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206 results

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Imaging readiness in the gene therapy era-exploring standardized protocols for response assessment.
Biswas A, Soo AKS, Kurian MA, Löbel U, D'Arco F, Batzios S, Sudhakar S, Mankad K; IMaging Assessment in Gene and Enzyme Replacement therapies (IMAGER) study group. Biswas A, et al. Among authors: kurian ma. J Inherit Metab Dis. 2025 Jan;48(1):e12828. doi: 10.1002/jimd.12828. Epub 2024 Dec 9. J Inherit Metab Dis. 2025. PMID: 39648747 No abstract available.
Avoiding Premature Diagnostic Closure: Lessons from Two Children with Neurotransmitter Disorders Associated with Dual Pathology.
Salazar-Villacorta A, Spaull R, Chowdhury S, Mukhtyar B, Chitre M, Armstrong R, Sa M, Chandratre S, Kini U, Chinthapalli R, Mankad K, Sudhakar S, Pope S, Heales S, Kurian MA. Salazar-Villacorta A, et al. Among authors: kurian ma. Mov Disord Clin Pract. 2024 Sep;11(9):1149-1152. doi: 10.1002/mdc3.14164. Epub 2024 Jul 31. Mov Disord Clin Pract. 2024. PMID: 39082248 Free PMC article. No abstract available.
UK research priority setting for childhood neurological conditions.
Cadwgan J, Goodwin J, Babcock B, Brick M, Chin R, Easton A, Green B, Hannan S, Inward RPD, Kinsella S, King C, Kurian MA, Levine P, Mallick A, Parr J, Partridge CA, Amin S, Lumsden D, Cross JH, Lim MJ; UK Childhood Neurological Disorders PSP Group. Cadwgan J, et al. Among authors: kurian ma. Dev Med Child Neurol. 2024 Dec;66(12):1590-1599. doi: 10.1111/dmcn.16021. Epub 2024 Jul 16. Dev Med Child Neurol. 2024. PMID: 39014885
Climate change and disorders of the nervous system.
Sisodiya SM, Gulcebi MI, Fortunato F, Mills JD, Haynes E, Bramon E, Chadwick P, Ciccarelli O, David AS, De Meyer K, Fox NC, Davan Wetton J, Koltzenburg M, Kullmann DM, Kurian MA, Manji H, Maslin MA, Matharu M, Montgomery H, Romanello M, Werring DJ, Zhang L, Friston KJ, Hanna MG. Sisodiya SM, et al. Among authors: kurian ma. Lancet Neurol. 2024 Jun;23(6):636-648. doi: 10.1016/S1474-4422(24)00087-5. Lancet Neurol. 2024. PMID: 38760101 Review.
Hyperkinetic Movement Disorder Caused by the Recurrent c.892C>T NACC1 Variant.
Komulainen-Ebrahim J, Kangas SM, López-Martín E, Feyma T, Scaglia F, Martínez-Delgado B, Kuismin O, Suo-Palosaari M, Carr L, Hinttala R, Kurian MA, Uusimaa J. Komulainen-Ebrahim J, et al. Among authors: kurian ma. Mov Disord Clin Pract. 2024 Jun;11(6):708-715. doi: 10.1002/mdc3.14051. Epub 2024 May 2. Mov Disord Clin Pract. 2024. PMID: 38698576 Free PMC article.
Neurodevelopmental and synaptic defects in DNAJC6 parkinsonism, amenable to gene therapy.
Abela L, Gianfrancesco L, Tagliatti E, Rossignoli G, Barwick K, Zourray C, Reid KM, Budinger D, Ng J, Counsell J, Simpson A, Pearson TS, Edvardson S, Elpeleg O, Brodsky FM, Lignani G, Barral S, Kurian MA. Abela L, et al. Among authors: kurian ma. Brain. 2024 Jun 3;147(6):2023-2037. doi: 10.1093/brain/awae020. Brain. 2024. PMID: 38242634 Free PMC article.
206 results