Botulinum toxins in clinical practice: Gaps in knowledge

Por Barbano, Richard L.
Publicado no Neurol Clin Pract (2016)

New triggers and non-motor findings in a family with rapid-onset dystonia-parkinsonism

Por Barbano, Richard L., Hill, Deborah F., Snively, Beverly M., Light, Laney S., Boggs, Niki, McCall, W. Vaughn, Stacy, Mark, Ozelius, Laurie, Sweadner, Kathleen J., Brashear, Allison
Publicado em 2012

Clinical and genetic features of cervical dystonia in a large multicenter cohort

Por LeDoux, Mark S., Vemula, Satya R., Xiao, Jianfeng, Thompson, Misty M., Perlmutter, Joel S., Wright, Laura J., Jinnah, H.A., Rosen, Ami R., Hedera, Peter, Comella, Cynthia L., Weissbach, Anne, Junker, Johanna, Jankovic, Joseph, Barbano, Richard L., Reich, Stephen G., Rodriguez, Ramon L., Berman, Brian D., Chouinard, Sylvain, Severt, Lawrence, Agarwal, Pinky, Stover, Natividad P.
Publicado no Neurol Genet (2016)

Clinical and Demographic Characteristics Related to Onset: Site and Spread of Cervical Dystonia

Por Norris, Scott A, Jinnah, H A, Espay, Alberto J., Klein, Christine, Brüggemann, Norbert, Barbano, Richard L., Malaty, Irene, Rodriguez, Ramon L., Vidailhet, Marie, Roze, Emmanuel, Reich, Stephen G., Berman, Brian D., LeDoux, Mark S., Richardson, Sarah Pirio, Agarwal, Pinky, Mari, Zoltan, Ondo, William, Shih, Ludy C, Fox, Susan, Berardelli, Alfredo, Testa, Claudia M, Chang, Florence CF, Troung, Daniel, Nahab, Fatta, Xie, Tao, Hallett, Mark, Rosen, Ami R, Wright, Laura J, Perlmutter, JS
Publicado no Mov Disord (2016)

Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry

Por Viollet, Louis, Glusman, Gustavo, Murphy, Kelley J., Newcomb, Tara M., Reyna, Sandra P., Sweney, Matthew, Nelson, Benjamin, Andermann, Frederick, Andermann, Eva, Acsadi, Gyula, Barbano, Richard L., Brown, Candida, Brunkow, Mary E., Chugani, Harry T., Cheyette, Sarah R., Collins, Abigail, DeBrosse, Suzanne D., Galas, David, Friedman, Jennifer, Hood, Lee, Huff, Chad, Jorde, Lynn B., King, Mary D., LaSalle, Bernie, Leventer, Richard J., Lewelt, Aga J., Massart, Mylynda B., Mérida, Mario R., Ptáček, Louis J., Roach, Jared C., Rust, Robert S., Renault, Francis, Sanger, Terry D., Sotero de Menezes, Marcio A., Tennyson, Rachel, Uldall, Peter, Zhang, Yue, Zupanc, Mary, Xin, Winnie, Silver, Kenneth, Swoboda, Kathryn J.
Publicado no PLoS One (2015)

Correction: Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry

Por Viollet, Louis, Glusman, Gustavo, Murphy, Kelley J., Newcomb, Tara M., Reyna, Sandra P., Sweney, Matthew, Nelson, Benjamin, Andermann, Frederick, Andermann, Eva, Acsadi, Gyula, Barbano, Richard L., Brown, Candida, Brunkow, Mary E., Chugani, Harry T., Cheyette, Sarah R., Collins, Abigail, DeBrosse, Suzanne D., Galas, David, Friedman, Jennifer, Hood, Lee, Huff, Chad, Jorde, Lynn B., King, Mary D., LaSalle, Bernie, Leventer, Richard J., Lewelt, Aga J., Massart, Mylynda B., Mérida, Mario R., Ptáček, Louis J., Roach, Jared C., Rust, Robert S., Renault, Francis, Sanger, Terry D., Sotero de Menezes, Marcio A., Tennyson, Rachel, Uldall, Peter, Zhang, Yue, Zupanc, Mary, Xin, Winnie, Silver, Kenneth, Swoboda, Kathryn J.
Publicado no PLoS One (2015)