Articles

• Strategic white matter tracts for processing speed deficits in age-related small vessel disease

  Marco Duering, Benno Gesierich, Stephan Seiler, Lukas Pirpamer, Mariya Gonik, Edith Hofer, Eric Jouvent, Edouard Duchesnay, Hugues Chabriat, Stefan Ropele, Reinhold Schmidt, Martin Dichgans

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• Antemortem MRI findings associated with microinfarcts at autopsy

  Mekala R. Raman, Gregory M. Preboske, Scott A. Przybelski, Jeffrey L. Gunter, Matthew L. Senjem, Prashanthi Vemuri, Matthew C. Murphy, Melissa E. Murray, Bradley F. Boeve, David S. Knopman, Ronald C. Petersen, Joseph E. Parisi, Dennis W. Dickson, Clifford R. Jack, Kejal Kantarci

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• Association of hypometabolism and amyloid levels in aging, normal subjects

  Val J. Lowe, Stephen D. Weigand, Matthew L. Senjem, Prashanthi Vemuri, Lennon Jordan, Kejal Kantarci, Bradley Boeve, Clifford R. Jack, David Knopman, Ronald C. Petersen

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• Topology of brainstem lesions associated with subjective visual vertical tilt

  Tae-Ho Yang, Sun-Young Oh, Kichang Kwak, Jong-Min Lee, Byoung-Soo Shin, Seul-Ki Jeong

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• Anti-agrin autoantibodies in myasthenia gravis

  Christiane Gasperi, Arthur Melms, Benedikt Schoser, Yina Zhang, Julia Meltoranta, Valerie Risson, Laurent Schaeffer, Bertold Schalke, Stephan Kröger

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• Paraparetic Guillain-Barré syndrome

  Bianca van den Berg, Christiaan Fokke, Judith Drenthen, Pieter A. van Doorn, Bart C. Jacobs

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• Lower motor neuron disease with respiratory failure caused by a novel MAPT mutation

  Alessio Di Fonzo, Dario Ronchi, Francesca Gallia, Fulvia Milena Cribiù, Ilaria Trezzi, Annalisa Vetro, Erika Della Mina, Ivan Limongelli, Riccardo Bellazzi, Ivana Ricca, Giuseppe Micieli, Elisa Fassone, Mafalda Rizzuti, Andreina Bordoni, Francesco Fortunato, Sabrina Salani, Gabriele Mora, Stefania Corti, Mauro Ceroni, Silvano Bosari, Orsetta Zuffardi, Nereo Bresolin, Eduardo Nobile-Orazio, Giacomo Pietro Comi

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• Congenital mirror movementsMutational analysis of RAD51 and DCC in 26 cases

  Aurélie Méneret, Christel Depienne, Florence Riant, Oriane Trouillard, Delphine Bouteiller, Massimo Cincotta, Pierre Bitoun, Julia Wickert, Isabelle Lagroua, Ana Westenberger, Alessandra Borgheresi, Diane Doummar, Marcello Romano, Simone Rossi, Luc Defebvre, Linda De Meirleir, Alberto J. Espay, Simona Fiori, Stephan Klebe, Chloé Quélin, Sabine Rudnik-Schöneborn, Ghislaine Plessis, Russell C. Dale, Susan Sklower Brooks, Karolina Dziezyc, Pierre Pollak, Jean-Louis Golmard, Marie Vidailhet, Alexis Brice, Emmanuel Roze

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• Expanding sialidosis spectrum by genome-wide screeningNEU1 mutations in adult-onset myoclonus

  Laura Canafoglia, Angela Robbiano, Davide Pareyson, Ferruccio Panzica, Lorenzo Nanetti, Anna Rita Giovagnoli, Anna Venerando, Cinzia Gellera, Silvana Franceschetti, Federico Zara

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• Motor protein mutations cause a new form of hereditary spastic paraplegia

  Andrés Caballero Oteyza, Esra Battaloğlu, Levent Ocek, Tobias Lindig, Jennifer Reichbauer, Adriana P. Rebelo, Michael A. Gonzalez, Yasar Zorlu, Burcak Ozes, Dagmar Timmann, Benjamin Bender, Günther Woehlke, Stephan Züchner, Ludger Schöls, Rebecca Schüle

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• Initial cognitive decline is associated with cortical thinning in early Parkinson disease

  Joana B. Pereira, Per Svenningsson, Daniel Weintraub, Kolbjørn Brønnick, Alexander Lebedev, Eric Westman, Dag Aarsland

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• Multimorbidity and the risk of restless legs syndrome in 2 prospective cohort studies

  András Szentkirályi, Henry Völzke, Wolfgang Hoffmann, Claudia Trenkwalder, Klaus Berger

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