Ezquerra M - Search Results

1

A novel MAPT mutation (P301T) associated with familial frontotemporal dementia.

Lladó A, Ezquerra M, Sánchez-Valle R, Rami L, Tolosa E, Molinuevo JL. Lladó A, et al. Among authors: ezquerra m. Eur J Neurol. 2007 Aug;14(8):e9-10. doi: 10.1111/j.1468-1331.2007.01763.x. Eur J Neurol. 2007. PMID: 17662000 No abstract available.

2

Alpha-antichymotrypsin gene polymorphism and risk for Alzheimer's disease in the Spanish population.

Ezquerra M, Blesa R, Tolosa E, Ballesta F, Oliva R. Ezquerra M, et al. Neurosci Lett. 1998 Jan 9;240(2):107-9. doi: 10.1016/s0304-3940(97)00924-5. Neurosci Lett. 1998. PMID: 9486483

3

Significant changes in the tau A0 and A3 alleles in progressive supranuclear palsy and improved genotyping by silver detection.

Oliva R, Tolosa E, Ezquerra M, Molinuevo JL, Valldeoriola F, Burguera J, Calopa M, Villa M, Ballesta F. Oliva R, et al. Among authors: ezquerra m. Arch Neurol. 1998 Aug;55(8):1122-4. doi: 10.1001/archneur.55.8.1122. Arch Neurol. 1998. PMID: 9708963

4

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: ezquerra m. Neurology. 1999 Jan 15;52(2):297-301. doi: 10.1212/wnl.52.2.297. Neurology. 1999. PMID: 9932947

5

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. Neurosci Lett. 1999 Nov 19;275(3):183-6. doi: 10.1016/s0304-3940(99)00738-7. Neurosci Lett. 1999. PMID: 10580705

6

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. Among authors: ezquerra m. Ann Neurol. 2000 Feb;47(2):242-5. Ann Neurol. 2000. PMID: 10665497

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. Among authors: ezquerra m. 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. Among authors: ezquerra m. Mov Disord. 2002 May;17(3):550-6. doi: 10.1002/mds.10076. Mov Disord. 2002. PMID: 12112206

9

Frequency of mutations in the presenilin and amyloid precursor protein genes in early-onset Alzheimer disease in Spain.

Lleó A, Blesa R, Queralt R, Ezquerra M, Molinuevo JL, Peña-Casanova J, Rojo A, Oliva R. Lleó A, et al. Among authors: ezquerra m. Arch Neurol. 2002 Nov;59(11):1759-63. doi: 10.1001/archneur.59.11.1759. Arch Neurol. 2002. PMID: 12433263

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. Arch Neurol. 2003 Aug;60(8):1149-51. doi: 10.1001/archneur.60.8.1149. Arch Neurol. 2003. PMID: 12925374

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