Cognitive-affective manifestations since premanifest phases of Spinocerebellar Ataxia Type 3/Machado-Joseph Disease by Bolzan, Gabriela, Müller Eyng, Maria E., Leotti, Vanessa B., Saraiva-Pereira, Maria L., Jardim, Laura B.

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The effect of bone marrow transplantation on oxidative stress in X-linked adrenoleukodystrophy by Rockenbach, Francieli J., Deon, Marion, Marchese, Daiane P., Manfredini, Vanusa, Mescka, Caroline, Ribas, Graziela S., Habekost, Clarissa T., Castro, Claudio G., Jardim, Laura B., Vargas, Carmen R.

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Globotriaosylceramide is correlated with oxidative stress and inflammation in Fabry patients treated with enzyme replacement therapy by Biancini, Giovana B., Vanzin, Camila S., Rodrigues, Daiane B., Deon, Marion, Ribas, Graziela S., Barschak, Alethéa G., Manfredini, Vanusa, Netto, Cristina B.O., Jardim, Laura B., Giugliani, Roberto, Vargas, Carmen R.

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Huntington's disease-like disorders in Latin America and the Caribbean by Walker, Ruth H., Gatto, Emilia M., Bustamante, M. Leonor, Bernal-Pacheco, Oscar, Cardoso, Francisco, Castilhos, Raphael M., Chana-Cuevas, Pedro, Cornejo-Olivas, Mario, Estrada-Bellmann, Ingrid, Jardim, Laura B., López-Castellanos, Ricardo, López-Contreras, Ricardo, Maia, Debora P., Mazzetti, Pilar, Miranda, Marcelo, Rodríguez-Violante, Mayela, Teive, Helio, Tumas, Vitor

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Protective effect of antioxidants on DNA damage in leukocytes from X-linked adrenoleukodystrophy patients by Marchetti, Desirèe P., Donida, Bruna, da Rosa, Helen T., Manini, Paula R., Moura, Dinara J., Saffi, Jenifer, Deon, Marion, Mescka, Caroline P., Coelho, Daniella M., Jardim, Laura B., Vargas, Carmen R.

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Akathisia: An unusual movement disorder in Machado–Joseph disease by Pedroso, José Luiz, Braga-Neto, Pedro, Felício, André C, Barsottini, Orlando G.P, Jardim, Laura B, Saraiva-Pereira, Maria Luiza

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Induction of lipid peroxidation and decrease of antioxidant defenses in symptomatic and asymptomatic patients with X‐linked adrenoleukodystrophy by Deon, Marion, Sitta, Angela, Barschak, Alethea G., Coelho, Daniela M., Pigatto, Maiara, Schmitt, Graziela O., Jardim, Laura B., Giugliani, Roberto, Wajner, Moacir, Vargas, Carmen R.

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Parkinson's disease and the heterozygous state for glucocerebrosidase mutations among Brazilians by Socal, Mariana P, Bock, Hugo, Michelin-Tirelli, Kristiane, Hilbig, Arlete, Saraiva-Pereira, Maria Luiza, Rieder, Carlos R.M, Jardim, Laura B

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Oxidative stress is induced in female carriers of X-linked adrenoleukodystrophy by Deon, Marion, Sitta, Angela, Barschak, Alethea G, Coelho, Daniela M, Terroso, Thatiana, Schmitt, Graziela O, Wanderley, Hector Y.C, Jardim, Laura B, Giugliani, Roberto, Wajner, Moacir, Vargas, Carmen R

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S100B and NSE serum concentrations in Machado Joseph disease by Tort, Adriano B.L., Portela, Luis V.C., Rockenbach, Isabel C., Monte, Thais L., Pereira, Maria L., Souza, Diogo O., Rieder, Carlos R.M., Jardim, Laura B.

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Impaired P50 sensory gating in Machado-Joseph disease by Ghisolfi, Eduardo S., Maegawa, Gustavo H.B., Becker, Jefferson, Paula Zanardo, Ana, Strimitzer, Ivo M., Prokopiuk, Alexandre S., Luiza Pereira, Maria, Carvalho, Thiago, Jardim, Laura B., Lara, Diogo R.

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Neurological phenotypes in spinocerebellar ataxia type 2: Role of mitochondrial polymorphism A10398G and other risk factors by Monte, Thais L, Pereira, Fernanda, da Rosa Reckziegel, Estela, Augustin, Marina Coutinho, Locks-Coelho, Lucas D, Santos, Amanda S.P, Pedroso, José L, Barsottini, Orlando, Vargas, Fernando R, Saraiva-Pereira, Maria-Luiza, Jardim, Laura B

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Akathisia: An unusual movement disorder in Machado-Joseph disease by Pedroso, José Luiz, Braga-Neto, Pedro, Felício, André C, Barsottini, Orlando G P, Jardim, Laura B, Saraiva-Pereira, Maria Luiza

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LRP10 genetic variants in familial Parkinson's disease and dementia with Lewy bodies: a genome-wide linkage and sequencing study by Quadri, Marialuisa, Mandemakers, Wim, Grochowska, Martyna M, Masius, Roy, Geut, Hanneke, Fabrizio, Edito, Kuipers, Demy, Minneboo, Michelle, Vergouw, Leonie J M, Yonova-Doing, Ekaterina, Simons, Erik, Zhao, Tianna, Chang, Hsiu-Chen, Parchi, Piero, Correia Guedes, Leonor, Thomas, Astrid, Brouwer, Rutger W W, Heijsman, Daphne, Ingrassia, Angela M T, Calandra Buonaura, Giovanna, Sarchioto, Marianna, Vanacore, Nicola, Olgiati, Simone, Wu-Chou, Yah-Huei, Yeh, Tu-Hsueh, Boon, Agnita J W, Hoogers, Susanne E, Ghazvini, Mehrnaz, IJpma, Arne S, van IJcken, Wilfred F J, Onofrj, Marco, Barone, Paolo, Nicholl, David J, De Mari, Michele, Barbosa, Egberto, De Michele, Giuseppe, Majoor-Krakauer, Danielle, van Swieten, John C, de Jong, Frank J, Ferreira, Joaquim J, Lu, Chin-Song, Meco, Giuseppe, Cortelli, Pietro, van de Berg, Wilma D J, Bonifati, Vincenzo, Mandemakers, Wim, Boon, Agnita J.W., Rood, Janneke P.A, Vergouw, Leonie J.M., de Jong, Frank J., van Swieten, John C., Mattace-Raso, Francesco U.S., Leenders, Klaus L., Ferreira, Joaquim J., Correia Guedes, Leonor, Puschmann, Andreas, Ygland, Emil, Nilsson, Christer, Chien, Hsin F., Barbosa, Egberto, Bannach Jardim, Laura, Rieder, Carlos R.M., Chang, Hsiu-Chen, Lu, Chin-Song, Wu-Chou, Yah-Huei, Yeh, Tu-Hsueh, Tassorelli, Cristina, Pacchetti, Claudio, Riboldazzi, Giulio, Bono, Giorgio, Comi, Cristoforo, Padovani, Alessandro, Borroni, Barbara, Raudino, Francesco, Tinazzi, Michele, Ferracci, Carlo, Dalla Libera, Alessio, Abbruzzese, Giovanni, Cortelli, Pietro, Marconi, Roberto, Guidi, Marco, Onofrj, Marco, Thomas, Astrid, Vanacore, Nicola, Meco, Giuseppe, Fabbrini, Giovanni, Berardelli, Alfredo, Stocchi, Fabrizio, Barone, Paolo, Picillo, Marina, De Michele, Giuseppe, De Mari, Michele, Dell'Aquila, Claudia, Iliceto, Gianni, Toni, Vincenzo, Trianni, Giorgio, Annesi, Grazia, Saddi, Valeria, Cossu, Gianni, Melis, Maurizio

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Clinical and molecular characterization of hereditary spastic paraplegias: A next-generation sequencing panel approach by Burguez, Daniela, Polese-Bonatto, Márcia, Scudeiro, Laís Alves Jacinto, Björkhem, Ingemar, Schöls, Ludger, Jardim, Laura Bannach, Matte, Ursula, Saraiva-Pereira, Maria Luiza, Siebert, Marina, Saute, Jonas Alex Morales

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Nerve conduction studies, electromyography and sympathetic skin response in Fabry's disease by Gomes, Irenio, Nora, Daniel B., Becker, Jefferson, Ehlers, João Arthur C., Schwartz, Ida V.D., Giugliani, Roberto, Ashton-Prolla, Patricia, Jardim, Laura

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