Mullan M - Search Results

1

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: mullan m. Brain. 1992 Jun;115 ( Pt 3):687-710. doi: 10.1093/brain/115.3.687. Brain. 1992. PMID: 1352725

2

Genetic characterization of a novel familial dementia.

Brown J, Smith S, Brun A, Collinge J, Gydesen S, Hardy J, Mullan M, Goate A. Brown J, et al. Among authors: mullan m. Ann N Y Acad Sci. 1991;640:181-3. doi: 10.1111/j.1749-6632.1991.tb00213.x. Ann N Y Acad Sci. 1991. PMID: 1776737

3

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: mullan m. J Neurol Sci. 1993 Feb;114(2):138-43. doi: 10.1016/0022-510x(93)90288-a. J Neurol Sci. 1993. PMID: 8445394

4

Familial Alzheimer's disease. A pedigree with a mis-sense mutation in the amyloid precursor protein gene (amyloid precursor protein 717 valine-->glycine).

Kennedy AM, Newman S, McCaddon A, Ball J, Roques P, Mullan M, Hardy J, Chartier-Harlin MC, Frackowiak RS, Warrington EK, et al. Kennedy AM, et al. Among authors: mullan m. Brain. 1993 Apr;116 ( Pt 2):309-24. doi: 10.1093/brain/116.2.309. Brain. 1993. PMID: 8461968

5

Sequencing of exons 16 and 17 of the beta-amyloid precursor protein gene in 14 families with early onset Alzheimer's disease fails to reveal mutations in the beta-amyloid sequence.

Crawford F, Hardy J, Mullan M, Goate A, Hughes D, Fidani L, Roques P, Rossor M, Chartier-Harlin MC. Crawford F, et al. Among authors: mullan m. Neurosci Lett. 1991 Nov 25;133(1):1-2. doi: 10.1016/0304-3940(91)90042-r. Neurosci Lett. 1991. PMID: 1791986

6

Screening for the APP codon 670/671 mutations in Alzheimer's disease.

Houlden H, Crawford F, Rossor M, Mullan M. Houlden H, et al. Among authors: mullan m. Neurosci Lett. 1993 May 14;154(1-2):161-2. doi: 10.1016/0304-3940(93)90196-r. Neurosci Lett. 1993. PMID: 8395665

7

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: mullan m. Hum Mol Genet. 1992 Jun;1(3):165-8. doi: 10.1093/hmg/1.3.165. Hum Mol Genet. 1992. PMID: 1303172

8

Segregation of a missense mutation in the amyloid precursor protein gene with familial Alzheimer's disease.

Goate A, Chartier-Harlin MC, Mullan M, Brown J, Crawford F, Fidani L, Giuffra L, Haynes A, Irving N, James L, et al. Goate A, et al. Among authors: mullan m. Nature. 1991 Feb 21;349(6311):704-6. doi: 10.1038/349704a0. Nature. 1991. PMID: 1671712

9

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: mullan m. Neurosci Lett. 1992 Mar 30;137(2):221-4. doi: 10.1016/0304-3940(92)90408-y. Neurosci Lett. 1992. PMID: 1584463

10

Alzheimer's disease. In search of the soluble.

Hardy J, Mullan M. Hardy J, et al. Among authors: mullan m. Nature. 1992 Sep 24;359(6393):268-9. doi: 10.1038/359268a0. Nature. 1992. PMID: 1406927 No abstract available.

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

344 results

Search Page

Filters