Baker M - Search Results

1

A family with a tau P301L mutation presenting with parkinsonism.

Walker RH, Friedman J, Wiener J, Hobler R, Gwinn-Hardy K, Adam A, DeWolfe J, Gibbs R, Baker M, Farrer M, Hutton M, Hardy J. Walker RH, et al. Among authors: baker m. Parkinsonism Relat Disord. 2002 Dec;9(2):121-3. doi: 10.1016/s1353-8020(02)00003-2. Parkinsonism Relat Disord. 2002. PMID: 12473404

2

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. Among authors: baker m. Ann Neurol. 1997 Jul;42(1):124-8. doi: 10.1002/ana.410420121. Ann Neurol. 1997. PMID: 9225696

3

Localization of frontotemporal dementia with parkinsonism in an Australian kindred to chromosome 17q21-22.

Baker M, Kwok JB, Kucera S, Crook R, Farrer M, Houlden H, Isaacs A, Lincoln S, Onstead L, Hardy J, Wittenberg L, Dodd P, Webb S, Hayward N, Tannenberg T, Andreadis A, Hallupp M, Schofield P, Dark F, Hutton M. Baker M, et al. Ann Neurol. 1997 Nov;42(5):794-8. doi: 10.1002/ana.410420516. Ann Neurol. 1997. PMID: 9392579

4

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. Among authors: baker m. Nat Med. 1998 Apr;4(4):452-5. doi: 10.1038/nm0498-452. Nat Med. 1998. PMID: 9546792

5

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. Among authors: baker m. Am J Med Genet. 1998 Mar 28;81(2):166-71. Am J Med Genet. 1998. PMID: 9613857

6

Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17.

Hutton M, Lendon CL, Rizzu P, Baker M, Froelich S, Houlden H, Pickering-Brown S, Chakraverty S, Isaacs A, Grover A, Hackett J, Adamson J, Lincoln S, Dickson D, Davies P, Petersen RC, Stevens M, de Graaff E, Wauters E, van Baren J, Hillebrand M, Joosse M, Kwon JM, Nowotny P, Che LK, Norton J, Morris JC, Reed LA, Trojanowski J, Basun H, Lannfelt L, Neystat M, Fahn S, Dark F, Tannenberg T, Dodd PR, Hayward N, Kwok JB, Schofield PR, Andreadis A, Snowden J, Craufurd D, Neary D, Owen F, Oostra BA, Hardy J, Goate A, van Swieten J, Mann D, Lynch T, Heutink P. Hutton M, et al. Among authors: baker m. Nature. 1998 Jun 18;393(6686):702-5. doi: 10.1038/31508. Nature. 1998. PMID: 9641683

7

Determination of the gene structure of human GFAP and absence of coding region mutations associated with frontotemporal dementia with parkinsonism linked to chromosome 17.

Isaacs A, Baker M, Wavrant-De Vrièze F, Hutton M. Isaacs A, et al. Among authors: baker m. Genomics. 1998 Jul 1;51(1):152-4. doi: 10.1006/geno.1998.5360. Genomics. 1998. PMID: 9693047 No abstract available.

8

No pathogenic mutations in the persyn gene in Parkinson's disease.

Lincoln S, Gwinn-Hardy K, Goudreau J, Chartier-Harlin MC, Baker M, Mouroux V, Richard F, Destée A, Becquet E, Amouyel P, Lynch T, Hardy J, Farrer M. Lincoln S, et al. Among authors: baker m. Neurosci Lett. 1999 Jan 4;259(1):65-6. doi: 10.1016/s0304-3940(98)00901-x. Neurosci Lett. 1999. PMID: 10027558

9

Association of an extended haplotype in the tau gene with progressive supranuclear palsy.

Baker M, Litvan I, Houlden H, Adamson J, Dickson D, Perez-Tur J, Hardy J, Lynch T, Bigio E, Hutton M. Baker M, et al. Hum Mol Genet. 1999 Apr;8(4):711-5. doi: 10.1093/hmg/8.4.711. Hum Mol Genet. 1999. PMID: 10072441

10

Low frequency of pathogenic mutations in the ubiquitin carboxy-terminal hydrolase gene in familial Parkinson's disease.

Lincoln S, Vaughan J, Wood N, Baker M, Adamson J, Gwinn-Hardy K, Lynch T, Hardy J, Farrer M. Lincoln S, et al. Among authors: baker m. Neuroreport. 1999 Feb 5;10(2):427-9. doi: 10.1097/00001756-199902050-00040. Neuroreport. 1999. PMID: 10203348

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