Masters CL - Search Results

1

Variable phenotype of Alzheimer's disease with spastic paraparesis.

Smith MJ, Kwok JB, McLean CA, Kril JJ, Broe GA, Nicholson GA, Cappai R, Hallupp M, Cotton RG, Masters CL, Schofield PR, Brooks WS. Smith MJ, et al. Among authors: masters cl. Ann Neurol. 2001 Jan;49(1):125-9. doi: 10.1002/1531-8249(200101)49:1<125::aid-ana21>3.0.co;2-1. Ann Neurol. 2001. PMID: 11198283

2

Soluble pool of Abeta amyloid as a determinant of severity of neurodegeneration in Alzheimer's disease.

McLean CA, Cherny RA, Fraser FW, Fuller SJ, Smith MJ, Beyreuther K, Bush AI, Masters CL. McLean CA, et al. Among authors: masters cl. Ann Neurol. 1999 Dec;46(6):860-6. doi: 10.1002/1531-8249(199912)46:6<860::aid-ana8>3.0.co;2-m. Ann Neurol. 1999. PMID: 10589538

3

Early-onset Alzheimer's disease caused by a novel mutation at codon 219 of the presenilin-1 gene.

Smith MJ, Gardner RJ, Knight MA, Forrest SM, Beyreuther K, Storey E, McLean CA, Cotton RG, Cappal R, Masters CL. Smith MJ, et al. Among authors: masters cl. Neuroreport. 1999 Feb 25;10(3):503-7. doi: 10.1097/00001756-199902250-00011. Neuroreport. 1999. PMID: 10208579

4

Irregular distribution of cytochrome c oxidase protein subunits in aging and Alzheimer's disease.

Ojaimi J, Masters CL, McLean C, Opeskin K, McKelvie P, Byrne E. Ojaimi J, et al. Among authors: masters cl. Ann Neurol. 1999 Oct;46(4):656-60. Ann Neurol. 1999. PMID: 10514105

5

Novel Leu723Pro amyloid precursor protein mutation increases amyloid beta42(43) peptide levels and induces apoptosis.

Kwok JB, Li QX, Hallupp M, Whyte S, Ames D, Beyreuther K, Masters CL, Schofield PR. Kwok JB, et al. Among authors: masters cl. Ann Neurol. 2000 Feb;47(2):249-53. doi: 10.1002/1531-8249(200002)47:2<249::aid-ana18>3.0.co;2-8. Ann Neurol. 2000. PMID: 10665499

6

Accumulation of insoluble alpha-synuclein in dementia with Lewy bodies.

Campbell BC, Li QX, Culvenor JG, Jäkälä P, Cappai R, Beyreuther K, Masters CL, McLean CA. Campbell BC, et al. Among authors: masters cl. Neurobiol Dis. 2000 Jun;7(3):192-200. doi: 10.1006/nbdi.2000.0286. Neurobiol Dis. 2000. PMID: 10860784

7

Gerstmann-Sträussler-Scheinker syndrome,fatal familial insomnia, and kuru: a review of these less common human transmissible spongiform encephalopathies.

Collins S, McLean CA, Masters CL. Collins S, et al. Among authors: masters cl. J Clin Neurosci. 2001 Sep;8(5):387-97. doi: 10.1054/jocn.2001.0919. J Clin Neurosci. 2001. PMID: 11535002 Review.

8

Creutzfeldt-Jakob disease in Australia 1970-1999.

Collins S, Boyd A, Lee JS, Lewis V, Fletcher A, McLean CA, Law M, Kaldor J, Smith MJ, Masters CL. Collins S, et al. Among authors: masters cl. Neurology. 2002 Nov 12;59(9):1365-71. doi: 10.1212/01.wnl.0000031793.11602.8c. Neurology. 2002. PMID: 12427885

9

Novel prion protein insert mutation associated with prolonged neurodegenerative illness.

Lewis V, Collins S, Hill AF, Boyd A, McLean CA, Smith M, Masters CL. Lewis V, et al. Among authors: masters cl. Neurology. 2003 May 27;60(10):1620-4. doi: 10.1212/01.wnl.0000065887.14609.0e. Neurology. 2003. PMID: 12771252

10

Commentary on the consensus recommendations for the post mortem diagnosis of Alzheimer's disease.

McLean CA, Beyreuther K, Masters CL. McLean CA, et al. Among authors: masters cl. Neurobiol Aging. 1997 Jul-Aug;18(4 Suppl):S89-90. doi: 10.1016/s0197-4580(97)00061-4. Neurobiol Aging. 1997. PMID: 9330993

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