Prevalence and Predictors of Vitamin D Insufficiency in Children: A Great Britain Population Based Study

por Absoud, Michael, Cummins, Carole, Lim, Ming J., Wassmer, Evangeline, Shaw, Nick
Publicado 2011

N-methyl-D-aspartate receptor antibody-mediated neurological disease: results of a UK-based surveillance study in children

por Wright, Sukhvir, Hacohen, Yael, Jacobson, Leslie, Agrawal, Shakti, Gupta, Rajat, Philip, Sunny, Smith, Martin, Lim, Ming, Wassmer, Evangeline, Vincent, Angela
Publicado en Arch Dis Child (2015)

Clinical trials of disease-modifying agents in pediatric MS: Opportunities, challenges, and recommendations from the IPMSSG

por Waubant, Emmanuelle, Banwell, Brenda, Wassmer, Evangeline, Sormani, Maria-Pia, Amato, Maria-Pia, Hintzen, Rogier, Krupp, Lauren, Rostásy, Kevin, Tenembaum, Silvia, Chitnis, Tanuja
Publicado en Neurology (2019)

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 en Neurol Neuroimmunol Neuroinflamm (2015)

International Pediatric MS Study Group Clinical Trials Summit: Meeting report

por Chitnis, Tanuja, Tardieu, Marc, Amato, Maria Pia, Banwell, Brenda, Bar-Or, Amit, Ghezzi, Angelo, Kornberg, Andrew, Krupp, Lauren B., Pohl, Daniela, Rostasy, Kevin, Tenembaum, Silvia, Waubant, Emmanuelle, Wassmer, Evangeline
Publicado 2013

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 2014

Surveillance for variant CJD: should more children with neurodegenerative diseases have autopsies?

por Verity, Christopher, Winstone, Anne Marie, Will, Robert, Powell, Alison, Baxter, Peter, de Sousa, Carlos, Gissen, Paul, Kurian, Manju, Livingston, John, McFarland, Robert, Pal, Suvankar, Pike, Michael, Robinson, Richard, Wassmer, Evangeline, Zuberi, Sameer
Publicado en Arch Dis Child (2019)

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 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 2011

Altered electroretinograms in patients with KCNJ10 mutations and EAST syndrome

por Thompson, Dorothy A, Feather, Sally, Stanescu, Horia C, Freudenthal, Bernard, Zdebik, Anselm A, Warth, Richard, Ognjanovic, Milos, Hulton, Sally A, Wassmer, Evangeline, van't Hoff, William, Russell-Eggitt, Isabelle, Dobbie, Angus, Sheridan, Eamonn, Kleta, Robert, Bockenhauer, Detlef
Publicado 2011

Recessive germline SDHA and SDHB mutations causing leukodystrophy and isolated mitochondrial complex II deficiency

por Alston, Charlotte L, Davison, James E, Meloni, Francesca, van der Westhuizen, Francois H, He, Langping, Hornig-Do, Hue-Tran, Peet, Andrew C, Gissen, Paul, Goffrini, Paola, Ferrero, Ileana, Wassmer, Evangeline, McFarland, Robert, Taylor, Robert W
Publicado 2012

A framework for measurement and harmonization of pediatric multiple sclerosis etiologic research studies: The Pediatric MS Tool-Kit

por Magalhaes, Sandra, Banwell, Brenda, Bar-Or, Amit, Fortier, Isabel, Hanwell, Heather E, Lim, Ming, Matt, Georg E, Neuteboom, Rinze F, O’Riordan, David L, Schneider, Paul K, Pugliatti, Maura, Shatenstein, Bryna, Tansey, Catherine M, Wassmer, Evangeline, Wolfson, Christina
Publicado en Mult Scler (2018)

Development and Validation of a Targeted Next-Generation Sequencing Gene Panel for Children With Neuroinflammation

por McCreary, Dara, Omoyinmi, Ebun, Hong, Ying, Mulhern, Ciara, Papadopoulou, Charalampia, Casimir, Marina, Hacohen, Yael, Nyanhete, Rodney, Ahlfors, Helena, Cullup, Thomas, Lim, Ming, Gilmour, Kimberly, Mankad, Kshitij, Wassmer, Evangeline, Berg, Stefan, Hemingway, Cheryl, Brogan, Paul, Eleftheriou, Despina
Publicado en JAMA Netw Open (2019)

Homozygous loss-of-function mutations in the gene encoding the dopamine transporter are associated with infantile parkinsonism-dystonia

por Kurian, Manju A., Zhen, Juan, Cheng, Shu-Yuan, Li, Yan, Mordekar, Santosh R., Jardine, Philip, Morgan, Neil V., Meyer, Esther, Tee, Louise, Pasha, Shanaz, Wassmer, Evangeline, Heales, Simon J.R., Gissen, Paul, Reith, Maarten E.A., Maher, Eamonn R.
Publicado 2009

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 2013

Mutations in CECR1 associated with a neutrophil signature in peripheral blood

por Belot, Alexandre, Wassmer, Evangeline, Twilt, Marinka, Lega, Jean-Christophe, Zeef, Leo AH, Oojageer, Anthony, Kasher, Paul R, Mathieu, Anne-Laure, Malcus, Christophe, Demaret, Julie, Fabien, Nicole, Collardeau-Frachon, Sophie, Mechtouff, Laura, Derex, Laurent, Walzer, Thierry, Rice, Gillian I, Durieu, Isabelle, Crow, Yanick J
Publicado 2014

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 en Dev Med Child Neurol (2013)

Use of Disease-Modifying Therapies in Pediatric Relapsing-Remitting Multiple Sclerosis in the United Kingdom

por Abdel-mannan, Omar A., Manchoon, Celeste, Rossor, Thomas, Southin, Justine-Clair, Tur, Carmen, Brownlee, Wallace, Byrne, Susan, Chitre, Manali, Coles, Alasdair, Forsyth, Rob, Kneen, Rachel, Mankad, Kshitij, Ram, Dipak, West, Siobhan, Wright, Sukhvir, Wassmer, Evangeline, Lim, Ming, Ciccarelli, Olga, Hemingway, Cheryl, Hacohen, Yael
Publicado en Neurol Neuroimmunol Neuroinflamm (2021)

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 en Am J Hum Genet (2016)

Radiologically isolated syndrome in children: Clinical and radiologic outcomes

por Makhani, Naila, Lebrun, Christine, Siva, Aksel, Brassat, David, Carra Dallière, Clarisse, de Seze, Jérôme, Du, Wei, Durand Dubief, Françoise, Kantarci, Orhun, Langille, Megan, Narula, Sona, Pelletier, Jean, Rojas, Juan Ignacio, Shapiro, Eugene D., Stone, Robert T., Tintoré, Mar, Uygunoglu, Ugur, Vermersch, Patrick, Wassmer, Evangeline, Okuda, Darin T., Pelletier, Daniel
Publicado en Neurol Neuroimmunol Neuroinflamm (2017)