Hereditary transthyretin amyloidosis: a comprehensive review with a focus on peripheral neuropathy von Poli, Loris, Labella, Beatrice, Cotti Piccinelli, Stefano, Caria, Filomena, Risi, Barbara, Damioli, Simona, Padovani, Alessandro, Filosto, Massimiliano

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Epileptic nystagmus as clinical manifestation of self‐limited focal epilepsy: Rethinking etiology and prognostic value and literature review von Sara, Brunetti, Isabella, Cocco, Simona, Damioli, Patrizia, Accorsi, Laura, Tassi, Lucio, Giordano

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A Comprehensive Update on Late-Onset Pompe Disease von Labella, Beatrice, Cotti Piccinelli, Stefano, Risi, Barbara, Caria, Filomena, Damioli, Simona, Bertella, Enrica, Poli, Loris, Padovani, Alessandro, Filosto, Massimiliano

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Leprosy Neuropathy in a Non-Endemic Area: A Clinical and Pathological Study von Cotti Piccinelli, Stefano, Tagliapietra, Matteo, Cavallaro, Tiziana, Labella, Beatrice, Risi, Barbara, Caria, Filomena, Damioli, Simona, Poli, Loris, Padovani, Alessandro, Ferrari, Sergio, Filosto, Massimiliano

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Juvenile-Onset Recurrent Rhabdomyolysis Due to Compound Heterozygote Variants in the ACADVL Gene von Labella, Beatrice, Lanzi, Gaetana, Cotti Piccinelli, Stefano, Caria, Filomena, Damioli, Simona, Risi, Barbara, Bertella, Enrica, Poli, Loris, Padovani, Alessandro, Filosto, Massimiliano

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Clinical Phenotype of Pediatric and Adult Patients With Spinal Muscular Atrophy With Four SMN2 Copies: Are They Really All Stable? von Ricci, Martina, Cicala, Gianpaolo, Capasso, Anna, Coratti, Giorgia, Fiori, Stefania, Cutrona, Costanza, D'Amico, Adele, Sansone, Valeria A., Bruno, Claudio, Messina, Sonia, Mongini, Tiziana, Coccia, Michela, Siciliano, Gabriele, Pegoraro, Elena, Masson, Riccardo, Filosto, Massimiliano, Comi, Giacomo P., Corti, Stefania, Ronchi, Dario, Maggi, Lorenzo, D'Angelo, Maria G., Vacchiano, Veria, Ticci, Chiara, Ruggiero, Lucia, Verriello, Lorenzo, Ricci, Federica S., Berardinelli, Angela L., Maioli, Maria Antonietta, Garibaldi, Matteo, Nigro, Vincenzo, Previtali, Stefano C., Pera, Maria Carmela, Tizzano, Eduardo, Pane, Marika, Tiziano, Francesco Danilo, Mercuri, Eugenio, Albamonte, Emilio, Antonaci, Laura, Bravetti, Chiara, Torri, Francesca, Turri, Mara, Bruno, Irene, Bonanno, Silvia, Trabacca, Antonio, Liguori, Rocco, Donati, Maria Alice, D'Errico, Eustachio, Varone, Antonio, Agosto, Caterina, Pini, Antonella, Politano, Luisa, Bertini, Enrico, Brolatti, Noemi, Sbarbati, Martina, D'Amario, Giulia, Dosi, Claudia, Magri, Francesca, Bello, Luca, Longo, Antonella, Simone, Isabella Laura, Picillo, Esther, Govoni, Alessandra, Piccinelli, Stefano Cotti, Gadaleta, Giulio, Bosco, Luca, Sacchini, Michele, Sframeli, Maria, Zoppi, Dario, Zambon, Alberto A., Procopio, Elena, Damioli, Simona, Padovani, Alessandro, Ricci, Giulia, Capece, Giuliana

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Efficacy and Safety of Bimagrumab in Sporadic Inclusion Body Myositis: Long-term Extension of RESILIENT von Amato, Anthony A., Hanna, Michael G., Machado, Pedro M., Badrising, Umesh A., Chinoy, Hector, Benveniste, Olivier, Karanam, Ananda Krishna, Wu, Min, Tankó, László B., Schubert-Tennigkeit, Agnes Annette, Papanicolaou, Dimitris A., Lloyd, Thomas E., Needham, Merrilee, Liang, Christina, Reardon, Katrina A., de Visser, Marianne, Ascherman, Dana P., Barohn, Richard J., Dimachkie, Mazen M., Miller, James A.L., Kissel, John T., Oskarsson, Björn, Joyce, Nanette C., Van den Bergh, Peter, Baets, Jonathan, De Bleecker, Jan L., Karam, Chafic, David, William S., Mirabella, Massimiliano, Nations, Sharon P., Jung, Hans H., Pegoraro, Elena, Maggi, Lorenzo, Rodolico, Carmelo, Filosto, Massimiliano, Shaibani, Aziz I., Sivakumar, Kumaraswamy, Goyal, Namita A., Mori-Yoshimura, Madoka, Yamashita, Satoshi, Suzuki, Naoki, Aoki, Masashi, Katsuno, Masahisa, Morihata, Hirokazu, Murata, Kenya, Nodera, Hiroyuki, Nishino, Ichizo, Romano, Carla D., Williams, Valerie S.L., Vissing, John, Zhang Auberson, Lixin

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Prognostic Usefulness of Motor Unit Number Index (MUNIX) in Patients Newly Diagnosed with Amyotrophic Lateral Sclerosis von Risi, Barbara, Cotti Piccinelli, Stefano, Gazzina, Stefano, Labella, Beatrice, Caria, Filomena, Damioli, Simona, Poli, Loris, Padovani, Alessandro, Filosto, Massimiliano

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Juvenile-Onset Recurrent Rhabdomyolysis Due to Compound Heterozygote Variants in the IACADVL/I Gene von Labella, Beatrice, Lanzi, Gaetana, Cotti Piccinelli, Stefano, Caria, Filomena, Damioli, Simona, Risi, Barbara, Bertella, Enrica, Poli, Loris, Padovani, Alessandro, Filosto, Massimiliano

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PURA-Related Developmental and Epileptic Encephalopathy von Johannesen, Katrine M., Gardella, Elena, Gjerulfsen, Cathrine E., Bayat, Allan, Rouhl, Rob P. W., Reijnders, Margot, Whalen, Sandra, Keren, Boris, Buratti, Julien, Courtin, Thomas, Wierenga, Klaas J., Isidor, Bertrand, Piton, Amelie, Faivre, Laurence, Garde, Aurore, Moutton, Sebastien, Tran-Mau-Them, Frederic, Denomme-Pichon, Anne-Sophie, Coubes, Christine, Larson, Austin, Esser, Michael J., Appendino, Juan Pablo, Al-Hertani, Walla, Gamboni, Beatriz, Mampel, Alejandra, Mayorga, Lia, Orsini, Alessandro, Bonuccelli, Alice, Suppiej, Agnese, Van-Gils, Julien, Vogt, Julie, Damioli, Simona, Giordano, Lucio, Moortgat, Stephanie, Wirrell, Elaine, Hicks, Sarah, Kini, Usha, Noble, Nathan, Stewart, Helen, Asakar, Shailesh, Cohen, Julie S., Naidu, SakkuBai R., Collier, Ashley, Brilstra, Eva H., Li, Mindy H., Brew, Casey, Bigoni, Stefania, Ognibene, Davide, Ballardini, Elisa, Ruivenkamp, Claudia, Faggioli, Raffaella, Afenjar, Alexandra, Rodriguez, Diana, Bick, David, Segal, Devorah, Coman, David, Gunning, Boudewijn, Devinsky, Orrin, Demmer, Laurie A., Grebe, Theresa, Pruna, Dario, Cursio, Ida, Greenhalgh, Lynn, Graziano, Claudio, Singh, Rahul Raman, Cantalupo, Gaetano, Willems, Marjolaine, Yoganathan, Sangeetha, Goes, Fernanda, Leventer, Richard J., Colavito, Davide, Olivotto, Sara, Scelsa, Barbara, Andrade, Andrea V., Ratke, Kelly, Tokarz, Farha, Khan, Atiya S., Ormieres, Clothilde, Benko, William, Keough, Karen, Keros, Sotirios, Hussain, Shanawaz, Franques, Ashlea, Varsalone, Felicia, Gronborg, Sabine, Mignot, Cyril, Heron, Delphine, Nava, Caroline, Isapof, Arnaud, Borlot, Felippe, Whitney, Robyn, Ronan, Anne, Foulds, Nicola, Somorai, Marta, Brandsema, John, Helbig, Katherine L., Helbig, Ingo, Ortiz-Gonzalez, Xilma R., Dubbs, Holly, Vitobello, Antonio

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Type I spinal muscular atrophy and disease modifying treatments: a nationwide study in children born since 2016 von Pera, Maria Carmela, Coratti, Giorgia, Pane, Marika, Masson, Riccardo, Sansone, Valeria Ada, D’Amico, Adele, Catteruccia, Michela, Agosto, Caterina, Varone, Antonio, Bruno, Claudio, Messina, Sonia, Ricci, Federica, Bruno, Irene, Procopio, Elena, Pini, Antonella, Siliquini, Sabrina, Zanin, Riccardo, Albamonte, Emilio, Berardinelli, Angela, Mastella, Chiara, Baranello, Giovanni, Previtali, Stefano Carlo, Trabacca, Antonio, Bravetti, Chiara, Gagliardi, Delio, Filosto, Massimiliano, de Sanctis, Roberto, Finkel, Richard, Mercuri, Eugenio, Gardani, Alice, Costantino, Maria Antonella, Bitetti, Ilaria, Franguel, Matteo Tuana, Sframeli, Maria, Magnolato, Andrea, Rausa, Myriam, Pagliaccia, Elena, Negri, Mirea, Del Monaco, Cesare, Berti, Beatrice, Leone, Daniela, Palermo, Concetta, Bertini, Enrico, Longo, Antonella, Dosi, Claudia, Carnicella, Sara, Morando, Simone, Brolatti, Noemi, Vento, Alessandra, Cavallina, Ilaria, Ferrante, Roberta, Bernasconi, Laura, Piastra, Marco, Genovese, Orazio, Forcina, Nicola, Benedetti, Francesca, Damioli, Simona, Fanelli, Lavinia, Stanca, Giulia, Norcia, Giulia, Sacchini, Matteo, Ticci, Chiara, Briganti, Elena

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Type I spinal muscular atrophy and disease modifying treatments: a nationwide study in children born since 2016Research in context von Maria Carmela Pera, Giorgia Coratti, Marika Pane, Riccardo Masson, Valeria Ada Sansone, Adele D’Amico, Michela Catteruccia, Caterina Agosto, Antonio Varone, Claudio Bruno, Sonia Messina, Federica Ricci, Irene Bruno, Elena Procopio, Antonella Pini, Sabrina Siliquini, Riccardo Zanin, Emilio Albamonte, Angela Berardinelli, Chiara Mastella, Giovanni Baranello, Stefano Carlo Previtali, Antonio Trabacca, Chiara Bravetti, Delio Gagliardi, Massimiliano Filosto, Roberto de Sanctis, Richard Finkel, Eugenio Mercuri, Alice Gardani, Maria Antonella Costantino, Ilaria Bitetti, Matteo Tuana Franguel, Maria Sframeli, Andrea Magnolato, Myriam Rausa, Elena Pagliaccia, Mirea Negri, Cesare Del Monaco, Beatrice Berti, Daniela Leone, Concetta Palermo, Enrico Bertini, Antonella Longo, Claudia Dosi, Sara Carnicella, Simone Morando, Noemi Brolatti, Alessandra Vento, Ilaria Cavallina, Roberta Ferrante, Laura Bernasconi, Marco Piastra, Orazio Genovese, Nicola Forcina, Francesca Benedetti, Simona Damioli, Lavinia Fanelli, Giulia Stanca, Giulia Norcia, Matteo Sacchini, Chiara Ticci, Elena Briganti

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PURA- Related Developmental and Epileptic Encephalopathy: Phenotypic and Genotypic Spectrum von Johannesen, Katrine M, Gardella, Elena, Gjerulfsen, Cathrine E, Bayat, Allan, Rouhl, Rob P W, Reijnders, Margot, Whalen, Sandra, Keren, Boris, Buratti, Julien, Courtin, Thomas, Wierenga, Klaas J, Isidor, Bertrand, Piton, Amélie, Faivre, Laurence, Garde, Aurore, Moutton, Sébastien, Tran-Mau-Them, Frédéric, Denommé-Pichon, Anne-Sophie, Coubes, Christine, Larson, Austin, Esser, Michael J, Appendino, Juan Pablo, Al-Hertani, Walla, Gamboni, Beatriz, Mampel, Alejandra, Mayorga, Lía, Orsini, Alessandro, Bonuccelli, Alice, Suppiej, Agnese, Van-Gils, Julien, Vogt, Julie, Damioli, Simona, Giordano, Lucio, Moortgat, Stephanie, Wirrell, Elaine, Hicks, Sarah, Kini, Usha, Noble, Nathan, Stewart, Helen, Asakar, Shailesh, Cohen, Julie S, Naidu, SakkuBai R, Collier, Ashley, Brilstra, Eva H, Li, Mindy H, Brew, Casey, Bigoni, Stefania, Ognibene, Davide, Ballardini, Elisa, Ruivenkamp, Claudia, Faggioli, Raffaella, Afenjar, Alexandra, Rodriguez, Diana, Bick, David, Segal, Devorah, Coman, David, Gunning, Boudewijn, Devinsky, Orrin, Demmer, Laurie A, Grebe, Theresa, Pruna, Dario, Cursio, Ida, Greenhalgh, Lynn, Graziano, Claudio, Singh, Rahul Raman, Cantalupo, Gaetano, Willems, Marjolaine, Yoganathan, Sangeetha, Góes, Fernanda, Leventer, Richard J, Colavito, Davide, Olivotto, Sara, Scelsa, Barbara, Andrade, Andrea V, Ratke, Kelly, Tokarz, Farha, Khan, Atiya S, Ormieres, Clothilde, Benko, William, Keough, Karen, Keros, Sotirios, Hussain, Shanawaz, Franques, Ashlea, Varsalone, Felicia, Grønborg, Sabine, Mignot, Cyril, Heron, Delphine, Nava, Caroline, Isapof, Arnaud, Borlot, Felippe, Whitney, Robyn, Ronan, Anne, Foulds, Nicola, Somorai, Marta, Brandsema, John, Helbig, Katherine L, Helbig, Ingo, Ortiz-González, Xilma R, Dubbs, Holly, Vitobello, Antonio

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Leprosy Neuropathy in a Non-Endemic Area: A Clinical and Pathological Study von Cotti Piccinelli, Stefano, Tagliapietra, Matteo, Cavallaro, Tiziana, Labella, Beatrice, Risi, Barbara, Caria, Filomena, Damioli, Simona, Poli, Loris, Padovani, Alessandro, Ferrari, Sergio, Filosto, Massimiliano

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Juvenile-Onset Recurrent Rhabdomyolysis Due to Compound Heterozygote Variants in the ACADVL Gene von Labella, Beatrice, Lanzi, Gaetana, Cotti Piccinelli, Stefano, Caria, Filomena, Damioli, Simona, Risi, Barbara, Bertella, Enrica, Poli, Loris, Padovani, Alessandro, Filosto, Massimiliano

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