[HTML][HTML] Amygdala pathology in amyotrophic lateral sclerosis and primary lateral sclerosis

RH Chipika, F Christidi, E Finegan, SLH Shing… - Journal of the …, 2020 - Elsevier
Temporal lobe studies in motor neuron disease overwhelmingly focus on white matter
alterations and cortical grey matter atrophy. Reports on amygdala involvement are …

[HTML][HTML] MRI data confirm the selective involvement of thalamic and amygdalar nuclei in amyotrophic lateral sclerosis and primary lateral sclerosis

RH Chipika, WF Siah, SLH Shing, E Finegan… - Data in brief, 2020 - Elsevier
A standardised imaging protocol was implemented to evaluate disease burden in specific
thalamic and amygdalar nuclei in 133 carefully phenotyped and genotyped motor neuron …

Basal ganglia involvement in amyotrophic lateral sclerosis

P Bede, M Elamin, S Byrne, RL McLaughlin, K Kenna… - Neurology, 2013 - AAN Enterprises
Objectives: To characterize the nature and extent of basal ganglia involvement in
amyotrophic lateral sclerosis (ALS) genotypes in vivo. Methods: Forty-four healthy controls …

Basal ganglia pathology in ALS is associated with neuropsychological deficits

J Machts, K Loewe, J Kaufmann, S Jakubiczka… - Neurology, 2015 - AAN Enterprises
Objectives: To evaluate basal ganglia changes along the amyotrophic lateral sclerosis (ALS)–
ALS–frontotemporal dementia (FTD) continuum using multiple, complementary imaging …

Brainstem–cortex disconnection in amyotrophic lateral sclerosis: bulbar impairment, genotype associations, asymptomatic changes and biomarker opportunities

M Tahedl, EL Tan, RH Chipika, JC Hengeveld… - Journal of …, 2023 - Springer
Background Bulbar dysfunction is a cardinal feature of ALS with important quality of life and
management implications. The objective of this study is the longitudinal evaluation of a large …

Genotype-associated cerebellar profiles in ALS: focal cerebellar pathology and cerebro-cerebellar connectivity alterations

P Bede, RH Chipika, F Christidi… - Journal of Neurology …, 2021 - jnnp.bmj.com
Objective Cerebellar disease burden and cerebro-cerebellar connectivity alterations are
poorly characterised in amyotrophic lateral sclerosis (ALS) despite the likely contribution of …

Multiparametric MRI study of ALS stratified for the C9orf72 genotype

P Bede, ALW Bokde, S Byrne, M Elamin… - Neurology, 2013 - AAN Enterprises
Objective: To describe the patterns of cortical and subcortical changes in amyotrophic lateral
sclerosis (ALS) stratified for the C9orf72 genotype. Methods: A prospective, single-center …

Widespread structural brain involvement in ALS is not limited to the C9orf72 repeat expansion

HJ Westeneng, R Walhout, M Straathof… - Journal of Neurology …, 2016 - jnnp.bmj.com
Background In patients with a C9orf72 repeat expansion (C9+), a neuroimaging phenotype
with widespread structural cerebral changes has been found. We aimed to investigate the …

Cortical atrophy in ALS is critically associated with neuropsychiatric and cognitive changes

E Mioshi, P Lillo, B Yew, S Hsieh, S Savage… - Neurology, 2013 - AAN Enterprises
Objective: To characterize the patterns of brain atrophy in patients with amyotrophic lateral
sclerosis (ALS) with and without cognitive and neuropsychiatric symptoms, in comparison to …

Tackling clinical heterogeneity across the amyotrophic lateral sclerosis–frontotemporal dementia spectrum using a transdiagnostic approach

RM Ahmed, M Bocchetta, EG Todd, NY Tse… - Brain …, 2021 - academic.oup.com
The disease syndromes of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia
(FTD) display considerable clinical, genetic and pathological overlap, yet mounting …