Pastor P - Search Results

1

5'-Upstream variants of CRHR1 and MAPT genes associated with age at onset in progressive supranuclear palsy and cortical basal degeneration.

Cruchaga C, Vidal-Taboada JM, Ezquerra M, Lorenzo E, Martinez-Lage P, Blazquez M, Tolosa E; Iberian Atypical Parkinsonism Study Group Researchers; Pastor P. Cruchaga C, et al. Among authors: pastor p. Neurobiol Dis. 2009 Feb;33(2):164-70. doi: 10.1016/j.nbd.2008.09.027. Epub 2008 Nov 1. Neurobiol Dis. 2009. PMID: 19022385

2

Alpha1-antichymotrypsin gene polymorphism and susceptibility to Parkinson's disease.

Muñoz E, Obach V, Oliva R, Martí MJ, Ezquerra M, Pastor P, Ballesta F, Tolosa E. Muñoz E, et al. Among authors: pastor p. Neurology. 1999 Jan 15;52(2):297-301. doi: 10.1212/wnl.52.2.297. Neurology. 1999. PMID: 9932947

3

Dopamine receptor D2 intronic polymorphism in patients with Parkinson's disease.

Pastor P, Muñoz E, Obach V, Martí MJ, Blesa R, Oliva R, Tolosa E. Pastor P, et al. Neurosci Lett. 1999 Oct 8;273(3):151-4. doi: 10.1016/s0304-3940(99)00633-3. Neurosci Lett. 1999. PMID: 10515181

4

Identification of a novel polymorphism in the promoter region of the tau gene highly associated to progressive supranuclear palsy in humans.

Ezquerra M, Pastor P, Valldeoriola F, Molinuevo JL, Blesa R, Tolosa E, Oliva R. Ezquerra M, et al. Among authors: pastor p. Neurosci Lett. 1999 Nov 19;275(3):183-6. doi: 10.1016/s0304-3940(99)00738-7. Neurosci Lett. 1999. PMID: 10580705

5

Significant association between the tau gene A0/A0 genotype and Parkinson's disease.

Pastor P, Ezquerra M, Muñoz E, Martí MJ, Blesa R, Tolosa E, Oliva R. Pastor P, et al. Ann Neurol. 2000 Feb;47(2):242-5. Ann Neurol. 2000. PMID: 10665497

6

A new mutation in the parkin gene in a patient with atypical autosomal recessive juvenile parkinsonism.

Muñoz E, Pastor P, Martí MJ, Oliva R, Tolosa E. Muñoz E, et al. Among authors: pastor p. Neurosci Lett. 2000 Jul 28;289(1):66-8. doi: 10.1016/s0304-3940(00)01248-9. Neurosci Lett. 2000. PMID: 10899410

7

Familial atypical progressive supranuclear palsy associated with homozigosity for the delN296 mutation in the tau gene.

Pastor P, Pastor E, Carnero C, Vela R, García T, Amer G, Tolosa E, Oliva R. Pastor P, et al. Among authors: pastor e. Ann Neurol. 2001 Feb;49(2):263-7. doi: 10.1002/1531-8249(20010201)49:2<263::aid-ana50>3.0.co;2-k. Ann Neurol. 2001. PMID: 11220749

8

Analysis of the coding and the 5' flanking regions of the alpha-synuclein gene in patients with Parkinson's disease.

Pastor P, Muñoz E, Ezquerra M, Obach V, Martí MJ, Valldeoriola F, Tolosa E, Oliva R. Pastor P, et al. Mov Disord. 2001 Nov;16(6):1115-9. doi: 10.1002/mds.1198. Mov Disord. 2001. PMID: 11748744

9

Further extension of the H1 haplotype associated with progressive supranuclear palsy.

Pastor P, Ezquerra M, Tolosa E, Muñoz E, Martí MJ, Valldeoriola F, Molinuevo JL, Calopa M, Oliva R. Pastor P, et al. Mov Disord. 2002 May;17(3):550-6. doi: 10.1002/mds.10076. Mov Disord. 2002. PMID: 12112206

10

Progressive supranuclear palsy: clinical and genetic aspects.

Pastor P, Tolosa E. Pastor P, et al. Curr Opin Neurol. 2002 Aug;15(4):429-37. doi: 10.1097/00019052-200208000-00005. Curr Opin Neurol. 2002. PMID: 12151839 Review.

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