Clinical relevance of voltage-gated potassium channel–complex antibodies in children

Por Hacohen, Yael, Singh, Rahul, Rossi, Meghan, Lang, Bethan, Hemingway, Cheryl, Lim, Ming, Vincent, Angela
Publicado no Neurology (2015)

Progressive neurologic disorder: Initial manifestation of hemophagocytic lymphohistiocytosis

Por Murphy, Claire, Nanthapisal, Sira, Gilmour, Kimberly, Laurent, Sue, D'Arco, Felice, Hemingway, Cheryl, Brogan, Paul, Eleftheriou, Despina
Publicado no Neurology (2016)

Myelin oligodendrocyte glycoprotein antibodies are associated with a non-MS course in children

Por Hacohen, Yael, Absoud, Michael, Deiva, Kumaran, Hemingway, Cheryl, Nytrova, Petra, Woodhall, Mark, Palace, Jacqueline, Wassmer, Evangeline, Tardieu, Marc, Vincent, Angela, Lim, Ming, Waters, Patrick
Publicado no Neurol Neuroimmunol Neuroinflamm (2015)

NMDA receptor antibodies associated with distinct white matter syndromes

Por Hacohen, Yael, Absoud, Michael, Hemingway, Cheryl, Jacobson, Leslie, Lin, Jean-Pierre, Pike, Mike, Pullaperuma, Sunil, Siddiqui, Ata, Wassmer, Evangeline, Waters, Patrick, Irani, Sarosh R., Buckley, Camilla, Vincent, Angela, Lim, Ming
Publicado em 2014

Paediatric UK demyelinating disease longitudinal study (PUDDLS)

Por Likeman Marcus, Kneen Rachel, Jardine Philip, Hemingway Cheryl, Gunny Roxanna, Foster Katharine, De Goede Christian, Chong Wui K, Cummins Carole, Absoud Michael, Lim Ming J, Pike Mike, Sibtain Naomi, Whitehouse William P, Wassmer Evangeline
Publicado em 2011-07-01

Paediatric UK demyelinating disease longitudinal study (PUDDLS)

Por Absoud, Michael, Cummins, Carole, Chong, Wui K, De Goede, Christian, Foster, Katharine, Gunny, Roxanna, Hemingway, Cheryl, Jardine, Philip, Kneen, Rachel, Likeman, Marcus, Lim, Ming J, Pike, Mike, Sibtain, Naomi, Whitehouse, William P, Wassmer, Evangeline
Publicado em 2011

Mutations in SLC25A22: hyperprolinaemia, vacuolated fibroblasts and presentation with developmental delay

Por Reid, Emma S., Williams, Hywel, Anderson, Glenn, Benatti, Malika, Chong, Kling, James, Chela, Ocaka, Louise, Hemingway, Cheryl, Little, Daniel, Brown, Richard, Parker, Alasdair, Holden, Simon, Footitt, Emma, Rahman, Shamima, Gissen, Paul, Mills, Philippa B., Clayton, Peter T.
Publicado no J Inherit Metab Dis (2017)

Acquired predisposition to mycobacterial disease due to autoantibodies to IFN-γ

Por Kampmann, Beate, Hemingway, Cheryl, Stephens, Alick, Davidson, Robert, Goodsall, Anna, Anderson, Suzanne, Nicol, Mark, Schölvinck, Elisabeth, Relman, David, Waddell, Simon, Langford, Paul, Sheehan, Brian, Semple, Lynn, Wilkinson, Katalin A., Wilkinson, Robert J., Ress, Stanley, Hibberd, Martin, Levin, Michael
Publicado em 2005

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

Genotypic and phenotypic spectrum of pyridoxine-dependent epilepsy (ALDH7A1 deficiency)

Por Mills, Philippa B., Footitt, Emma J., Mills, Kevin A., Tuschl, Karin, Aylett, Sarah, Varadkar, Sophia, Hemingway, Cheryl, Marlow, Neil, Rennie, Janet, Baxter, Peter, Dulac, Olivier, Nabbout, Rima, Craigen, William J., Schmitt, Bernhard, Feillet, François, Christensen, Ernst, De Lonlay, Pascale, Pike, Mike G., Hughes, M. Imelda, Struys, Eduard A., Jakobs, Cornelis, Zuberi, Sameer M., Clayton, Peter T.
Publicado em 2010

Paediatric autoimmune encephalopathies: clinical features, laboratory investigations and outcomes in patients with or without antibodies to known central nervous system autoantigen...

Por Hacohen, Yael, Wright, Sukhvir, Waters, Patrick, Agrawal, Shakti, Carr, Lucinda, Cross, Helen, De Sousa, Carlos, DeVile, Catherine, Fallon, Penny, Gupta, Rajat, Hedderly, Tammy, Hughes, Elaine, Kerr, Tim, Lascelles, Karine, Lin, Jean-Pierre, Philip, Sunny, Pohl, Keith, Prabahkar, Prab, Smith, Martin, Williams, Ruth, Clarke, Antonia, Hemingway, Cheryl, Wassmer, Evangeline, Vincent, Angela, Lim, Ming J
Publicado em 2013

Utility and safety of rituximab in pediatric autoimmune and inflammatory CNS disease

Por Dale, Russell C., Brilot, Fabienne, Duffy, Lisa V., Twilt, Marinka, Waldman, Amy T., Narula, Sona, Muscal, Eyal, Deiva, Kumaran, Andersen, Erik, Eyre, Michael R., Eleftheriou, Despina, Brogan, Paul A., Kneen, Rachel, Alper, Gulay, Anlar, Banu, Wassmer, Evangeline, Heineman, Kirsten, Hemingway, Cheryl, Riney, Catherine J., Kornberg, Andrew, Tardieu, Marc, Stocco, Amber, Banwell, Brenda, Gorman, Mark P., Benseler, Susanne M., Lim, Ming
Publicado em 2014

Delineation of the movement disorders associated with FOXG1 mutations

Por Papandreou, Apostolos, Schneider, Ruth B., Augustine, Erika F., Ng, Joanne, Mankad, Kshitij, Meyer, Esther, McTague, Amy, Ngoh, Adeline, Hemingway, Cheryl, Robinson, Robert, Varadkar, Sophia M., Kinali, Maria, Salpietro, Vincenzo, O'Driscoll, Margaret C., Basheer, S. Nigel, Webster, Richard I., Mohammad, Shekeeb S., Pula, Shpresa, McGowan, Marian, Trump, Natalie, Jenkins, Lucy, Elmslie, Frances, Scott, Richard H., Hurst, Jane A., Perez-Duenas, Belen, Paciorkowski, Alexander R., Kurian, Manju A.
Publicado no Neurology (2016)

Mutations in SNORD118 cause the cerebral microangiopathy leukoencephalopathy with calcifications and cysts

Por Jenkinson, Emma M., Rodero, Mathieu P., Kasher, Paul R., Uggenti, Carolina, Oojageer, Anthony, Goosey, Laurence C., Rose, Yohann, Kershaw, Christopher J., Urquhart, Jill E., Williams, Simon G., Bhaskar, Sanjeev S., O’Sullivan, James, Baerlocher, Gabriela M., Haubitz, Monika, Aubert, Geraldine, Barañano, Kristin W., Barnicoat, Angela J., Battini, Roberta, Berger, Andrea, Blair, Edward M., Brunstrom-Hernandez, Janice E., Buckard, Johannes A., Cassiman, David M., Caumes, Rosaline, Cordelli, Duccio M., De Waele, Liesbeth M., Fay, Alexander J., Ferreira, Patrick, Fletcher, Nicholas A., Fryer, Alan E., Goel, Himanshu, Hemingway, Cheryl A., Henneke, Marco, Hughes, Imelda, Jefferson, Rosalind J., Kumar, Ram, Lagae, Lieven, Landrieu, Pierre G., Lourenço, Charles M., Malpas, Timothy J., Mehta, Sarju G., Metz, Imke, Naidu, Sakkubai, Õunap, Katrin, Panzer, Axel, Prabhakar, Prab, Quaghebeur, Geraldine, Schiffmann, Raphael, Sherr, Elliott H., Sinnathuray, Kanaga R., Soh, Calvin, Stewart, Helen S., Stone, John, Van Esch, Hilde, Van Mol, Christine E.G., Vanderver, Adeline, Wakeling, Emma L., Whitney, Andrea, Pavitt, Graham D., Griffiths-Jones, Sam, Rice, Gillian I., Revy, Patrick, van der Knaap, Marjo S., Livingston, John H., O’Keefe, Raymond T., Crow, Yanick J.
Publicado no Nat Genet (2016)