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Muscle & Nerve|September 25, 2004
Cytoplasmic body myopathy masquerading as motor neuron diseaseArun V Krishnan, Roger Pamphlett, David Burke, et al.
Journal of Neuroscience Methods|August 2, 2005
Detection of mutations in whole genome-amplified DNA from laser-microdissected neuronsRoger Pamphlett, Paul R Heath, Hazel Holden, et al.
Scientific Reports|March 17, 2015
Exome sequencing of case-unaffected-parents trios reveals recessive and de novo genetic variants in sporadic ALSKaryn Meltz Steinberg, Bing Yu, Daniel C Koboldt, et al.
Acta Neuropathologica|December 2, 2021
Microglia and monocytes in inflammatory CNS disease: integrating phenotype and functionAlanna G Spiteri, Claire L Wishart, Roger Pamphlett, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|May 12, 2015
Whole genome analyses reveal no pathogenetic single nucleotide or structural differences between monozygotic twins discordant for amyotrophic lateral sclerosisKaryn Meltz Steinberg, Thomas J Nicholas, Daniel C Koboldt, et al.
Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia|April 28, 2009
What lies beneath the tent? JC-virus cerebellar granule cell neuronopathy complicating sarcoidosisRon Granot, Richard Lawrence, Michael Barnett, et al.
Plos One|October 29, 2020
The distribution of toxic metals in the human retina and optic nerve head: Implications for age-related macular degenerationRoger Pamphlett, Svetlana Cherepanoff, Lay Khoon Too, et al.
Pathology|January 15, 2011
Overview and recent advances in neuropathology. Part 2: NeurodegenerationColin L Masters, Jillian J Kril, Glenda M Halliday, et al.
Neurobiology of Aging|May 3, 2013
Mutation analysis and immunopathological studies of PFN1 in familial and sporadic amyotrophic lateral sclerosisShu Yang, Jennifer A Fifita, Kelly L Williams, et al.
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