Menéndez M - Search Results

1

Analysis of the Micro-RNA-133 and PITX3 genes in Parkinson's disease.

de Mena L, Coto E, Cardo LF, Díaz M, Blázquez M, Ribacoba R, Salvador C, Pastor P, Samaranch L, Moris G, Menéndez M, Corao AI, Alvarez V. de Mena L, et al. Among authors: menendez m. Am J Med Genet B Neuropsychiatr Genet. 2010 Sep;153B(6):1234-9. doi: 10.1002/ajmg.b.31086. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 20468068

2

Amyloid precursor protein gene (APP) variation in late-onset Alzheimer's disease.

Miar A, Alvarez V, Corao AI, Díaz M, Alonso B, Martínez C, Calatayud MT, Menéndez M, Morís G, Coto E. Miar A, et al. Among authors: menendez m. J Mol Neurosci. 2011 Sep;45(1):5-9. doi: 10.1007/s12031-011-9510-x. Epub 2011 Mar 22. J Mol Neurosci. 2011. PMID: 21424791

3

A search for SNCA 3' UTR variants identified SNP rs356165 as a determinant of disease risk and onset age in Parkinson's disease.

Cardo LF, Coto E, de Mena L, Ribacoba R, Lorenzo-Betancor O, Pastor P, Samaranch L, Mata IF, Díaz M, Moris G, Menéndez M, Corao AI, Alvarez V. Cardo LF, et al. Among authors: menendez m. J Mol Neurosci. 2012 Jul;47(3):425-30. doi: 10.1007/s12031-011-9669-1. Epub 2011 Nov 11. J Mol Neurosci. 2012. PMID: 22076805

4

Mutational screening of PARKIN identified a 3' UTR variant (rs62637702) associated with Parkinson's disease.

de Mena L, Samaranch LL, Coto E, Cardo LF, Ribacoba R, Lorenzo-Betancor O, Pastor P, Wang L, Irigoyen J, Mata IF, Díaz M, Moris G, Menéndez M, Corao AI, Lorenzo E, Alvarez V. de Mena L, et al. Among authors: menendez m. J Mol Neurosci. 2013 Jun;50(2):264-9. doi: 10.1007/s12031-012-9942-y. Epub 2012 Dec 30. J Mol Neurosci. 2013. PMID: 23275044

5

Alpha-synuclein transcript isoforms in three different brain regions from Parkinson's disease and healthy subjects in relation to the SNCA rs356165/rs11931074 polymorphisms.

Cardo LF, Coto E, de Mena L, Ribacoba R, Mata IF, Menéndez M, Moris G, Alvarez V. Cardo LF, et al. Among authors: menendez m. Neurosci Lett. 2014 Mar 6;562:45-9. doi: 10.1016/j.neulet.2014.01.009. Epub 2014 Jan 10. Neurosci Lett. 2014. PMID: 24418406

6

The screening of the 3'UTR sequence of LRRK2 identified an association between the rs66737902 polymorphism and Parkinson's disease.

Cardo LF, Coto E, Ribacoba R, Mata IF, Moris G, Menéndez M, Alvarez V. Cardo LF, et al. Among authors: menendez m. J Hum Genet. 2014 Jun;59(6):346-8. doi: 10.1038/jhg.2014.26. Epub 2014 Apr 24. J Hum Genet. 2014. PMID: 24758914

7

MiRNA profile in the substantia nigra of Parkinson's disease and healthy subjects.

Cardo LF, Coto E, Ribacoba R, Menéndez M, Moris G, Suárez E, Alvarez V. Cardo LF, et al. Among authors: menendez m. J Mol Neurosci. 2014 Dec;54(4):830-6. doi: 10.1007/s12031-014-0428-y. Epub 2014 Oct 5. J Mol Neurosci. 2014. PMID: 25284245

8

Myocyte enhancing factor-2A in Alzheimer's disease: genetic analysis and association with MEF2A-polymorphisms.

González P, Alvarez V, Menéndez M, Lahoz CH, Martínez C, Corao AI, Calatayud MT, Peña J, García-Castro M, Coto E. González P, et al. Among authors: menendez m. Neurosci Lett. 2007 Jan 3;411(1):47-51. doi: 10.1016/j.neulet.2006.09.055. Epub 2006 Nov 16. Neurosci Lett. 2007. PMID: 17112666

9

FGF20 rs12720208 SNP and microRNA-433 variation: no association with Parkinson's disease in Spanish patients.

de Mena L, Cardo LF, Coto E, Miar A, Díaz M, Corao AI, Alonso B, Ribacoba R, Salvador C, Menéndez M, Morís G, Alvarez V. de Mena L, et al. Among authors: menendez m. Neurosci Lett. 2010 Jul 19;479(1):22-5. doi: 10.1016/j.neulet.2010.05.019. Epub 2010 May 13. Neurosci Lett. 2010. PMID: 20471450

10

SPG7 mutational screening in spastic paraplegia patients supports a dominant effect for some mutations and a pathogenic role for p.A510V.

Sánchez-Ferrero E, Coto E, Beetz C, Gámez J, Corao AI, Díaz M, Esteban J, del Castillo E, Moris G, Infante J, Menéndez M, Pascual-Pascual SI, López de Munaín A, Garcia-Barcina MJ, Alvarez V; Genetics of Spastic Paraplegia study group. Sánchez-Ferrero E, et al. Among authors: menendez m. Clin Genet. 2013 Mar;83(3):257-62. doi: 10.1111/j.1399-0004.2012.01896.x. Epub 2012 May 21. Clin Genet. 2013. PMID: 22571692

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