Substance abuse may hasten motor onset of Huntington disease: Evaluating the Enroll-HD database

Por Schultz, Jordan L., Kamholz, John A., Moser, David J., Feely, Shawna M.E., Paulsen, Jane S., Nopoulos, Peg C.
Publicado no Neurology (2017)

Charcot Marie Tooth (CMT) Subtypes and Genetic Testing Strategies

Por Saporta, Anita S.D., Sottile, Stephanie L., Miller, Lindsey J., Feely, Shawna M.E., Siskind, Carly E, Shy, Michael E.
Publicado em 2011

PMP22 expression in dermal nerve myelin from patients with CMT1A

Por Katona, Istvan, Wu, Xingyao, Feely, Shawna M. E., Sottile, Stephanie, Siskind, Carly E., Miller, Lindsey J., Shy, Michael E., Li, Jun
Publicado em 2009

Deficits in stepping response time are associated with impairments in balance and mobility in people with Huntington disease

Por Goldberg, Allon, Schepens, Stacey L., Feely, Shawna M. E., Garbern, James Y., Miller, Lindsey J., Siskind, Carly E., Conti, Gerry E
Publicado em 2010

Psychometrics evaluation of Charcot-Marie-Tooth Neuropathy Score (CMTNSv2) second version, using Rasch analysis

Por Sadjadi, Reza, Reilly, Mary M., Shy, Michael E., Pareyson, Davide, Laura, Matilde, Murphy, Sinead, Feely, Shawna M.E., Grider, Tiffany, Bacon, Chelsea, Piscosquito, Giuseppe, Calabrese, Daniela, Burns, Ted M.
Publicado no J Peripher Nerv Syst (2014)

Absence of Dystrophin Related Protein-2 disrupts Cajal bands in a patient with Charcot-Marie-Tooth disease

Por Brennan, Kathryn M., Bai, Yunhong, Pisciotta, Chiara, Wang, Suola, Feely, Shawna M.E., Hoegger, Mark, Gutmann, Laurie, Moore, Steven A., Gonzalez, Michael, Sherman, Diane L., Brophy, Peter J., Züchner, Stephan, Shy, Michael E.
Publicado no Neuromuscul Disord (2015)

High-Dosage Ascorbic Acid Treatment in Charcot-Marie-Tooth Disease Type 1A: Results of a Randomized, Double-Masked, Controlled Trial

Por Lewis, Richard A., McDermott, Michael P., Herrmann, David N., Hoke, Ahmet, Clawson, Lora L., Siskind, Carly, Feely, Shawna M. E., Miller, Lindsey J., Barohn, Richard J., Smith, Patricia, Luebbe, Elizabeth, Wu, Xingyao, Shy, Michael E.
Publicado em 2013

Missense Mutations in the Copper Transporter Gene ATP7A Cause X-Linked Distal Hereditary Motor Neuropathy

Por Kennerson, Marina L., Nicholson, Garth A., Kaler, Stephen G., Kowalski, Bartosz, Mercer, Julian F.B., Tang, Jingrong, Llanos, Roxana M., Chu, Shannon, Takata, Reinaldo I., Speck-Martins, Carlos E., Baets, Jonathan, Almeida-Souza, Leonardo, Fischer, Dirk, Timmerman, Vincent, Taylor, Philip E., Scherer, Steven S., Ferguson, Toby A., Bird, Thomas D., De Jonghe, Peter, Feely, Shawna M.E., Shy, Michael E., Garbern, James Y.
Publicado em 2010