Manju A Kurian
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Explore the profile of Manju A Kurian including associated specialties, affiliations and a list of published articles.
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177
Citations
4401
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Recent Articles
1.
Cif L, Cif L, Demailly D, Demailly D, Lin J, Lin J, et al.
ArXiv
. 2025 Feb;
PMID: 39990802
Heterozygous mutations in are associated with an early-onset, progressive and often complex dystonia (DYT28). Key characteristics of typical disease include focal motor features at disease presentation, evolving through a caudocranial...
2.
Alhaque S, Budinger D, Garavaglia B, Zorzi G, Barral S, Kurian M
Stem Cell Res
. 2025 Feb;
84:103669.
PMID: 39919432
Adenylyl cyclase 5 (ADCY5)-related diseases are a rare group of genetic disorders that commonly present in childhood. Heterozygous mutations in ADCY5 lead to ADCY5-related dyskinesia, comprising a wide array of...
3.
Biswas A, Soo A, Kurian M, Lobel U, DArco F, Batzios S, et al.
J Inherit Metab Dis
. 2024 Dec;
48(1):e12828.
PMID: 39648747
No abstract available.
4.
Couto B, Galosi S, Steel D, Kurian M, Friedman J, Gorodetsky C, et al.
Mov Disord
. 2024 Aug;
39(9):1446-1467.
PMID: 39119747
Acute presentation of severe motor disorders is a diagnostic and management challenge. We define severe acute motor exacerbations (SAME) as acute/subacute motor symptoms that persist for hours-to-days with a severity...
5.
Salazar-Villacorta A, Spaull R, Chowdhury S, Mukhtyar B, Chitre M, Armstrong R, et al.
Mov Disord Clin Pract
. 2024 Jul;
11(9):1149-1152.
PMID: 39082248
No abstract available.
6.
Cadwgan J, Goodwin J, Babcock B, Brick M, Chin R, Easton A, et al.
Dev Med Child Neurol
. 2024 Jul;
66(12):1590-1599.
PMID: 39014885
Aim: To identify research priorities regarding the effectiveness of interventions for children and young people (CYP) with childhood neurological conditions (CNCs). These include common conditions such as epilepsies and cerebral...
7.
Spaull R, Soo A, Batzios S, Footitt E, Whiteley R, Mink J, et al.
Neurology
. 2024 Jul;
103(3):e209615.
PMID: 38976822
Objectives: Neuronal ceroid lipofuscinosis type 2 (CLN2-disease) is an inherited childhood-onset neurodegenerative condition, with classical early features of speech delay, epilepsy, myoclonus, ataxia, and motor regression. This study aimed to...
8.
Sisodiya S, Gulcebi M, Fortunato F, Mills J, Haynes E, Bramon E, et al.
Lancet Neurol
. 2024 May;
23(6):636-648.
PMID: 38760101
Anthropogenic climate change is affecting people's health, including those with neurological and psychiatric diseases. Currently, making inferences about the effect of climate change on neurological and psychiatric diseases is challenging...
9.
Komulainen-Ebrahim J, Kangas S, Lopez-Martin E, Feyma T, Scaglia F, Martinez-Delgado B, et al.
Mov Disord Clin Pract
. 2024 May;
11(6):708-715.
PMID: 38698576
Background: Genetic syndromes of hyperkinetic movement disorders associated with epileptic encephalopathy and intellectual disability are becoming increasingly recognized. Recently, a de novo heterozygous NACC1 (nucleus accumbens-associated 1) missense variant was...
10.
Araujo Salomao R, Rezende Filho F, Borges V, Kurian M, Ferraz H, Breedveld G, et al.
Parkinsonism Relat Disord
. 2024 Apr;
123:106103.
PMID: 38582019
Neurodegeneration with brain iron accumulation (NBIA) encompasses a clinically and genetically heterogeneous group of rare disorders. Here, we report clinical, neuroimaging and genetic studies in twenty three Brazilian NBIA patients....