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31 publications found
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Determining the incidence of familiality in ALS: A study of temporal trends in Ireland from 1994 to 2016
“Switchboard” malfunction in motor neuron diseases: Selective pathology of thalamic nuclei in amyotrophic lateral sclerosis and primary lateral sclerosis.
Amygdala pathology in amyotrophic lateral sclerosis and primary lateral sclerosis.
Evolving diagnostic criteria in primary lateral sclerosis: The clinical and radiological basis of “probable PLS”.
MRI data confirm the selective involvement of thalamic and amygdalar nuclei in amyotrophic lateral sclerosis and primary lateral sclerosis.
Genotype-associated cerebellar profiles in ALS: focal cerebellar pathology and cerebro-cerebellar connectivity alterations
Infratentorial pathology in frontotemporal dementia: cerebellar grey and white matter alterations in FTD phenotypes
Whole genome sequencing analysis reveals post-zygotic mutation variability in monozygotic twins discordant for amyotrophic lateral sclerosis
Cognitive and neuropsychiatric endophenotypes in amyotrophic lateral sclerosis
Radiological correlates of pseudobulbar affect: Corticobulbar and cerebellar components in primary lateral sclerosis
Brainstem-cortex disconnection in amyotrophic lateral sclerosis: bulbar impairment, genotype associations, asymptomatic changes and biomarker opportunities
Not a benign motor neuron disease: longitudinal imaging captures relentless motor connectome disintegration in primary lateral sclerosis
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