New vascular classification of port-wine stains: improving prediction of Sturge–Weber risk

por Waelchli, R, Aylett, SE, Robinson, K, Chong, WK, Martinez, AE, Kinsler, VA
Publicado 2014

Extending the spectrum of AKT1 mosaicism: not just the Proteus syndrome

por Polubothu, S., Al‐Olabi, L., Wilson, L., Chong, W.K., Kinsler, V.A.
Publicado 2016

Classification of neurological abnormalities in children with congenital melanocytic naevus syndrome identifies magnetic resonance imaging as the best predictor of clinical outcome

por Waelchli, R., Aylett, S.E., Atherton, D., Thompson, D.J., Chong, W.K., Kinsler, V.A.
Publicado 2015

Volume reduction of caudate nucleus is associated with movement coordination deficits in patients with hippocampal atrophy due to perinatal hypoxia-ischaemia

por Geva, Sharon, Jentschke, Sebastian, Argyropoulos, Georgios P.D., Chong, W.K., Gadian, David G., Vargha-Khadem, Faraneh
Publicado 2020

Hippocampal and diencephalic pathology in developmental amnesia

por Dzieciol, Anna M., Bachevalier, Jocelyne, Saleem, Kadharbatcha S., Gadian, David G., Saunders, Richard, Chong, W.K. Kling, Banks, Tina, Mishkin, Mortimer, Vargha-Khadem, Faraneh
Publicado 2017

Melanoma in congenital melanocytic naevi

por Kinsler, V.A., O'Hare, P., Bulstrode, N., Calonje, J.E., Chong, W.K., Hargrave, D., Jacques, T., Lomas, D., Sebire, N.J., Slater, O.
Publicado 2017

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

PLA2G6-associated neurodegeneration (PLAN): Further expansion of the clinical, radiological and mutation spectrum associated with infantile and atypical childhood-onset disease

por Illingworth, M.A., Meyer, E., Chong, W.K., Manzur, A.Y., Carr, L.J., Younis, R., Hardy, C., McDonald, F., Childs, A.M., Stewart, B., Warren, D., Kneen, R., King, M.D., Hayflick, S.J., Kurian, M.A.
Publicado 2014

Syndrome of Hepatic Cirrhosis, Dystonia, Polycythemia, and Hypermanganesemia Caused by Mutations in SLC30A10, a Manganese Transporter in Man

por Tuschl, Karin, Clayton, Peter T., Gospe, Sidney M., Gulab, Shamshad, Ibrahim, Shahnaz, Singhi, Pratibha, Aulakh, Roosy, Ribeiro, Reinaldo T., Barsottini, Orlando G., Zaki, Maha S., Del Rosario, Maria Luz, Dyack, Sarah, Price, Victoria, Rideout, Andrea, Gordon, Kevin, Wevers, Ron A., Chong, W.K. ‘‘Kling’’, Mills, Philippa B.
Publicado 2016

Deep sequencing reveals persistence of cell-associated mumps vaccine virus in chronic encephalitis

por Morfopoulou, Sofia, Mee, Edward T., Connaughton, Sarah M., Brown, Julianne R., Gilmour, Kimberly, Chong, WK ‘Kling’, Duprex, W. Paul, Ferguson, Deborah, Hubank, Mike, Hutchinson, Ciaran, Kaliakatsos, Marios, McQuaid, Stephen, Paine, Simon, Plagnol, Vincent, Ruis, Christopher, Virasami, Alex, Zhan, Hong, Jacques, Thomas S., Schepelmann, Silke, Qasim, Waseem, Breuer, Judith
Publicado 2016

Clinical and molecular characterization of KCNT1-related severe early-onset epilepsy

por McTague, Amy, Nair, Umesh, Malhotra, Sony, Meyer, Esther, Trump, Natalie, Gazina, Elena V., Papandreou, Apostolos, Ngoh, Adeline, Ackermann, Sally, Ambegaonkar, Gautam, Appleton, Richard, Desurkar, Archana, Eltze, Christin, Kneen, Rachel, Kumar, Ajith V., Lascelles, Karine, Montgomery, Tara, Ramesh, Venkateswaran, Samanta, Rajib, Scott, Richard H., Tan, Jeen, Whitehouse, William, Poduri, Annapurna, Scheffer, Ingrid E., Chong, W.K. “Kling”, Cross, J. Helen, Topf, Maya, Petrou, Steven, Kurian, Manju A.
Publicado 2018