Authors: Reid, E Dearlove, AM Osborn, O Rogers, MT Rubinsztein, DC

Citation: E. Reid et al., A locus for autosomal dominant "pure" hereditary spastic paraplegia maps to chromosome 19q13, AM J HU GEN, 66(2), 2000, pp. 728-732

Authors: Reid, E Grayson, C Rubinsztein, DC Rogers, MT Rubinsztein, JS

Citation: E. Reid et al., Subclinical cognitive impairment in autosomal dominant "pure" hereditary spastic paraplegia, J MED GENET, 36(10), 1999, pp. 797-798

Authors: Reid, E Grayson, C Rogers, MT Rubinsztein, DC

Citation: E. Reid et al., Locus-phenotype correlations in autosomal dominant pure hereditary spasticparaplegia - A clinical and molecular genetic study of 28 United Kingdom families, BRAIN, 122, 1999, pp. 1741-1755

Authors: Bushby, KMD Pollitt, C Johnson, MA Rogers, MT Chinnery, PF

Citation: Kmd. Bushby et al., Muscle pain as a prominent feature of facioscapulohumeral muscular dystrophy (FSHD): four illustrative case reports, NEUROMUSC D, 8(8), 1998, pp. 574-579

Authors: Rogers, MT

Citation: Mt. Rogers, The 92nd Annual Conference of the Dickens Fellowship: July 23-29, 1998, DICKENSIAN, 94(446), 1998, pp. 215-224