Progressive hepatic mitochondrial dysfunction in premanifest Huntington's disease

Hepatic mitochondrial dysfunction in manifest and premanifest Huntington disease

(2013) S. H. Stuwe et al.   NEUROLOGY

Hepatic mitochondrial dysfunction in Friedreich Ataxia

(2011) Sven H Stüwe et al.   BMC Neurology

Potential endpoints for clinical trials in premanifest and early Huntington's disease in the TRACK-HD study: analysis of 24 month observational data

(2011) Sarah J Tabrizi et al.   LANCET NEUROLOGY

PGC-1alpha downstream transcription factors NRF-1 and TFAM are genetic modifiers of Huntington disease

(2011) Elahe Taherzadeh-Fard et al.   Molecular Neurodegeneration

Mitochondrial haplogroup H correlates with ATP levels and age at onset in Huntington disease

(2010) Larissa Arning et al.   JOURNAL OF MOLECULAR MEDICINE-JMM

Neurocognitive signs in prodromal Huntington disease.

(2010) Julie C. Stout et al.   NEUROPSYCHOLOGY

Role of mitochondrial dysfunction in the pathogenesis of Huntington's disease

(2009) Rodrigo A. Quintanilla et al.   BRAIN RESEARCH BULLETIN