Author/Creator: Collinge, J - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Collinge, J

1. 022 Voxelwise analysis of cerebral diffusion tensor imaging in prion diseases. Issue 3 (9th February 2012)

Authors:: Porter, M C; Hyare, H; De Vita, E; Thompson, A; Lukic, A; Yousry, T; Rudge, P; Mead, S; Collinge, J; Thornton, J
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 83:Issue 3(2012)
Page Start:: e1
Record Type:: Journal Article
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2. Association of a null allele of SPRN with variant Creutzfeldt–Jakob disease. Issue 12 (19th September 2008)

Authors:: Beck, J A; Campbell, T A; Adamson, G; Poulter, M; Uphill, J B; Molou, E; Collinge, J; Mead, S
Journal:: Journal of medical genetics
Issue:: Volume 45:Issue 12(2008)
Page Start:: 813
Record Type:: Journal Article
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3. Corticobasal syndrome associated with a novel 1048_1049insG progranulin mutation. Issue 11 (28th October 2009)

Authors:: Rohrer, J D; Beck, J; Warren, J D; King, A; Sarraj, S Al; Holton, J; Revesz, T; Collinge, J; Mead, S
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 80:Issue 11(2009)
Page Start:: 1297
Record Type:: Journal Article
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4. Distinct neuropsychological profiles correspond to distribution of cortical thinning in inherited prion disease caused by insertional mutation. Issue 1 (17th August 2011)

Authors:: Alner, K; Hyare, H; Mead, S; Rudge, P; Wroe, S; Rohrer, J D; Ridgway, G R; Ourselin, S; Clarkson, M; Hunt, H; Fox, N C; Webb, T; Collinge, J; Cipolotti, L
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 83:Issue 1(2012)
Page Start:: 109
Record Type:: Journal Article
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5. Familial Alzheimer's disease and inherited prion disease in the UK are poorly ascertained. Issue 9 (27th August 2010)

Authors:: Stevens, J C; Beck, J; Lukic, A; Ryan, N; Abbs, S; Collinge, J; Fox, N C; Mead, S
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 82:Issue 9(2011)
Page Start:: 1054
Record Type:: Journal Article
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6. Familial Pick's disease and dementia in frontal lobe degeneration of non-Alzheimer type are not variants of prion disease. Issue 6 (June 1994)

Authors:: Collinge, J; Palmer, M S; Sidle, K C; Mahal, S P; Campbell, T; Brown, J; Hardy, J; Brun, A E; Gustafson, L; Bakker, E
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 57:Issue 6(1994)
Page Start:: 762
Record Type:: Journal Article
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7. Familial prion disease in a Hungarian family with a novel 144-base pair insertion in the prion protein gene. Issue 3 (16th February 2007)

Authors:: Kovács, T; Beck, J A; Papp, M I; Lantos, P L; Arányi, Z; Szirmai, I G; Farsang, M; Stuke, A; Csillik, A; Collinge, J
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 78:Issue 3(2007)
Page Start:: 321
Record Type:: Journal Article
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8. High levels of disease related prion protein in the ileum in variant Creutzfeldt-Jakob disease. Issue 10 (14th September 2005)

Authors:: Joiner, S; Linehan, J M; Brandner, S; Wadsworth, J D F; Collinge, J
Journal:: Gut
Issue:: Volume 54:Issue 10(2005)
Page Start:: 1506
Record Type:: Journal Article
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9. Inherited prion disease (PrP lysine 200) in Britain: two case reports. Issue 6873 (30th January 1993)

Authors:: Collinge, J; Palmer, M S; Campbell, T; Sidle, K C; Carroll, D; Harding, A
Journal:: BMJ
Issue:: Volume 306:Issue 6873(1993)
Page Start:: 301
Record Type:: Journal Article
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10. Irregular presence of abnormal prion protein in appendix in variant Creutzfeldt-Jakob disease. Issue 5 (1st November 2002)

Authors:: Joiner, S; Linehan, J; Brandner, S; Wadsworth, J D F; Collinge, J
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 73:Issue 5(2002)
Page Start:: 597
Record Type:: Journal Article
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