EVALUATION OF MYOCARDIAL BLOOD PERFUSION IN MAN WITH RADIOACTIVE POTASSIUM OR RUBIDIUM AND PRECORDIAL COUNTING von DONATO, L, BARTOLOMEI, G, GIORDANI, R

Volltext

Serum spermidine oxidase activity in patients with insulin-dependent diabetes mellitus and microvascular complications von Seghieri, Giuseppe, Gironi, Alfredo, Niccolai, Margherita, Mammini, Piero, Alviggi, Lorenzo, Giorgio, Lamberto A., Caselli, Paolo, Bartolomei, Giancarlo

Volltext

Raised plasma fibronectin concentration is related to the presence of diabetic retinopathy von Giorgio, Lamberto A., Seghieri, Giuseppe, Gironi, Alfredo, Mammini, Piero, Bartoli, Umberto, Bartolomei, Giancarlo

Volltext

Genome-wide Analyses Identify KIF5A as a Novel ALS Gene von Kenna, Kevin P., Chia, Ruth, Dominov, Janice A., Nalls, Mike A., van Vugt, Joke J.F.A., Simone, Isabella, Caredda, Carla, Milia, Antonio, Floris, Gianluca, Caponnetto, Claudia, Mandich, Paola, Mora, Gabriele, Sideri, Riccardo, Penco, Silvana, Mandrioli, Jessica, Trojsi, Francesca, Ticca, Anna, Ortu, Enzo, Pugliatti, Maura, Benigni, Michele, Brunetti, Maura, Marrali, Giuseppe, Riva, Nilo, Conforti, Francesca L., Messina, Sonia, D’Alfonso, Sandra, Baloh, Robert H., Penny, Michelle, Moreno, Cristiane de Araujo Martins, Chung, Wendy K., Cirulli, Elizabeth T., Harris, Tim, Krueger, Brian J., Lasseigne, Brittany N., McKenna-Yasek, Diane, Myers, Richard M., Pulst, Stefan M., Raphael, Alya R., Rouleau, Guy A., Sapp, Peter C., Waite, Lindsay L., Wang, Quanli, Ostrow, Lyle W., Baas, Frank, Zaitlen, Noah, Hornstein, Eran, Patsopoulos, Nikolaos A., Kaye, Julia, Wyman, Stacia, LeNail, Alexander, Baxi, Emily, LeNail, Alex, Benatar, Michael, Hussain, Sumaira, Swenson, Andrea, Jackson, Carlayne, So, Yuen, Wuu, Joanne, Silani, Vincenzo, Fogh, Isabella, Cereda, Cristina, Ceroni, Mauro, Mazzini, Letizia, Maderna, Luca, Sorarù, Gianni, Bernard, Emilien, Laaksovirta, Hannu, McKenna-Yasek, Diane, Asress, Seneshaw, Al-Sarraj, Safa, Scholz, Sonja W., MacGowan, Daniel J.L., Kirby, Janine, Pioro, Erik P., Pamphlett, Roger, Dunckley, Travis L., Troncoso, Juan C., Moisse, Matthieu, Drory, Vivian E., Turner, Martin R., Blair, Ian P., de Carvalho, Mamede, Hide, Winston, Glass, Jonathan, Mill, Jonathan, Newhouse, Stephen, Pulit, Sara, Robberecht, Wim, Shaw, Pamela, van den Berg, Leonard, Williams, Kelly L., Zatz, Mayana, Rothstein, Jeffrey D., Simmons, Zachary, Van Damme, Philip, Sabatelli, Mario, Trojanowski, John Q., Brown, Robert H., Veldink, Jan H., Tienari, Pentti

Volltext

A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD von Renton, Alan E., Majounie, Elisa, Waite, Adrian, Simón-Sánchez, Javier, Rollinson, Sara, Gibbs, J. Raphael, Schymick, Jennifer C., Laaksovirta, Hannu, van Swieten, John C., Myllykangas, Liisa, Kalimo, Hannu, Paetau, Anders, Abramzon, Yevgeniya, Remes, Anne M., Kaganovich, Alice, Scholz, Sonja W., Duckworth, Jamie, Ding, Jinhui, Harmer, Daniel W., Hernandez, Dena G., Johnson, Janel O., Mok, Kin, Ryten, Mina, Trabzuni, Danyah, Guerreiro, Rita J., Orrell, Richard W., Neal, James, Murray, Alex, Pearson, Justin, Jansen, Iris E., Sondervan, David, Seelaar, Harro, Blake, Derek, Young, Kate, Halliwell, Nicola, Callister, Janis Bennion, Toulson, Greg, Richardson, Anna, Gerhard, Alex, Snowden, Julie, Mann, David, Neary, David, Nalls, Michael A., Peuralinna, Terhi, Jansson, Lilja, Isoviita, Veli-Matti, Kaivorinne, Anna-Lotta, Hölttä-Vuori, Maarit, Ikonen, Elina, Sulkava, Raimo, Benatar, Michael, Wuu, Joanne, Chiò, Adriano, Restagno, Gabriella, Borghero, Giuseppe, Sabatelli, Mario, Heckerman, David, Rogaeva, Ekaterina, Zinman, Lorne, Rothstein, Jeffrey D., Sendtner, Michael, Drepper, Carsten, Eichler, Evan E., Alkan, Can, Abdullaev, Ziedulla, Pack, Svetlana D., Dutra, Amalia, Pak, Evgenia, Hardy, John, Singleton, Andrew, Williams, Nigel M., Heutink, Peter, Pickering-Brown, Stuart, Morris, Huw R., Tienari, Pentti J., Traynor, Bryan J.

Volltext

Mutations in the Matrin 3 gene cause familial amyotrophic lateral sclerosis von Johnson, Janel O, Pioro, Erik P, Boehringer, Ashley, Chia, Ruth, Feit, Howard, Renton, Alan E, Pliner, Hannah A, Abramzon, Yevgeniya, Marangi, Giuseppe, Winborn, Brett J, Gibbs, J Raphael, Nalls, Michael A, Morgan, Sarah, Shoai, Maryam, Hardy, John, Pittman, Alan, Orrell, Richard W, Malaspina, Andrea, Sidle, Katie C, Fratta, Pietro, Harms, Matthew B, Baloh, Robert H, Pestronk, Alan, Weihl, Conrad C, Rogaeva, Ekaterina, Zinman, Lorne, Drory, Vivian E, Borghero, Giuseppe, Mora, Gabriele, Calvo, Andrea, Rothstein, Jeffrey D, Drepper, Carsten, Sendtner, Michael, Singleton, Andrew B, Taylor, J Paul, Cookson, Mark R, Restagno, Gabriella, Sabatelli, Mario, Bowser, Robert, Chiò, Adriano, Traynor, Bryan J

Volltext

Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis von Noyce, Alastair J., Hemani, Gibran, Mora, Gabriele, Bartolomei, Ilaria, Benigni, Michele, Borghero, Giuseppe, Brunetti, Maura, Calvo, Andrea, Cammarosano, Stefania, Cannas, Antonino, Caponnetto, Claudia, Casale, Federico, Cavallaro, Sebastiano, Chiò, Adriano, Colletti, Tiziana, Conforti, Francesca L., Conte, Amelia, Corrado, Lucia, Costantino, Emanuela, D'Alfonso, Sandra, Femiano, Cinzia, Ferrarese, Carlo, Fini, Nicola, Floris, Gianluca, Grassano, Maurizio, Lattante, Serena, Logroscino, Giancarlo, Loi, Daniela, Mancardi, Gianluigi, Mandich, Paola, Manera, Umberto, Marinou, Kalliopi, Marrali, Giuseppe, Marrosu, Maria Giovanna, Mazzini, Letizia, Melis, Maurizio, Messina, Sonia, Mora, Gabriele, Occhineri, Patrizia, Origone, Paola, Pani, Carla, Petrucci, Antonio, Pirisi, Angelo, Restagno, Gabriella, Ricci, Claudia, Riva, Nilo, Sabatelli, Mario, Santarelli, Marialuisa, Spataro, Rossella, Tanel, Raffaella, Tremolizzo, Lucio, Volanti, Paolo, Zollino, Marcella, Arepalli, Sampath, Bowser, Robert, Broach, James, Camu, William, Chia, Ruth, Chiò, Adriano, Ding, Jinhui, Dunckley, Travis L., Eicher, John D., Faghri, Faraz, Feldman, Eva, Fratta, Pietro, Geiger, Joshua T., Gerhard, Glenn, Hardy, John, Harms, Matthew B., Heiman‐Patterson, Terry D., Kamel, Freya, MacGowan, Daniel J.L., Maragakis, Nicholas J., Murphy, Natalie A., Myllykangas, Liisa, Nalls, Mike A., Nicolas, Aude, Orrell, Richard W., Pamphlett, Roger, Pickering‐Brown, Stuart, Pioro, Erik, Pliner, Hannah A., Pulst, Stefan M., Ravits, John M., Rothstein, Jeffrey D., Salvi, Erika, Sendtner, Michael, Simmons, Zachary, Stone, David C., Sulkava, Raimo, Troncoso, Juan C., Van Damme, Philip, Van Deerlin, Vivianna M., Van Den Bosch, Ludo, Zinman, Lorne, Tienari, Pentti J., Stone, David J., Nalls, Mike A., Singleton, Andrew B., Traynor, Bryan J.

Volltext

Genetic counselling in ALS: facts, uncertainties and clinical suggestions von Chiò, Adriano, Battistini, Stefania, Calvo, Andrea, Caponnetto, Claudia, Conforti, Francesca L, Corbo, Massimo, Giannini, Fabio, Mandrioli, Jessica, Mora, Gabriele, Sabatelli, Mario, Ajmone, Clara, Mastro, Enza, Pain, Debora, Mandich, Paola, Penco, Silvana, Restagno, Gabriella, Zollino, Marcella, Surbone, Antonella

Volltext

TBK1 is associated with ALS and ALS-FTD in Sardinian patients von Borghero, Giuseppe, MD, Pugliatti, Maura, MD, PhD, Marrosu, Francesco, MD, Marrosu, Maria Giovanna, MD, Murru, Maria Rita, MSc, Floris, Gianluca, MD, Cannas, Antonino, MD, Occhineri, Patrizia, MD, Cau, Tea B., MD, Loi, Daniela, MD, Ticca, Anna, MD, Traccis, Sebastiano, MD, Manera, Umberto, MD, Canosa, Antonio, MD, PhD, Moglia, Cristina, MD, PhD, Calvo, Andrea, MD, PhD, Barberis, Marco, MSc, Brunetti, Maura, MSc, Gibbs, J.Raphael, PhD, Renton, Alan E., PhD, Errichiello, Edoardo, MSc, Zoledziewska, Magdalena, PhD, Mulas, Antonella, PhD, Qian, Yong, PhD, Din, Jun, PhD, Pliner, Hannah A., PhD, Traynor, Bryan J., MD, PhD, Chiò, Adriano, MD, FAAN

Volltext

C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS population von Sabatelli, Mario, Conforti, Francesca Luisa, Zollino, Marcella, Mora, Gabriele, Monsurrò, Maria Rosaria, Volanti, Paolo, Marinou, Kalliopi, Salvi, Fabrizio, Corbo, Massimo, Giannini, Fabio, Battistini, Stefania, Penco, Silvana, Lunetta, Christian, Quattrone, Aldo, Gambardella, Antonio, Logroscino, Giancarlo, Simone, Isabella, Bartolomei, Ilaria, Pisano, Fabrizio, Tedeschi, Gioacchino, Conte, Amelia, Spataro, Rossella, La Bella, Vincenzo, Caponnetto, Claudia, Mancardi, Gianluigi, Mandich, Paola, Sola, Patrizia, Mandrioli, Jessica, Renton, Alan E, Majounie, Elisa, Abramzon, Yevgeniya, Marrosu, Francesco, Marrosu, Maria Giovanna, Murru, Maria Rita, Sotgiu, Maria Alessandra, Pugliatti, Maura, Rodolico, Carmelo, Moglia, Cristina, Calvo, Andrea, Ossola, Irene, Brunetti, Maura, Traynor, Bryan J, Borghero, Giuseppe, Restagno, Gabriella, Chiò, Adriano

Volltext

Erythropoietin in amyotrophic lateral sclerosis: a multicentre, randomised, double blind, placebo controlled, phase III study von Lauria, Giuseppe, Dalla Bella, Eleonora, Antonini, Giovanni, Borghero, Giuseppe, Capasso, Margherita, Caponnetto, Claudia, Chiò, Adriano, Corbo, Massimo, Eleopra, Roberto, Fazio, Raffaella, Filosto, Massimiliano, Giannini, Fabio, Granieri, Enrico, La Bella, Vincenzo, Logroscino, Giancarlo, Mandrioli, Jessica, Mazzini, Letizia, Monsurrò, Maria Rosaria, Mora, Gabriele, Pietrini, Vladimiro, Quatrale, Rocco, Rizzi, Romana, Salvi, Fabrizio, Siciliano, Gabriele, Sorarù, Gianni, Volanti, Paolo, Tramacere, Irene, Filippini, Graziella

Volltext

Mechanism-free repurposing of drugs for C9orf72-related ALS/FTD using large-scale genomic data von Saez-Atienzar, Sara, Souza, Cleide dos Santos, Chia, Ruth, Burciu, Camelia, Gibbs, J. Raphael, Jones, Ashley, Dewan, Ramita, Pensato, Viviana, Corrado, Lucia, van Vugt, Joke J.F.A., van Rheenen, Wouter, Camu, William, Cusi, Daniele, Ding, Jinhui, Drepper, Carsten, Drory, Vivian E., Gerhard, Glenn, Gibbs, J. Raphael, Gibson, Summer B., Hardy, John, Landers, John E., Guissart, Claire, MacGowan, Daniel JL, Mouzat, Kevin, Myllykangas, Liisa, Pulst, Stefan M., Ravits, John M., Renton, Alan E., Rogaeva, Ekaterina, Salvi, Erika, Scholz, Sonja W., Tienari, Pentti J., Valori, Miko, Van Damme, Philip, Zinman, Lorne, Barberis, Marco, Bersano, Enrica, Bisogni, Giulia, Canale, Fabrizio, Carrera, Paola, Casale, Federico, Colletti, Tiziana, Conforti, Francesca L., Ferrarese, Carlo, Greco, Lucia, La Bella, Vincenzo, Marrosu, Maria Giovanna, Messina, Sonia, Moglia, Cristina, Passaniti, Carla, Petrelli, Cristina, Petrucci, Antonio, Russo, Massimo, Salvi, Fabrizio, Santarelli, Marialuisa, Sideri, Riccardo, Vasta, Rosario, Zucchi, Elisabetta, Ticozzi, Nicola, Tiloca, Cinzia, Peverelli, Silvia, Taroni, Franco, Pensato, Viviana, Castellotti, Barbara, Comi, Giacomo P., Corrado, Lucia, Sorarù, Gianni, Corcia, Philippe, Vourc'h, Patrick, Gotkine, Marc, Drory, Vivian, Berg, Leonard H., Andersen, Peter, Tiloca, Cinzia, Verde, Federico, Al Khleifat, Ahmad, Piccinelli, Stefano Cotti, Padovani, Alessandro, Calvo, Andrea, Canosa, Antonio, Lunetta, Christian, Cardinali, Patrizio, Scarpini, Elio, Comi, Giacomo P., Pinter, Giuseppe Lauria, Taroni, Franco, Bella, Eleonora Dalla, Adeleye, Adelani, McGrath Martinez, Elisa, Soltis, Anthony R., Sukumar, Gauthaman, Viollet, Coralie, McLaughlin, Russell, Sorarù, Gianni, Ratti, Antonia, Doucet-O’Hare, Tara, Nath, Avindra, Siciliano, Gabriele, Glass, Jonathan D., Ferraiuolo, Laura

Volltext

ATXN2 is a modifier of phenotype in ALS patients of Sardinian ancestry von Borghero, Giuseppe, Pugliatti, Maura, Marrosu, Francesco, Marrosu, Maria Giovanna, Murru, Maria Rita, Floris, Gianluca, Cannas, Antonino, Parish, Leslie D, Cau, Tea B, Loi, Daniela, Ticca, Anna, Traccis, Sebastiano, Manera, Umberto, Canosa, Antonio, Moglia, Cristina, Calvo, Andrea, Barberis, Marco, Brunetti, Maura, Renton, Alan E, Nalls, Mike A, Traynor, Bryan J, Restagno, Gabriella, Chiò, Adriano

Volltext

Intravenous Thrombolysis with rt-PA in Acute Ischemic Stroke Patients Aged Older than 80 Years in Italy von Toni, Danilo, Lorenzano, Svetlana, Agnelli, Giancarlo, Guidetti, Donata, Orlandi, Giovanni, Semplicini, Andrea, Toso, Vito, Caso, Valeria, Malferrari, Giovanni, Fanucchi, Simona, Bartolomei, Luigi, Prencipe, Massimiliano

Volltext

HFE p.H63D polymorphism does not influence ALS phenotype and survival von Chiò, Adriano, Mora, Gabriele, Sabatelli, Mario, Caponnetto, Claudia, Lunetta, Christian, Traynor, Bryan J, Johnson, Janel O, Nalls, Mike A, Calvo, Andrea, Moglia, Cristina, Borghero, Giuseppe, Monsurrò, Maria Rosaria, La Bella, Vincenzo, Volanti, Paolo, Simone, Isabella, Salvi, Fabrizio, Logullo, Francesco O, Nilo, Riva, Giannini, Fabio, Mandrioli, Jessica, Tanel, Raffaella, Murru, Maria Rita, Mandich, Paola, Zollino, Marcella, Conforti, Francesca L, Penco, Silvana, Brunetti, Maura, Barberis, Marco, Restagno, Gabriella

Volltext

ATNX2 is not a regulatory gene in Italian amyotrophic lateral sclerosis patients with C9ORF72 GGGGCC expansion von Chiò, Adriano, Mora, Gabriele, Sabatelli, Mario, Caponnetto, Claudia, Lunetta, Christian, Traynor, Bryan J, Johnson, Janel O, Nalls, Mike A, Calvo, Andrea, Moglia, Cristina, Borghero, Giuseppe, Trojsi, Francesca, La Bella, Vincenzo, Volanti, Paolo, Simone, Isabella, Salvi, Fabrizio, Logullo, Francesco O, Riva, Nilo, Carrera, Paola, Giannini, Fabio, Mandrioli, Jessica, Tanel, Raffaella, Capasso, Margherita, Tremolizzo, Lucio, Battistini, Stefania, Murru, Maria Rita, Origone, Paola, Zollino, Marcella, Penco, Silvana, Mazzini, Letizia, D'Alfonso, Sandra, Restagno, Gabriella, Brunetti, Maura, Barberis, Marco, Conforti, Francesca L

Volltext

Le genre, une nouvelle approche du fait religieux - La chancellerie consulaire française (XVIe-XXe siècle) : attributions, organisation, agents, usagers - Penser l’hégémonie et la... von Bartolomei, Arnaud, Biagianti, Annalisa, Camillocci, Daniela Solfaroli, Ciavolella, Riccardo, Duval, Sylvie, Frosini, Fabio, Gazzetta, Liviana, Gouic, Olivier Le, Grenet, Mathieu, Guyard, Nicolas, Hufton, Olwen, Jesné, Fabrice, Jestin, Mathieu, Jusseaume, Anne, Laqua-O’Donnell, Simone, Liguori, Guido, Massé, Alexandre, Mignemi, Niccolò, Muller, Caroline, Paci, Deborah, Pera, Isabella, Schirru, Giancarlo, Sudda, Magali Della, Tafuro, Azzurra, Tippelskirch, Xenia von, Ulbert, Jörg

Volltext