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Journal of Neurology, Neurosurgery, and Psychiatry|April 1, 1997
Spinal and cutaneous schwannomatosis is a variant form of type 2 neurofibromatosis: a clinical and molecular studyD G Evans, S Mason, S M Huson, et al.Nature Genetics|May 1, 1993
A tandem duplication in the D-loop of human mitochondrial DNA is associated with deletions in mitochondrial myopathiesM Brockington, M G Sweeney, S R Hammans, et al.American Journal of Human Genetics|October 1, 1992
Evidence against an X-linked locus close to DXS7 determining visual loss susceptibility in British and Italian families with Leber hereditary optic neuropathyM G Sweeney, M B Davis, A Lashwood, et al.Journal of Neurology, Neurosurgery, and Psychiatry|August 1, 1994
Debrisoquine hydroxylase gene polymorphism in familial Parkinson's diseaseV Planté-Bordeneuve, M B Davis, D M Maraganore, et al.Movement Disorders : Official Journal of the Movement Disorder Society|May 1, 1994
Tyrosine hydroxylase polymorphism in familial and sporadic Parkinson's diseaseV Planté-Bordeneuve, M B Davis, D M Maraganore, et al.Journal of the Neurological Sciences|March 1, 1994
Platelet mitochondrial function in Leber's hereditary optic neuropathyP R Smith, J M Cooper, G G Govan, et al.Movement Disorders : Official Journal of the Movement Disorder Society|January 1, 1988
The diverse neurological features of Niemann-Pick disease type C: a report of two casesR J Coleman, S A Robb, B D Lake, et al.The Quarterly Journal of Medicine|July 1, 1993
Mitochondrial DNA transfer RNA mutation Leu(UUR)A-->G 3260: a second family with myopathy and cardiomyopathyM G Sweeney, M Brockington, M J Weston, et al.Brain : a Journal of Neurology|December 1, 1991
Irish (Donegal) amyloidosis is associated with the transthyretinALA60 (Appalachian) variantH Staunton, M B Davis, R J Guiloff, et al.American Journal of Human Genetics|July 1, 1996
Evidence against an X-linked visual loss susceptibility locus in Leber hereditary optic neuropathyR M Chalmers, M B Davis, M G Sweeney, et al.Pageof 21