Results: 1-16 |
Results: 16

Authors: Storey, E Thal, S Johnson, C Grey, M Madray, H Hodgson, M Pfeiffer, C
Citation: E. Storey et al., Reinforcement of occupational history taking: A success story, TEACH L MED, 13(3), 2001, pp. 176-182

Authors: Hand, PJ Gardner, RJM Knight, MA Forrest, SM Storey, E
Citation: Pj. Hand et al., Clinical features of a large Australian pedigree with episodic ataxia type1, MOVEMENT D, 16(5), 2001, pp. 938-939

Authors: Hodgson, MJ Bracker, A Yang, C Storey, E Jarvis, BJ Milton, D Lummus, Z Bernstein, D Cole, S
Citation: Mj. Hodgson et al., Hypersensitivity pneumonitis in a metal-working environment, AM J IND M, 39(6), 2001, pp. 616-628

Authors: Gardner, RJM Coleman, LT Mitchell, LA Smith, LJ Harvey, AS Scheffer, IE Storey, E Nowotny, MJ Sloane, RA Lubitz, L
Citation: Rjm. Gardner et al., Near-total absence of the cerebellum, NEUROPEDIAT, 32(2), 2001, pp. 62-68

Authors: Amor, DJ Delatycki, MB Gardner, RJM Storey, E
Citation: Dj. Amor et al., New variant of familial cerebellar ataxia with hypergonadotropic hypogonadism and sensorineural deafness, AM J MED G, 99(1), 2001, pp. 29-33

Authors: Poon, MA Stuckey, S Storey, E
Citation: Ma. Poon et al., MRI evidence of cerebellar and hippocampal involvement in Creutzfeldt-Jakob disease, NEURORADIOL, 43(9), 2001, pp. 746-749

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

Authors: Brodaty, H Ames, D Boundy, KL Hecker, J Snowdon, J Storey, E Yates, MW
Citation: H. Brodaty et al., Pharmacological treatment of cognitive deficits in Alzheimer's disease, MED J AUST, 175(6), 2001, pp. 324-329

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

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

Authors: Smith, MJ Gardner, RJM Knight, MA Forrest, SM Beyreuther, K Storey, E McLean, CA Cotton, RGH Cappal, R Masters, CL
Citation: Mj. Smith et al., Early-onset Alzheimer's disease caused by a novel mutation at codon 219 ofthe presenilin-1 gene, NEUROREPORT, 10(3), 1999, pp. 503-507

Authors: Storey, E Katz, M Brickman, Y Beyreuther, K Masters, CL
Citation: E. Storey et al., Amyloid precursor protein of Alzheimer's disease: evidence for a stable, full-length, trans-membrane pool in primary neuronal cultures, EUR J NEURO, 11(5), 1999, pp. 1779-1788

Authors: Storey, E Cappai, R
Citation: E. Storey et R. Cappai, The amyloid precursor protein of Alzheimer's disease and the A beta peptide, NEUROP AP N, 25(2), 1999, pp. 81-97

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

Authors: Storey, E Forrest, SM Shaw, JH Mitchell, P Gardner, RJM
Citation: E. Storey et al., Spinocerebellar ataxia type 2 - Clinical features of a pedigree displayingprominent frontal-executive dysfunction, ARCH NEUROL, 56(1), 1999, pp. 43-50

Authors: Storey, E
Citation: E. Storey, Dominantly inherited ataxias. Part I, J CL NEUROS, 5(3), 1998, pp. 257-264
Risultati: 1-16 |