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Neurologic Wilson's disease 由 Matthew T. Lorincz

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The Dyskinesia Impairment Scale: a new instrument to measure dystonia and choreoathetosis in dyskinetic cerebral palsy 由 Elegast Monbaliu, Els Ortibus, Jos De Cat, Bernard Dan, Lieve Heyrman, Peter Prinzie, Paul De Cock, Hilde Feys

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Clinical patterns of dystonia and choreoathetosis in participants with dyskinetic cerebral palsy 由 Elegast Monbaliu, Paul De Cock, Els Ortibus, Lieve Heyrman, Katrijn Klingels, Hilde Feys

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Linkage of Benign Familial Infantile Convulsions to Chromosome 16p12-q12 Suggests Allelism to the Infantile Convulsions and Choreoathetosis Syndrome 由 Roberto Caraballo, Sylvana Pavek, Arnaud Lemainque, Marguerite Gastaldi, Bernard Échenne, Jacques Motté, Pierre Genton, Ricardo Cersósimo, Véronique Humbertclaude, Natalio Fejerman, Anthony P. Monaco, Mark G. Lathrop, Jacques Rochette, Pierre Szepetowski

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The Neurological Presentation of Ceruloplasmin Gene Mutations 由 Alisdair McNeill, Massimo Pandolfo, Jens Kuhn, Huifang Shang, Hiroaki Miyajima

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Genetics of an X-Linked Disorder of Uric Acid Metabolism and Cerebral Function 由 William L. Nyhan, Joseph J. Pesek, Lawrence Sweetman, Donald G. Carpenter, C H Carter

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PROGRESSIVE FAMILIAL CHOREOATHETOSIS WITH CUTANEOUS TELANGIECTASIA 由 C. E. Wells, G. MILTON SHY

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Acidúria glutárica tipo 1: variabilidade fenotípica. Estudo de seis pacientes 由 Erasmo Barbante Casella, Antônio Umberto Bresolin, Marcelo Valente, Durval Anibal Daniel, José Jorge Machado, María Aparecida Vieira, Adriana Gomes Tenório, Néstor Chamoles

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Familial Infantile Convulsions and Paroxysmal Choreoathetosis: A New Neurological Syndrome Linked to the Pericentromeric Region of Human Chromosome 16 由 Pierre Szepetowski, Jacques Rochette, Patrick Berquin, Charles Piussan, G.M. Lathrop, Anthony P. Monaco

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Dentato-rubro-pallido-luysian atrophy: a clinico-pathological study. 由 Ryo Iizuka, Keizo Hirayama, K Maehara

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PRRT2 Mutations Cause Benign Familial Infantile Epilepsy and Infantile Convulsions with Choreoathetosis Syndrome 由 Sarah E. Heron, Bronwyn E. Grinton, Sara Kivity, Zaid Afawi, Sameer M. Zuberi, James N. Hughes, Clair Pridmore, Bree Hodgson, Xenia Iona, Lynette G. Sadleir, James T. Pelekanos, Eric Herlenius, Hadassa Goldberg‐Stern, Haim Bassan, Eric Haan, Amos D. Korczyn, Alison Gardner, Mark Corbett, Jozef Gécz, Paul Q. Thomas, John C. Mulley, Samuel F. Berkovic, Ingrid E. Scheffer, Leanne M. Dibbens

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Movement disorders induced by peripheral trauma 由 José Cláudio Marinho da Nóbrega, Cynthia Campos, João Carlos Papaterra Limongi, Manoel Jacobsen Teixeira, Tchia Yeng Lin

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Dyskinesia induced by phenytoin 由 Maria Augusta Montenegro, ANNA ELISA SCOTONI, Fernando Cendes

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Movement disorders due to bilirubin toxicity 由 Jessica Rose, Rachel Vassar

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Familial <i>PRRT2</i> mutation with heterogeneous paroxysmal disorders including paroxysmal torticollis and hemiplegic migraine 由 Russell C. Dale, A. Gardiner, Jayne Antony, Henry Houlden

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Coreoatetose paroxística cinesiogênica: relato de um caso tratado com carbamazepina 由 Paulo Eduardo Mestrinelli Carrilho, Egberto Reis Barbosa, Mônica Santoro Haddad, Luiz Roberto Comerlatti, João Carlos Papaterra Limongi, Milberto Scaff

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GLUT1 deficiency syndrome 2013: Current state of the art 由 Valentina De Giorgis, Pierangelo Veggiotti

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<i>PRRT2</i> mutations in familial infantile seizures, paroxysmal dyskinesia, and hemiplegic migraine 由 Carla Marini, Valerio Conti, Davide Mei, Domenica Battaglia, Donatella Lettori, Emma Losito, G. Bruccini, Gaetano Tortorella, Renzo Guerrini

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Transcription factor haploinsufficiency: when half a loaf is not enough 由 Jonathan G. Seidman, Christine E. Seidman

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Pediatric Anti-N-methyl-D-Aspartate Receptor Encephalitis—Clinical Analysis and Novel Findings in a Series of 20 Patients 由 Thaís Armangué, Maarten J. Titulaer, Ignacio Málaga, Luís Bataller, Iñigo Gabilondo, Francesc Graus, Josep Dalmau

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