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Browsing publications by Dr Tuomo Polvikoski

Newcastle AuthorsTitleYearFull text
Dr Sabine Specht
Dr Jennifer Duff
Dr Richard Charlton
Dr Tuomo Polvikoski
Dr Rita Barresi
et al.
A cryptic intronic LAMA2 insertion in a boy with mild congenital muscular dystrophy type 1A2021
Jack Collier
Dr Monika Olahova
Dr Nuria Martinez Lopez
Dr Tuomo Polvikoski
Dr Andrew Schaefer
et al.
Developmental consequences of defective Atg7-mediated autophagy in humans2021
Professor Johannes Attems
Dr Lauren Walker
Dr Kirsty McAleese
Dr Tuomo Polvikoski
Professor Ian McKeith
et al.
Neuropathological consensus criteria for the evaluation of Lewy pathology in post-mortem brains: a multi-centre study2021
Dr Timothy Williams
Dr Mark Baker
Dr Tuomo Polvikoski
Professor Bert van den Berg
TDP-43 proteinopathies: A new wave of neurodegenerative diseases2021
Dr Daniel Erskine
Dr Amy Reeve
Dr Tuomo Polvikoski
Dr Andrew Schaefer
Professor Robert Taylor
et al.
Lewy body pathology is more prevalent in older individuals with mitochondrial disease than controls2020
Dr Ren Ding
Dr Yoshiki Hase
Kamar Ameen-Ali
Michael Ndung'U
William Stevenson
et al.
Loss of capillary pericytes and the blood–brain barrier in white matter in poststroke and vascular dementias and Alzheimer’s disease2020
Professor Fiona Matthews
Dr Tuomo Polvikoski
Professor Carol Brayne
Putative risk alleles for LATE‐NC with hippocampal sclerosis in population‐representative autopsy cohorts2020
Dr Yoshiki Hase
Dr Tuomo Polvikoski
Dr Michael Firbank
Dr Lucinda Craggs
William Stevenson
et al.
Small vessel disease pathological changes in neurodegenerative and vascular dementias concomitant with autonomic dysfunction2020
Dr Yoshiki Hase
Dr Tuomo Polvikoski
Dr Mai Hase
William Stevenson
Dr Louise Allan
et al.
Carotid artery disease in post-stroke survivors and effects of enriched environment on stroke pathology in a mouse model of carotid artery stenosis2019
Dr Veronika Boczonadi
Dr Monika Olahova
Dr Boglárka Bánsági
Dr Andreas Roos
Dr Vankateswara Ramesh
et al.
Correction: Mitochondrial oxodicarboxylate carrier deficiency is associated with mitochondrial DNA depletion and spinal muscular atrophy–like disease (Genetics in Medicine, (2018), 20, 10, (1224-1235), 10.1038/gim.2017.251)2019
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