Authors:
Reid, E
Escayg, A
Dearlove, AM
Lee, DD
Meisler, MH
Rubinsztein, DC
Citation: E. Reid et al., The spastic paraplegia SPG10 locus: narrowing of critical region and exclusion of sodium channel gene SCN8A as a candidate, J MED GENET, 38(1), 2001, pp. 65-67
Authors:
Lindsey, JC
Lusher, ME
McDermott, CJ
White, KD
Reid, E
Rubinsztein, DC
Bashir, R
Hazan, J
Shaw, PJ
Bushby, KMD
Citation: Jc. Lindsey et al., Mutation analysis of the spastin gene (SPG4) in patients with hereditary spastic paraparesis, J MED GENET, 37(10), 2000, pp. 759-765
Citation: E. Reid, 13(th) Bioanalytical Forum - Drug level measurement in the mass spectrometry era - Guildford (United Kingdom), August 31-September 3, 1999 - Foreword, CHROMATOGR, 52, 2000, pp. S7-S7
Citation: Uat. Brinkman et al., Unorthodox temperature conditions: Opinions and supplementary observationsfrom bioanalytical forum participants, CHROMATOGR, 52, 2000, pp. S57-S59
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:
Proe, MF
Craig, J
Griffiths, J
Wilson, A
Reid, E
Citation: Mf. Proe et al., Comparison of biomass production in coppice and single stem woodland management systems on an imperfectly drained gley soil in central Scotland, BIO BIOENER, 17(2), 1999, pp. 141-151
Authors:
Lowe, GDO
Rumley, A
Woodward, M
Reid, E
Rumley, J
Citation: Gdo. Lowe et al., Activated protein C resistance and the FV : R(506)Q mutation in a random population sample - Associations with cardiovascular risk factors and coagulation variables, THROMB HAEM, 81(6), 1999, pp. 918-924
Authors:
Reid, E
Dearlove, AM
Whiteford, ML
Rhodes, M
Rubinsztein, DC
Citation: E. Reid et al., Autosomal dominant spastic paraplegia - Refined SPG8 locus and additional genetic heterogeneity, NEUROLOGY, 53(8), 1999, pp. 1844-1849
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:
Reid, E
Dearlove, AM
Rhodes, M
Rubinsztein, DC
Citation: E. Reid et al., A new locus for autosomal dominant "pure" hereditary spastic paraplegia mapping to chromosome 12q13, and evidence for further genetic heterogeneity, AM J HU GEN, 65(3), 1999, pp. 757-763