Rossor M - Search Results

1

Phenotypic variability in the brains of a family with a prion disease characterized by a 144-base pair insertion in the prion protein gene.

King A, Doey L, Rossor M, Mead S, Collinge J, Lantos P. King A, et al. Among authors: rossor m. Neuropathol Appl Neurobiol. 2003 Apr;29(2):98-105. doi: 10.1046/j.1365-2990.2003.00423.x. Neuropathol Appl Neurobiol. 2003. PMID: 12662318

2

A pathogenic progranulin mutation and C9orf72 repeat expansion in a family with frontotemporal dementia.

Lashley T, Rohrer JD, Mahoney C, Gordon E, Beck J, Mead S, Warren J, Rossor M, Revesz T. Lashley T, et al. Among authors: rossor m. Neuropathol Appl Neurobiol. 2014 Jun;40(4):502-13. doi: 10.1111/nan.12100. Neuropathol Appl Neurobiol. 2014. PMID: 24286341 Free PMC article.

3

Familial Alzheimer's disease with the amyloid precursor protein position 717 mutation and sporadic Alzheimer's disease have the same cytoskeletal pathology.

Lantos PL, Luthert PJ, Hanger D, Anderton BH, Mullan M, Rossor M. Lantos PL, et al. Among authors: rossor m. Neurosci Lett. 1992 Mar 30;137(2):221-4. doi: 10.1016/0304-3940(92)90408-y. Neurosci Lett. 1992. PMID: 1584463

4

A new variant of prion disease.

Collinge J, Rossor M. Collinge J, et al. Among authors: rossor m. Lancet. 1996 Apr 6;347(9006):916-7. doi: 10.1016/s0140-6736(96)91407-5. Lancet. 1996. PMID: 8598749 No abstract available.

5

Duplication of amyloid precursor protein (APP), but not prion protein (PRNP) gene is a significant cause of early onset dementia in a large UK series.

McNaughton D, Knight W, Guerreiro R, Ryan N, Lowe J, Poulter M, Nicholl DJ, Hardy J, Revesz T, Lowe J, Rossor M, Collinge J, Mead S. McNaughton D, et al. Among authors: rossor m. Neurobiol Aging. 2012 Feb;33(2):426.e13-21. doi: 10.1016/j.neurobiolaging.2010.10.010. Epub 2010 Dec 28. Neurobiol Aging. 2012. PMID: 21193246 Free PMC article.

6

Pick's disease is associated with mutations in the tau gene.

Pickering-Brown S, Baker M, Yen SH, Liu WK, Hasegawa M, Cairns N, Lantos PL, Rossor M, Iwatsubo T, Davies Y, Allsop D, Furlong R, Owen F, Hardy J, Mann D, Hutton M. Pickering-Brown S, et al. Among authors: rossor m. Ann Neurol. 2000 Dec;48(6):859-67. Ann Neurol. 2000. PMID: 11117542

7

HECTD2, a candidate susceptibility gene for Alzheimer's disease on 10q.

Lloyd SE, Rossor M, Fox N, Mead S, Collinge J. Lloyd SE, et al. Among authors: rossor m. BMC Med Genet. 2009 Sep 15;10:90. doi: 10.1186/1471-2350-10-90. BMC Med Genet. 2009. PMID: 19754925 Free PMC article.

8

Genetic characterization of a familial non-specific dementia originating in Jutland, Denmark.

Brown J, Gydesen S, Sorensen SA, Brun A, Smith S, Houlden H, Twells R, Mullan M, Rossor M, Collinge J, et al. Brown J, et al. Among authors: rossor m. J Neurol Sci. 1993 Feb;114(2):138-43. doi: 10.1016/0022-510x(93)90288-a. J Neurol Sci. 1993. PMID: 8445394

9

Familial progressive supranuclear palsy.

Brown J, Lantos P, Stratton M, Roques P, Rossor M. Brown J, et al. Among authors: rossor m. J Neurol Neurosurg Psychiatry. 1993 May;56(5):473-6. doi: 10.1136/jnnp.56.5.473. J Neurol Neurosurg Psychiatry. 1993. PMID: 8505637 Free PMC article.

10

Familial non-specific dementia maps to chromosome 3.

Brown J, Ashworth A, Gydesen S, Sorensen A, Rossor M, Hardy J, Collinge J. Brown J, et al. Among authors: rossor m. Hum Mol Genet. 1995 Sep;4(9):1625-8. doi: 10.1093/hmg/4.9.1625. Hum Mol Genet. 1995. PMID: 8541850

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 Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

624 results

Search Page

Filters