Articoli con mandati relativi all'accesso pubblico - evangeline wassmerUlteriori informazioni
Non disponibili pubblicamente: 5
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Paediatric neuromyelitis optica: clinical, MRI of the brain and prognostic features
M Absoud, MJ Lim, R Appleton, A Jacob, J Kitley, MI Leite, MG Pike, ...
Journal of Neurology, Neurosurgery & Psychiatry 86 (4), 470-472, 2015
Mandati: Health Research Board, Ireland
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Autoantibody biomarkers in childhood-acquired demyelinating syndromes: results from a national surveillance cohort
Y Hacohen, M Absoud, M Woodhall, C Cummins, CG De Goede, ...
Journal of Neurology, Neurosurgery & Psychiatry 85 (4), 456-461, 2014
Mandati: National Institute for Health Research, UK, Multiple Sclerosis Society, UK
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The natural history of variable subtypes in pediatric-onset TUBB4A-related leukodystrophy
F Gavazzi, B Charsar, E Hamilton, JA Erler, V Patel, S Woidill, ...
Molecular Genetics and Metabolism 144 (3), 109048, 2025
Mandati: Fonds de recherche du Québec - Santé
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Neurological and Psychiatric Manifestations of COVID-19 in UK Children: A Prospective National Cohort Study
STJ Ray, O Abdel-Mannan, M Sa, C Fuller, GK Wood, K Psyden, M Yoong, ...
Mandati: UK Medical Research Council, National Institute for Health Research, UK …
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O9-5 Childhood optic neuritis: clinical features and outcome
M Absoud, C Cummins, N Desai, A Gika, N McSweeney, P Munot, ...
European Journal of Paediatric Neurology 13, S22-S23, 2009
Mandati: German Research Foundation
Disponibili pubblicamente: 91
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Mutations in ADAR1 cause Aicardi-Goutières syndrome associated with a type I interferon signature
GI Rice, PR Kasher, GMA Forte, NM Mannion, SM Greenwood, ...
Nature genetics 44 (11), 1243-1248, 2012
Mandati: US National Institutes of Health
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Mutations involved in Aicardi-Goutieres syndrome implicate SAMHD1 as regulator of the innate immune response
GI Rice, J Bond, A Asipu, RL Brunette, IW Manfield, IM Carr, JC Fuller, ...
Nature genetics 41 (7), 829-832, 2009
Mandati: US National Institutes of Health
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Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1
YJ Crow, DS Chase, J Lowenstein Schmidt, M Szynkiewicz, GMA Forte, ...
American journal of medical genetics Part A 167 (2), 296-312, 2015
Mandati: US National Institutes of Health, European Commission
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Clinical and molecular phenotype of Aicardi-Goutieres syndrome
G Rice, T Patrick, R Parmar, CF Taylor, A Aeby, J Aicardi, R Artuch, ...
The American Journal of Human Genetics 81 (4), 713-725, 2007
Mandati: Cancer Research UK
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Comprehensive rare variant analysis via whole-genome sequencing to determine the molecular pathology of inherited retinal disease
KJ Carss, G Arno, M Erwood, J Stephens, A Sanchis-Juan, S Hull, K Megy, ...
The American Journal of Human Genetics 100 (1), 75-90, 2017
Mandati: British Heart Foundation, UK Medical Research Council, National Institute …
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Disease course and treatment responses in children with relapsing myelin oligodendrocyte glycoprotein antibody–associated disease
Y Hacohen, YY Wong, C Lechner, M Jurynczyk, S Wright, B Konuskan, ...
JAMA neurology 75 (4), 478-487, 2018
Mandati: National Institute for Health Research, UK
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Utility and safety of rituximab in pediatric autoimmune and inflammatory CNS disease
RC Dale, F Brilot, LV Duffy, M Twilt, AT Waldman, S Narula, E Muscal, ...
Neurology 83 (2), 142-150, 2014
Mandati: US National Institutes of Health, National Institute for Health Research, UK
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Paediatric autoimmune encephalopathies: clinical features, laboratory investigations and outcomes in patients with or without antibodies to known central nervous system …
Y Hacohen, S Wright, P Waters, S Agrawal, L Carr, H Cross, C De Sousa, ...
Journal of Neurology, Neurosurgery & Psychiatry 84 (7), 748-755, 2013
Mandati: Wellcome Trust
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Homozygous loss-of-function mutations in the gene encoding the dopamine transporter are associated with infantile parkinsonism-dystonia
MA Kurian, J Zhen, SY Cheng, Y Li, SR Mordekar, P Jardine, NV Morgan, ...
The Journal of clinical investigation 119 (6), 1595-1603, 2009
Mandati: US National Institutes of Health
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Tyrosine hydroxylase deficiency: a treatable disorder of brain catecholamine biosynthesis
MA Willemsen, MM Verbeek, EJ Kamsteeg, JF de Rijk-van Andel, A Aeby, ...
Brain 133 (6), 1810-1822, 2010
Mandati: Swiss National Science Foundation
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Myelin oligodendrocyte glycoprotein antibodies are associated with a non-MS course in children
Y Hacohen, M Absoud, K Deiva, C Hemingway, P Nytrova, M Woodhall, ...
Neuroimmunology & Neuroinflammation 2 (2), e81, 2015
Mandati: National Institute for Health Research, UK
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Clinical and molecular characterisation of hereditary dopamine transporter deficiency syndrome: an observational cohort and experimental study
MA Kurian, Y Li, J Zhen, E Meyer, N Hai, HJ Christen, GF Hoffmann, ...
The Lancet Neurology 10 (1), 54-62, 2011
Mandati: US National Institutes of Health
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Diagnostic algorithm for relapsing acquired demyelinating syndromes in children
Y Hacohen, K Mankad, WK Chong, F Barkhof, A Vincent, M Lim, ...
Neurology 89 (3), 269-278, 2017
Mandati: National Institute for Health Research, UK
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Neurological manifestations of SARS-CoV-2 infection in hospitalised children and adolescents in the UK: a prospective national cohort study
STJ Ray, O Abdel-Mannan, M Sa, C Fuller, GK Wood, K Pysden, M Yoong, ...
The Lancet Child & Adolescent Health 5 (9), 631-641, 2021
Mandati: UK Medical Research Council, National Institute for Health Research, UK …
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Paediatric acquired demyelinating syndromes: incidence, clinical and magnetic resonance imaging features
M Absoud, MJ Lim, WK Chong, CG De Goede, K Foster, R Gunny, ...
Multiple Sclerosis Journal 19 (1), 76-86, 2013
Mandati: Multiple Sclerosis Society, UK
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