Poulter M - Search Results

1

Inherited prion disease with 144 base pair gene insertion. 2. Clinical and pathological features.

Collinge J, Brown J, Hardy J, Mullan M, Rossor MN, Baker H, Crow TJ, Lofthouse R, Poulter M, Ridley R, et al. Collinge J, et al. Among authors: poulter m. Brain. 1992 Jun;115 ( Pt 3):687-710. doi: 10.1093/brain/115.3.687. Brain. 1992. PMID: 1352725

2

Inherited prion disease with six octapeptide repeat insertional mutation--molecular analysis of phenotypic heterogeneity.

Mead S, Poulter M, Beck J, Webb TE, Campbell TA, Linehan JM, Desbruslais M, Joiner S, Wadsworth JD, King A, Lantos P, Collinge J. Mead S, et al. Among authors: poulter m. Brain. 2006 Sep;129(Pt 9):2297-317. doi: 10.1093/brain/awl226. Brain. 2006. PMID: 16923955

3

Insertions in the prion protein gene in atypical dementias.

Owen F, Poulter M, Collinge J, Leach M, Shah T, Lofthouse R, Chen YF, Crow TJ, Harding AE, Hardy J, et al. Owen F, et al. Among authors: poulter m. Exp Neurol. 1991 May;112(2):240-2. doi: 10.1016/0014-4886(91)90075-n. Exp Neurol. 1991. PMID: 1674696

4

An in-frame insertion in the prion protein gene in familial Creutzfeldt-Jakob disease.

Owen F, Poulter M, Shah T, Collinge J, Lofthouse R, Baker H, Ridley R, McVey J, Crow TJ. Owen F, et al. Among authors: poulter m. Brain Res Mol Brain Res. 1990 Apr;7(3):273-6. doi: 10.1016/0169-328x(90)90038-f. Brain Res Mol Brain Res. 1990. PMID: 2159587

5

A dementing illness associated with a novel insertion in the prion protein gene.

Owen F, Poulter M, Collinge J, Leach M, Lofthouse R, Crow TJ, Harding AE. Owen F, et al. Among authors: poulter m. Brain Res Mol Brain Res. 1992 Mar;13(1-2):155-7. doi: 10.1016/0169-328x(92)90056-h. Brain Res Mol Brain Res. 1992. PMID: 1349721

6

Inherited prion disease with 144 base pair gene insertion. 1. Genealogical and molecular studies.

Poulter M, Baker HF, Frith CD, Leach M, Lofthouse R, Ridley RM, Shah T, Owen F, Collinge J, Brown J, et al. Poulter M, et al. Brain. 1992 Jun;115 ( Pt 3):675-85. doi: 10.1093/brain/115.3.675. Brain. 1992. PMID: 1352724

7

Prion dementia without characteristic pathology.

Collinge J, Owen F, Poulter M, Leach M, Crow TJ, Rossor MN, Hardy J, Mullan MJ, Janota I, Lantos PL. Collinge J, et al. Among authors: poulter m. Lancet. 1990 Jul 7;336(8706):7-9. doi: 10.1016/0140-6736(90)91518-f. Lancet. 1990. PMID: 1973256

8

Distinct glycoform ratios of protease resistant prion protein associated with PRNP point mutations.

Hill AF, Joiner S, Beck JA, Campbell TA, Dickinson A, Poulter M, Wadsworth JD, Collinge J. Hill AF, et al. Among authors: poulter m. Brain. 2006 Mar;129(Pt 3):676-85. doi: 10.1093/brain/awl013. Epub 2006 Jan 16. Brain. 2006. PMID: 16415305

9

Inherited prion disease with 4-octapeptide repeat insertion: disease requires the interaction of multiple genetic risk factors.

Kaski DN, Pennington C, Beck J, Poulter M, Uphill J, Bishop MT, Linehan JM, O'Malley C, Wadsworth JD, Joiner S, Knight RS, Ironside JW, Brandner S, Collinge J, Mead S. Kaski DN, et al. Among authors: poulter m. Brain. 2011 Jun;134(Pt 6):1829-38. doi: 10.1093/brain/awr079. Brain. 2011. PMID: 21616973

10

Aminoacid polymorphism in human prion protein and age at death in inherited prion disease.

Baker HE, Poulter M, Crow TJ, Frith CD, Lofthouse R, Ridley RM. Baker HE, et al. Among authors: poulter m. Lancet. 1991 May 25;337(8752):1286. doi: 10.1016/0140-6736(91)92953-y. Lancet. 1991. PMID: 1674080 No abstract available.

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