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 no Neuroimage Clin (2016)

Paediatric cerebrovascular CT angiography—towards better image quality

Por Thust, Stefanie C., Chong, Wui Khean Kling, Gunny, Roxana, Mazumder, Asif, Poitelea, Marius, Welsh, Anna, Ederies, Ash, Mankad, Kshitij
Publicado no Quant Imaging Med Surg (2014)

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 em 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 no Orphanet J Rare Dis (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 no Epilepsia (2016)

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 em 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 no Dev Med Child Neurol (2013)