Glibenclamide in the treatment for gestational diabetes mellitus in a compared study to insulin von Silva, Jean C, Bertini, Anna M, Taborda, Wladimir, Becker, Felipe, Bebber, Fernanda R L, Aquim, Gabriela M D C, Viesi, Juliana M Z

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Glibenclamida no tratamento do diabete melito gestacional em estudo comparado à insulina von Silva, Jean C., Bertini, Anna M., Taborda, Wladimir, Becker, Felipe, Bebber, Fernanda R.L., Aquim, Gabriela M.D.C., Viesi, Juliana M.Z.

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Glibenclamida no tratamento do diabete melito gestacional em estudo comparado à insulina von Silva, Jean C., Bertini, Anna M., Taborda, Wladimir, Becker, Felipe, Bebber, Fernanda R.L., Aquim, Gabriela M.D.C., Viesi, Juliana M.Z.

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Levosimendan for Hemodynamic Support after Cardiac Surgery von Landoni, Giovanni, Lomivorotov, Vladimir V, Alvaro, Gabriele, Lobreglio, Rosetta, Pisano, Antonio, Guarracino, Fabio, Calabrò, Maria G, Grigoryev, Evgeny V, Likhvantsev, Valery V, Salgado-Filho, Marcello F, Bianchi, Alessandro, Pasyuga, Vadim V, Baiocchi, Massimo, Pappalardo, Federico, Monaco, Fabrizio, Boboshko, Vladimir A, Abubakirov, Marat N, Amantea, Bruno, Lembo, Rosalba, Brazzi, Luca, Verniero, Luigi, Bertini, Pietro, Scandroglio, Anna M, Bove, Tiziana, Belletti, Alessandro, Michienzi, Maria G, Shukevich, Dmitriy L, Zabelina, Tatiana S, Bellomo, Rinaldo, Zangrillo, Alberto

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Mechanisms inducing low bone density in duchenne muscular dystrophy in mice and humans von Rufo, Anna, Del Fattore, Andrea, Capulli, Mattia, Carvello, Francesco, De Pasquale, Loredana, Ferrari, Serge, Pierroz, Dominique, Morandi, Lucia, De Simone, Michele, Rucci, Nadia, Bertini, Enrico, Bianchi, Maria Luisa, De Benedetti, Fabrizio, Teti, Anna

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Randomized phase 2 trial and open-label extension of domagrozumab in Duchenne muscular dystrophy von Wagner, Kathryn R., Abdel-Hamid, Hoda Z., Mah, Jean K., Campbell, Craig, Guglieri, Michela, Muntoni, Francesco, Takeshima, Yasuhiro, McDonald, Craig M., Kostera-Pruszczyk, Anna, Karachunski, Peter, Butterfield, Russell J., Mercuri, Eugenio, Fiorillo, Chiara, Bertini, Enrico S., Tian, Cuixia, Statland, Jeffery, Sadosky, Alesia B., Purohit, Vivek S., Sherlock, Sarah P., Palmer, Jeffrey P., Binks, Michael, Charnas, Lawrence, Marraffino, Shannon, Wong, Brenda L.

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Ataluren in patients with nonsense mutation Duchenne muscular dystrophy (ACT DMD): a multicentre, randomised, double-blind, placebo-controlled, phase 3 trial von McDonald, Craig M, Campbell, Craig, Torricelli, Ricardo Erazo, Finkel, Richard S, Flanigan, Kevin M, Goemans, Nathalie, Heydemann, Peter, Kaminska, Anna, Kirschner, Janbernd, Muntoni, Francesco, Osorio, Andrés Nascimento, Schara, Ulrike, Sejersen, Thomas, Shieh, Perry B, Sweeney, H Lee, Topaloglu, Haluk, Tulinius, Már, Vilchez, Juan J, Voit, Thomas, Wong, Brenda, Elfring, Gary, Kroger, Hans, Luo, Xiaohui, McIntosh, Joseph, Ong, Tuyen, Riebling, Peter, Souza, Marcio, Spiegel, Robert J, Peltz, Stuart W, Mercuri, Eugenio, Alfano, Lindsay N, Eagle, Michelle, James, Meredith K, Lowes, Linda, Mayhew, Anna, Mazzone, Elena S, Nelson, Leslie, Rose, Kristy J, Abdel-Hamid, Hoda Z, Apkon, Susan D, Barohn, Richard J, Bertini, Enrico, Bloetzer, Clemens, de Vaud, Lausanne Canton, Butterfield, Russell J, Chabrol, Brigitte, Chae, Jong-Hee, Jongno-gu, Daehak-ro, Comi, Giacomi Pietro, Darras, Basil T, Dastgir, Jahannaz, Desguerre, Isabelle, Escobar, Raul G, Finanger, Erika, Guglieri, Michela, Hughes, Imelda, Iannaccone, Susan T, Jones, Kristi J, Karachunski, Peter, Kudr, Martin, Lotze, Timothy, Mah, Jean K, Mathews, Katherine, Nevo, Yoram, Parsons, Julie, Péréon, Yann, de Queiroz Campos Araujo, Alexandra Prufer, Renfroe, J Ben, de Resende, Maria Bernadete Dutra, Ryan, Monique, Selby, Kathryn, Tennekoon, Gihan, Vita, Giuseppe

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Mediterranean winter rainfall in phase with African monsoons during the past 1.36 million years von Wagner, Bernd, Vogel, Hendrik, Francke, Alexander, Friedrich, Tobias, Donders, Timme, Lacey, Jack H., Leng, Melanie J., Regattieri, Eleonora, Sadori, Laura, Wilke, Thomas, Zanchetta, Giovanni, Albrecht, Christian, Bertini, Adele, Combourieu-Nebout, Nathalie, Cvetkoska, Aleksandra, Giaccio, Biagio, Grazhdani, Andon, Hauffe, Torsten, Holtvoeth, Jens, Joannin, Sebastien, Jovanovska, Elena, Just, Janna, Kouli, Katerina, Kousis, Ilias, Koutsodendris, Andreas, Krastel, Sebastian, Lagos, Markus, Leicher, Niklas, Levkov, Zlatko, Lindhorst, Katja, Masi, Alessia, Melles, Martin, Mercuri, Anna M., Nomade, Sebastien, Nowaczyk, Norbert, Panagiotopoulos, Konstantinos, Peyron, Odile, Reed, Jane M., Sagnotti, Leonardo, Sinopoli, Gaia, Stelbrink, Björn, Sulpizio, Roberto, Timmermann, Axel, Tofilovska, Slavica, Torri, Paola, Wagner-Cremer, Friederike, Wonik, Thomas, Zhang, Xiaosen

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Safety and efficacy of olesoxime in patients with type 2 or non-ambulatory type 3 spinal muscular atrophy: a randomised, double-blind, placebo-controlled phase 2 trial von Bertini, Enrico, Prof, Dessaud, Eric, PhD, Mercuri, Eugenio, Prof, Muntoni, Francesco, Prof, Kirschner, Janbernd, Prof, Reid, Carol, PhD, Lusakowska, Anna, MD, Comi, Giacomo P, Prof, Cuisset, Jean-Marie, MD, Abitbol, Jean-Louis, MD, Scherrer, Bruno, PhD, Ducray, Patricia Sanwald, PhD, Buchbjerg, Jeppe, MSc, Vianna, Eduardo, PhD, van der Pol, W Ludo, MD, Vuillerot, Carole, MD, Blaettler, Thomas, MD, Fontoura, Paulo, MD

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Biallelic Mutations in TBCD, Encoding the Tubulin Folding Cofactor D, Perturb Microtubule Dynamics and Cause Early-Onset Encephalopathy von Flex, Elisabetta, Niceta, Marcello, Cecchetti, Serena, Thiffault, Isabelle, Au, Margaret G., Capuano, Alessandro, Piermarini, Emanuela, Ivanova, Anna A., Francis, Joshua W., Chillemi, Giovanni, Chandramouli, Balasubramanian, Carpentieri, Giovanna, Haaxma, Charlotte A., Ciolfi, Andrea, Pizzi, Simone, Douglas, Ganka V., Levine, Kara, Sferra, Antonella, Dentici, Maria Lisa, Pfundt, Rolph R., Le Pichon, Jean-Baptiste, Farrow, Emily, Baas, Frank, Piemonte, Fiorella, Dallapiccola, Bruno, Graham, John M., Saunders, Carol J., Bertini, Enrico, Kahn, Richard A., Koolen, David A., Tartaglia, Marco

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Abatement of 2,4-D by H2O2 solar photolysis and solar photo-Fenton-like process with minute Fe(III) concentrations von Serra-Clusellas, Anna, De Angelis, Laura, Lin, Chung-Ho, Vo, Phuc, Bayati, Mohamed, Sumner, Lloyd, Lei, Zhentian, Amaral, Nathalia B., Bertini, Liliana M., Mazza, Jose, Pizzio, Luis R., Stripeikis, Jorge D., Rengifo-Herrera, Julián A., Fidalgo de Cortalezzi, María M.

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Ataluren treatment of patients with nonsense mutation dystrophinopathy von Bushby, Katharine, Finkel, Richard, Wong, Brenda, Barohn, Richard, Campbell, Craig, Comi, Giacomo P., Connolly, Anne M., Day, John W., Flanigan, Kevin M., Goemans, Nathalie, Jones, Kristi J., Mercuri, Eugenio, Quinlivan, Ros, Renfroe, James B., Russman, Barry, Ryan, Monique M., Tulinius, Mar, Voit, Thomas, Moore, Steven A., Lee Sweeney, H., Abresch, Richard T., Coleman, Kim L., Eagle, Michelle, Florence, Julaine, Gappmaier, Eduard, Glanzman, Allan M., Henricson, Erik, Barth, Jay, Elfring, Gary L., Reha, Allen, Spiegel, Robert J., O'donnell, Michael W., Peltz, Stuart W., Mcdonald, Craig M.

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Pollen-based paleoenvironmental and paleoclimatic change at Lake Ohrid (south-eastern Europe) during the past 500 ka von Sadori, Laura, Koutsodendris, Andreas, Panagiotopoulos, Konstantinos, Masi, Alessia, Bertini, Adele, Combourieu-Nebout, Nathalie, Francke, Alexander, Kouli, Katerina, Joannin, Sébastien, Mercuri, Anna Maria, Peyron, Odile, Torri, Paola, Wagner, Bernd, Zanchetta, Giovanni, Sinopoli, Gaia, Donders, Timme H.

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Diagnosis and management of spinal muscular atrophy: Part 1: Recommendations for diagnosis, rehabilitation, orthopedic and nutritional care von Mercuri, Eugenio, Finkel, Richard S., Muntoni, Francesco, Wirth, Brunhilde, Montes, Jacqueline, Main, Marion, Mazzone, Elena S., Vitale, Michael, Snyder, Brian, Quijano-Roy, Susana, Bertini, Enrico, Davis, Rebecca Hurst, Meyer, Oscar H., Simonds, Anita K., Schroth, Mary K., Graham, Robert J., Kirschner, Janbernd, Iannaccone, Susan T., Crawford, Thomas O., Woods, Simon, Qian, Ying, Sejersen, Thomas, Muntoni, Francesco, Wirth, Brunhilde, Tiziano, Francesco Danilo, Kirschner, Janbernd, Tizzano, Eduardo, Topaloglu, Haluk, Swoboda, Kathy, Laing, Nigel, Kayoko, Saito, Prior, Thomas, Chung, Wendy K., Wu, Shou-Mei, Montes, Jacqueline, Mazzone, Elena, Main, Marion, Coleman, Caron, Gee, Richard, Glanzman, Allan, Kroksmark, Anna-Karin, Krosschell, Kristin, Nelson, Leslie, Rose, Kristy, Stępień, Agnieszka, Vuillerot, Carole, Vitale, Michael, Snyder, Brian, Quijano-Roy, Susana, Dubousset, Jean, Farrington, David, Flynn, Jack, Halanski, Matthew, Hasler, Carol, Miladi, Lotfi, Reilly, Christopher, Roye, Benjamin, Sponseller, Paul, Yazici, Muharrem, Hurst, Rebecca, Bertini, Enrico, Tarrant, Stacey, Barja, Salesa, Bertoli, Simona, Crawford, Thomas, Foust, Kevin, Kyle, Barbara, Rodan, Lance, Roper, Helen, Seffrood, Erin, Swoboda, Kathryn, Szlagatys-Sidorkiewicz, Agnieszka

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Gene expression profiling in the early phases of DMD: a constant molecular signature characterizes DMD muscle from early postnatal life throughout disease progression von Pescatori, Mario, Broccolini, Aldobrando, Minetti, Carlo, Bertini, Enrico, Bruno, Claudio, D'amico, Adele, Bernardini, Camilla, Mirabella, Massimiliano, Silvestri, Gabriella, Giglio, Vincenzo, Modoni, Anna, Pedemonte, Marina, Tasca, Giorgio, Galluzzi, Giuliana, Mercuri, Eugenio, Tonali, Pietro A, Ricci, Enzo

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Intensity Modulated Radiation Therapy With Simultaneous Integrated Boost in Patients With Brain Oligometastases: A Phase 1 Study (ISIDE-BM-1) von Ferro, Marica, MD, Chiesa, Silvia, MD, Macchia, Gabriella, MD, Cilla, Savino, PhD, Bertini, Federica, MD, Frezza, Giovanni, MD, Farioli, Andrea, MD, Cammelli, Silvia, MD, Balducci, Mario, MD, Ianiro, Anna, PhD, Angelini, Anna Lisa, PhD, Compagnone, Gaetano, PhD, Valentini, Vincenzo, MD, Deodato, Francesco, MD, Morganti, Alessio G., MD

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Disease characteristics of MCT8 deficiency: an international, retrospective, multicentre cohort study von Groeneweg, Stefan, van Geest, Ferdy S, Abacı, Ayhan, Alcantud, Alberto, Ambegaonkar, Gautam P, Armour, Christine M, Bakhtiani, Priyanka, Barca, Diana, Bertini, Enrico S, van Beynum, Ingrid M, Brunetti-Pierri, Nicola, Bugiani, Marianna, Cappa, Marco, Cappuccio, Gerarda, Castellotti, Barbara, Castiglioni, Claudia, Chatterjee, Krishna, de Coo, Irenaeus F M, Coutant, Régis, Craiu, Dana, Crock, Patricia, DeGoede, Christian, Demir, Korcan, Dica, Alice, Dimitri, Paul, Dolcetta-Capuzzo, Anna, Dremmen, Marjolein H G, Dubey, Rachana, Enderli, Anina, Fairchild, Jan, Gallichan, Jonathan, George, Belinda, Gevers, Evelien F, Hackenberg, Annette, Halász, Zita, Heinrich, Bianka, Huynh, Tony, Kłosowska, Anna, van der Knaap, Marjo S, van der Knoop, Marieke M, Konrad, Daniel, Koolen, David A, Krude, Heiko, Lawson-Yuen, Amy, Lebl, Jan, Linder-Lucht, Michaela, Lorea, Cláudia F, Lourenço, Charles M, Lunsing, Roelineke J, Lyons, Greta, Malikova, Jana, Mancilla, Edna E, McGowan, Anne, Mericq, Veronica, Lora, Felipe M, Moran, Carla, Müller, Katalin E, Oliver-Petit, Isabelle, Paone, Laura, Paul, Praveen G, Polak, Michel, Porta, Francesco, Poswar, Fabiano O, Reinauer, Christina, Rozenkova, Klara, Menevse, Tuba S, Simm, Peter, Simon, Anna, Singh, Yogen, Spada, Marco, van der Spek, Jet, Stals, Milou A M, Stoupa, Athanasia, Subramanian, Gopinath M, Tonduti, Davide, Turan, Serap, den Uil, Corstiaan A, Vanderniet, Joel, van der Walt, Adri, Wémeau, Jean-Louis, Wierzba, Jolante, de Wit, Marie-Claire Y, Wolf, Nicole I, Wurm, Michael, Zibordi, Federica, Zung, Amnon, Zwaveling-Soonawala, Nitash, Visser, W Edward

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LYRM7 mutations cause a multifocal cavitating leukoencephalopathy with distinct MRI appearance von Dallabona, Cristina, Abbink, Truus E M, Carrozzo, Rosalba, Torraco, Alessandra, Legati, Andrea, van Berkel, Carola G M, Niceta, Marcello, Langella, Tiziana, Verrigni, Daniela, Rizza, Teresa, Diodato, Daria, Piemonte, Fiorella, Lamantea, Eleonora, Fang, Mingyan, Zhang, Jianguo, Martinelli, Diego, Bevivino, Elsa, Dionisi-Vici, Carlo, Vanderver, Adeline, Philip, Sunny G, Kurian, Manju A, Verma, Ishwar C, Bijarnia-Mahay, Sunita, Jacinto, Sandra, Furtado, Fatima, Accorsi, Patrizia, Ardissone, Anna, Moroni, Isabella, Ferrero, Ileana, Tartaglia, Marco, Goffrini, Paola, Ghezzi, Daniele, van der Knaap, Marjo S, Bertini, Enrico

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Clinical, biochemical, and genetic features associated with VARS2‐related mitochondrial disease von Bruni, Francesco, Di Meo, Ivano, Bellacchio, Emanuele, Webb, Bryn D., McFarland, Robert, Chrzanowska‐Lightowlers, Zofia M.A., He, Langping, Skorupa, Ewa, Moroni, Isabella, Ardissone, Anna, Walczak, Anna, Tyynismaa, Henna, Isohanni, Pirjo, Mandel, Hanna, Prokisch, Holger, Haack, Tobias, Bonnen, Penelope E., Bertini, Enrico, Pronicka, Ewa, Ghezzi, Daniele, Taylor, Robert W., Diodato, Daria

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The NorthStar Ambulatory Assessment in Duchenne muscular dystrophy: considerations for the design of clinical trials von Ricotti, Valeria, Ridout, Deborah A, Pane, Marika, Main, Marion, Mayhew, Anna, Mercuri, Eugenio, Manzur, Adnan Y, Muntoni, Francesco

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