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Poor stimulus discriminability as a common neuropsychological deficit between ADHD and reading ability in young children: a moderated mediation model von Lúcio, P. S., Salum, G. A., Rohde, L. A., Swardfager, W., Gadelha, A., Vandekerckhove, J., Pan, P. M., Polanczyk, G. V., do Rosário, M. C., Jackowski, A. P., Mari, J. J., Cogo-Moreira, H.

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Outrageous prices of orphan drugs: a call for collaboration von Luzzatto, Lucio, Hyry, Hanna I, Schieppati, Arrigo, Costa, Enrico, Simoens, Steven, Schaefer, Franz, Roos, Jonathan C P, Merlini, Giampaolo, Kääriäinen, Helena, Garattini, Silvio, Hollak, Carla E, Remuzzi, Giuseppe, Barbui, Tiziano, Benigni, Ariela, Costa, Enrico, Daina, Erica, Garattini, Silvio, Gramaglia, Donatella, Hollak, Carla E M, Hyry, Hanna, Kaarinen, Helena, Licht, Christoph, Luzzatto, Lucio, Merlini, Giampaolo, Notaro, Rosario, Remuzzi, Giuseppe, Schaefer, Franz, Schieppati, Arrigo, Simoens, Steven

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Polymorphism of the complement receptor 1 gene correlates with the hematologic response to eculizumab in patients with paroxysmal nocturnal hemoglobinuria von Rondelli, Tommaso, Risitano, Antonio M, Peffault de Latour, Régis, Sica, Michela, Peruzzi, Benedetta, Ricci, Patrizia, Barcellini, Wilma, Iori, Anna Paola, Boschetti, Carla, Valle, Veronica, Frémeaux-Bacchi, Veronique, De Angioletti, Maria, Socie, Gerard, Luzzatto, Lucio, Notaro, Rosario

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The complement receptor 2/factor H fusion protein TT30 protects paroxysmal nocturnal hemoglobinuria erythrocytes from complement-mediated hemolysis and C3 fragment von RISITANO, Antonio M, NOTARO, Rosario, LUZZATTO, Lucio, MICHAEL HOLERS, V, PASCARIELLO, Caterina, SICA, Michela, VECCHIO, Luigi Del, HORVATH, Christopher J, FRIDKIS-HARELI, Masha, SELLERI, Carmine, LINDORFER, Margaret A, TAYLOR, Ronald P

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The Influence of Ecosystem and Phylogeny on Tropical Tree Crown Size and Shape von Shenkin, Alexander, Bentley, Lisa Patrick, Oliveras, Imma, Salinas, Norma, Adu-Bredu, Stephen, Marimon-Junior, Ben Hur, Marimon, Beatriz S., Peprah, Theresa, Choque, Efrain Lopez, Trujillo Rodriguez, Lucio, Clemente Arenas, Edith Rosario, Adonteng, Christian, Seidu, John, Passos, Fabio Barbosa, Reis, Simone Matias, Blonder, Benjamin, Silman, Miles, Enquist, Brian J., Asner, Gregory P., Malhi, Yadvinder

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Design and Construction of the Full-Length Prototype of the 11-T Dipole Magnet for the High Luminosity LHC Project at CERN von Savary, Frederic, Bordini, Bernardo, Fiscarelli, Lucio, Foussat, A. P., Grand-Clement, Ludovic, Lackner, Friedrich, Loffler, C. H., Semeraro, Michela, Smekens, David, Ramos, Delio Duarte, Prin, Herve, Principe, Rosario, Bottura, Luca, Rossi, Lucio, Bermudez, Susana Izquierdo

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Neuroimaging findings in Mowat–Wilson syndrome: a study of 54 patients von Garavelli, Livia, Ivanovski, Ivan, Caraffi, Stefano Giuseppe, Santodirocco, Daniela, Pollazzon, Marzia, Cordelli, Duccio Maria, Abdalla, Ebtesam, Accorsi, Patrizia, Adam, Margaret P., Baldo, Chiara, Bayat, Allan, Belligni, Elga, Bonvicini, Federico, Breckpot, Jeroen, Callewaert, Bert, Cocchi, Guido, Cuturilo, Goran, Devriendt, Koenraad, Dinulos, Mary Beth, Djuric, Olivera, Epifanio, Roberta, Faravelli, Francesca, Formisano, Debora, Giordano, Lucio, Grasso, Marina, Grønborg, Sabine, Iodice, Alessandro, Iughetti, Lorenzo, Lacombe, Didier, Maggi, Massimo, Malbora, Baris, Mammi, Isabella, Moutton, Sebastien, Møller, Rikke, Muschke, Petra, Napoli, Manuela, Pantaleoni, Chiara, Pascarella, Rosario, Pellicciari, Alessandro, Poch-Olive, Maria Luisa, Raviglione, Federico, Rivieri, Francesca, Russo, Carmela, Savasta, Salvatore, Scarano, Gioacchino, Selicorni, Angelo, Silengo, Margherita, Sorge, Giovanni, Tarani, Luigi, Tone, Luis Gonzaga, Toutain, Annick, Trimouille, Aurelien, Valera, Elvis Terci, Vergano, Samantha Schrier, Zanotta, Nicoletta, Zollino, Marcella, Dobyns, William B, Paciorkowski, Alex R

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Author Correction: Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes von Cortese, Andrea, Zhu, Yi, Rebelo, Adriana P., Negri, Sara, Courel, Steve, Abreu, Lisa, Bacon, Chelsea J., Bai, Yunhong, Bis-Brewer, Dana M., Bugiardini, Enrico, Buglo, Elena, Danzi, Matt C., Feely, Shawna M. E., Athanasiou-Fragkouli, Alkyoni, Haridy, Nourelhoda A., Isasi, Rosario, Khan, Alaa, Laurà, Matilde, Magri, Stefania, Pipis, Menelaos, Pisciotta, Chiara, Powell, Eric, Rossor, Alexander M., Saveri, Paola, Sowden, Janet E., Tozza, Stefano, Vandrovcova, Jana, Dallman, Julia, Grignani, Elena, Marchioni, Enrico, Scherer, Steven S., Tang, Beisha, Lin, Zhiqiang, Al-Ajmi, Abdullah, Schüle, Rebecca, Synofzik, Matthis, Maisonobe, Thierry, Stojkovic, Tanya, Auer-Grumbach, Michaela, Abdelhamed, Mohamed A., Hamed, Sherifa A., Zhang, Ruxu, Manganelli, Fiore, Santoro, Lucio, Taroni, Franco, Pareyson, Davide, Houlden, Henry, Herrmann, David N., Reilly, Mary M., Shy, Michael E., Zhai, R. Grace, Zuchner, Stephan

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Biallelic mutations in SORD cause a common and potentially treatable hereditary neuropathy with implications for diabetes (vol 16, pg 613, 2020) von Cortese, Andrea, Zhu, Yi, Rebelo, Adriana P., Negri, Sara, Courel, Steve, Abreu, Lisa, Bacon, Chelsea J., Bai, Yunhong, Bis-Brewer, Dana M., Bugiardini, Enrico, Buglo, Elena, Danzi, Matt C., Feely, Shawna M. E., Athanasiou-Fragkouli, Alkyoni, Haridy, Nourelhoda A., Isasi, Rosario, Khan, Alaa, Laura, Matilde, Magri, Stefania, Pipis, Menelaos, Pisciotta, Chiara, Powell, Eric, Rossor, Alexander M., Saveri, Paola, Sowden, Janet E., Tozza, Stefano, Vandrovcova, Jana, Dallman, Julia, Grignani, Elena, Marchioni, Enrico, Scherer, Steven S., Tang, Beisha, Lin, Zhiqiang, Al-Ajmi, Abdullah, Schule, Rebecca, Synofzik, Matthis, Maisonobe, Thierry, Stojkovic, Tanya, Auer-Grumbach, Michaela, Abdelhamed, Mohamed A., Hamed, Sherifa A., Zhang, Ruxu, Manganelli, Fiore, Santoro, Lucio, Taroni, Franco, Pareyson, Davide, Houlden, Henry, Herrmann, David N., Reilly, Mary M., Shy, Michael E., Zhai, R. Grace, Zuchner, Stephan

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Knockdown resistance mutations (kdr) and insecticide susceptibility to DDT and pyrethroids in Anopheles gambiae from Equatorial Guinea von Moreno, M, Vicente, J.L, Cano, J, Berzosa, P.J, de Lucio, A, Nzambo, S, Bobuakasi, L, Buatiche, J.N, Ondo, M, Micha, F, Do Rosario, V.E, Pinto, J, Benito, A

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The complement receptor 2/factor H fusion protein TT30 protects paroxysmal nocturnal hemoglobinuria erythrocytes from complement-mediated hemolysis and C3 fragment opsonization von Risitano, Antonio M., Notaro, Rosario, Pascariello, Caterina, Sica, Michela, del Vecchio, Luigi, Horvath, Christopher J., Fridkis-Hareli, Masha, Selleri, Carmine, Lindorfer, Margaret A., Taylor, Ronald P., Luzzatto, Lucio, Holers, V. Michael

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A Preliminary Investigation on a Multimodal Controller and Freehand Based Interaction in Virtual Reality von Capece, Nicola, Gruosso, Monica, Erra, Ugo, Catena, Rosario, Manfredi, Gilda

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Chromosome Instability and Progression in Urothelial Cell Carcinoma of the Bladder von Santos, Lúcio, Pereira, Sofia, Leite, Rosário P., Suoto, Marta, Amaro, Teresina, Criado, Begoña

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Age: “A Natural Anesthetic” in Pain Perception during the Transrectal Ultrasound-Guided Prostate Biopsy Procedure von Dell'atti, Lucio, Borea, Pier Andrea, Russo, Gian Rosario

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Maternally transmitted severe glucose 6-phosphate dehydrogenase deficiency is an embryonic lethal von Longo, Letizia, Vanegas, Olga Camacho, Patel, Meghavi, Rosti, Vittorio, Li, Haiqing, Waka, John, Merghoub, Taha, Pandolfi, Pier Paolo, Notaro, Rosario, Manova, Katia, Luzzatto, Lucio

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Dopamine Receptor Expression and Function in Clinically Nonfunctioning Pituitary Tumors: Comparison with the Effectiveness of Cabergoline Treatment von Pivonello, Rosario, Matrone, Carmela, Filippella, Mariagiovanna, Cavallo, Luigi M., Di Somma, Carolina, Cappabianca, Paolo, Colao, Annamaria, Annunziato, Lucio, Lombardi, Gaetano

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