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467 results on '"Riva, Enrica"'

2. Design and Development of Patient-Specific Medical Devices for Maxillofacial Surgery Through 3D Modeling, Topology Optimization, and Additive Manufacturing

Author

Favi, Claudio, Riva, Enrica, Fortese, Giovanni, Varazzani, Andrea, Chaari, Fakher, Series Editor, Gherardini, Francesco, Series Editor, Ivanov, Vitalii, Series Editor, Haddar, Mohamed, Series Editor, Cavas-Martínez, Francisco, Editorial Board Member, di Mare, Francesca, Editorial Board Member, Kwon, Young W., Editorial Board Member, Trojanowska, Justyna, Editorial Board Member, Xu, Jinyang, Editorial Board Member, Carfagni, Monica, editor, Furferi, Rocco, editor, Di Stefano, Paolo, editor, and Governi, Lapo, editor

Published
2024
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9. Point of view of the Italians pediatric scientific societies about the pediatric care during the COVID-19 lockdown: what has changed and future prospects for restarting

Author

Lubrano, Riccardo, Villani, Alberto, Berrettini, Stefano, Caione, Paolo, Chiara, Alberto, Costantino, Antonella, Formigari, Roberto, Franzoni, Emilio, Gattinara, Guido Castelli, Giustardi, Arturo, La Marca, Giancarlo, Lionetti, Paolo, Lima, Mario, Maffei, Claudio, Malamisura, Monica, Manzoni, Giantonio, Marseglia, Gian Luigi, Memeo, Antonio, Mosca, Fabio, Perricone, Giovanna, Peruzzi, Licia, Piacentini, Giorgio, Pozzobon, Gabriella, Riva, Enrica, Tesoro, Simonetta, Zampino, Giuseppe, Zanetto, Federica, Zecca, Marco, and Bloise, Silvia

Published
2020
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10. Fish consumption in mid-childhood and its relationship to neuropsychological outcomes measured in 7–9 year old children using a NUTRIMENTHE neuropsychological battery

Author

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, and Emmett, P.M.

Published
2016
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12. Severe Hypertriglyceridemia in a Newborn with Monogenic Lipoprotein Lipase Deficiency: An Unconventional Therapeutic Approach with Exchange Transfusion

Author

Pugni, Lorenza, Riva, Enrica, Pietrasanta, Carlo, Rabacchi, Claudio, Bertolini, Stefano, Pederiva, Cristina, Mosca, Fabio, Calandra, Sebastiano, Zschocke, Johannes, Editor-in-chief, Gibson, K Michael, Editor-in-chief, Gibson, K. Michael, editor, Brown, Garry, editor, Morava, Eva, editor, and Peters, Verena, editor

Published
2014
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17. Rapid Growth and Childhood Obesity Are Strongly Associated with LysoPC(14:0)

Author

Rzehak, Peter, Hellmuth, Christian, Uhl, Olaf, Kirchberg, Franca F., Peissner, Wolfgang, Harder, Ulrike, Grote, Veit, Weber, Martina, Xhonneux, Annick, Langhendries, Jean-Paul, Ferre, Natalia, Closa-Monasterolo, Ricardo, Verduci, Elvira, Riva, Enrica, Socha, Piotr, Gruszfeld, Dariusz, and Koletzko, Berthold

Published
2014

25. Electrolyte abnormalities in cystic fibrosis: systematic review of the literature

Author

Scurati-Manzoni, Elisabetta, Fossali, Emilio F., Agostoni, Carlo, Riva, Enrica, Simonetti, Giacomo D., Zanolari-Calderari, Maura, Bianchetti, Mario G., and Lava, Sebastiano A.G.

Subjects
Cystic fibrosis -- Research -- Risk factors -- Complications and side effects -- Patient outcomes -- Care and treatment, Hypokalemia -- Risk factors -- Research, Alkalosis -- Research -- Risk factors, Health
Abstract

Background Cystic fibrosis per se can sometimes lead to hyponatremia, hypokalemia, hypochloremia or hyperbicarbonatemia. This tendency was first documented 60 years ago and has subsequently been confirmed in single case reports or small case series, most of which were retrospective. However, this issue has not been addressed analytically. We have therefore systematically reviewed and analyzed the available literature on this subject. Methods This was a systematic review of the literature. Results The reports included in this review cover 172 subacute and 90 chronic cases of electrolyte imbalances in patients with cystic fibrosis. The male:female ratio was 1.57. Electrolyte abnormalities were mostly associated with clinically inapparent fluid volume depletion, mainly affected patients aged ≤ 2.5 years, frequently tended to recur and often were found before the diagnosis of cystic fibrosis was established. Subacute presentation often included an history of heat exposure, vomiting, excessive sweating and pulmonary infection. History of chronic presentation, in contrast, was often inconspicuous. The tendency to hypochloremia, hypokalemia and metabolic alkalosis was similar between subacute and chronic patients, with hyponatremia being more pronounced (P < 0.02) in subacute compared to chronic presentations. Subacute cases were treated parenterally; chronic ones were usually managed with oral salt supplementation. Retention of urea and creatinine was documented in 38% of subacute cases. Conclusions The findings of our review suggest that physicians should be aware that electrolyte abnormalities can occur both as a presenting and a recurring feature of cystic fibrosis. Keywords Cystic fibrosis * Hypokalemia * Hyponatremia * Metabolic alkalosis, Introduction Hyponatremia, hypokalemia, hypochloremia or hyperbicarbonatemia are conditions that can be found in cystic fibrosis patients on drug treatment [1, 2]. Hyponatremia and hypokalemia can also be found in cystic [...]

Published
2014
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26. Front-of-pack (FOP) labelling systems to improve the quality of nutrition information to prevent obesity: NutrInform Battery vs Nutri-Score

Author

Carruba, Michele O., primary, Caretto, Antonio, additional, De Lorenzo, Antonino, additional, Fatati, Giuseppe, additional, Ghiselli, Andrea, additional, Lucchin, Lucio, additional, Maffeis, Claudio, additional, Malavazos, Alexis, additional, Malfi, Giuseppe, additional, Riva, Enrica, additional, Ruocco, Chiara, additional, Santini, Ferruccio, additional, Silano, Marco, additional, Valerio, Alessandra, additional, Vania, Andrea, additional, and Nisoli, Enzo, additional

Published
2021
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34. Additional file 1 of Point of view of the Italians pediatric scientific societies about the pediatric care during the COVID-19 lockdown: what has changed and future prospects for restarting

Author

Lubrano, Riccardo, Villani, Alberto, Berrettini, Stefano, Caione, Paolo, Chiara, Alberto, Costantino, Antonella, Formigari, Roberto, Franzoni, Emilio, Gattinara, Guido Castelli, Giustardi, Arturo, Marca, Giancarlo La, Lionetti, Paolo, Lima, Mario, Maffei, Claudio, Malamisura, Monica, Giantonio Manzoni, Marseglia, Gian Luigi, Memeo, Antonio, Mosca, Fabio, Perricone, Giovanna, Peruzzi, Licia, Piacentini, Giorgio, Pozzobon, Gabriella, Riva, Enrica, Tesoro, Simonetta, Zampino, Giuseppe, Zanetto, Federica, Zecca, Marco, and Bloise, Silvia

Abstract

Additional file 1. Fiarped questionnaire.

Published
2020
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37. Increased Breastfeeding Rates in Italy

Author

Giovannini, Marcello, Banderali, Giuseppe, Agostoni, Carlo, Scaglioni, Silvia, Silano, Marco, Riva, Enrica, Davis, Margarett K., editor, Isaacs, Charles E., editor, Hanson, Lars Å., editor, and Wright, Anne L., editor

Published
2002
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50. A European multicenter study of phenylalanine hydroxylase deficiency: classification of 105 mutations and a general system for genotype-based prediction of metabolic phenotype

Author

Guldberg, Per, Rey, Francoise, Zschocke, Johannes, Romano, Valentino, Francois, Baudouin, Michiels, Luc, Ullrich, Kurt, Hoffmann, Georg F., Burgard, Peter, Schmidt, Hildgund, Meli, Concetta, Riva, Enrica, Dianzani, Irma, Ponzone, Alberto, Rey, Jean, and Guttler, Flemming

Subjects
Europe -- Health aspects, Genetic disorders -- Research, Phenylalanine -- Physiological aspects, Metabolic diseases -- Genetic aspects, Phenylketonuria -- Genetic aspects, Disease susceptibility -- Genetic aspects, Biological sciences
Abstract

A European multicenter study of phenylalanine hydroxylase deficiency has led to a general system for prediction of metabolic phenotype based on genotype and to classification of 105 mutations. Mild hyperphenylalaninemia (MHP) and phenylketonuria (PKU) are allelic disorders caused by mutations in the gene coding for phenylalanine hydroxylase (PAH). Both mutations were found in 686 patients in seven locations in Europe. Based on the phenotypic characteristics of 297 functionally hemizygous patients, 105 of the mutations were assigned to one of four arbitrary phenotype categories. Data show that the PAH-mutation genotype is the primary determinant of metabolic phenotype in most PAH-deficiency patients. The disorder is autosomal recessive.

Published
1998

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