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Results: 1-17 |
Results: 17
A meta-analysis of genomic screens in multiple sclerosis
Authors: Pericak-Vance, MA Rimmler, JB Saunders, AM Martin, ER Haines, JL Garcia, ME Oksenberg, JR Barcellos, LF Lincoln, R Goodkin, DE Hauser, SL Compston, DAS Sawcer, SJ Clayton, D Jones, HB Walker, N Goodfellow, PPN Bulman, D Sadovnick, D Ebers, GC Dyment, D Willer, C Risch, N
Citation: Ma. Pericak-vance et al., A meta-analysis of genomic screens in multiple sclerosis, MULT SCLER, 7(1), 2001, pp. 3-11
Remyelination of demyelinated CNS axons by transplanted human Schwann cells: The deleterious effect of contaminating fibroblasts
Authors: Brierley, CMH Crang, AJ Iwashita, Y Gilson, JM Scolding, NJ Compston, DAS Blakemore, WF
Citation: Cmh. Brierley et al., Remyelination of demyelinated CNS axons by transplanted human Schwann cells: The deleterious effect of contaminating fibroblasts, CELL TRANSP, 10(3), 2001, pp. 305-315
Detection of optic nerve atrophy following a single episode of unilateral optic neuritis by MRI using a fat-saturated short-echo fast FLAIR sequence
Authors: Hickman, SJ Brex, PA Brierley, CMH Silver, NC Barker, GJ Scolding, NJ Compston, DAS Moseley, IF Plant, GT Miller, DH
Citation: Sj. Hickman et al., Detection of optic nerve atrophy following a single episode of unilateral optic neuritis by MRI using a fat-saturated short-echo fast FLAIR sequence, NEURORADIOL, 43(2), 2001, pp. 123-128
Patterns of disease in concordant parent-child pairs with multiple sclerosis
Authors: Hupperts, R Broadley, S Mander, A Clayton, D Compston, DAS Robertson, NP
Citation: R. Hupperts et al., Patterns of disease in concordant parent-child pairs with multiple sclerosis, NEUROLOGY, 57(2), 2001, pp. 290-295
Infratentorial hypointense lesion volume on T1-weighted magnetic resonanceimaging correlates with disability in patients with chronic cerebellar ataxia due to multiple sclerosis
Authors: Hickman, SJ Brierley, CMH Silver, NC Moseley, IF Scolding, NJ Compston, DAS Miller, DH
Citation: Sj. Hickman et al., Infratentorial hypointense lesion volume on T1-weighted magnetic resonanceimaging correlates with disability in patients with chronic cerebellar ataxia due to multiple sclerosis, J NEUR SCI, 187(1-2), 2001, pp. 35-39
No association between multiple sclerosis and the Notch3 gene responsible for cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL)
Authors: Broadley, SA Sawcer, SJ Chataway, SJS Coraddu, F Coles, A Gray, J Roxburgh, R Clayton, D Compston, DAS
Citation: Sa. Broadley et al., No association between multiple sclerosis and the Notch3 gene responsible for cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL), J NE NE PSY, 71(1), 2001, pp. 97-99
Multiple sclerosis: Ethics, outcome variables and clinical scales
Authors: Coles, AJ Compston, DAS
Citation: Aj. Coles et Das. Compston, Multiple sclerosis: Ethics, outcome variables and clinical scales, CLINICAL TRIALS IN NEUROLOGY, 2001, pp. 359-370
Multiple sclerosis and tonsillectomy: no evidence for an influence on the development of disease or clinical phenotype
Authors: Broadley, SA Deans, J Chataway, SJS Sawcer, SJ Compston, DAS
Citation: Sa. Broadley et al., Multiple sclerosis and tonsillectomy: no evidence for an influence on the development of disease or clinical phenotype, MULT SCLER, 6(2), 2000, pp. 121-123
Normal polyclonal immunoglobulins ('IVIg') inhibit microglial phagocytosisin vitro
Authors: Stangel, M Joly, E Scolding, NJ Compston, DAS
Citation: M. Stangel et al., Normal polyclonal immunoglobulins ('IVIg') inhibit microglial phagocytosisin vitro, J NEUROIMM, 106(1-2), 2000, pp. 137-144
Autoimmune disease in first-degree relatives of patients with multiple sclerosis - A UK survey
Authors: Broadley, SA Deans, J Sawcer, SJ Clayton, D Compston, DAS
Citation: Sa. Broadley et al., Autoimmune disease in first-degree relatives of patients with multiple sclerosis - A UK survey, BRAIN, 123, 2000, pp. 1102-1111
Urinary, faecal and sexual dysfunction in patients with multiple sclerosis
Authors: Hennessey, A Robertson, NP Swingler, R Compston, DAS
Citation: A. Hennessey et al., Urinary, faecal and sexual dysfunction in patients with multiple sclerosis, J NEUROL, 246(11), 1999, pp. 1027-1032
Identification of A2B5-positive putative oligodendrocyte progenitor cells and A2B5-positive astrocytes in adult human white matter
Authors: Scolding, NJ Rayner, PJ Compston, DAS
Citation: Nj. Scolding et al., Identification of A2B5-positive putative oligodendrocyte progenitor cells and A2B5-positive astrocytes in adult human white matter, NEUROSCIENC, 89(1), 1999, pp. 1-4
Recall antigen presentation by gamma-interferon-activated microglia results in T cell activation and propagation of the immune response
Authors: Hall, GL Girdlestone, J Compston, DAS Wing, MG
Citation: Gl. Hall et al., Recall antigen presentation by gamma-interferon-activated microglia results in T cell activation and propagation of the immune response, J NEUROIMM, 98(2), 1999, pp. 105-111
Comparison of C1q-receptors on rat microglia and peritoneal macrophages
Authors: Wing, MG Seilly, DJ Nicholas, RS Rahman, S Zajicek, J Lachmann, PJ Compston, DAS
Citation: Mg. Wing et al., Comparison of C1q-receptors on rat microglia and peritoneal macrophages, J NEUROIMM, 94(1-2), 1999, pp. 74-81
Quantitative MRI in patients with secondary progressive MS treated with monoclonal antibody Campath 1H
Authors: Paolillo, A Coles, AJ Molyneux, PD Gawne-Cain, M MacManus, D Barker, GJ Compston, DAS Miller, DH
Citation: A. Paolillo et al., Quantitative MRI in patients with secondary progressive MS treated with monoclonal antibody Campath 1H, NEUROLOGY, 53(4), 1999, pp. 751-757
Moyamoya disease presenting as Valsalva related partial seizures
Authors: Robertson, NP Compston, DAS Kirkpatrick, P
Citation: Np. Robertson et al., Moyamoya disease presenting as Valsalva related partial seizures, J NE NE PSY, 66(1), 1999, pp. 111-111
Prognosis in multiple sclerosis: genetic factors
Authors: Robertson, NP Compston, DAS
Citation: Np. Robertson et Das. Compston, Prognosis in multiple sclerosis: genetic factors, FRONTIERS IN MULTIPLE SCLEROSIS, VOL 2, 1999, pp. 51-61
Risultati: 1-17 |