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Early-onset versus late-onset Alzheimer's disease: the case of the missing APOE ɛ4 allele.
van der Flier WM, Pijnenburg YA, Fox NC, Scheltens P. van der Flier WM, et al. Lancet Neurol. 2011 Mar;10(3):280-8. doi: 10.1016/S1474-4422(10)70306-9. Epub 2010 Dec 22. Lancet Neurol. 2011. PMID: 21185234
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
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
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
Clinical features of sporadic and familial Alzheimer's disease.
Rossor MN, Fox NC, Freeborough PA, Harvey RJ. Rossor MN, et al. Neurodegeneration. 1996 Dec;5(4):393-7. doi: 10.1006/neur.1996.0052. Neurodegeneration. 1996. PMID: 9117552 Review.
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
Slowing the progression of Alzheimer disease: monitoring progression.
Rossor MN, Fox NC, Freeborough PA, Roques PK. Rossor MN, et al. Alzheimer Dis Assoc Disord. 1997;11 Suppl 5:S6-9. Alzheimer Dis Assoc Disord. 1997. PMID: 9348422
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.
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