Brown J - Search Results

1

Clinical features of frontotemporal dementia due to the intronic tau 10(+16) mutation.

Janssen JC, Warrington EK, Morris HR, Lantos P, Brown J, Revesz T, Wood N, Khan MN, Cipolotti L, Fox NC, Rossor MN. Janssen JC, et al. Among authors: brown j. Neurology. 2002 Apr 23;58(8):1161-8. doi: 10.1212/wnl.58.8.1161. Neurology. 2002. PMID: 11971081

2

Familial progressive supranuclear palsy.

Brown J, Lantos P, Stratton M, Roques P, Rossor M. Brown J, et al. 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.

3

Familial dementia lacking specific pathological features presenting with clinical features of corticobasal degeneration.

Brown J, Lantos PL, Rossor MN. Brown J, et al. J Neurol Neurosurg Psychiatry. 1998 Oct;65(4):600-3. doi: 10.1136/jnnp.65.4.600. J Neurol Neurosurg Psychiatry. 1998. PMID: 9771798 Free PMC article.

4

Mutation in the tau exon 10 splice site region in familial frontotemporal dementia.

Morris HR, Perez-Tur J, Janssen JC, Brown J, Lees AJ, Wood NW, Hardy J, Hutton M, Rossor MN. Morris HR, et al. Among authors: brown j. Ann Neurol. 1999 Feb;45(2):270-1. Ann Neurol. 1999. PMID: 9989634 No abstract available.

5

A novel tau mutation (N296N) in familial dementia with swollen achromatic neurons and corticobasal inclusion bodies.

Spillantini MG, Yoshida H, Rizzini C, Lantos PL, Khan N, Rossor MN, Goedert M, Brown J. Spillantini MG, et al. Among authors: brown j. Ann Neurol. 2000 Dec;48(6):939-43. doi: 10.1002/1531-8249(200012)48:6<939::aid-ana17>3.3.co;2-t. Ann Neurol. 2000. PMID: 11117553

6

Inherited prion disease with 144 base pair gene insertion. 2. Clinical and pathological features.

Collinge J, Brown J, Hardy J, Mullan M, Rossor MN, Baker H, Crow TJ, Lofthouse R, Poulter M, Ridley R, et al. Collinge J, et al. Among authors: brown j. Brain. 1992 Jun;115 ( Pt 3):687-710. doi: 10.1093/brain/115.3.687. Brain. 1992. PMID: 1352725

7

Frontal lobe or 'nonspecific' dementias are genetically heterogeneous.

Ashworth A, Brown J, Gydesen S, Sorensen SA, Rossor MN, Hardy J, Collinge J. Ashworth A, et al. Among authors: brown j. Neurology. 1995 Sep;45(9):1781. doi: 10.1212/wnl.45.9.1781. Neurology. 1995. PMID: 7675248 No abstract available.

8

The genetics of Alzheimer's disease.

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

9

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. Hum Mol Genet. 1995 Sep;4(9):1625-8. doi: 10.1093/hmg/4.9.1625. Hum Mol Genet. 1995. PMID: 8541850

10

Familial dementia with swollen achromatic neurons and corticobasal inclusion bodies: a clinical and pathological study.

Brown J, Lantos PL, Roques P, Fidani L, Rossor MN. Brown J, et al. J Neurol Sci. 1996 Jan;135(1):21-30. doi: 10.1016/0022-510x(95)00236-u. J Neurol Sci. 1996. PMID: 8926492

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

21,095 results

Search Page

Filters