Management of Posterior Fossa Dissecting Aneurysms

Por Winston Chong, W. K.
Publicado em 2008

Acute laryngeal stridor with respiratory arrest in drug induced systemic lupus erythematosus.

Por Chong, W. K., Dewhurst, A. G., Dathan, J. R.
Publicado em 1988

3T MRI - 3D DSA Fusion Technique on Posterior Cerebral Artery Dissecting Aneurysm: Understanding a Potential Pathophysiologic Mechanism

Por Chong, W.K.W., Lee, S.K., Terbrugge, K.G.
Publicado em 2006

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 no Br J Dermatol (2016)

Painful and painless ophthalmoplegia with cavernous sinus pseudotumour.

Por Ganesan, V, Lin, J P, Chong, W K, Kirkham, F J, Surtees, R A
Publicado em 1996

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 no Br J Dermatol (2015)

Dystonia with Brain Manganese Accumulation Resulting From SLC30A10 Mutations: A New Treatable Disorder

Por Stamelou, Maria, Tuschl, Karin, Chong, W K, Burroughs, Andrew K, Mills, Philippa B, Bhatia, Kailash P, Clayton, Peter T
Publicado em 2012

The technique of laparoscopic cholecystectomy in children.

Por Davidoff, A M, Branum, G D, Murray, E A, Chong, W K, Ware, R E, Kinney, T R, Pappas, T N, Meyers, W C
Publicado em 1992

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 no Cortex (2017)

Correlation of MRI and neuropathology in AIDS.

Por Everall, I P, Chong, W K, Wilkinson, I D, Paley, M N, Chinn, R J, Hall-Craggs, M A, Scaravilli, F, Lantos, P L, Luthert, P J, Harrison, M J
Publicado em 1997

ImmunoglobuliN in the Treatment of Encephalitis (IgNiTE): protocol for a multicentre randomised controlled trial

Por Iro, M A, Sadarangani, M, Absoud, M, Chong, W K, Clark, C A, Easton, A, Gray, V, Kneen, R, Lim, M, Pike, M, Solomon, T, Vincent, A, Willis, L, Yu, L-M, Pollard, A J
Publicado no BMJ Open (2016)

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 em 2014

Over- and Underdosage of SOX3 Is Associated with Infundibular Hypoplasia and Hypopituitarism

Por Woods, Kathryn S., Cundall, Maria, Turton, James, Rizotti, Karine, Mehta, Ameeta, Palmer, Rodger, Wong, Jacqueline, Chong, W. K., Al-Zyoud, Mahmoud, El-Ali, Maryam, Otonkoski, Timo, Martinez-Barbera, Juan-Pedro, Thomas, Paul Q., Robinson, Iain C., Lovell-Badge, Robin, Woodward, Karen J., Dattani, Mehul T.
Publicado em 2005

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., “Kling” Chong, W.K., Mills, Philippa B.
Publicado em 2012

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 no Am J Hum Genet (2016)

Mutations in PROSC Disrupt Cellular Pyridoxal Phosphate Homeostasis and Cause Vitamin-B(6)-Dependent Epilepsy

Por Darin, Niklas, Reid, Emma, Prunetti, Laurence, Samuelsson, Lena, Husain, Ralf A., Wilson, Matthew, El Yacoubi, Basma, Footitt, Emma, Chong, W.K., Wilson, Louise C., Prunty, Helen, Pope, Simon, Heales, Simon, Lascelles, Karine, Champion, Mike, Wassmer, Evangeline, Veggiotti, Pierangelo, de Crécy-Lagard, Valérie, Mills, Philippa B., Clayton, Peter T.
Publicado no Am J Hum Genet (2016)

Novel mutations expand the clinical spectrum of DYNC1H1-associated spinal muscular atrophy

Por Scoto, Mariacristina, Rossor, Alexander M., Harms, Matthew B., Cirak, Sebahattin, Calissano, Mattia, Robb, Stephanie, Manzur, Adnan Y., Martínez Arroyo, Amaia, Rodriguez Sanz, Aida, Mansour, Sahar, Fallon, Penny, Hadjikoumi, Irene, Klein, Andrea, Yang, Michele, De Visser, Marianne, Overweg-Plandsoen, W.C.G. (Truus), Baas, Frank, Taylor, J. Paul, Benatar, Michael, Connolly, Anne M., Al-Lozi, Muhammad T., Nixon, John, de Goede, Christian G.E.L., Foley, A. Reghan, Mcwilliam, Catherine, Pitt, Matthew, Sewry, Caroline, Phadke, Rahul, Hafezparast, Majid, Chong, W.K. “Kling”, Mercuri, Eugenio, Baloh, Robert H., Reilly, Mary M., Muntoni, Francesco
Publicado no Neurology (2015)

Mutations in SLC39A14 disrupt manganese homeostasis and cause childhood-onset parkinsonism–dystonia

Por Tuschl, Karin, Meyer, Esther, Valdivia, Leonardo E., Zhao, Ningning, Dadswell, Chris, Abdul-Sada, Alaa, Hung, Christina Y., Simpson, Michael A., Chong, W. K., Jacques, Thomas S., Woltjer, Randy L., Eaton, Simon, Gregory, Allison, Sanford, Lynn, Kara, Eleanna, Houlden, Henry, Cuno, Stephan M., Prokisch, Holger, Valletta, Lorella, Tiranti, Valeria, Younis, Rasha, Maher, Eamonn R., Spencer, John, Straatman-Iwanowska, Ania, Gissen, Paul, Selim, Laila A. M., Pintos-Morell, Guillem, Coroleu-Lletget, Wifredo, Mohammad, Shekeeb S., Yoganathan, Sangeetha, Dale, Russell C., Thomas, Maya, Rihel, Jason, Bodamer, Olaf A., Enns, Caroline A., Hayflick, Susan J., Clayton, Peter T., Mills, Philippa B., Kurian, Manju A., Wilson, Stephen W.
Publicado no Nat Commun (2016)