[HTML][HTML] Widespread subcortical grey matter degeneration in primary lateral sclerosis: a multimodal imaging study with genetic profiling

E Finegan, SLH Shing, RH Chipika, MA Doherty… - NeuroImage: Clinical, 2019 - Elsevier
Background Primary lateral sclerosis (PLS) is a low incidence motor neuron disease which
carries a markedly better prognosis than amyotrophic lateral sclerosis (ALS). Despite …

[HTML][HTML] Cerebellar pathology in motor neuron disease: neuroplasticity and neurodegeneration

RH Chipika, G Mulkerrin, PF Pradat… - Neural regeneration …, 2022 - journals.lww.com
Amyotrophic lateral sclerosis is a relentlessly progressive multi-system condition. The
clinical picture is dominated by upper and lower motor neuron degeneration, but extra-motor …

Respiratory therapies for amyotrophic lateral sclerosis: a state of the art review

P Sales de Campos, WL Olsen… - Chronic respiratory …, 2023 - journals.sagepub.com
Amyotrophic lateral sclerosis (ALS) is a neurodegenerative condition noteworthy for upper
and lower motor neuron death. Involvement of respiratory motor neuron pools leads to …

A cross-sectional, quantitative videofluoroscopic analysis of swallowing physiology and function in individuals with amyotrophic lateral sclerosis

AA Waito, EK Plowman, CEA Barbon… - Journal of Speech …, 2020 - ASHA
Purpose To date, research characterizing swallowing changes in individuals with
amyotrophic lateral sclerosis (ALS) has primarily relied on subjective descriptions. Thus, the …

[HTML][HTML] Propagation patterns in motor neuron diseases: Individual and phenotype-associated disease-burden trajectories across the UMN-LMN spectrum of MNDs

M Tahedl, SLH Shing, E Finegan, RH Chipika… - Neurobiology of …, 2022 - Elsevier
Motor neuron diseases encompass a divergent group of conditions with considerable
differences in clinical manifestations, survival, and genetic vulnerability. One of the key …

[HTML][HTML] Rice bran, an off-shoot to newer therapeutics in neurological disorders

T Behl, S Kumar, A Sehgal, S Singh, S Kumari… - Biomedicine & …, 2021 - Elsevier
Normal brain functioning involves the interaction of interconnected molecular and cellular
activities, which appear to alter normal to abnormal brain functioning when worsened …

[HTML][HTML] Alterations in somatosensory, visual and auditory pathways in amyotrophic lateral sclerosis: an under-recognised facet of ALS

RH Chipika, G Mulkerrin, A Murad, J Lope… - Journal of integrative …, 2022 - imrpress.com
Background: While amyotrophic lateral sclerosis (ALS) is widely recognised as a multi-
network disorder with extensive frontotemporal and cerebellar involvement, sensory …

Validating automatic diadochokinesis analysis methods across dysarthria severity and syllable task in amyotrophic lateral sclerosis

C Tanchip, DL Guarin, S McKinlay, C Barnett… - Journal of Speech …, 2022 - ASHA
Purpose: Oral diadochokinesis (DDK) is a standard dysarthria assessment task. To extract
automatic and semi-automatic DDK measurements, numerous DDK analysis algorithms …

Reliability and validity of speech & pause measures during passage reading in ALS

C Barnett, JR Green, R Marzouqah… - … Lateral Sclerosis and …, 2020 - Taylor & Francis
Objective: The use of speech measures is becoming a common practice in the assessment
of bulbar disease progression in amyotrophic lateral sclerosis (ALS). This study aimed to …

[HTML][HTML] Infratentorial pathology in frontotemporal dementia: cerebellar grey and white matter alterations in FTD phenotypes

MC McKenna, RH Chipika, S Li Hi Shing, F Christidi… - Journal of …, 2021 - Springer
The contribution of cerebellar pathology to cognitive and behavioural manifestations is
increasingly recognised, but the cerebellar profiles of FTD phenotypes are relatively poorly …