POLG1-Related and other “Mitochondrial Parkinsonisms”: an Overview

Is It ADEM, POLG, or Both?

(2010) Mandy O. Harris et al.   ARCHIVES OF NEUROLOGY

POLG1 Variations Presenting as Multiple Sclerosis

(2010) Andoni Echaniz-Laguna et al.   ARCHIVES OF NEUROLOGY

Maternal inheritance and mitochondrial DNA variants in familial Parkinson's disease

(2010) David K Simon et al.   BMC Medical Genetics

Role of Histidine 932 of the Human Mitochondrial DNA Polymerase in Nucleotide Discrimination and Inherited Disease

(2010) Dipanwita Batabyal et al.   JOURNAL OF BIOLOGICAL CHEMISTRY

POLG, but notPEO1, is a frequent cause of cerebellar ataxia in Central Europe

(2010) Julia Schicks et al.   MOVEMENT DISORDERS

Polymerase Gamma 1 Mutations

(2010) Margherita Milone et al.   NEUROLOGIST

POLG1 polyglutamine tract variants associated with Parkinson's disease

(2010) Johanna Eerola et al.   NEUROSCIENCE LETTERS

Variations of the CAG trinucleotide repeat in DNA polymerase gamma (POLG1) is associated with Parkinson's disease in Sweden

(2010) Anna Anvret et al.   NEUROSCIENCE LETTERS

Genetic variation of the mitochondrial complex I subunit NDUFV2 and Parkinson’s disease

(2010) Kenya Nishioka et al.   PARKINSONISM & RELATED DISORDERS

Diagnostic Approach to Mitochondrial Disorders: the Need for a Reliable Biomarker

(2009) M. Mancuso et al.   CURRENT MOLECULAR MEDICINE

Impaired mitochondrial dynamics and function in the pathogenesis of Parkinson's disease

(2009) Hansruedi Büeler   EXPERIMENTAL NEUROLOGY

The unfolding clinical spectrum of POLG mutations

(2009) M J Blok et al.   JOURNAL OF MEDICAL GENETICS

Sustained dopaminergic response of parkinsonism and depression in POLG-associated parkinsonism

(2009) Matthis Synofzik et al.   MOVEMENT DISORDERS

Mitochondrial ND3 as the novel causative gene for Leber hereditary optic neuropathy and dystonia

(2009) Kang Wang et al.   NEUROGENETICS

Electron transfer mediators and other metabolites and cofactors in the treatment of mitochondrial dysfunction

(2009) Daniele Orsucci et al.   NUTRITION REVIEWS

DNA polymerase gamma and mitochondrial disease: Understanding the consequence of POLG mutations

(2008) Sherine S.L. Chan et al.   BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS

Molecular and clinical genetics of mitochondrial diseases due toPOLGmutations

(2008) Lee-Jun C. Wong et al.   HUMAN MUTATION

Mitochondrial DNA polymorphisms and haplogroups in Parkinson’s disease and control individuals with a similar genetic background

(2008) Helen Latsoudis et al.   JOURNAL OF HUMAN GENETICS

Mitochondrial DNA single deletion in a patient with postural tremor

(2008) Michelangelo Mancuso et al.   MOVEMENT DISORDERS

OPA1 IN MULTIPLE MITOCHONDRIAL DNA DELETION DISORDERS

(2008) J. D. Stewart et al.   NEUROLOGY

Additive effects of POLG1 and ANT1 mutations in a complex encephalomyopathy

(2008) Giuliana Galassi et al.   NEUROMUSCULAR DISORDERS

Two novel POLG1 mutations in a patient with progressive external ophthalmoplegia, levodopa-responsive pseudo-orthostatic tremor and parkinsonism

(2008) Federica Invernizzi et al.   NEUROMUSCULAR DISORDERS

Alpha-synuclein pathology and Parkinsonism associated withPOLG1mutations and multiple mitochondrial DNA deletions

(2008)   NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY

Parkinsonism associated with the homozygous W748S mutation in the POLG1 gene

(2008) A.M. Remes et al.   PARKINSONISM & RELATED DISORDERS

Prevalence of mitochondrial DNA disease in adults

(2007) Andrew M. Schaefer et al.   ANNALS OF NEUROLOGY

The mtDNA A8344G “MERRF” mutation is not a common cause of sporadic Parkinson disease in Italian population

(2007) Michelangelo Mancuso et al.   PARKINSONISM & RELATED DISORDERS