A. E. Harding
Publications by Year
Research Areas
Mitochondrial Function and Pathology, Genetic Neurodegenerative Diseases, Metabolism and Genetic Disorders, Hereditary Neurological Disorders, Neurological diseases and metabolism
Most-Cited Works
- → Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy(1991)2,802 cited
- → Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies(1988)1,839 cited
- A new mitochondrial disease associated with mitochondrial DNA heteroplasmy.(1990)
- → CLASSIFICATION OF THE HEREDITARY ATAXIAS AND PARAPLEGIAS(1983)955 cited
- → The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation(1995)482 cited
- Clinical features and classification of inherited ataxias.(1993)
- → Debrisoquine hydroxylase gene polymorphism and susceptibility to Parkinson's disease(1992)421 cited
- → THE CLINICAL FEATURES OF MITOCHONDRIAL MYOPATHY(1986)418 cited
- → Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA(1992)412 cited
- Primary pathogenic mtDNA mutations in multigeneration pedigrees with Leber hereditary optic neuropathy.(1996)