Mitochondrial dysfunction and free radical damage in the Huntington R6/2 transgenic mouse

Sarah J. Tabrizi, J. M. Workman, Paul Hart, +5

Annals of Neurology

Antioxidant treatment improves in vivo cardiac and skeletal muscle bioenergetics in patients with Friedreich's ataxia

Raffaele Lodi, Paul Hart, B. Rajagopalan, +8

Annals of Neurology

Lipid PeroxidationMolecular BiologyAntioxidant TreatmentRedox BiologyOxidative Stress +18

Antioxidant Treatment of Patients With Friedreich Ataxia

Paul Hart, Raffaele Lodi, B. Rajagopalan, +8

Archives of Neurology

Coenzyme Q₁₀ and vitamin E deficiency in Friedreich’s ataxia: predictor of efficacy of vitamin E and coenzyme Q₁₀ therapy

Jonathan M. Cooper, L.V. Prasad Korlipara, Paul Hart, +2

European Journal of Neurology

Mitochondrial dysfunction and free radical damage in the Huntington R6/2 transgenic mouse

Sarah J. Tabrizi, J. M. Workman, Paul Hart, +5

Annals of Neurology

Mitochondrial DysfunctionGeneticsCell DeathMouse BrainsRedox Biology +16

The Silver Syndrome Variant of Hereditary Spastic Paraplegia Maps to Chromosome 11q12-q14, with Evidence for Genetic Heterogeneity within This Subtype

Harshad B. Patel, Paul Hart, Thomas T. Warner, +4

The American Journal of Human Genetics

Allelic VariantMendelian DisorderGenetic DisorderSilver Syndrome VariantGenetics +8

Suppression of pendular nystagmus by smoking cannabis in a patient with multiple sclerosis

Frank Schön, Paul Hart, Timothy L. Hodgson, +4

Neurology

Cannabis UseEarly 1960SNeuropsychologyOphthalmologyNeurological Disorder +11

Role of Oxidative Damage in Friedreich's Ataxia

J. L. Bradley, Saffron Homayoun, Paul Hart, +2

Neurochemical Research

Lipid PeroxidationOxidative DamageNeuroprotectionNeurologyNeuroscience +4

International cooperative ataxia rating scale (ICARS): Appropriate for studies of Friedreich's ataxia?

Stefan Cano, Jeremy Hobart, Paul Hart, +3

Movement Disorders

SPG3A mutation screening in English families with early onset autosomal dominant hereditary spastic paraplegia

Philip A. Wilkinson, Paul Hart, Harshad B. Patel, +2

Journal of the Neurological Sciences

Rare DiseasesMendelian DisorderSpg3a MutationGenetic DisorderGenetics +5