Resultats de la cerca - Evangeline Wassmer

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  1. 1
    Prevalence and Predictors of Vitamin D Insufficiency in Children: A Great Britain Population Based Study

    Prevalence and Predictors of Vitamin D Insufficiency in Children: A Great Britain Population Based Study per Michael Absoud, Carole Cummins, Ming Lim, Evangeline Wassmer, Nick Shaw

    Publicat 2011
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  2. 2
    Pediatric optic neuritis

    Pediatric optic neuritis per E. Ann Yeh, Jennifer Graves, Leslie Benson, Evangeline Wassmer, Amy Waldman

    Publicat 2016
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  3. 3
    Paediatric multiple sclerosis: a new era in diagnosis and treatment

    Paediatric multiple sclerosis: a new era in diagnosis and treatment per Sophie Duignan, Wallace Brownlee, Evangeline Wassmer, Cheryl Hemingway, Ming Lim, Olga Ciccarelli, Yael Hacohen

    Publicat 2019
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  4. 4
    Diagnostic algorithm for relapsing acquired demyelinating syndromes in children

    Diagnostic algorithm for relapsing acquired demyelinating syndromes in children per Yael Hacohen, Kshitij Mankad, W.K. Chong, Frederik Barkhof, Angela Vincent, Ming Lim, Evangeline Wassmer, Olga Ciccarelli, Cheryl Hemingway

    Publicat 2017
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  5. 5
    Myelin oligodendrocyte glycoprotein and aquaporin‐4 antibodies are highly specific in children with acquired demyelinating syndromes

    Myelin oligodendrocyte glycoprotein and aquaporin‐4 antibodies are highly specific in children with acquired demyelinating syndromes per Sophie Duignan, Sukhvir Wright, Thomas Rossor, John Cazabon, Kimberly Gilmour, Olga Ciccarelli, Evangeline Wassmer, Ming Lim, Cheryl Hemingway, Yael Hacohen

    Publicat 2018
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  6. 6
    ‘Leukodystrophy‐like’ phenotype in children with myelin oligodendrocyte glycoprotein antibody‐associated disease

    ‘Leukodystrophy‐like’ phenotype in children with myelin oligodendrocyte glycoprotein antibody‐associated disease per Yael Hacohen, Thomas Rossor, Kshitij Mankad, W.K. Chong, Andrew Lux, Evangeline Wassmer, Ming Lim, Frederik Barkhof, Olga Ciccarelli, Cheryl Hemingway

    Publicat 2017
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  7. 7
    N-methyl-D-aspartate receptor antibody-mediated neurological disease: results of a UK-based surveillance study in children

    N-methyl-D-aspartate receptor antibody-mediated neurological disease: results of a UK-based surveillance study in children per Sukhvir Wright, Yael Hacohen, Leslie Jacobson, Shakti Agrawal, Rajat Das Gupta, Sunny Philip, Martin A. Smith, Ming Lim, Evangeline Wassmer, Angela Vincent

    Publicat 2015
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  8. 8
    Improved performance of the 2017 McDonald criteria for diagnosis of multiple sclerosis in children in a real-life cohort

    Improved performance of the 2017 McDonald criteria for diagnosis of multiple sclerosis in children in a real-life cohort per Yael Hacohen, Wallace Brownlee, Kshitij Mankad, W.K. Chong, Alan J. Thompson, Ming Lim, Evangeline Wassmer, Cheryl Hemingway, Frederik Barkhof, Olga Ciccarelli

    Publicat 2019
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  9. 9
    Myelin oligodendrocyte glycoprotein antibodies are associated with a non-MS course in children

    Myelin oligodendrocyte glycoprotein antibodies are associated with a non-MS course in children per Yael Hacohen, Michael Absoud, Kumaran Deiva, Cheryl Hemingway, Petra Nytrová, Mark Woodhall, Jacqueline Palace, Evangeline Wassmer, Marc Tardieu, Angela Vincent, Ming Lim, Patrick Waters

    Publicat 2015
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  10. 10
    Early predictors of epilepsy and subsequent relapse in children with acute disseminated encephalomyelitis

    Early predictors of epilepsy and subsequent relapse in children with acute disseminated encephalomyelitis per Thomas Rossor, Christina Benetou, Sukhvir Wright, Sophie Duignan, Karine Lascelles, Robert Robinson, Krishna B. Das, Olga Ciccarelli, Evangeline Wassmer, Cheryl Hemingway, Ming Lim, Yael Hacohen

    Publicat 2019
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  11. 11
    E.U. paediatric MOG consortium consensus: Part 1 – Classification of clinical phenotypes of paediatric myelin oligodendrocyte glycoprotein antibody-associated disorders

    E.U. paediatric MOG consortium consensus: Part 1 – Classification of clinical phenotypes of paediatric myelin oligodendrocyte glycoprotein antibody-associated disorders per Arlette L. Bruijstens, Christian Lechner, Lorraine Flet‐Berliac, Kumaran Deiva, Rinze F. Neuteboom, Cheryl Hemingway, Evangeline Wassmer, E.U. paediatric Mog consortium, Arlette L. Bruijstens, Eva‐Maria Wendel, Christian Lechner, Markus Breu, Lorraine Flet‐Berliac, Aliénor de Chalus, Marco Capobianco, Laetitia Giorgi, Cheryl Hemingway, Evangeline Wassmer, Ming Lim, Ronny Wickström, Thaís Armangué, Kumaran Deiva, Rinze F. Neuteboom

    Publicat 2020
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  12. 12
    E.U. paediatric MOG consortium consensus: Part 4 – Outcome of paediatric myelin oligodendrocyte glycoprotein antibody-associated disorders

    E.U. paediatric MOG consortium consensus: Part 4 – Outcome of paediatric myelin oligodendrocyte glycoprotein antibody-associated disorders per Arlette L. Bruijstens, Markus Breu, Eva‐Maria Wendel, Evangeline Wassmer, Ming Lim, Rinze F. Neuteboom, Ronny Wickström, E.U. paediatric Mog consortium, Arlette L. Bruijstens, Eva‐Maria Wendel, Christian Lechner, Markus Breu, Lorraine Flet‐Berliac, Aliénor de Chalus, Marco Capobianco, Laetitia Giorgi, Cheryl Hemingway, Evangeline Wassmer, Ming Lim, Ronny Wickström, Thaís Armangué, Kumaran Deiva, Rinze F. Neuteboom

    Publicat 2020
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  13. 13
    International Pediatric MS Study Group Clinical Trials Summit

    International Pediatric MS Study Group Clinical Trials Summit per Tanuja Chitnis, Marc Tardieu, Maria Pia Amato, Brenda Banwell, Amit Bar‐Or, Angelo Ghezzi, Andrew J. Kornberg, Lauren Krupp, Daniela Pohl, Kevin Rostásy, Silvia Tenembaum, Emmanuelle Waubant, Evangeline Wassmer

    Publicat 2013
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  14. 14
    Neuromyelitis optica relapses: Race and rate, immunosuppression and impairment

    Neuromyelitis optica relapses: Race and rate, immunosuppression and impairment per George Tackley, Fanny O’Brien, João Carlos da Rocha, Mark Woodhall, Patrick Waters, Saleel Chandratre, Christopher Halfpenny, Cheryl Hemingway, Evangeline Wassmer, Warren W. Wasiewski, Maria Isabel Leite, Jacqueline Palace

    Publicat 2016
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  15. 15
    NMDA receptor antibodies associated with distinct white matter syndromes

    NMDA receptor antibodies associated with distinct white matter syndromes per Yael Hacohen, Michael Absoud, Cheryl Hemingway, Leslie Jacobson, Jean‐Pierre Lin, Mike Pike, Sunil Pullaperuma, Ata Siddiqui, Evangeline Wassmer, Patrick Waters, Sarosh R. Irani, Camilla Buckley, Angela Vincent, Ming Lim

    Publicat 2014
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  16. 16
    Outcome and recurrence 1 year after pediatric arterial ischemic stroke in a population‐based cohort

    Outcome and recurrence 1 year after pediatric arterial ischemic stroke in a population‐based cohort per Andrew A. Mallick, Vijeya Ganesan, Fenella J. Kirkham, Penny Fallon, Tammy Hedderly, Tony McShane, Alasdair Parker, Evangeline Wassmer, Elizabeth Wraige, Sam Amin, Hannah B Edwards, Mario Cortina‐Borja, Finbar O’Callaghan

    Publicat 2016
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  17. 17
    Altered electroretinograms in patients with KCNJ10 mutations and EAST syndrome

    Altered electroretinograms in patients with KCNJ10 mutations and EAST syndrome per Dorothy Thompson, Sally Feather, Horia Stanescu, Bernard Freudenthal, Anselm A. Zdebik, Richard Warth, Miloš Ognjanović, Sally A. Hulton, Evangeline Wassmer, William van’t Hoff, Isabelle Russell‐Eggitt, Angus Dobbie, Eamonn Sheridan, Robert Kleta, Detlef Böckenhauer

    Publicat 2011
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  18. 18
    Paediatric acute disseminated encephalomyelitis followed by optic neuritis: disease course, treatment response and outcome

    Paediatric acute disseminated encephalomyelitis followed by optic neuritis: disease course, treatment response and outcome per Yu Yi M. Wong, Yael Hacohen, Thaís Armangué, Evangeline Wassmer, Hélène Verhelst, Cheryl Hemingway, E Daniëlle van Pelt, Coriene E. Catsman‐Berrevoets, Rogier Q. Hintzen, Kumaran Deiva, Ming Lim, Kevin Rostásy, Rinze F. Neuteboom

    Publicat 2018
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  19. 19
    Homozygous loss-of-function mutations in the gene encoding the dopamine transporter are associated with infantile parkinsonism-dystonia

    Homozygous loss-of-function mutations in the gene encoding the dopamine transporter are associated with infantile parkinsonism-dystonia per Manju A. Kurian, Juan Zhen, Shuyuan Cheng, Yan Li, Santosh Mordekar, Philip Jardine, Neil V. Morgan, Esther Meyer, Louise Tee, Shanaz Pasha, Evangeline Wassmer, Simon Heales, Paul Gissen, Maarten E. A. Reith, Eamonn R. Maher

    Publicat 2009
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  20. 20
    Recessive germline<i>SDHA</i>and<i>SDHB</i>mutations causing leukodystrophy and isolated mitochondrial complex II deficiency

    Recessive germline<i>SDHA</i>and<i>SDHB</i>mutations causing leukodystrophy and isolated mitochondrial complex II deficiency per Charlotte L. Alston, James Davison, Francesca Meloni, Francois H. van der Westhuizen, Langping He, Hue‐Tran Hornig‐Do, Andrew C. Peet, Paul Gissen, P Goffrini, Ileana Ferrero, Evangeline Wassmer, Robert McFarland, Robert W. Taylor

    Publicat 2012
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