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

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

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

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

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Hippocampal and diencephalic pathology in developmental amnesia von Dzieciol, Anna M., Bachevalier, Jocelyne, Saleem, Kadharbatcha S., Gadian, David G., Saunders, Richard, Chong, W.K. Kling, Banks, Tina, Mishkin, Mortimer, Vargha-Khadem, Faraneh

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Immunotherapy-responsive childhood neurodegeneration with systemic and central nervous system inflammation von Sa, Mario, Hacohen, Yael, Alderson, Lucy, Chong, W.K. Kling, Anderson, Glenn, Jacques, Thomas S., Neubauer, David, Szczepanik, Elzbieta, Lim, Ming, Kaliakatsos, Marios

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MR determination of neonatal spinal canal depth von Arthurs, Owen, Thayyil, Sudhin, Wade, Angie, Chong, W.K. ‘Kling’, Sebire, Neil J, Taylor, Andrew M

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Cerebellar Involvement in the Phakomatoses von Chong, W.K. ‘Kling’

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Normal MRI neuroimaging and acute dancing eyes syndrome von Dale, Russell C, Church, Andrew J, Wyatt, Mike C, Sharma, Sanjiv, Chong, Kling WK, Cox, Tim CS

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

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