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

Parkinson's Disease and Parkinsonism: Neuropathology

(2013) D. W. Dickson   Cold Spring Harbor Perspectives in Medicine

Cerebellar Ataxia in Patients With Mitochondrial DNA Disease

(2012) Nichola Zoe Lax et al.   JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY

Thalamic noradrenaline in Parkinson's disease: Deficits suggest role in motor and non-motor symptoms

(2012) Christian Pifl et al.   MOVEMENT DISORDERS

Toxin Models of Mitochondrial Dysfunction in Parkinson's Disease

(2011) Terina N. Martinez et al.   ANTIOXIDANTS & REDOX SIGNALING

Sensory neuronopathy in patients harbouring recessive polymerase γ mutations

(2011) Nichola Z. Lax et al.   BRAIN

Proposal for the standardisation of multi-centre trials in nuclear medicine imaging: prerequisites for a European 123I-FP-CIT SPECT database

(2011) John Caddell Dickson et al.   EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING

Structural Basis of Defects in the Sacsin HEPN Domain Responsible for Autosomal Recessive Spastic Ataxia of Charlevoix-Saguenay (ARSACS)

(2011) Guennadi Kozlov et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

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

(2010) Charalampos Tzoulis et al.   BRAIN

Gamma oscillations in the hippocampus require high complex I gene expression and strong functional performance of mitochondria

(2010) Oliver Kann et al.   BRAIN

Prevalence of hereditary ataxia and spastic paraplegia in southeast Norway: a population-based study

(2009) A. K. Erichsen et al.   BRAIN

The 18F-FDG PET Cingulate Island Sign and Comparison to 123I- -CIT SPECT for Diagnosis of Dementia with Lewy Bodies

(2009) S. M. Lim et al.   JOURNAL OF NUCLEAR MEDICINE

Nature of Mitochondrial DNA Deletions in Substantia Nigra Neurons

(2008) Amy K. Reeve et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Infantile-onset spinocerebellar ataxia and mitochondrial recessive ataxia syndrome are associated with neuronal complex I defect and mtDNA depletion

(2008) A. H. Hakonen et al.   HUMAN MOLECULAR GENETICS

Neurodegenerative parkinsonism and progressive external ophthalmoplegia with a Twinkle mutation

(2008) Wim Vandenberghe et al.   MOVEMENT DISORDERS