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Browsing publications by Dr Tuomo Polvikoski

Newcastle AuthorsTitleYearFull text
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
Dr Tuomo Polvikoski
Prediction models for dementia and neuropathology in the oldest old: the Vantaa 85+ cohort study2019
Dr Lizzie Harris
Dr Chiara Marini Bettolo
Dr Ana Topf
Dr Rita Barresi
Dr Tuomo Polvikoski
et al.
MEGF10 related myopathies: A new case with adult onset disease with prominent respiratory failure and review of reported phenotypes2018
Dr Tuomo Polvikoski
Dr Thais Minett
Professor Fiona Matthews
Professor Carol Brayne
Hippocampal sclerosis, hippocampal neuron loss patterns and TDP-43 in the aged population2018
Dr Veronika Boczonadi
Dr Monika Olahova
Dr Boglarka Bansagi
Dr Andreas Roos
Dr Vankateswara Ramesh
et al.
Mitochondrial oxodicarboxylate carrier deficiency is associated with mitochondrial DNA depletion and spinal muscular atrophy–like disease2018
Dr Lizzie Harris
Dr Umar Burki
Dr Chiara Marini Bettolo
Dr Marta Bertoli
Dr Teresinha Evangelista
et al.
Complex phenotypes associated with STIM1 mutations in both coiled coil and EF-hand domains2017
Dr Aiqing Chen
Dr Rufus Akinyemi
Dr Yoshiki Hase
Dr Michael Firbank
Michael Ndung'U
et al.
Frontal white matter hyperintensities, clasmatodendrosis and gliovascular abnormalities in ageing and post-stroke dementia2016
Dr Tracey Willis
Dr Claire Wood
Dr Tuomo Polvikoski
Dr Rita Barresi
Professor Hanns Lochmuller
et al.
Muscle hypertrophy as the presenting sign in a patient with a complete FHL1 deletion2016
Sebastian Figueroa Bonaparte
Dr Rita Barresi
Dr Tuomo Polvikoski
Dr Timothy Williams
Dr Ana Topf
et al.
Mutational spectrum and phenotypic variability of VCP-related neurological disease in the UK2016
Professor Fiona Matthews
Dr Tuomo Polvikoski
Old-age hippocampal sclerosis associates with GRN and TMEM106B but not with ABCC9 variation in population-based cohorts2016
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