational Biomedicine and Neuroscience (DiBraiN), University of Study of Bari, 70124 Bari, Italy., Gabriele M; Department of Translational Biomedicine and Neuroscience (DiBraiN), University of Study of Bari, 70124 Bari, Italy., Pepe I; Department of Translational Biomedicine and Neuroscience (DiBraiN), University of Study of Bari, 70124 Bari, Italy., Centrone C; Department of Translational Biomedicine and Neuroscience (DiBraiN), University of Study of Bari, 70124 Bari, Italy., Cataldi S; Department of Translational Biomedicine and Neuroscience (DiBraiN), University of Study of Bari, 70124 Bari, Italy., Fischetti F; Department of Translational Biomedicine and Neuroscience (DiBraiN), University of Study of Bari, 70124 Bari, Italy.

Publikováno v: Journal of functional morphology and kinesiology [J Funct Morphol Kinesiol] 2024 Oct 02; Vol. 9 (4). Date of Electronic Publication: 2024 Oct 02.

DNA identification of skeletal remains by investigator’s intuition

Autor: Ricci, U., Centrone, C., Gerundino, F., Pelo, E.

Publikováno v: In Forensic Science International: Genetics Supplement Series December 2019 7(1):156-157

Presentation of the Consensus Document 2019 on the genetic analysis of Cystic Fibrosis

Autor: Lucarelli M., Angioni A., Baffico M., Bombieri C., Bonizzato A., Borgo G., Castaldo G., Castellani C., Centrone C., Coiana A., D'Apice M. R., Girgenti C. D., Egiziano S., Favarato M., Ferlisi A., Melotti P., Minicucci L., Pelo E., Ragusa A., Ravani A., Savoldi G., Seia M., Termini L.

The causative gene of Cystic Fibrosis (CF) is the Cystic Fibrosis Transmembrane conductance Regulator (CFTR). Although monogenic, CF has a complex genotype - phenotype relationship mainly originated by the high number of CFTR variants, the challengin

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http://hdl.handle.net/11588/875505

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Clinical outcomes of a large cohort of individuals with the F508del/5T;TG12 CFTR genotype.

Autor: Tosco A; Paediatric Unit, Department of Translational Medical Sciences, Cystic Fibrosis Regional Reference Center, University of Naples Federico II, Naples, Italy., Castaldo A; Paediatric Unit, Department of Translational Medical Sciences, Cystic Fibrosis Regional Reference Center, University of Naples Federico II, Naples, Italy., Colombo C; Cystic Fibrosis Regional Reference Center, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, University of Milan, Department of Pathophysiology and Transplantation, Milan, Italy., Claut L; Cystic Fibrosis Regional Reference Center, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, University of Milan, Department of Pathophysiology and Transplantation, Milan, Italy., Carnovale V; Department of Translational Medical Science, Cystic Fibrosis Center, Adult Unit, University of Naples 'Federico II', Italy., Iacotucci P; Department of Translational Medical Science, Cystic Fibrosis Center, Adult Unit, University of Naples 'Federico II', Italy., Lucarelli M; Dept of Experimental Medicine, Sapienza University of Rome, Rome, Italy; Pasteur Institute, Cenci Bolognetti Foundation, Sapienza University of Rome, Rome, Italy., Cimino G; Cystic Fibrosis Regional Reference Center, A.O.U. Policlinico Umberto I, Rome, Italy., Fabrizzi B; Cystic Fibrosis Regional Reference Center, Mother - Child Department, United Hospitals, Ancona, Italy., Caporelli N; Cystic Fibrosis Regional Reference Center, Mother - Child Department, United Hospitals, Ancona, Italy., Majo F; Cystic Fibrosis Centre, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy., Ciciriello F; Cystic Fibrosis Centre, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy., Padoan R; Cystic Fibrosis Regional Support Center, Department of Pediatrics, University of Brescia, ASST Spedali Civili Brescia, Brescia, Italy., Poli P; Cystic Fibrosis Regional Support Center, Department of Pediatrics, University of Brescia, ASST Spedali Civili Brescia, Brescia, Italy., Taccetti G; Meyer Children's Hospital, Cystic Fibrosis Regional Reference Center, Department of Paediatric Medicine, Viale Gaetano Pieraccini 24, Florence, Italy., Centrone C; Diagnostic Genetics Unit, Careggi University Hospital, Florence, Italy., Casciaro R; IRCCS Istituto Giannina Gaslini, Genova, Italy., Castellani C; IRCCS Istituto Giannina Gaslini, Genova, Italy., Salvatore D; Cystic Fibrosis Center, Hospital San Carlo, Potenza, Italy., Colangelo C; Cystic Fibrosis Center, Hospital San Carlo, Potenza, Italy., Bonomi P; Freelance Statistician, Milan, Italy., Castaldo G; Department of Molecular Medicine and Medical Biotechnology, University of Naples, Naples, Italy; CEINGE-Advanced Biotechnology, Naples, Italy., Terlizzi V; Meyer Children's Hospital, Cystic Fibrosis Regional Reference Center, Department of Paediatric Medicine, Viale Gaetano Pieraccini 24, Florence, Italy. Electronic address: vito.terlizzi@meyer.it.

Publikováno v: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society [J Cyst Fibros] 2022 Sep; Vol. 21 (5), pp. 850-855. Date of Electronic Publication: 2022 May 04.