Enteral Levodopa Therapy in Advanced Parkinson's Disease with Gastroparesis

Por Venkitachalam, Anil, Lazarescu, Adriana, Suchowersky, Oksana
Publicado no Mov Disord Clin Pract (2015)

Hyperkinetic movement disorders

Por Suchowersky, Oksana, Comella, Cynthia, Goetz, Christopher G.
Publicado em c201

Episodic Ataxia Secondary to CEP290 Compound Heterozygous Mutations: A Case Report

Por Hamed, Moath, Shetty, Aakash, Dzwiniel, Tara, Buller, Mark, Koskinen, Lotta, Suchowersky, Oksana
Publicado no Mov Disord Clin Pract (2019)

Impact of belief in neuroprotection on therapeutic intervention in Parkinson disease

Por Elble, Rodger J., Suchowersky, Oksana, Shaftman, Stephanie, Weiner, William J., Huang, Peng, Tilley, Barbara
Publicado em 2010

Engagement with genetic discrimination: concerns and experiences in the context of Huntington disease

Por Bombard, Yvonne, Penziner, Elizabeth, Suchowersky, Oksana, Guttman, Mark, Paulsen, Jane S, Bottorff, Joan L, Hayden, Michael R
Publicado em 2007

Walking with Music Is a Safe and Viable Tool for Gait Training in Parkinson's Disease: The Effect of a 13-Week Feasibility Study on Single and Dual Task Walking

Por de Bruin, Natalie, Doan, Jon B., Turnbull, George, Suchowersky, Oksana, Bonfield, Stephan, Hu, Bin, Brown, Lesley A.
Publicado em 2010

Obstacle Avoidance amongst Parkinson Disease Patients Is Challenged in a Threatening Context

Por Doan, Jon B., de Bruin, Natalie, Pellis, Sergio M., Suchowersky, Oksana, Whishaw, Ian Q., Brown, Lesley A.
Publicado no J Neurodegener Dis (2013)

No Sex Differences in Use of Dopaminergic Medication in Early Parkinson Disease in the US and Canada - Baseline Findings of a Multicenter Trial

Por Umeh, Chizoba C., Pérez, Adriana, Augustine, Erika F., Dhall, Rohit, Dewey, Richard B., Mari, Zoltan, Simon, David K., Wills, Anne-Marie A., Christine, Chadwick W., Schneider, Jay S., Suchowersky, Oksana
Publicado no PLoS One (2014)

Sex Differences in Clinical Features of Early, Treated Parkinson’s Disease

Por Augustine, Erika F., Pérez, Adriana, Dhall, Rohit, Umeh, Chizoba C., Videnovic, Aleksandar, Cambi, Franca, Wills, Anne-Marie A., Elm, Jordan J., Zweig, Richard M., Shulman, Lisa M., Nance, Martha A., Bainbridge, Jacquelyn, Suchowersky, Oksana
Publicado no PLoS One (2015)

POLR3A variants in hereditary spastic paraplegia and ataxia

Por Gauquelin, Laurence, Tétreault, Martine, Thiffault, Isabelle, Farrow, Emily, Miller, Neil, Yoo, Byunggil, Bareke, Eric, Yoon, Grace, Suchowersky, Oksana, Dupré, Nicolas, Tarnopolsky, Mark, Brais, Bernard, Wolf, Nicole I, Majewski, Jacek, Rouleau, Guy A, Gan-Or, Ziv, Bernard, Geneviève
Publicado no Brain (2018)

Channelopathies Are a Frequent Cause of Genetic Ataxias Associated with Cerebellar Atrophy

Por Gauquelin, Laurence, Hartley, Taila, Tarnopolsky, Mark, Dyment, David A., Brais, Bernard, Geraghty, Michael T., Tétreault, Martine, Ahmed, Sohnee, Rojas, Samantha, Choquet, Karine, Majewski, Jacek, Bernier, François, Innes, Allan Micheil, Rouleau, Guy, Suchowersky, Oksana, Boycott, Kym M., Yoon, Grace
Publicado no Mov Disord Clin Pract (2020)

The R941L mutation in MYH14 disrupts mitochondrial fission and associates with peripheral neuropathy

Por Almutawa, Walaa, Smith, Christopher, Sabouny, Rasha, Smit, Ryan B., Zhao, Tian, Wong, Rachel, Lee-Glover, Laurie, Desrochers-Goyette, Justine, Ilamathi, Hema Saranya, Suchowersky, Oksana, Germain, Marc, Mains, Paul E., Parboosingh, Jillian S., Pfeffer, Gerald, Innes, A. Micheil, Shutt, Timothy E.
Publicado no EBioMedicine (2019)

Hospitalization in Parkinson disease: A survey of National Parkinson Foundation Centers

Por Chou, Kelvin L., Zamudio, Jorge, Schmidt, Peter, Price, Catherine C., Parashos, Sotirios A., Bloem, Bastiaan R., Lyons, Kelly E., Christine, Chadwick W., Pahwa, Rajesh, Bodis-Wollner, Ivan, Oertel, Wolfgang H., Suchowersky, Oksana, Aminoff, Michael J., Malaty, Irene A., Friedman, Joseph H., Okun, Michael S.
Publicado em 2011

Exome Sequencing as a Diagnostic Tool for Pediatric-Onset Ataxia

Por Sawyer, Sarah L, Schwartzentruber, Jeremy, Beaulieu, Chandree L, Dyment, David, Smith, Amanda, Chardon, Jodi Warman, Yoon, Grace, Rouleau, Guy A, Suchowersky, Oksana, Siu, Victoria, Murphy, Lisa, Hegele, Robert A, Marshall, Christian R, Bulman, Dennis E, Majewski, Jacek, Tarnopolsky, Mark, Boycott, Kym M
Publicado no Hum Mutat (2014)

Canadian guideline for Parkinson disease

Por Grimes, David, Fitzpatrick, Megan, Gordon, Joyce, Miyasaki, Janis, Fon, Edward A., Schlossmacher, Michael, Suchowersky, Oksana, Rajput, Alexander, Lafontaine, Anne Louise, Mestre, Tiago, Appel-Cresswell, Silke, Kalia, Suneil K., Schoffer, Kerrie, Zurowski, Mateusz, Postuma, Ronald B., Udow, Sean, Fox, Susan, Barbeau, Pauline, Hutton, Brian
Publicado no CMAJ (2019)

Assessing non-Mendelian Inheritance in Inherited Axonopathies

Por Bis-Brewer, Dana M., Gan-Or, Ziv, Sleiman, Patrick, Hakonarson, Hakon, Fazal, Sarah, Courel, Steve, Cintra, Vivian, Tao, Feifei, Estiar, Mehrdad A., Tarnopolsky, Mark, Boycott, Kym M., Yoon, Grace, Suchowersky, Oksana, Dupré, Nicolas, Cheng, Andrew, Lloyd, Thomas E., Rouleau, Guy, Schüle, Rebecca, Züchner, Stephan
Publicado no Genet Med (2020)

Management of the hospitalized patient with Parkinson’s disease: Current state of the field and need for guidelines✩

Por Aminoff, Michael J., Christine, Chad W., Friedman, Joseph H., Chou, Kelvin L., Lyons, Kelly E., Pahwa, Rajesh, Bloem, Bastian R., Parashos, Sotirios A., Price, Catherine C., Malaty, Irene A., Iansek, Robert, Bodis-Wollner, Ivan, Suchowersky, Oksana, Oertel, Wolfgang H., Zamudio, Jorge, Oberdorf, Joyce, Schmidt, Peter, Okun, Michael S.
Publicado em 2010

Levodopa-Carbidopa Intestinal Gel in Advanced Parkinson'd Disease: Final 12-Month, Open-Label Results

Por Fernandez, Hubert H, Standaert, David G, Hauser, Robert A, Lang, Anthony E, Fung, Victor SC, Klostermann, Fabian, Lew, Mark F, Odin, Per, Steiger, Malcolm, Yakupov, Eduard Z, Chouinard, Sylvain, Suchowersky, Oksana, Dubow, Jordan, Hall, Coleen M, Chatamra, Krai, Robieson, Weining Z, Benesh, Janet A, Espay, Alberto J
Publicado no Mov Disord (2015)

Clinical and genetic study of hereditary spastic paraplegia in Canada

Por Chrestian, Nicolas, Dupré, Nicolas, Gan-Or, Ziv, Szuto, Anna, Chen, Shiyi, Venkitachalam, Anil, Brisson, Jean-Denis, Warman-Chardon, Jodi, Ahmed, Sohnee, Ashtiani, Setareh, MacDonald, Heather, Mohsin, Noreen, Mourabit-Amari, Karim, Provencher, Pierre, Boycott, Kym M., Stavropoulos, Dimitri J., Dion, Patrick A., Ray, Peter N., Suchowersky, Oksana, Rouleau, Guy A., Yoon, Grace
Publicado no Neurol Genet (2016)

Mutations in BICD2, which Encodes a Golgin and Important Motor Adaptor, Cause Congenital Autosomal-Dominant Spinal Muscular Atrophy

Por Neveling, Kornelia, Martinez-Carrera, Lilian A., Hölker, Irmgard, Heister, Angelien, Verrips, Aad, Hosseini-Barkooie, Seyyed Mohsen, Gilissen, Christian, Vermeer, Sascha, Pennings, Maartje, Meijer, Rowdy, te Riele, Margot, Frijns, Catharina J.M., Suchowersky, Oksana, MacLaren, Linda, Rudnik-Schöneborn, Sabine, Sinke, Richard J., Zerres, Klaus, Lowry, R. Brian, Lemmink, Henny H., Garbes, Lutz, Veltman, Joris A., Schelhaas, Helenius J., Scheffer, Hans, Wirth, Brunhilde
Publicado em 2013