Zobrazeno 1 - 10
of 108
pro vyhledávání: '"Quaghebeur, Gerardine"'
Autor:
Boccard, Sandra G.J., Fernandes, Henrique M., Jbabdi, Saad, Van Hartevelt, Tim J., Kringelbach, Morten L., Quaghebeur, Gerardine, Moir, Liz, Mancebo, Victor Piqueras, Pereira, Erlick A.C., Fitzgerald, James J., Green, Alexander L., Stein, John, Aziz, Tipu Z.
Publikováno v:
In World Neurosurgery February 2016 86:361-370
Autor:
Kuklisova-Murgasova, Maria, Cifor, Amalia, Napolitano, Raffaele, Papageorghiou, Aris, Quaghebeur, Gerardine, Rutherford, Mary A., Hajnal, Joseph V., Noble, J. Alison, Schnabel, Julia A.
Publikováno v:
In Medical Image Analysis December 2013 17(8):1137-1150
Autor:
Kuklisova-Murgasova, Maria, Quaghebeur, Gerardine, Rutherford, Mary A., Hajnal, Joseph V., Schnabel, Julia A.
Publikováno v:
In Medical Image Analysis December 2012 16(8):1550-1564
Autor:
Alston, Charlotte L., Heidler, Juliana, Dibley, Marris G., Kremer, Laura S., Taylor, Lucie S., Fratter, Carl, French, Courtney E., Glasgow, Ruth I.C., Feichtinger, René G., Delon, Isabelle, Pagnamenta, Alistair T., Dolling, Helen, Lemonde, Hugh, Aiton, Neil, Bjørnstad, Alf, Henneke, Lisa, Gärtner, Jutta, Thiele, Holger, Tauchmannova, Katerina, Quaghebeur, Gerardine, Houstek, Josef, Sperl, Wolfgang, Raymond, F. Lucy, Prokisch, Holger, Mayr, Johannes A., McFarland, Robert, Poulton, Joanna, Ryan, Michael T., Wittig, Ilka, Henneke, Marco, Taylor, Robert W.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______518::50931f8bcae7e46a007bd91d34330653
https://mediatum.ub.tum.de/1525534
https://mediatum.ub.tum.de/1525534
Autor:
Pagnamenta, Alistair T., Howard, Malcolm F., Wisniewski, Eva, Popitsch, Niko, Knight, Samantha J.L., Keays, David A., Quaghebeur, Gerardine, Cox, Helen, Cox, Phillip, Balla, Tamas, Taylor, Jenny C., Kini, Usha
Publikováno v:
Human Molecular Genetics
Polymicrogyria (PMG) is a structural brain abnormality involving the cerebral cortex that results from impaired neuronal migration and although several genes have been implicated, many cases remain unsolved. In this study, exome sequencing in a famil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::64ab33e6800458762b7cab3af8a7c0df
http://europepmc.org/articles/PMC4459391
http://europepmc.org/articles/PMC4459391
Autor:
Liao, Chunyan, Ashley, Neil, Diot, Alan, Morten, Karl, Phadwal, Kanchan, Williams, Andrew, Fearnley, Ian, Rosser, Lyndon, Lowndes, Jo, Fratter, Carl, Ferguson, David J.P., Vay, Laura, Quaghebeur, Gerardine, Moroni, Isabella, Bianchi, Stefania, Lamperti, Costanza, Downes, Susan M., Sitarz, Kamil S., Flannery, Padraig J., Carver, Janet, Dombi, Eszter, East, Daniel, Laura, Matilde, Reilly, Mary M., Mortiboys, Heather, Prevo, Remko, Campanella, Michelangelo, Daniels, Matthew J., Zeviani, Massimo, Yu-Wai-Man, Patrick, Simon, Anna Katharina, Votruba, Marcela, Poulton, Joanna
Publikováno v:
Neurology
Liao, C, Ashley, N, Diot, A, Morten, K, Phadwal, K, Williams, A, Fearnley, I, Rosser, L, Lowndes, J, Fratter, C, Ferguson, D J P, Vay, L, Quaghebeur, G, Moroni, I, Bianchi, S, Lamperti, C, Downes, S M, Sitarz, K S, Flannery, P J, Carver, J, Dombi, E, East, D, Laura, M, Reilly, M M, Mortiboys, H, Prevo, R, Campanella, M, Daniels, M J, Zeviani, M, Yu-Wai-Man, P, Simon, A K, Votruba, M & Poulton, J 2017, ' Dysregulated mitophagy and mitochondrial organization in optic atrophy due to OPA1 mutations ', Neurology, vol. 88, no. 2, pp. 131-142 . https://doi.org/10.1212/WNL.0000000000003491
Digital.CSIC. Repositorio Institucional del CSIC
instname
Liao, C, Ashley, N, Diot, A, Morten, K, Phadwal, K, Williams, A, Fearnley, I, Rosser, L, Lowndes, J, Fratter, C, Ferguson, D J P, Vay, L, Quaghebeur, G, Moroni, I, Bianchi, S, Lamperti, C, Downes, S M, Sitarz, K S, Flannery, P J, Carver, J, Dombi, E, East, D, Laura, M, Reilly, M M, Mortiboys, H, Prevo, R, Campanella, M, Daniels, M J, Zeviani, M, Yu-Wai-Man, P, Simon, A K, Votruba, M & Poulton, J 2017, ' Dysregulated mitophagy and mitochondrial organization in optic atrophy due to OPA1 mutations ', Neurology, vol. 88, no. 2, pp. 131-142 . https://doi.org/10.1212/WNL.0000000000003491
Digital.CSIC. Repositorio Institucional del CSIC
instname
© 2016 The Author(s).
[Objective]: To investigate mitophagy in 5 patients with severe dominantly inherited optic atrophy (DOA), caused by depletion of OPA1 (a protein that is essential for mitochondrial fusion), compared with healthy controls.
[Objective]: To investigate mitophagy in 5 patients with severe dominantly inherited optic atrophy (DOA), caused by depletion of OPA1 (a protein that is essential for mitochondrial fusion), compared with healthy controls.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::405f90410b7c65c0cc88235b04994e56
Autor:
Cusack, Stephen, Evans, Rupert, Richards, Peter, Quaghebeur, Gerardine, McGeehan, D. F., Maryosh, J. A. A., Tennant, W. G., Robertson, C. E.
Publikováno v:
BMJ: British Medical Journal, 1989 Sep . 299(6702), 790-791.
Externí odkaz:
https://www.jstor.org/stable/29705445
Autor:
Quaghebeur, Gerardine, Richards, Peter
Publikováno v:
BMJ: British Medical Journal, 1989 Aug 01. 299(6696), 410-410.
Externí odkaz:
https://www.jstor.org/stable/29704998
Akademický článek
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Akademický článek
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