Charalampos Tzoulis

Papers authored by Charalampos Tzoulis

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2014 Iselin Marie Wedding, Jeanette Koht, Gia Tuong Thi Tran, Doriana Misceo, Kaja Kristine Selmer, Asbj Holmgren, Eirik Frengen, Laurence Bindoff

, Chantal M. E. Tallaksen, Charalampos Tzoulis

Spastic paraplegia type 7 is Associated with multiple mitochondrial DNA deletions

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I. F. M. de Coo (René), L. de Meirleir (Linda), J. Uusimaa (Johanna), I. de Angst (Isabel), Kalliopi Sofou, Irenaeus F. M. De Coo, Pirjo Isohanni, K. Sofou (Kalliopi), M. K. Isohanni (Matti), Elsebet Ostergaard, M. Ostergaard, Karin Naess, Linda De Meirleir, K. Naess (Karin), Charalampos Tzoulis

and 15 other authors

A multicenter study on Leigh syndrome: Disease course and predictors of survival

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2013 Kristoffer Haugarvoll, Charalampos Tzoulis

, Gia T. Tran, Bjørn Karlsen, Bernt A. Engelsen, Per M. Knappskog, Laurence A. Bindoff

Myoclonus-dystonia and epilepsy in a family with a novel epsilon-sarcoglycan mutation

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Charalampos Tzoulis

, Stefan Johansson, Bjørn Ivar Haukanes, Helge Boman, Per Morten Knappskog, Laurence A. Bindoff

Novel SACS Mutations Identified by Whole Exome Sequencing in a Norwegian Family with Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay

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Charalampos Tzoulis

, Christian Vedeler, Mette Haugen, Anette Storstein, Gia Tuong Tran, Ivar Otto Gjerde, Martin Biermann, Thomas Schwarzlmüller, Laurence A. Bindoff

Progressive striatal necrosis associated with anti-NMDA receptor antibodies

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Charalampos Tzoulis

, Gia Tuong Tran, Thomas Schwarzlmüller, Karsten Specht, Kristoffer Haugarvoll, Novin Balafkan, Peer K. Lilleng, Hrvoje Miletic, Martin Biermann, B. Martin, Laurence A. Bindoff

Severe nigrostriatal degeneration without clinical parkinsonism in patients with polymerase gamma mutations

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Kristoffer Haugarvoll, Stefan Johansson, Charalampos Tzoulis

, Bjørn Ivar Haukanes, Cecilie Bredrup, Gesche Neckelmann, Helge Boman, Per Morten Knappskog, Laurence A. Bindoff

MRI characterisation of adult onset alpha-methylacyl-coA racemase deficiency diagnosed by exome sequencing

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2012 Charalampos Tzoulis

, Laurence A. Bindoff

Acute mitochondrial encephalopathy reflects neuronal energy failure irrespective of which genome the genetic defect affects

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Novin Balafkan, Charalampos Tzoulis

, Bernd Müller, Kristoffer Haugarvoll, Ole-Bjørn Tysnes, Jan Petter Larsen, Laurence A. Bindoff

Number of CAG repeats in POLG1 and its association with Parkinson disease in the Norwegian population

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Charalampos Tzoulis

, Ivar Otto Gjerde, Eirik Søfteland, Gesche Neckelmann, Eivind Strøm, Olav Karsten Vintermyr, Lisbeth Sviland, Martin Biermann

Erdheim–Chester disease presenting with an intramedullary spinal cord lesion

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2011 Charalampos Tzoulis

, Gia Tuong Tran, Ivar Otto Gjerde, Jan Aasly, Gesche Neckelmann, Jana Rydland, Viktoria Varga, Pia Wadel-Andersen, Laurence A. Bindoff

Leukoencephalopathy with brainstem and spinal cord involvement caused by a novel mutation in the DARS2 gene

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2010 Petter S. Sanaker, Marina Toompuu, Vanessa E. Hogan, Langping He, Charalampos Tzoulis

, Zofia M. A. Chrzanowska-Lightowlers, Robert W. Taylor, Laurence A. Bindoff

Differences in RNA processing underlie the tissue specific phenotype of ISCU myopathy

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Charalampos Tzoulis

, Gesche Neckelmann, Sverre J. Mørk, Bernt E. Engelsen, Carlo Viscomi, Gunnar Moen, Lars Ersland, Massimo Zeviani, Laurence A. Bindoff

Localized cerebral energy failure in DNA polymerase gamma-associated encephalopathy syndromes

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This paper was not found in any repository, but could be made available legally by the author.

2009 Arne Gramstad, Laurence A. Bindoff

, Atle Lillebø, Charalampos Tzoulis

, Bernt A. Engelsen

Neuropsychological performance in patients with POLG1 mutations and the syndrome of mitochondrial spinocerebellar ataxia and epilepsy

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C. Tzoulis

, M. Papingji, T. Fiskestrand, L. S. Røste, L. A. Bindoff

Mitochondrial DNA depletion in progressive external ophthalmoplegia caused byPOLG1mutations

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2008 Charalampos Tzoulis

, Laurence A. Bindoff

Serial Diffusion Imaging in a Case of Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes

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Charalampos Tzoulis

, Paola S. Denora, Filippo M. Santorelli, Laurence A. Bindoff

Hereditary spastic paraplegia caused by the novel mutation 1047insC in the SPG7 gene

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B. A. Engelsen, C. Tzoulis

, B. Karlsen, A. Lillebo, L. M. Laegreid, J. Aasly, M. Zeviani, L. A. Bindoff

POLG1 mutations cause a syndromic epilepsy with occipital lobe predilection

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This paper was not found in any repository; the policy of its publisher is unknown or unclear.

2006 Charalampos Tzoulis

[A 90-year-old woman with acute hemiparesis].

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Ch Tzoulis

, H. Naess, L. Thomassen

Migrainous cerebral infarction in a previously healthy 93-year-old female patient with no risk factors for stroke

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Papers authored by Charalampos Tzoulis