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Glucose transporter-1 deficiency syndrome: the expanding clinical and genetic spectrum of a treatable disorder.
Brain. 2010 Mar;133(Pt 3):655-70. doi: 10.1093/brain/awp336. Epub 2010 Feb 2.
Brain. 2010.
PMID: 20129935
Stomatin-deficient cryohydrocytosis results from mutations in SLC2A1: a novel form of GLUT1 deficiency syndrome.
Flatt JF, Guizouarn H, Burton NM, Borgese F, Tomlinson RJ, Forsyth RJ, Baldwin SA, Levinson BE, Quittet P, Aguilar-Martinez P, Delaunay J, Stewart GW, Bruce LJ.
Flatt JF, et al. Among authors: forsyth rj.
Blood. 2011 Nov 10;118(19):5267-77. doi: 10.1182/blood-2010-12-326645. Epub 2011 Jul 26.
Blood. 2011.
PMID: 21791420
Free article.
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Natural History of Vanishing White Matter.
Hamilton EMC, van der Lei HDW, Vermeulen G, Gerver JAM, Lourenço CM, Naidu S, Mierzewska H, Gemke RJBJ, de Vet HCW, Uitdehaag BMJ, Lissenberg-Witte BI; VWM Research Group; van der Knaap MS.
Hamilton EMC, et al.
Ann Neurol. 2018 Aug;84(2):274-288. doi: 10.1002/ana.25287. Epub 2018 Sep 6.
Ann Neurol. 2018.
PMID: 30014503
Free PMC article.
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Disease Course and Treatment Responses in Children With Relapsing Myelin Oligodendrocyte Glycoprotein Antibody-Associated Disease.
Hacohen Y, Wong YY, Lechner C, Jurynczyk M, Wright S, Konuskan B, Kalser J, Poulat AL, Maurey H, Ganelin-Cohen E, Wassmer E, Hemingway C, Forsyth R, Hennes EM, Leite MI, Ciccarelli O, Anlar B, Hintzen R, Marignier R, Palace J, Baumann M, Rostásy K, Neuteboom R, Deiva K, Lim M.
Hacohen Y, et al.
JAMA Neurol. 2018 Apr 1;75(4):478-487. doi: 10.1001/jamaneurol.2017.4601.
JAMA Neurol. 2018.
PMID: 29305608
Free PMC article.
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RARS2 mutations in a sibship with infantile spasms.
Ngoh A, Bras J, Guerreiro R, Meyer E, McTague A, Dawson E, Mankad K, Gunny R, Clayton P, Mills PB, Thornton R, Lai M, Forsyth R, Kurian MA.
Ngoh A, et al.
Epilepsia. 2016 May;57(5):e97-e102. doi: 10.1111/epi.13358. Epub 2016 Apr 8.
Epilepsia. 2016.
PMID: 27061686
Free PMC article.
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Complement factor I deficiency: A potentially treatable cause of fulminant cerebral inflammation.
Altmann T, Torvell M, Owens S, Mitra D, Sheerin NS, Morgan BP, Kavanagh D, Forsyth R.
Altmann T, et al.
Neurol Neuroimmunol Neuroinflamm. 2020 Feb 25;7(3):e689. doi: 10.1212/NXI.0000000000000689. Print 2020 May.
Neurol Neuroimmunol Neuroinflamm. 2020.
PMID: 32098865
Free PMC article.
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Prion-like α-synuclein pathology in the brain of infants with Krabbe disease.
Hatton C, Ghanem SS, Koss DJ, Abdi IY, Gibbons E, Guerreiro R, Bras J; International DLB Genetics Consortium; Walker L, Gelpi E, Heywood W, Outeiro TF, Attems J, McFarland R, Forsyth R, El-Agnaf OM, Erskine D.
Hatton C, et al.
Brain. 2022 May 24;145(4):1257-1263. doi: 10.1093/brain/awac002.
Brain. 2022.
PMID: 34999780
Free PMC article.
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Evolution of brain MRI lesions in paediatric myelin-oligodendrocyte glycoprotein antibody-associated disease (MOGAD) and its relevance to disease course.
Abdel-Mannan O, Champsas D, Tur C, Lee V, Manivannan S, Usman H, Skippen A, Desai I, Chitre M, Forsyth R, Kneen R, Ram D, Ramdas S, Rossor T, West S, Wright S, Palace J, Wassmer E, Hemingway C, Lim MJ, Mankad K, Ciccarelli O, Hacohen Y; UK-Childhood Neuroinflammatory Disease Network.
Abdel-Mannan O, et al.
J Neurol Neurosurg Psychiatry. 2024 Apr 12;95(5):426-433. doi: 10.1136/jnnp-2023-332542.
J Neurol Neurosurg Psychiatry. 2024.
PMID: 37979966
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Brown-Vialetto-Van Laere Syndrome as a Mimic of Neuroimmune Disorders: 3 Cases From the Clinic and Review of the Literature.
Allison T, Roncero I, Forsyth R, Coffman K, Pichon JL.
Allison T, et al.
J Child Neurol. 2017 May;32(6):528-532. doi: 10.1177/0883073816689517. Epub 2017 Jan 24.
J Child Neurol. 2017.
PMID: 28116953
Review.
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Risk and causes of death in children with a seizure disorder.
Nesbitt V, Kirkpatrick M, Pearson G, Colver A, Forsyth R.
Nesbitt V, et al.
Dev Med Child Neurol. 2012 Jul;54(7):612-7. doi: 10.1111/j.1469-8749.2012.04295.x. Epub 2012 Apr 14.
Dev Med Child Neurol. 2012.
PMID: 22500675
Free article.
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