Charalampos Tzoulis
Charalampos Tzoulis
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Sitert av
The spectrum of clinical disease caused by the A467T and W748S POLG mutations: a study of 26 cases
C Tzoulis, BA Engelsen, W Telstad, J Aasly, M Zeviani, S Winterthun, ...
Brain 129 (7), 1685-1692, 2006
A multicenter study on Leigh syndrome: disease course and predictors of survival
K Sofou, IFM De Coo, P Isohanni, E Ostergaard, K Naess, L De Meirleir, ...
Orphanet journal of rare diseases 9 (1), 1-16, 2014
Defective mitochondrial DNA homeostasis in the substantia nigra in Parkinson disease
C Dölle, I Flønes, GS Nido, H Miletic, N Osuagwu, S Kristoffersen, ...
Nature communications 7 (1), 13548, 2016
POLG1 mutations cause a syndromic epilepsy with occipital lobe predilection
BA Engelsen, C Tzoulis, B Karlsen, A Lillebø, LM Lægreid, J Aasly, ...
Brain 131 (3), 818-828, 2008
The NADPARK study: A randomized phase I trial of nicotinamide riboside supplementation in Parkinson’s disease
B Brakedal, C Dölle, F Riemer, Y Ma, GS Nido, GO Skeie, AR Craven, ...
Cell metabolism 34 (3), 396-407. e6, 2022
Neuronal complex I deficiency occurs throughout the Parkinson’s disease brain, but is not associated with neurodegeneration or mitochondrial DNA damage
IH Flønes, E Fernandez-Vizarra, M Lykouri, B Brakedal, GO Skeie, ...
Acta neuropathologica 135, 409-425, 2018
Glitazone use associated with reduced risk of Parkinson's disease
B Brakedal, I Flønes, SF Reiter, Ø Torkildsen, C Dölle, J Assmus, ...
Movement Disorders 32 (11), 1594-1599, 2017
Practical guidance for CD management involving treatment of botulinum toxin: a consensus statement
A Albanese, G Abbruzzese, D Dressler, W Duzynski, S Khatkova, MJ Marti, ...
Journal of neurology 262, 2201-2213, 2015
Severe nigrostriatal degeneration without clinical parkinsonism in patients with polymerase gamma mutations
C Tzoulis, GT Tran, T Schwarzlmüller, K Specht, K Haugarvoll, N Balafkan, ...
Brain 136 (8), 2393-2404, 2013
Molecular pathogenesis of polymerase gamma–related neurodegeneration
C Tzoulis, GT Tran, J Coxhead, B Bertelsen, PK Lilleng, N Balafkan, ...
Annals of neurology 76 (1), 66-81, 2014
Localized cerebral energy failure in DNA polymerase gamma-associated encephalopathy syndromes
C Tzoulis, G Neckelmann, SJ Mørk, BE Engelsen, C Viscomi, G Moen, ...
Brain 133 (5), 1428-1437, 2010
Serial diffusion imaging in a case of mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes
C Tzoulis, LA Bindoff
Stroke 40 (2), e15-e17, 2009
The angiogenic switch leads to a metabolic shift in human glioblastoma
KM Talasila, GV Røsland, HR Hagland, E Eskilsson, IH Flønes, S Fritah, ...
Neuro-oncology 19 (3), 383-393, 2017
Phenotype-genotype correlations in Leigh syndrome: new insights from a multicentre study of 96 patients
K Sofou, IFM de Coo, E Ostergaard, P Isohanni, K Naess, L De Meirleir, ...
Journal of medical genetics 55 (1), 21-27, 2018
Spastic paraplegia type 7 is associated with multiple mitochondrial DNA deletions
IM Wedding, J Koht, GT Tran, D Misceo, KK Selmer, A Holmgren, ...
PloS one 9 (1), e86340, 2014
The clinical spectrum and natural history of early-onset diseases due to DNA polymerase gamma mutations
O Hikmat, C Tzoulis, WK Chong, L Chentouf, C Klingenberg, C Fratter, ...
Genetics in Medicine 19 (11), 1217-1225, 2017
MRI characterisation of adult onset alpha-methylacyl-coA racemase deficiency diagnosed by exome sequencing
K Haugarvoll, S Johansson, C Tzoulis, BI Haukanes, C Bredrup, ...
Orphanet journal of rare diseases 8, 1-10, 2013
Ultradeep mapping of neuronal mitochondrial deletions in Parkinson's disease
GS Nido, C Dölle, I Flønes, HA Tuppen, G Alves, OB Tysnes, K Haugarvoll, ...
Neurobiology of aging 63, 120-127, 2018
Understanding the epilepsy in POLG related disease
O Hikmat, T Eichele, C Tzoulis, LA Bindoff
International journal of molecular sciences 18 (9), 1845, 2017
Increased levels of cell-free mitochondrial DNA in the cerebrospinal fluid of patients with multiple sclerosis
KN Varhaug, CA Vedeler, KM Myhr, JH Aarseth, C Tzoulis, LA Bindoff
Mitochondrion 34, 32-35, 2017
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Artikler 1–20