Novel surface features for automated detection of focal cortical dysplasias in paediatric epilepsy

por Adler, Sophie, Wagstyl, Konrad, Gunny, Roxana, Ronan, Lisa, Carmichael, David, Cross, J Helen, Fletcher, Paul C., Baldeweg, Torsten
Publicado 2016

Towards in vivo focal cortical dysplasia phenotyping using quantitative MRI

por Adler, Sophie, Lorio, Sara, Jacques, Thomas S., Benova, Barbora, Gunny, Roxana, Cross, J. Helen, Baldeweg, Torsten, Carmichael, David W.
Publicado 2017

MRI profiling of focal cortical dysplasia using multi‐compartment diffusion models

por Lorio, Sara, Adler, Sophie, Gunny, Roxana, D’Arco, Felice, Kaden, Enrico, Wagstyl, Konrad, Jacques, Thomas S., Clark, Chris A., Cross, Judith Helen, Baldeweg, Torsten, Carmichael, David W.
Publicado 2020

Oxygen dependency of mitochondrial metabolism indicates outcome of newborn brain injury

por Bale, Gemma, Mitra, Subhabrata, de Roever, Isabel, Sokolska, Magdalena, Price, David, Bainbridge, Alan, Gunny, Roxana, Uria-Avellanal, Cristina, Kendall, Giles S, Meek, Judith, Robertson, Nicola J, Tachtsidis, Ilias
Publicado 2018

Post mortem magnetic resonance imaging in the fetus, infant and child: A comparative study with conventional autopsy (MaRIAS Protocol)

por Thayyil, Sudhin, Sebire, Neil J, Chitty, Lyn S, Wade, Angie, Olsen, Oystein, Gunny, Roxana S, Offiah, Amaka, Saunders, Dawn E, Owens, Catherine M, Chong, WK 'Kling', Robertson, Nicola J, Taylor, Andrew M
Publicado 2011

HIBCH mutations can cause Leigh-like disease with combined deficiency of multiple mitochondrial respiratory chain enzymes and pyruvate dehydrogenase

por Ferdinandusse, Sacha, Waterham, Hans R, Heales, Simon JR, Brown, Garry K, Hargreaves, Iain P, Taanman, Jan-Willem, Gunny, Roxana, Abulhoul, Lara, Wanders, Ronald JA, Clayton, Peter T, Leonard, James V, Rahman, Shamima
Publicado 2013

RARS2 mutations in a sibship with infantile spasms

por Ngoh, Adeline, Bras, Jose, Guerreiro, Rita, Meyer, Esther, McTague, Amy, Dawson, Eleanor, Mankad, Kshitij, Gunny, Roxana, Clayton, Peter, Mills, Philippa B., Thornton, Rachel, Lai, Ming, Forsyth, Robert, Kurian, Manju A.
Publicado 2016

Multimodal computational neocortical anatomy in pediatric hippocampal sclerosis

por Adler, Sophie, Blackwood, Mallory, Northam, Gemma B., Gunny, Roxana, Hong, Seok‐Jun, Bernhardt, Boris C., Bernasconi, Andrea, Bernasconi, Neda, Jacques, Thomas, Tisdall, Martin, Carmichael, David W., Cross, J. Helen, Baldeweg, Torsten
Publicado 2018

Quantitative MRI susceptibility mapping reveals cortical signatures of changes in iron, calcium and zinc in malformations of cortical development in children with drug-resistant ep...

por Lorio, Sara, Sedlacik, Jan, So, Po-Wah, Parkes, Harold G., Gunny, Roxana, Löbel, Ulrike, Li, Yao-Feng, Ogunbiyi, Olumide, Mistry, Talisa, Dixon, Emma, Adler, Sophie, Cross, J. Helen, Baldeweg, Torsten, Jacques, Thomas S., Shmueli, Karin, Carmichael, David W
Publicado 2021

Paediatric acquired demyelinating syndromes: incidence, clinical and magnetic resonance imaging features

por Absoud, Michael, Lim, Ming J, Chong, Wui K, De Goede, Christian G, Foster, Katharine, Gunny, Roxana, Hemingway, Cheryl, Jardine, Philip E, Kneen, Rachel, Likeman, Marcus, Nischal, Ken K, Pike, Michael G, Sibtain, Naomi A, Whitehouse, William P, Cummins, Carole, Wassmer, Evangeline
Publicado 2013

Neurological features of epilepsy, ataxia, sensorineural deafness, tubulopathy syndrome

por Cross, J Helen, Arora, Ruchi, Heckemann, Rolf A, Gunny, Roxana, Chong, Kling, Carr, Lucinda, Baldeweg, Torsten, Differ, Ann-Marie, Lench, Nicholas, Varadkar, Sophie, Sirimanna, Tony, Wassmer, Evangeline, Hulton, Sally A, Ognjanovic, Milos, Ramesh, Venkateswaran, Feather, Sally, Kleta, Robert, Hammers, Alexander, Bockenhauer, Detlef
Publicado 2013