Harvey RJ - Search Results

1

Chromosome 14 familial Alzheimer's disease: the clinical and neuropathological characteristics of a family with a leucine-->serine (L250S) substitution at codon 250 of the presenilin 1 gene.

Harvey RJ, Ellison D, Hardy J, Hutton M, Roques PK, Collinge J, Fox NC, Rossor MN. Harvey RJ, et al. J Neurol Neurosurg Psychiatry. 1998 Jan;64(1):44-9. doi: 10.1136/jnnp.64.1.44. J Neurol Neurosurg Psychiatry. 1998. PMID: 9436726 Free PMC article.

2

Pathogenic presenilin 1 mutations (P436S & I143F) in early-onset Alzheimer's disease in the UK. Mutations in brief no. 223. Online.

Palmer MS, Beck JA, Campbell TA, Humphries CB, Roques PK, Fox NC, Harvey R, Rossor MN, Collinge J. Palmer MS, et al. Hum Mutat. 1999;13(3):256. doi: 10.1002/(sici)1098-1004(1999)13:3<256::aid-humu11>3.0.co;2-p. Hum Mutat. 1999. PMID: 10090481

3

Clinicopathological features of familial Alzheimer's disease associated with the M139V mutation in the presenilin 1 gene. Pedigree but not mutation specific age at onset provides evidence for a further genetic factor.

Fox NC, Kennedy AM, Harvey RJ, Lantos PL, Roques PK, Collinge J, Hardy J, Hutton M, Stevens JM, Warrington EK, Rossor MN. Fox NC, et al. Among authors: harvey rj. Brain. 1997 Mar;120 ( Pt 3):491-501. doi: 10.1093/brain/120.3.491. Brain. 1997. PMID: 9126060

4

Intracranial volume and Alzheimer disease: evidence against the cerebral reserve hypothesis.

Jenkins R, Fox NC, Rossor AM, Harvey RJ, Rossor MN. Jenkins R, et al. Among authors: harvey rj. Arch Neurol. 2000 Feb;57(2):220-4. doi: 10.1001/archneur.57.2.220. Arch Neurol. 2000. PMID: 10681081 Clinical Trial.

5

Alzheimer's disease due to an intronic presenilin-1 (PSEN1 intron 4) mutation: A clinicopathological study.

Janssen JC, Hall M, Fox NC, Harvey RJ, Beck J, Dickinson A, Campbell T, Collinge J, Lantos PL, Cipolotti L, Stevens JM, Rossor MN. Janssen JC, et al. Among authors: harvey rj. Brain. 2000 May;123 ( Pt 5):894-907. doi: 10.1093/brain/123.5.894. Brain. 2000. PMID: 10775535

6

Autopsy-confirmed familial early-onset Alzheimer disease caused by the l153V presenilin 1 mutation.

Janssen JC, Lantos PL, Fox NC, Harvey RJ, Beck J, Dickinson A, Campbell TA, Collinge J, Hanger DP, Cipolotti L, Stevens JM, Rossor MN. Janssen JC, et al. Among authors: harvey rj. Arch Neurol. 2001 Jun;58(6):953-8. doi: 10.1001/archneur.58.6.953. Arch Neurol. 2001. PMID: 11405810

7

Early onset familial Alzheimer's disease: Mutation frequency in 31 families.

Janssen JC, Beck JA, Campbell TA, Dickinson A, Fox NC, Harvey RJ, Houlden H, Rossor MN, Collinge J. Janssen JC, et al. Among authors: harvey rj. Neurology. 2003 Jan 28;60(2):235-9. doi: 10.1212/01.wnl.0000042088.22694.e3. Neurology. 2003. PMID: 12552037

8

The prevalence and causes of dementia in people under the age of 65 years.

Harvey RJ, Skelton-Robinson M, Rossor MN. Harvey RJ, et al. J Neurol Neurosurg Psychiatry. 2003 Sep;74(9):1206-9. doi: 10.1136/jnnp.74.9.1206. J Neurol Neurosurg Psychiatry. 2003. PMID: 12933919 Free PMC article.

9

Does early-onset Alzheimer disease constitute a distinct subtype? The contribution of molecular genetics.

Harvey RJ, Rossor MN. Harvey RJ, et al. Alzheimer Dis Assoc Disord. 1995;9 Suppl 1:S7-13. Alzheimer Dis Assoc Disord. 1995. PMID: 7546599 Review.

10

Clinical features of sporadic and familial Alzheimer's disease.

Rossor MN, Fox NC, Freeborough PA, Harvey RJ. Rossor MN, et al. Among authors: harvey rj. Neurodegeneration. 1996 Dec;5(4):393-7. doi: 10.1006/neur.1996.0052. Neurodegeneration. 1996. PMID: 9117552 Review.

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