Fox NC - Search Results

1

Longitudinal (¹⁸F)AV-1451 PET imaging in a patient with frontotemporal dementia due to a Q351R MAPT mutation.

Convery RS, Jiao J, Clarke MTM, Moore KM, Koriath CAM, Woollacott IOC, Weston PSJ, Gunn R, Rabiner I, Cash DM, Rossor MN, Warren JD, Fox NC, Ourselin S, Bocchetta M, Rohrer JD. Convery RS, et al. Among authors: fox nc. J Neurol Neurosurg Psychiatry. 2020 Jan;91(1):106-108. doi: 10.1136/jnnp-2019-320904. Epub 2019 Aug 22. J Neurol Neurosurg Psychiatry. 2020. PMID: 31439620 Free PMC article. No abstract available.

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

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.

5

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

6

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.

7

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

8

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

9

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.

10

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. Among authors: fox nc. 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.

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