Rossor M - Search Results

1

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

2

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

3

Molecular genetic characterisation of frontotemporal dementia on chromosome 3.

Ashworth A, Lloyd S, Brown J, Gydesen S, Sorensen SA, Brun A, Englund E, Humphreys C, Housman D, Badura M, Stanton V Jr, Taylor K, Cameron J, Munroe D, Johansson J, Rossor M, Fisher EM, Collinge J. Ashworth A, et al. Among authors: rossor m. Dement Geriatr Cogn Disord. 1999;10 Suppl 1:93-101. doi: 10.1159/000051222. Dement Geriatr Cogn Disord. 1999. PMID: 10436350

4

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.

5

Screening for mutations in the open reading frame and promoter of the beta-amyloid precursor protein gene in familial Alzheimer's disease: identification of a further family with APP717 Val-->Ile.

Fidani L, Rooke K, Chartier-Harlin MC, Hughes D, Tanzi R, Mullan M, Roques P, Rossor M, Hardy J, Goate A. Fidani L, et al. Among authors: rossor m. Hum Mol Genet. 1992 Jun;1(3):165-8. doi: 10.1093/hmg/1.3.165. Hum Mol Genet. 1992. PMID: 1303172

6

The genetics of Alzheimer's disease.

Kennedy AM, Brown J, Rossor M. Kennedy AM, et al. Among authors: rossor m. Baillieres Clin Neurol. 1994 Aug;3(2):217-40. Baillieres Clin Neurol. 1994. PMID: 7952845 Review.

7

Confirmation that familial clustering and age of onset in late onset Alzheimer's disease are determined at the apolipoprotein E locus.

Houlden H, Crook R, Hardy J, Roques P, Collinge J, Rossor M. Houlden H, et al. Among authors: rossor m. Neurosci Lett. 1994 Jun 20;174(2):222-4. doi: 10.1016/0304-3940(94)90026-4. Neurosci Lett. 1994. PMID: 7970184

8

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.

9

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.

10

Chromosome 3 linked frontotemporal dementia (FTD-3).

Gydesen S, Brown JM, Brun A, Chakrabarti L, Gade A, Johannsen P, Rossor M, Thusgaard T, Grove A, Yancopoulou D, Spillantini MG, Fisher EM, Collinge J, Sorensen SA. Gydesen S, et al. Among authors: rossor m. Neurology. 2002 Nov 26;59(10):1585-94. doi: 10.1212/01.wnl.0000034763.54161.1f. Neurology. 2002. PMID: 12451202

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