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Life (Basel, Switzerland)|June 28, 2023
Serum Neurofilaments in Motor Neuron Disease and Their Utility in Differentiating ALS, PMA and PLSGavin McCluskey, Karen E Morrison, Colette Donaghy, et al.
Neuroimage. Clinical|November 12, 2019
Brainstem pathology in amyotrophic lateral sclerosis and primary lateral sclerosis: A longitudinal neuroimaging studyPeter Bede, Rangariroyashe H Chipika, Eoin Finegan, et al.
Neuroimage. Clinical|December 5, 2019
Widespread subcortical grey matter degeneration in primary lateral sclerosis: a multimodal imaging study with genetic profilingEoin Finegan, Stacey Li Hi Shing, Rangariroyashe H Chipika, et al.
Journal of Neurology|July 21, 2019
The clinical and radiological profile of primary lateral sclerosis: a population-based studyEoin Finegan, Rangariroyashe H Chipika, Stacey Li Hi Shing, et al.
Nature Genetics|February 28, 2006
ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosisMatthew J Greenway, Peter M Andersen, Carsten Russ, et al.
Brain Imaging and Behavior|January 7, 2021
Extra-motor cerebral changes and manifestations in primary lateral sclerosisEoin Finegan, Stacey Li Hi Shing, Rangariroyashe H Chipika, et al.
Journal of the Neurological Sciences|July 31, 2020
Evolving diagnostic criteria in primary lateral sclerosis: The clinical and radiological basis of "probable PLS"Eoin Finegan, Stacey Li Hi Shing, We Fong Siah, et al.
Data in Brief|September 18, 2020
Imaging and clinical data indicate considerable disease burden in 'probable' PLS: Patients with UMN symptoms for 2-4 yearsEoin Finegan, We Fong Siah, Stacey Li Hi Shing, et al.
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