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QJM : Monthly Journal of the Association of Physicians|March 12, 2005
Borna disease virus and the evidence for human pathogenicity: a systematic reviewR M Chalmers, D Rh Thomas, R L SalmonVeterinary Parasitology|February 9, 1999
Detection of Cryptosporidium oocysts in wild mammals of mainland BritainA P Sturdee, R M Chalmers, S A BullArchives of Ophthalmology (Chicago, Ill. : 1960)|September 1, 1988
Treatment of chronic macular edema with acetazolamideS N Cox, E Hay, A C BirdThe Biochemical Journal|January 1, 1991
Comparison of benzyl alcohol dehydrogenases and benzaldehyde dehydrogenases from the benzyl alcohol and mandelate pathways in Acinetobacter calcoaceticus and from the TOL-plasmid-encoded toluene pathway in Pseudomonas putida. N-terminal amino acid sequences, amino acid compositions and immunological cross-reactionsR M Chalmers, J N Keen, C A FewsonJournal of Neurology, Neurosurgery, and Psychiatry|April 1, 1997
Autosomal recessive inheritance of hereditary motor and sensory neuropathy with optic atrophyR M Chalmers, P Riordan-Eva, N W WoodMuscle & Nerve. Supplement|January 1, 1995
Mitochondrial DNA diseases: genotype and phenotype in Leber's hereditary optic neuropathyA E Harding, P Riordan-Eva, G G GovanJournal of Medical Genetics|December 1, 1989
Genetic heterogeneity and mitochondrial DNA heteroplasmy in Leber's hereditary optic neuropathyI J Holt, D H Miller, A E HardingRevue Neurologique|January 1, 1992
[Demonstration of genetic mutation in most of the amyloid neuropathies with sporadic occurrence]D Adams, M Reilly, A E Harding, et al.Journal of Medical Genetics|March 1, 1990
Pontobulbar palsy and neurosensory deafness (Brown-Vialetto-Van Laere syndrome) with possible autosomal dominant inheritanceS A Hawkins, N C Nevin, A E HardingBrain : a Journal of Neurology|June 1, 1994
Autosomal dominant cerebellar ataxia with pigmentary macular dystrophy. A clinical and genetic study of eight familiesT P Enevoldson, M D Sanders, A E HardingPageof 56