Pastor P - Search Results

1

TREM2 R47H variant and risk of essential tremor: a cross-sectional international multicenter study.

Ortega-Cubero S, Lorenzo-Betancor O, Lorenzo E, Agúndez JA, Jiménez-Jiménez FJ, Ross OA, Wurster I, Mielke C, Lin JJ, Coria F, Clarimon J, Ezquerra M, Brighina L, Annesi G, Alonso-Navarro H, García-Martin E, Gironell A, Marti MJ, Yueh KC, Wszolek ZK, Sharma M, Berg D, Krüger R, Pastor MA, Pastor P. Ortega-Cubero S, et al. Among authors: pastor p, pastor ma. Parkinsonism Relat Disord. 2015 Mar;21(3):306-9. doi: 10.1016/j.parkreldis.2014.12.010. Epub 2014 Dec 24. Parkinsonism Relat Disord. 2015. PMID: 25585992 Free PMC article.

2

Identification of Spanish familial Parkinson's disease and screening for the Ala53Thr mutation of the alpha-synuclein gene in early onset patients.

Muñoz E, Oliva R, Obach V, Martí MJ, Pastor P, Ballesta F, Tolosa E. Muñoz E, et al. Among authors: pastor p. Neurosci Lett. 1997 Oct 10;235(1-2):57-60. doi: 10.1016/s0304-3940(97)00710-6. Neurosci Lett. 1997. PMID: 9389595

3

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

4

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

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

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

8

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

9

Relative high frequency of the c.255delA parkin gene mutation in Spanish patients with autosomal recessive parkinsonism.

Muñoz E, Tolosa E, Pastor P, Martí MJ, Valldeoriola F, Campdelacreu J, Oliva R. Muñoz E, et al. Among authors: pastor p. J Neurol Neurosurg Psychiatry. 2002 Nov;73(5):582-4. doi: 10.1136/jnnp.73.5.582. J Neurol Neurosurg Psychiatry. 2002. PMID: 12397156 Free PMC article.

10

A novel mutation in the PSEN2 gene (T430M) associated with variable expression in a family with early-onset Alzheimer disease.

Ezquerra M, Lleó A, Castellví M, Queralt R, Santacruz P, Pastor P, Molinuevo JL, Blesa R, Oliva R. Ezquerra M, et al. Among authors: pastor p. Arch Neurol. 2003 Aug;60(8):1149-51. doi: 10.1001/archneur.60.8.1149. Arch Neurol. 2003. PMID: 12925374

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