Resultats de la cerca - McCarthy, Allan
- Mostrar 1 - 13 resultats de 13
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Failure of Sequential Pallidal and Motor Thalamus DBS for Rapid‐Onset Dystonia‐Parkinsonism (DYT12) per Fearon, Conor, McKinley, John, McCarthy, Allan, Rebelo, Pedro, Goggin, Carole, Magennis, Brian, Aziz, Tipu, Green, Alexander L., Lynch, Timothy
Publicat 2017Text -
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Ondine's Curse in Frontotemporal Dementia with Parkinsonism Linked to Chromosome 17 Caused by MAPT Variants per Williams, Laura, Olszewska, Diana A., Fearon, Conor, Magennis, Brian, McCarthy, Allan, Rowland, Lewis P., Mayeux, Richard, Page, Rory, Fahn, Stanley, Beausang, Alan, Lynch, Tim
Publicat 2021Text -
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EBV driven natural killer cell disease of the central nervous system presenting as subacute cognitive decline per Brett, Francesca M., Flavin, Richard, Chen, Daphne, Loftus, Teresa, Looby, Seamus, McCarthy, Allan, de Gascun, Cillian, Jaffe, Elaine S., Nor, Nurul, Javadpour, Mohsen, McCabe, Dominick
Publicat 2017Text -
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Association Between Glucocerebrosidase Mutations and Parkinson's Disease in Ireland per Olszewska, Diana A., McCarthy, Allan, Soto-Beasley, Alexandra I., Walton, Ronald L., Magennis, Brian, McLaughlin, Russell L., Hardiman, Orla, Ross, Owen A., Lynch, Tim
Publicat 2020Text -
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Exonic Re-Sequencing of the Chromosome 2q24.3 Parkinson’s Disease Locus per Labbé, Catherine, Ogaki, Kotaro, Lorenzo-Betancor, Oswaldo, Carrasquillo, Minerva M., Heckman, Michael G., McCarthy, Allan, Soto-Ortolaza, Alexandra I., Walton, Ronald L., Lynch, Timothy, Siuda, Joanna, Opala, Grzegorz, Krygowska-Wajs, Anna, Barcikowska, Maria, Czyzewski, Krzysztof, Dickson, Dennis W., Uitti, Ryan J., Wszolek, Zbigniew K., Ross, Owen A.
Publicat 2015Text -
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Closing the tau loop: the missing tau mutation per McCarthy, Allan, Lonergan, Roisin, Olszewska, Diana A., O’Dowd, Sean, Cummins, Gemma, Magennis, Brian, Fallon, Emer M., Pender, Niall, Huey, Edward D., Cosentino, Stephanie, O’Rourke, Killian, Kelly, Brendan D., O’Connell, Martin, Delon, Isabelle, Farrell, Michael, Spillantini, Maria Grazia, Rowland, Lewis P., Fahn, Stanley, Craig, Peter, Hutton, Michael, Lynch, Tim
Publicat 2015Text -
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Mutations in the SPG7 gene cause chronic progressive external ophthalmoplegia through disordered mitochondrial DNA maintenance per Pfeffer, Gerald, Gorman, Gráinne S, Griffin, Helen, Kurzawa-Akanbi, Marzena, Blakely, Emma L., Wilson, Ian, Sitarz, Kamil, Moore, David, Murphy, Julie L., Alston, Charlotte L., Pyle, Angela, Coxhead, Jon, Payne, Brendan, Gorrie, George H., Longman, Cheryl, Hadjivassiliou, Marios, McConville, John, Dick, David, Imam, Ibrahim, Hilton, David, Norwood, Fiona, Baker, Mark R., Jaiser, Stephan R., Yu-Wai-Man, Patrick, Farrell, Michael, McCarthy, Allan, Lynch, Timothy, McFarland, Robert, Schaefer, Andrew M., Turnbull, Douglass M., Horvath, Rita, Taylor, Robert W., Chinnery, Patrick F.
Publicat 2014Text -
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DNAJC13 p.Asn855Ser mutation screening in Parkinson’s disease and pathologically confirmed Lewy body disease patients per Lorenzo-Betancor, Oswaldo, Ogaki, Kotaro, Soto-Ortolaza, Alexandra I., Labbé, Catherine, Walton, Ronald L., Strongosky, Audrey J., van Gerpen, Jay A., Uitti, Ryan J., McLean, Pamela, Springer, Wolfdieter, Siuda, Joanna, Opala, Grzegorz, Krygowska-Wajs, Anna, Barcikowska, Maria, Czyzewski, Krzysztof, McCarthy, Allan, Lynch, Timothy, Puschmann, Andreas, Rektorová, Irena, Sanotsky, Yanosh, Vilarino-Guell, Carles, Farrer, Matthew J., Ferman, Tanis J., Boeve, Bradley F., Petersen, Ronald C., Parisi, Joseph E., Graff-Radford, Neill R., Dickson, Dennis W., Wszolek, Zbigniew K., Ross, Owen A.
Publicat 2015Text