Mullan M - Search Results

1

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

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: 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

3

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

4

Screening for the beta-amyloid precursor protein mutation (APP717: Val----Ile) in extended pedigrees with early onset Alzheimer's disease.

Chartier-Harlin MC, Crawford F, Hamandi K, Mullan M, Goate A, Hardy J, Backhovens H, Martin JJ, Broeckhoven CV. Chartier-Harlin MC, et al. Among authors: mullan m. Neurosci Lett. 1991 Aug 5;129(1):134-5. doi: 10.1016/0304-3940(91)90738-f. Neurosci Lett. 1991. PMID: 1922963

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

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

7

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

8

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

9

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.

10

Genetic linkage studies suggest that Alzheimer's disease is not a single homogeneous disorder.

St George-Hyslop PH, Haines JL, Farrer LA, Polinsky R, Van Broeckhoven C, Goate A, McLachlan DR, Orr H, Bruni AC, Sorbi S, Rainero I, Foncin JF, Pollen D, Cantu JM, Tupler R, Voskresenskaya N, Mayeux R, Growden J, Fried VA, Myers RH, Nee L, Backhovens H, Martin JJ, Rossor M, Owen MJ, Mullan M, Percy ME, Karlinsky H, Rich S, Heston L, Montesi M, Mortilla M, Nacmias N, Gusella JF, Hardy JA; FAD Collaborative Study Group, et al. St George-Hyslop PH, et al. Among authors: mullan m. Nature. 1990 Sep 13;347(6289):194-7. doi: 10.1038/347194a0. Nature. 1990. PMID: 2395471

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