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Results:
1-16
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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
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