Fox NC - Search Results

1

The pattern of atrophy in familial Alzheimer disease: volumetric MRI results from the DIAN study.

Cash DM, Ridgway GR, Liang Y, Ryan NS, Kinnunen KM, Yeatman T, Malone IB, Benzinger TL, Jack CR Jr, Thompson PM, Ghetti BF, Saykin AJ, Masters CL, Ringman JM, Salloway SP, Schofield PR, Sperling RA, Cairns NJ, Marcus DS, Xiong C, Bateman RJ, Morris JC, Rossor MN, Ourselin S, Fox NC; Dominantly Inherited Alzheimer Network (DIAN). Cash DM, et al. Among authors: fox nc. Neurology. 2013 Oct 15;81(16):1425-33. doi: 10.1212/WNL.0b013e3182a841c6. Epub 2013 Sep 18. Neurology. 2013. PMID: 24049139 Free PMC article.

2

Atrophy of the hippocampal formation in early familial Alzheimer's disease. A longitudinal MRI study of at-risk members of a family with an amyloid precursor protein 717Val-Gly mutation.

Fox NC, Warrington EK, Stevens JM, Rossor MN. Fox NC, et al. Ann N Y Acad Sci. 1996 Jan 17;777:226-32. doi: 10.1111/j.1749-6632.1996.tb34423.x. Ann N Y Acad Sci. 1996. PMID: 8624089

3

Visualisation and quantification of rates of atrophy in Alzheimer's disease.

Fox NC, Freeborough PA, Rossor MN. Fox NC, et al. Lancet. 1996 Jul 13;348(9020):94-7. doi: 10.1016/s0140-6736(96)05228-2. Lancet. 1996. PMID: 8676724

4

Incomplete penetrance of familial Alzheimer's disease in a pedigree with a novel presenilin-1 gene mutation.

Rossor MN, Fox NC, Beck J, Campbell TC, Collinge J. Rossor MN, et al. Among authors: fox nc. Lancet. 1996 Jun 1;347(9014):1560. doi: 10.1016/s0140-6736(96)90715-1. Lancet. 1996. PMID: 8684135 No abstract available.

5

Non-Alzheimer dementias in young patients.

Harvey RJ, Roques P, Fox NC, Rossor MN. Harvey RJ, et al. Among authors: fox nc. Br J Psychiatry. 1996 Mar;168(3):384-5. doi: 10.1192/bjp.168.3.384b. Br J Psychiatry. 1996. PMID: 8833704 No abstract available.

6

Presymptomatic hippocampal atrophy in Alzheimer's disease. A longitudinal MRI study.

Fox NC, Warrington EK, Freeborough PA, Hartikainen P, Kennedy AM, Stevens JM, Rossor MN. Fox NC, et al. Brain. 1996 Dec;119 ( Pt 6):2001-7. doi: 10.1093/brain/119.6.2001. Brain. 1996. PMID: 9010004

7

Clinical features of sporadic and familial Alzheimer's disease.

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

8

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. Brain. 1997 Mar;120 ( Pt 3):491-501. doi: 10.1093/brain/120.3.491. Brain. 1997. PMID: 9126060

9

Slowing the progression of Alzheimer disease: monitoring progression.

Rossor MN, Fox NC, Freeborough PA, Roques PK. Rossor MN, et al. Among authors: fox nc. Alzheimer Dis Assoc Disord. 1997;11 Suppl 5:S6-9. Alzheimer Dis Assoc Disord. 1997. PMID: 9348422

10

Cerebral and cerebellar atrophy on serial magnetic resonance imaging in an initially symptom free subject at risk of familial prion disease.

Fox NC, Freeborough PA, Mekkaoui KF, Stevens JM, Rossor MN. Fox NC, et al. BMJ. 1997 Oct 4;315(7112):856-7. doi: 10.1136/bmj.315.7112.856. BMJ. 1997. PMID: 9353507 Free PMC article. No abstract available.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

604 results

Search Page