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Results:
1-12
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Results: 12
Authors:
Farrer, M
Maraganore, DM
Lockhart, P
Singleton, A
Lesnick, TG
de Andrade, M
West, A
de Silva, R
Hardy, J
Hernandez, D
Citation: M. Farrer et al., alpha-synuclein gene haplotypes are associated with Parkinson's disease, HUM MOL GEN, 10(17), 2001, pp. 1847-1851
Authors:
Khan, N
Graham, E
Dixon, P
Morris, C
Mander, A
Clayton, D
Vaughan, J
Quinn, N
Lees, A
Daniel, S
Wood, N
de Silva, R
Citation: N. Khan et al., Parkinson's disease is not associated with combined alpha-synuclein/apolipoprotein E susceptibility genotype, ANN NEUROL, 49(5), 2001, pp. 665-668
Authors:
de Silva, R
Weiler, M
Morris, HR
Martin, ER
Wood, NW
Lees, AJ
Citation: R. De Silva et al., Strong association of a novel Tau promoter haplotype in progressive supranuclear palsy, NEUROSCI L, 311(3), 2001, pp. 145-148
Authors:
Bandopadhyay, R
de Silva, R
Khan, N
Graham, E
Vaughan, J
Engelender, S
Ross, C
Morris, H
Morris, C
Wood, NW
Daniel, S
Lees, A
Citation: R. Bandopadhyay et al., No pathogenic mutations in the synphilin-1 gene in Parkinson's disease, NEUROSCI L, 307(2), 2001, pp. 125-127
Authors:
Senanayake, B
de Silva, R
Bone, I
Citation: B. Senanayake et al., Seven recurrences of spinal inflammation, J ROY S MED, 94(3), 2001, pp. 134-135
Teaching and learning school mathematics by building on students' out-of-school mathematics practice
Authors:
Masingila, JO
de Silva, R
Citation: Jo. Masingila et R. De Silva, Teaching and learning school mathematics by building on students' out-of-school mathematics practice, SOCIOCULTURAL RESEARCH ON MATHEMATICS EDUCATION, 2001, pp. 329-344
Authors:
Zerr, I
Brandel, JP
Masullo, C
Wientjens, D
de Silva, R
Zeidler, M
Granieri, E
Sampaolo, S
van Duijn, C
Delasnerie-Laupretre, N
Will, R
Poser, S
Citation: I. Zerr et al., European surveillance on Creutzfeldt-Jakob disease: a case-control study for medical risk factors, J CLIN EPID, 53(7), 2000, pp. 747-754
Authors:
Unlu, M
de Lange, RPJ
de Silva, R
Kalaria, R
Clair, DS
Citation: M. Unlu et al., Detection of complement factor B in the cerebrospinal fluid of patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy disease using two-dimensional gel electrophoresis and mass spectrometry, NEUROSCI L, 282(3), 2000, pp. 149-152
Authors:
Monckton, DG
Cayuela, ML
Gould, FK
Brook, GJR
de Silva, R
Ashizawa, T
Citation: Dg. Monckton et al., Very large (CAG)(n) DNA repeat expansions in the sperm of two spinocerebellar ataxia type 7 males, HUM MOL GEN, 8(13), 1999, pp. 2473-2478
Authors:
de Silva, R
Duncan, R
Patterson, J
Gillham, R
Hadley, D
Citation: R. De Silva et al., Regional cerebral perfusion and amytal distribution during the Wada test, J NUCL MED, 40(5), 1999, pp. 747-752
Authors:
Seneviratne, U
de Silva, R
Citation: U. Seneviratne et R. De Silva, Lambert-Eaton myasthenic syndrome, POSTG MED J, 75(887), 1999, pp. 516-520
Authors:
de Silva, R
Petty, R
Loudon, M
Frew, C
Cooke, A
Davidson, R
Citation: R. De Silva et al., Friedreich's ataxia in a pedigree with apparent autosomal dominant spinocerebellar degeneration, J NE NE PSY, 66(1), 1999, pp. 117-118
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