Items where Author is "Shy, Michael E."

Yes

Eschbach, Judith and Sinniger, Jérôme and Bouitbir, Jamal and Fergani, Anissa and Schlagowski, Anna-Isabel and Zoll, Joffrey and Geny, Bernard and René, Frédérique and Larmet, Yves and Marion, Vincent and Baloh, Robert H. and Harms, Matthew B. and Shy, Michael E. and Messadeq, Nadia and Weydt, Patrick and Loeffler, Jean-Philippe and Ludolph, Albert C. and Dupuis, Luc. (2013) Dynein mutations associated with hereditary motor neuropathies impair mitochondrial morphology and function with age. Neurobiology of disease, 58. pp. 220-230.

Kennerson, Marina L. and Nicholson, Garth A. and Kaler, Stephen G. and Kowalski, Bartosz and Mercer, Julian F. B. and Tang, Jingrong and Llanos, Roxana M. and Chu, Shannon and Takata, Reinaldo I. and Speck-Martins, Carlos E. and Baets, Jonathan and Almeida-Souza, Leonardo and Fischer, Dirk and Timmerman, Vincent and Taylor, Philip E. and Scherer, Steven S. and Ferguson, Toby A. and Bird, Thomas D. and De Jonghe, Peter and Feely, Shawna M. E. and Shy, Michael E. and Garbern, James Y.. (2010) Missense mutations in the copper transporter gene ATP7A cause X-linked distal hereditary motor neuropathy. American journal of human genetics, Vol. 86, H. 3. pp. 343-352.