Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Roberto Della Casa"'
Autor:
Vincenza Gragnaniello, Federica Deodato, Serena Gasperini, Maria Alice Donati, Clementina Canessa, Simona Fecarotta, Antonia Pascarella, Giuseppe Spadaro, Daniela Concolino, Alberto Burlina, Giancarlo Parenti, Pietro Strisciuglio, Agata Fiumara, Roberto Della Casa
Publikováno v:
Italian Journal of Pediatrics, Vol 48, Iss 1, Pp 1-14 (2022)
Abstract Background Classic infantile onset of Pompe disease (c-IOPD) leads to hypotonia and hypertrophic cardiomyopathy within the first days to weeks of life and, without treatment, patients die of cardiorespiratory failure in their first 1–2 yea
Externí odkaz:
https://doaj.org/article/61af1ccf535f4399a2639a84afdb50e6
Autor:
Alessandro Rossi, Chiara Simeoli, Mariacarolina Salerno, Rosario Ferrigno, Roberto Della Casa, Annamaria Colao, Pietro Strisciuglio, Giancarlo Parenti, Rosario Pivonello, Daniela Melis
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-8 (2020)
Abstract Background Glycogen storage disease type I (GSDI) is an inborn error of carbohydrate metabolism caused by mutations of either the G6PC gene (GSDIa) or the SLC37A4 gene (GSDIb). Glucose 6-phosphate (G6P) availability has been shown to modulat
Externí odkaz:
https://doaj.org/article/881d60d9f267492191ae50bab927516d
Autor:
Rossella Parini, Paola De Lorenzo, Andrea Dardis, Alberto Burlina, Alessandra Cassio, Paolo Cavarzere, Daniela Concolino, Roberto Della Casa, Federica Deodato, Maria Alice Donati, Agata Fiumara, Serena Gasperini, Francesca Menni, Veronica Pagliardini, Michele Sacchini, Marco Spada, Roberta Taurisano, Maria Grazia Valsecchi, Maja Di Rocco, Bruno Bembi
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-12 (2018)
Abstract Background Enzyme replacement therapy (ERT) has deeply modified the clinical history of Infantile Onset Pompe Disease (IOPD). However, its long-term effectiveness is still not completely defined. Available data shows a close relationship bet
Externí odkaz:
https://doaj.org/article/605b3b5eb28d4b7a99de8697eff78483
Autor:
Mariacarolina Salerno, Annamaria Colao, Roberto Della Casa, Pietro Strisciuglio, Rosario Pivonello, A. Rossi, Chiara Simeoli, Daniela Melis, Rosario Ferrigno, Giancarlo Parenti
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-8 (2020)
Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
Background Glycogen storage disease type I (GSDI) is an inborn error of carbohydrate metabolism caused by mutations of either the G6PC gene (GSDIa) or the SLC37A4 gene (GSDIb). Glucose 6-phosphate (G6P) availability has been shown to modulate 11β-hy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::26064fcd5d1f662084d47bb2428bf6a5
http://link.springer.com/article/10.1186/s13023-020-01377-w
http://link.springer.com/article/10.1186/s13023-020-01377-w
Autor:
Francesca, Cenzato, Milani, Gregorio P., Angela, Amigoni, Francesca, Sperotto, Bianchetti, Mario G., Carlo, Agostoni, Giovanni, Montini, Farello, Giovanni, Francesco, Chiarelli, Greco, Rita, Franco Di Lollo, Fabio Rocco Forte, Sergio, Manieri, Luigi, Carpino, Mimma, Caloiero, Anastasia, Cirisano, Salvatore, Bragh(`(o)), Roberto Della Casa, Felice, Nunziata, Carmine, Pecoraro, Rosario, Pacifico, Marcello, Lanari, Chiara, Ghizzi, Laura, Serra, Marcello, Stella, Giuseppe, Maggiore, Roberto, Fiorini, Icilio, Dodi, Andrea, Morelli, Lorenzo, Lughetti, Andrea, Cella, Gianluca, Vergine, Alessandro De Fanti, Danica, Dragovic, Daniele, Santori, Giorgio, Cozzi, Paola, Cogo, Marilena, Raponi, Riccardo, Lubrano, Mauro de Martinis, Antonio, Gatto, Maria Antonietta Barbieri, Antonino, Reale, Giorgio, Bracaglia, Emanuela, Piccotti, Riccardo, Borea, Alberto, Gaiero, Laura, Martelli, Alberto, Arrighini, Paola, Cianci, Claudio, Cavalli, Leonardina De Santis, Benedetta Chiara Pietra, Andrea, Biondi, Marco, Sala, Pogliani, Laura M., Simonetta, Cherubini, Marta, Bellini, Paola, Bruni, Giovanni, Traina, Paola, Tommasi, Paolo Del Barba, Sergio, Arrigoni, Salvini, Filippo M., Luca, Bernardo, Giuseppe, Bertolozzi, Silvia, Fasoli, Gian Luigi Marseglia, Emilio, Palumbo, Annalisa, Bosco, Gianpaolo, Mirri, Elisabetta, Fabiani, Ermanno, Ruffini, Luisa, Pieragostini, Martina, Fornaro, Gabriele, Ripanti, Donnina, Pannoni, Felici, Enrico, Anna, Perona, Eleonora, Tappi, Oscar Nis Haitink, Ivana, Rabbone, Pina Teresa Capalbo, Antonio, Urbino, Andrea, Guala, Gianluca, Cosi, Maria Gabriella Barracchia, Baldassarre, Martire, Fabio, Cardinale, Fulvio, Moramarco, Carmelo, Perrone, Angelo, Campanozzi, Valerio, Cecinati, Alessandro, Canetto, Ciro, Clemente, Antonio, Cualbu, Fabio, Narducci, Giuseppina, Mula, Pasquale, Bulciolu, Roberto, Antonucci, Giuseppe, Gramaglia, Giuseppe, Cavaleri, Carmelo, Salpietro, Giovanni, Corsello, Rosario, Salvo, Marcello, Palmeri, Maria Assunta Vitale, Ambra, Morgano, Susanna, Falorni, Diego, Peroni, Stefano, Masi, Alessio, Bertini, Angelina, Vaccaro, Pierluigi, Vasarri, Petra, Reinstadler, Massimo, Soffiati, Maurizio, Stefanelli, VERROTTI di PIANELLA, Alberto, Catherine, Bertone, Stefano, Marzini, Liviana Da Dalt, Simone, Rugolotto, Floriana, Scozzola, Luca Ecclesio Livio, Mauro, Cinquetti, Davide, Silvagni, Massimo Bellettato and
Urinary tract infections (UTIs) are among the most frequent bacterial diseases in infants and children. Physician adherence to recommendations is notoriously often poor, but no data are available on UTIs management in the emergency setting. In this m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::518af26f8bf82ca6c525bb62ef449194
https://hdl.handle.net/11585/900339
https://hdl.handle.net/11585/900339
Autor:
Deianira Pedoto, Alfredo Diana, Roberto Della Casa, Francesca Paciello, Flavio Quarantiello, Maria Laura Pennacchio
Publikováno v:
Pediatric Infectious Disease Journal. 40:e276-e278
Primary pyomyositis is a bacterial muscle infection which may lead to abscess formation and severe complications. Although this condition has long been considered "tropical" and rare, mostly affecting immunocompromised patients, cases of pyomyositis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82b6e869795c6b2ba3b5f0918e7306c6
https://doi.org/10.1097/inf.0000000000003113
https://doi.org/10.1097/inf.0000000000003113
Autor:
Vincenza Gragnaniello, Federica Deodato, Serena Gasperini, Maria Alice Donati, Clementina Canessa, Simona Fecarotta, Antonia Pascarella, Giuseppe Spadaro, Daniela Concolino, Alberto Burlina, Giancarlo Parenti, Pietro Strisciuglio, Agata Fiumara, Roberto Della Casa
Publikováno v:
Italian journal of pediatrics. 48(1)
Background Classic infantile onset of Pompe disease (c-IOPD) leads to hypotonia and hypertrophic cardiomyopathy within the first days to weeks of life and, without treatment, patients die of cardiorespiratory failure in their first 1–2 years of lif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f88fee145192a0a9cdc14ae65a1fafac
https://pubmed.ncbi.nlm.nih.gov/35248118
https://pubmed.ncbi.nlm.nih.gov/35248118
Autor:
W.W.M. Pim Pijnappel, Roberto Della Casa, Ans T. van der Ploeg, Lucio Santoro, Liliana Vercelli, Marcella Coletta, Olimpia Musumeci, Marianthi Karali, Andrea Dardis, Annamaria Carissimo, Nadia Minopoli, Edoardo Nusco, Francesca Gatto, Antonietta Tarallo, Tiziana Mongini, Sandro Banfi, Roberta Taurisano, Giancarlo Parenti, Lucia Ruggiero, Carla Damiano, Antonio Toscano, Simona Fecarotta, Emma Acampora, Bruno Bembi, Federica Deodato
Publikováno v:
Genetics in medicine (2018): 1–10. doi:10.1038/s41436-018-0103-8
info:cnr-pdr/source/autori:Tarallo A.; Carissimo A.; Gatto F.; Nusco E.; Toscano A.; Musumeci O.; Coletta M.; Karali M.; Acampora E.; Damiano C.; Minopoli N.; Fecarotta S.; della Casa R.; Mongini T.; Vercelli L.; Santoro L.; Ruggiero L.; Deodato F.; Taurisano R.; Bembi B.; Dardis A.; Banfi S.; Pijnappel W.W.P.; van der Ploeg A.T.; Parenti G./titolo:microRNAs as biomarkers in Pompe disease/doi:10.1038%2Fs41436-018-0103-8/rivista:Genetics in medicine/anno:2018/pagina_da:1/pagina_a:10/intervallo_pagine:1–10/volume
Genetics in Medicine, 21(3), 591-600. Lippincott Williams & Wilkins
info:cnr-pdr/source/autori:Tarallo A.; Carissimo A.; Gatto F.; Nusco E.; Toscano A.; Musumeci O.; Coletta M.; Karali M.; Acampora E.; Damiano C.; Minopoli N.; Fecarotta S.; della Casa R.; Mongini T.; Vercelli L.; Santoro L.; Ruggiero L.; Deodato F.; Taurisano R.; Bembi B.; Dardis A.; Banfi S.; Pijnappel W.W.P.; van der Ploeg A.T.; Parenti G./titolo:microRNAs as biomarkers in Pompe disease/doi:10.1038%2Fs41436-018-0103-8/rivista:Genetics in medicine/anno:2018/pagina_da:1/pagina_a:10/intervallo_pagine:1–10/volume
Genetics in Medicine, 21(3), 591-600. Lippincott Williams & Wilkins
PURPOSE: We studied microRNAs as potential biomarkers for Pompe disease. METHODS: We analyzed microRNA expression by small RNA-seq in tissues from the disease murine model at two different ages (3 and 9 months), and in plasma from Pompe patients. RES
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1fcda52c7f58c88ad9e3a6b33934c2bd
https://doi.org/10.1038/s41436-018-0103-8
https://doi.org/10.1038/s41436-018-0103-8
Autor:
Francesco Mattioli, Roberto Della Casa
Publikováno v:
Italus Hortus. 26:1-18
For the benefit of a younger audience, the cherry can be further enhanced by freeing it from the fruit group and allowing it to become part of the world of desserts and special treats. On the contrary, the localisms, traditions, and seasonality which
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::69a57cd2ff9f1251110212d3ecc825a5
https://doi.org/10.26353/j.itahort/2019.1.118
https://doi.org/10.26353/j.itahort/2019.1.118
Autor:
Pierre, Quartier, Ekaterina, Alexeeva, Constantin, Tamàs, Vyacheslav, Chasnyk, Nico, Wulffraat, Karin, Palmblad, Carine, Wouters, Hermine, Brunner, Katherine, Marzan, Rayfel, Schneider, Gerd, Horneff, Martini, Alberto, Jordi, Anton, Xiaoling, Wei, Alan, Slade, Ruperto, Nicolino, Ken, Abrams, Wolfgang, Emminger, Andrea, Ulbrich, Sugarka, Fodor, Lien, Desomer, Bernard, Lauwerys, Bénédicte, Brichard, Cécile, Boulanger, Gabriel, Levy, Laurence, Goffin, Phu Quoc Le, Marcia, Bandeira, Christina Feitosa Pelajo, Sheila Knupp Feitosa, Christianne, Costa, Marta Cristine Felix Rodrigues, Clovis Artur Almeida da Silva, Lucia Maria Mattei de, Katia, Kozu, Ronald, Laxer, Kristin, Houghton, Lori, Tucker, Kimberly, Morishita, Agnes, Mogenet, Richard, Mouy, Brigitte Bader Meunier, Candice, Meyzer, Michaela, Semeraro, Ouafa, Ben‐brahim, Isabelle, Kone‐paut, Caroline, Galeotti, Linda, Rossi, Perrine, Dusser, Bilade, Cherquaoui, Alexandre, Belot, Agnes, Duquesne, Freychet, Caroline, Laurent, Audrey, Marine, Desjonqueres, Ivan, Foeldvari, Antonia, Kienast, Barbara, Willig, Deborah, Barthel, Joachim, Peitz, Stefanie, Wintrich, Tilman Felix Geikowski, Anna Carina Schulz, Markus, Hufnagel, Marc, Hirdes, Rouven, Kubicki, Janbernd, Kirschner, Ales, Janda, Andre, Jacob, Cornelia, Emerich, Anna, Raab, Gonza, Ngoumou, Kirsten, Minden, Mareike, Lieber, Sae‐Lim von Stuckrad, Jasmin Kuemmerle Deschner, Sandra, Hansmann, Tom, Schleich, Ines Maria Magunia, Joachim, Riethmuller, Nicole, Anders, Hartwig, Lehmann, Jan de Laffolie, Thomas, Lutz, Juergen, Grulich‐henn, Johannes, Pfeil, Astrid, Helling‐bakki, Ralf, Trauzeddel, Daniel, Haselbusch, Henryk, Kolbeck, Elisabeth, Weissbarth‐riedel, Anja, Froehlich, Andrea, Ponyi, Diana, Garan, Ilonka, Orban, Krisztina, Sevcic, Yonatan, Butbul, Riva, Brik, Philip, Hashkes, Ori, Toker, Ruby, Haviv, Yosef, Uziel, Rubi, Haviv, Veronica, Moshe, Michal, Rothschild, Liora, Harel, Gil, Amarilyo, Rotem, Tal, Mohamad Hamad Said, Irit, Tirosh, Shiri, Spielman, Maya, Gerstein, Ravelli, Angelo, Schiappapietra, Benedetta, Varnier, GIULIA CAMILLA, Finetti, Martina, Marasini, Maurizio, Caorsi, Roberta, Rosina, Silvia, Federici, Silvia, Irene, Pontikaki, Pier Luigi Meroni, Valeri, Gerloni, Nicola, Ughi, Tania, Ubiali, Maria, Alessio, Roberto Della Casa, Sebastiaan Jozef Vastert, Joost Frans Swart, van Royen‐Kerhof, A., Ellen, Schatorje, Van Iperen‐Schutte, G., Lidia, Rutkowska‐sak, Izabela, Szczygielska, Malgorzata, Kwiatkowska, Maria, Marusak‐banacka, Piotr, Gietka, Kseniya, Isaeva, Rina, Denisova, Ludmila, Snegireva, Margarita, Dubko, Mikhail, Kostik, Natalia, Buchinskaia, Olga, Kalashnikova, Sergey, Avrusin, Vera, Masalova, Esmeralda Nunez Cuadros, Gisela, Diez, Rocio Galindo Zavala, Rosa Bou Torrent, Estibaliz, Iglesias, Joan, Calzada, Violeta, Bittermann, Alina Lucica Boteanu, Maria Luz Gamir, Inmaculada, Calvo, Berta, Lopez, Isabel, Gonzalez, Laura, Fernandez, Daniel Clemente Garulo, Juan Carlos Lopez Robledillo, Rosa, Merino, Rosa, Alcobendas, Agustin, Remesal, Sara, Murias, Magnusson, Bo, Ozgur, Kasapcopur, Kenan, Barut, Amra, Adrovic, Sezgin, Sahin, Muferet, Erguven, Refia Gozdenur Savci, Seza, Ozen, Selcan, Demir, Yelda, Bilginer, Zehra Serap Avci, Ezgi Deriz Batu, Andreas, Reiff, Anusha, Ramanatham, Diana, Brown, Bracha, Shaham, Shirley, Parks, Michal, Cidon, Gloria, Higgins, Charles, Spencer, Jenny, Rossette, Karla, Jones, Sharon Bout Tabaku, Shelli, Farley, Shoghik, Akoghlanian
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::cec0dcf8696b3828689854500b78a1d0
http://hdl.handle.net/11588/821370
http://hdl.handle.net/11588/821370