Genetic Counseling in Huntington's Disease: Potential New Challenges on Horizon? by Simone Migliore, Joseph Jankovic, Ferdinando Squitieri

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Safer Attitude to Risky Decision-Making in Premanifest Huntington’s Disease Subjects by Giulia D’Aurizio, Simone Migliore, Giuseppe Curcio, Ferdinando Squitieri

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Current Diagnostic Methods and Non-Coding RNAs as Possible Biomarkers in Huntington’s Disease by Miguel Pellegrini, Guendalina Bergonzoni, Federica Perrone, Ferdinando Squitieri, Marta Biagioli

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Mitochondrial Respiration Changes in R6/2 Huntington’s Disease Model Mice during Aging in a Brain Region Specific Manner by Johannes Burtscher, Alba Di Pardo, Vittorio Maglione, Christoph Schwarzer, Ferdinando Squitieri

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Emotion recognition and inhibitory control in manifest and pre-manifest Huntington's disease: evidence from a new Stroop task by Thomas Hunefeldt, Sabrina Maffi, Simone Migliore, Ferdinando Squitieri, Marta Olivetti Belardinelli

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Sleep Quality and Related Clinical Manifestations in Huntington Disease by Sabrina Maffi, Eugenia Scaricamazza, Simone Migliore, Melissa Casella, Consuelo Ceccarelli, Ferdinando Squitieri

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Deep white matter in Huntington's disease. by Owen Phillips, Ferdinando Squitieri, Cristina Sanchez-Castaneda, Francesca Elifani, Carlo Caltagirone, Umberto Sabatini, Margherita Di Paola

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Nitric oxide dysregulation in platelets from patients with advanced Huntington disease. by Albino Carrizzo, Alba Di Pardo, Vittorio Maglione, Antonio Damato, Enrico Amico, Luigi Formisano, Carmine Vecchione, Ferdinando Squitieri

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Juvenile Huntington disease in Argentina by Emilia Mabel Gatto, Virginia Parisi, José Luis Etcheverry, Ana Sanguinetti, Lorena Cordi, Adrian Binelli, Gabriel Persi, Ferdinando Squitieri

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A Novel Triplet-Primed PCR Assay to Detect the Full Range of Trinucleotide CAG Repeats in the Huntingtin Gene (<i>HTT</i>) by Alessandro De Luca, Annunziata Morella, Federica Consoli, Sergio Fanelli, Julie R. Thibert, Sarah Statt, Gary J. Latham, Ferdinando Squitieri

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Tractography of the corpus callosum in Huntington's disease. by Owen Phillips, Cristina Sanchez-Castaneda, Francesca Elifani, Vittorio Maglione, Alba Di Pardo, Carlo Caltagirone, Ferdinando Squitieri, Umberto Sabatini, Margherita Di Paola

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Cognitive and behavioral associated changes in manifest Huntington disease: A retrospective cross‐sectional study by Simone Migliore, Giulia D’Aurizio, Sabrina Maffi, Consuelo Ceccarelli, Giovanni Ristori, Silvia Romano, Anna Castaldo, Caterina Mariotti, Giuseppe Curcio, Ferdinando Squitieri

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Cognitive Reserve in Early Manifest Huntington Disease Patients: Leisure Time Is Associated with Lower Cognitive and Functional Impairment by Simone Migliore, Giulia D’Aurizio, Eugenia Scaricamazza, Sabrina Maffi, Consuelo Ceccarelli, Giovanni Ristori, Silvia Romano, Anna Castaldo, Mario Fichera, Giuseppe Curcio, Ferdinando Squitieri

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Generation of induced pluripotent stem cell line, CSSi004-A (2962), from a patient diagnosed with Huntington's disease at the presymptomatic stage by Eris Bidollari, Giovannina Rotundo, Daniela Ferrari, Ornella Candido, Laura Bernardini, Federica Consoli, Alessandro De Luca, Iolanda Santimone, Giuseppe Lamorte, Andrea Ilari, Ferdinando Squitieri, Angelo Luigi Vescovi, Jessica Rosati

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Generation of the induced pluripotent stem cell line CSSi006-A (3681) from a patient affected by advanced-stage Juvenile Onset Huntington's Disease by Giovannina Rotundo, Eris Bidollari, Daniela Ferrari, Iolanda Spasari, Laura Bernardini, Federica Consoli, Alessandro De Luca, Iolanda Santimone, Giuseppe Lamorte, Simone Migliore, Ferdinando Squitieri, Angelo Luigi Vescovi, Jessica Rosati

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GLUT-1 changes in paediatric Huntington disease brain cortex and fibroblasts: an observational case-control studyResearch in context by Antonella Tramutola, Hannah S. Bakels, Federica Perrone, Michela Di Nottia, Tommaso Mazza, Maria Pia Abruzzese, Martina Zoccola, Sara Pagnotta, Rosalba Carrozzo, Susanne T. de Bot, Marzia Perluigi, Willeke M.C. van Roon-Mom, Ferdinando Squitieri

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“Spazio Huntington”: Tracing the Early Motor, Cognitive and Behavioral Profiles of Kids with Proven Pediatric Huntington Disease and Expanded Mutations > 80 CAG Repeats by Federica Graziola, Sabrina Maffi, Melissa Grasso, Giacomo Garone, Simone Migliore, Eugenia Scaricamazza, Consuelo Ceccarelli, Melissa Casella, Ludovica Busi, Barbara D’Alessio, Alessandro De Luca, Giovanna Stefania Colafati, Umberto Sabatini, Alessandro Capuano, Ferdinando Squitieri

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Known Drugs Identified by Structure-Based Virtual Screening Are Able to Bind Sigma-1 Receptor and Increase Growth of Huntington Disease Patient-Derived Cells by Theo Battista, Gianmarco Pascarella, David Sasah Staid, Gianni Colotti, Jessica Rosati, Annarita Fiorillo, Alessia Casamassa, Angelo Luigi Vescovi, Barbara Giabbai, Marta Stefania Semrau, Sergio Fanelli, Paola Storici, Ferdinando Squitieri, Veronica Morea, Andrea Ilari

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Generation of induced pluripotent stem cell line CSSi008-A (4698) from a patient affected by advanced stage of Dentato-Rubral-Pallidoluysian atrophy (DRPLA) by Eris Bidollari, Giovannina Rotundo, Filomena Altieri, Mariangela Amicucci, Daniele Wiquel, Daniela Ferrari, Marina Goldoni, Laura Bernardini, Federica Consoli, Alessandro De Luca, Sergio Fanelli, Giuseppe Lamorte, Leonardo D'Agruma, Angelo Luigi Vescovi, Ferdinando Squitieri, Jessica Rosati

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International Guidelines for the Treatment of Huntington's Disease by Anne-Catherine Bachoud-Lévi, Joaquim Ferreira, Renaud Massart, Katia Youssov, Anne Rosser, Monica Busse, David Craufurd, David Craufurd, Ralf Reilmann, Ralf Reilmann, Giuseppe De Michele, Daniela Rae, Ferdinando Squitieri, Klaus Seppi, Charles Perrine, Clarisse Scherer-Gagou, Olivier Audrey, Christophe Verny, Jean-Marc Burgunder

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