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Results: 1-15 |
Results: 15
Accuracy of estimation of rock mass moduli
Authors: Glynn, ME Nicholson, GA Warriner, JB
Citation: Me. Glynn et al., Accuracy of estimation of rock mass moduli, T I MIN M-A, 110, 2001, pp. A66-A68
Accuracy of estimation of rock mass moduli (vol 110, pg A66, 2001)
Authors: Glynn, ME Nicholson, GA Warriner, JB
Citation: Me. Glynn et al., Accuracy of estimation of rock mass moduli (vol 110, pg A66, 2001), T I MIN M-A, 110, 2001, pp. A132-A132
Mutations in SPTLC1, encoding serine palmitoyltransferase, long chain basesubunit-1, cause hereditary sensory neuropathy type I
Authors: Dawkins, JL Hulme, DJ Brahmbhatt, SB Auer-Grumbach, M Nicholson, GA
Citation: Jl. Dawkins et al., Mutations in SPTLC1, encoding serine palmitoyltransferase, long chain basesubunit-1, cause hereditary sensory neuropathy type I, NAT GENET, 27(3), 2001, pp. 309-312
Clinical and pathological features of a parkinsonian syndrome in a family with an Ala53Thr alpha-synuclein mutation
Authors: Spira, PJ Sharpe, DM Halliday, G Cavanagh, J Nicholson, GA
Citation: Pj. Spira et al., Clinical and pathological features of a parkinsonian syndrome in a family with an Ala53Thr alpha-synuclein mutation, ANN NEUROL, 49(3), 2001, pp. 313-319
Variable phenotype of Alzheimer's disease with spastic paraparesis
Authors: Smith, MJ Kwok, JBJ McLean, CA Kril, JJ Broe, GA Nicholson, GA Cappai, R Hallupp, M Cotton, RGH Masters, CL Schofield, PR Brooks, WS
Citation: Mj. Smith et al., Variable phenotype of Alzheimer's disease with spastic paraparesis, ANN NEUROL, 49(1), 2001, pp. 125-129
A new autosomal dominant pure cerebellar ataxia
Authors: Storey, E Gardner, RJM Knight, MA Kennerson, ML Tuck, RR Forrest, SM Nicholson, GA
Citation: E. Storey et al., A new autosomal dominant pure cerebellar ataxia, NEUROLOGY, 57(10), 2001, pp. 1913-1915
Dominant intermediate Charcot-Marie-Tooth neuropathy maps to chromosome 19p12-p13.2
Authors: Kennerson, ML Zhu, D Gardner, RJM Storey, E Merory, J Robertson, SP Nicholson, GA
Citation: Ml. Kennerson et al., Dominant intermediate Charcot-Marie-Tooth neuropathy maps to chromosome 19p12-p13.2, AM J HU GEN, 69(4), 2001, pp. 883-888
Hereditary sensory neuropathy type I: Haplotype analysis shows founders insouthern England and Europe
Authors: Nicholson, GA Dawkins, JL Blair, IP Auer-Grumbach, M Brahmbhatt, SB Hulme, DJ
Citation: Ga. Nicholson et al., Hereditary sensory neuropathy type I: Haplotype analysis shows founders insouthern England and Europe, AM J HU GEN, 69(3), 2001, pp. 655-659
Ancestral origins of the Machado-Joseph disease mutation: A worldwide haplotype study
Authors: Gaspar, C Lopes-Cendes, I Hayes, S Goto, J Arvidsson, K Dias, A Silveira, I Maciel, P Coutinho, P Lima, M Zhou, YX Soong, BW Watanabe, M Giunti, P Stevanin, G Riess, O Sasaki, H Hsieh, M Nicholson, GA Brunt, E Higgins, JJ Lauritzen, M Tranebjaerg, L Volpini, V Wood, N Ranum, L Tsuji, S Brice, A Sequeiros, J Rouleau, GA
Citation: C. Gaspar et al., Ancestral origins of the Machado-Joseph disease mutation: A worldwide haplotype study, AM J HU GEN, 68(2), 2001, pp. 523-528
Exclusion of NFIL3 as the gene causing hereditary sensory neuropathy type I by mutation analysis
Authors: Hulme, DJ Blair, IP Dawkins, JL Nicholson, GA
Citation: Dj. Hulme et al., Exclusion of NFIL3 as the gene causing hereditary sensory neuropathy type I by mutation analysis, HUM GENET, 106(6), 2000, pp. 594-596
Frequency of spinocerebellar ataxia types 1, 2, 3, 6, and 7 in Australian patients with spinocerebellar ataxia
Authors: Storey, E du Sart, D Shaw, JH Lorentzos, P Kelly, L Gardner, RJM Forrest, SM Biros, I Nicholson, GA
Citation: E. Storey et al., Frequency of spinocerebellar ataxia types 1, 2, 3, 6, and 7 in Australian patients with spinocerebellar ataxia, AM J MED G, 95(4), 2000, pp. 351-357
Clinical syndromes associated with tomacula or myelin swellings in sural nerve biopsies
Authors: Sander, S Ouvrier, RA McLeod, JG Nicholson, GA Pollard, JD
Citation: S. Sander et al., Clinical syndromes associated with tomacula or myelin swellings in sural nerve biopsies, J NE NE PSY, 68(4), 2000, pp. 483-488
Carbon sequestration in wood and paper products
Authors: Skog, KE Nicholson, GA
Citation: Ke. Skog et Ga. Nicholson, Carbon sequestration in wood and paper products, USDA ROCKY, (59), 2000, pp. 79-88
Clinical and genetic study of Friedreich ataxia in an Australian population
Authors: Delatycki, MB Paris, DBBP Gardner, RJM Nicholson, GA Nassif, N Storey, E MacMillan, JC Collins, V Williamson, R Forrest, SM
Citation: Mb. Delatycki et al., Clinical and genetic study of Friedreich ataxia in an Australian population, AM J MED G, 87(2), 1999, pp. 168-174
Different patterns of obstetric complications in myotonic dystrophy in relation to the disease status of the fetus
Authors: Rudnik-Schoneborn, S Nicholson, GA Morgan, G Rohrig, D Zerres, K
Citation: S. Rudnik-schoneborn et al., Different patterns of obstetric complications in myotonic dystrophy in relation to the disease status of the fetus, AM J MED G, 80(4), 1998, pp. 314-321
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