Perez-Tur J - Search Results

1

The genetic and pathological classification of familial frontotemporal dementia.

Morris HR, Khan MN, Janssen JC, Brown JM, Perez-Tur J, Baker M, Ozansoy M, Hardy J, Hutton M, Wood NW, Lees AJ, Revesz T, Lantos P, Rossor MN. Morris HR, et al. Arch Neurol. 2001 Nov;58(11):1813-6. doi: 10.1001/archneur.58.11.1813. Arch Neurol. 2001. PMID: 11708988

2

Complete analysis of the presenilin 1 gene in early onset Alzheimer's disease.

Hutton M, Busfield F, Wragg M, Crook R, Perez-Tur J, Clark RF, Prihar G, Talbot C, Phillips H, Wright K, Baker M, Lendon C, Duff K, Martinez A, Houlden H, Nichols A, Karran E, Roberts G, Roques P, Rossor M, Venter JC, Adams MD, Cline RT, Phillips CA, Goate A, et al. Hutton M, et al. Neuroreport. 1996 Feb 29;7(3):801-5. doi: 10.1097/00001756-199602290-00029. Neuroreport. 1996. PMID: 8733749

3

A further presenilin 1 mutation in the exon 8 cluster in familial Alzheimer's disease.

Perez-Tur J, Croxton R, Wright K, Phillips H, Zehr C, Crook R, Hutton M, Hardy J, Karran E, Roberts GW, Lancaster S, Haltia T. Perez-Tur J, et al. Neurodegeneration. 1996 Sep;5(3):207-12. doi: 10.1006/neur.1996.0028. Neurodegeneration. 1996. PMID: 8910898

4

Early-onset Alzheimer's disease with a presenilin-1 mutation at the site corresponding to the Volga German presenilin-2 mutation.

Crook R, Ellis R, Shanks M, Thal LJ, Perez-Tur J, Baker M, Hutton M, Haltia T, Hardy J, Galasko D. Crook R, et al. Ann Neurol. 1997 Jul;42(1):124-8. doi: 10.1002/ana.410420121. Ann Neurol. 1997. PMID: 9225696

5

The role of presenilin 1 in the genetics of Alzheimer's disease.

Clark RF, Hutton M, Talbot C, Wragg M, Lendon C, Busfield F, Han SW, Perez-Tur J, Adams M, Fuldner R, Roberts G, Karran E, Hardy J, Goate A. Clark RF, et al. Cold Spring Harb Symp Quant Biol. 1996;61:551-8. Cold Spring Harb Symp Quant Biol. 1996. PMID: 9246481

6

Increased Abeta42(43) from cell lines expressing presenilin 1 mutations.

Mehta ND, Refolo LM, Eckman C, Sanders S, Yager D, Perez-Tur J, Younkin S, Duff K, Hardy J, Hutton M. Mehta ND, et al. Ann Neurol. 1998 Feb;43(2):256-8. doi: 10.1002/ana.410430217. Ann Neurol. 1998. PMID: 9485068

7

Low frequency of alpha-synuclein mutations in familial Parkinson's disease.

Farrer M, Wavrant-De Vrieze F, Crook R, Boles L, Perez-Tur J, Hardy J, Johnson WG, Steele J, Maraganore D, Gwinn K, Lynch T. Farrer M, et al. Ann Neurol. 1998 Mar;43(3):394-7. doi: 10.1002/ana.410430320. Ann Neurol. 1998. PMID: 9506559

8

A variant of Alzheimer's disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1.

Crook R, Verkkoniemi A, Perez-Tur J, Mehta N, Baker M, Houlden H, Farrer M, Hutton M, Lincoln S, Hardy J, Gwinn K, Somer M, Paetau A, Kalimo H, Ylikoski R, Pöyhönen M, Kucera S, Haltia M. Crook R, et al. Nat Med. 1998 Apr;4(4):452-5. doi: 10.1038/nm0498-452. Nat Med. 1998. PMID: 9546792

9

Cloning and characterization of the presenilin-2 gene promoter.

Pennypacker KR, Fuldner R, Xu R, Hernandez H, Dawbarn D, Mehta N, Perez-Tur J, Baker M, Hutton M. Pennypacker KR, et al. Brain Res Mol Brain Res. 1998 May;56(1-2):57-65. doi: 10.1016/s0169-328x(98)00028-x. Brain Res Mol Brain Res. 1998. PMID: 9602061

10

Exclusion of genetic linkage to 4q21-23 and 17q21 in a family with Lewy body parkinsonism.

Hardy J, Pérez-Tur J, Baker M, Farrer M, Crook R, Hutton M, Johnson WG, Gwinn K, Muenter M, Rocca WA, Maraganore D. Hardy J, et al. Am J Med Genet. 1998 Mar 28;81(2):166-71. Am J Med Genet. 1998. PMID: 9613857

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