Ezquerra M - 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: ezquerra m. 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

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

3

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

4

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

5

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

6

A novel intronic mutation in the DDP1 gene in a family with X-linked dystonia-deafness syndrome.

Ezquerra M, Campdelacreu J, Muñoz E, Tolosa E, Martí MJ. Ezquerra M, et al. Arch Neurol. 2005 Feb;62(2):306-8. doi: 10.1001/archneur.62.2.306. Arch Neurol. 2005. PMID: 15710860

7

LRRK2 mutations in Spanish patients with Parkinson disease: frequency, clinical features, and incomplete penetrance.

Gaig C, Ezquerra M, Marti MJ, Muñoz E, Valldeoriola F, Tolosa E. Gaig C, et al. Among authors: ezquerra m. Arch Neurol. 2006 Mar;63(3):377-82. doi: 10.1001/archneur.63.3.377. Arch Neurol. 2006. PMID: 16533964

8

No evidence of CRHR1 gene involvement in progressive supranuclear palsy.

Campdelacreu J, Gaig C, Ezquerra M, Muñoz E, Martí MJ, Valldeoriola F, Tolosa E. Campdelacreu J, et al. Among authors: ezquerra m. Neurosci Lett. 2006 Nov 27;409(1):61-4. doi: 10.1016/j.neulet.2006.09.017. Epub 2006 Sep 28. Neurosci Lett. 2006. PMID: 17010515

9

G2019S LRRK2 mutation causing Parkinson's disease without Lewy bodies.

Gaig C, Martí MJ, Ezquerra M, Rey MJ, Cardozo A, Tolosa E. Gaig C, et al. Among authors: ezquerra m. J Neurol Neurosurg Psychiatry. 2007 Jun;78(6):626-8. doi: 10.1136/jnnp.2006.107904. Epub 2007 Jan 8. J Neurol Neurosurg Psychiatry. 2007. PMID: 17210620 Free PMC article.

10

Screening for the LRRK2 G2019S and codon-1441 mutations in a pathological series of parkinsonian syndromes and frontotemporal lobar degeneration.

Gaig C, Ezquerra M, Martí MJ, Valldeoriola F, Muñoz E, Lladó A, Rey MJ, Cardozo A, Molinuevo JL, Tolosa E. Gaig C, et al. Among authors: ezquerra m. J Neurol Sci. 2008 Jul 15;270(1-2):94-8. doi: 10.1016/j.jns.2008.02.010. Epub 2008 Mar 19. J Neurol Sci. 2008. PMID: 18353371

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