Fox NC - Search Results

1

Neurological manifestations of autosomal dominant familial Alzheimer's disease: a comparison of the published literature with the Dominantly Inherited Alzheimer Network observational study (DIAN-OBS).

Tang M, Ryman DC, McDade E, Jasielec MS, Buckles VD, Cairns NJ, Fagan AM, Goate A, Marcus DS, Xiong C, Allegri RF, Chhatwal JP, Danek A, Farlow MR, Fox NC, Ghetti B, Graff-Radford NR, Laske C, Martins RN, Masters CL, Mayeux RP, Ringman JM, Rossor MN, Salloway SP, Schofield PR, Morris JC, Bateman RJ; Dominantly Inherited Alzheimer Network (DIAN). Tang M, et al. Among authors: fox nc. Lancet Neurol. 2016 Dec;15(13):1317-1325. doi: 10.1016/S1474-4422(16)30229-0. Epub 2016 Oct 21. Lancet Neurol. 2016. PMID: 27777020 Free PMC article. Review.

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.

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