Zobrazeno 1 - 10
of 120
pro vyhledávání: '"Alice Re"'
Autor:
Valentina Rovelli, Vittoria Ercoli, Alice Re Dionigi, Sabrina Paci, Elisabetta Salvatici, Juri Zuvadelli, Giuseppe Banderali
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 36, Iss , Pp 100998- (2023)
Background: Dietary intervention is to date the mainstay treatment to prevent toxic phenylalanine (Phe) accumulation in PKU patients. Despite success preventing central nervous system damage, there is increasing evidence of possible other unfavorable
Externí odkaz:
https://doaj.org/article/9a6b60d4535844958c4f28996717c080
Autor:
Giulia Tomagra, Alice Re, Veronica Varzi, Pietro Aprà, Adam Britel, Claudio Franchino, Sofia Sturari, Nour-Hanne Amine, Remco H. S. Westerink, Valentina Carabelli, Federico Picollo
Publikováno v:
Biosensors, Vol 13, Iss 12, p 1033 (2023)
MicroGraphited-Diamond-Multi Electrode Arrays (μG-D-MEAs) can be successfully used to reveal, in real time, quantal exocytotic events occurring from many individual neurosecretory cells and/or from many neurons within a network. As μG-D-MEAs arrays
Externí odkaz:
https://doaj.org/article/4531c5589f8d46369a6956802afc7efc
Autor:
Valentina Rovelli, Graziella Cefalo, Vittoria Ercoli, Juri Zuvadelli, Turri Olivia, Daniela Graziani, Alberti Luisella, Davide Bassi, Alice Re Dionigi, Raed Selmi, Sabrina Paci, Elisabetta Salvatici, Giuseppe Banderali
Publikováno v:
Endocrinology, Diabetes & Metabolism, Vol 6, Iss 2, Pp n/a-n/a (2023)
Abstract Background Hyperphenylalaninemias (HPA) are due to several gene mutations, of which the PAH gene is the most frequently involved. Prevalence and incidence of disease vary between populations, with genotype/phenotype correlations not always c
Externí odkaz:
https://doaj.org/article/b8f12589c5bd4c2cba0716180c4abc04
Autor:
Valentina Rovelli, Juri Zuvadelli, Marta Piotto, Andrea Scopari, Alice Re Dionigi, Vittoria Ercoli, Sabrina Paci, Graziella Cefalo, Elisabetta Salvatici, Giuseppe Banderali
Publikováno v:
Italian Journal of Pediatrics, Vol 48, Iss 1, Pp 1-6 (2022)
Abstract Background Pompe disease (PD) is a disorder of glycogen metabolism conditioning a progressive and life conditioning myopathy. Enzyme replacement therapy (ERT) is currently the best treatment option for PD, but is not resolutive. While other
Externí odkaz:
https://doaj.org/article/708b2dcf88fb41cda20947b356c935fd
Autor:
Valentina Rovelli, Juri Zuvadelli, Vittoria Ercoli, Chiara Montanari, Sabrina Paci, Alice Re Dionigi, Andrea Scopari, Elisabetta Salvatici, Graziella Cefalo, Giuseppe Banderali
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 27, Iss , Pp 100759- (2021)
Background: COVID19 pandemic urged the need to take severe measures for reducing the epidemic spread. Lockdowns were imposed throughout countries and even Inborn errors of metabolism (IEMs) affected patients had to face it and adapt, with management
Externí odkaz:
https://doaj.org/article/d1a0e0dd2e0c4622b67093aa0e0647d0
Autor:
Rovelli, Valentina, Ercoli, Vittoria, Dionigi, Alice Re, Paci, Sabrina, Salvatici, Elisabetta, Zuvadelli, Juri, Banderali, Giuseppe
Publikováno v:
In Molecular Genetics and Metabolism Reports September 2023 36
Autor:
Goyens, Philippe, Carlier, Clotilde, Hoyos, Joana, Poncelet, Pascale, Dain, Elena, Martin, Françoise, Xhonneux, Annick, Langhendries, Jean-Paul, Van Hees, Jean-Noel, Rousseaux, Deborah, Closa-Monasterolo, Ricardo, Escribano, Joaquin, Luque, Veronica, Mendez, Georgina, Ferre, Natalia, Zaragoza-Jordana, Marta, Giovannini, Marcello, Riva, Enrica, Agostoni, Carlo, Scaglioni, Silvia, Verduci, Elvira, Vecchi, Fiammetta, Dionigi, Alice Re, Arrizza, Chiara, Mariani, Benedetta, Socha, Jerzy, Socha, Piotr, Stolarczyk, Anna, Szott, Katarzyna, Dobrzańska, Anna, Gruszfeld, Dariusz, Kowalik, Agnieszka, Janas, Roman, Pietraszek, Ewa, Perrin, Emmanuel, von Kries, Rüdiger, Groebe, Helfried, Reith, Anna, Hofmann, Renate, Koletzko, Berthold, Grote, Veit, Weber, Martina, Rzehak, Peter, Schiess, Sonia, Beyer, Jeannette, Fritsch, Michaela, Handel, Uschi, Pawellek, Ingrid, Verwied-Jorky, Sabine, Hannibal, Iris, Demmelmair, Hans, Haile, Gudrun, Kirchberg, Franca, Akopjan, Lusine, Campoy (PI), Cristina, Pérez, Miguel, Catena, Andrés, Torres-Espínola, Francisco J., Cristina Martínez-Zaldívar, Mª, Brandi, Pilar, Victoria Escolano-Margarit, Mª, Gudrun, Haile, Krauss-Estchmann, Susan, Décsi, Tamas, Csábi, Györgyi, Györey, Esther, Gispert-Llaurado, M., Perez-Garcia, Miguel, Escribano, J., Closa-Monasterolo, R., Luque, V., Grote, V., Weber, M., Torres-Espínola, F.J., Czech-Kowalska, J., Verduci, E., Martin, F., Piqueras, M.J., Koletzko, B., Decsi, T., Campoy, Cristina, Emmett, P.M.
Publikováno v:
In Clinical Nutrition December 2016 35(6):1301-1307
Autor:
Annick, Xhonneux, Jean-Paul, Langhendries, Françoise, Martin, Laurence, Seidel, Adelin, Albert, Elena, Dain, Martina, Totzauer, Veit, Grote, Veronica, Luque, Ricardo, Closa-Monasterolo, Alice Re, Dionigi, Elvira, Verduci, Darius, Gruszfeld, Piotr, Socha, Berthold, Koletzko
Publikováno v:
Maternal and Child Health Journal. 26:1274-1282
Background Maternal perception of child weight status in children with overweight or obesity has received a lot of attention but data on paternal perception of children from presumably healthy cohorts are lacking. Objective We aimed to investigate pa
Publikováno v:
Climate
Volume 11
Issue 3
Pages: 56
Volume 11
Issue 3
Pages: 56
Extreme sea levels and coastal flooding are projected to be among the most uncertain and severe consequences of climate change. In response, a wide development of coastal vulnerability assessment methodologies has been observed in research to support
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe8a94e843e2164c34d38d55e798e455
https://hdl.handle.net/11583/2976607
https://hdl.handle.net/11583/2976607
Autor:
Valentina Rovelli, Graziella Cefalo, Vittoria Ercoli, Juri Zuvadelli, Turri Olivia, Daniela Graziani, Alberti Luisella, Davide Bassi, Alice Re Dionigi, Raed Selmi, Sabrina Paci, Elisabetta Salvatici, Giuseppe Banderali
Publikováno v:
Endocrinology, Diabetes & Metabolism. 6
Hyperphenylalaninemias (HPA) are due to several gene mutations, of which the PAH gene is the most frequently involved. Prevalence and incidence of disease vary between populations, with genotype/phenotype correlations not always capable to correctly