Alonso-Montes C - Search Results

1

New polymorphisms in human MEF2C gene as potential modifier of hypertrophic cardiomyopathy.

Alonso-Montes C, Naves-Diaz M, Fernandez-Martin JL, Rodriguez-Reguero J, Moris C, Coto E, Cannata-Andia JB, Rodriguez I. Alonso-Montes C, et al. Mol Biol Rep. 2012 Sep;39(9):8777-85. doi: 10.1007/s11033-012-1740-7. Epub 2012 Jun 21. Mol Biol Rep. 2012. PMID: 22718505

2

Prevalence and spectrum of mutations in the sarcomeric troponin T and I genes in a cohort of Spanish cardiac hypertrophy patients.

García-Castro M, Reguero JR, Morís C, Alonso-Montes C, Berrazueta JR, Sainz R, Alvarez V, Coto E. García-Castro M, et al. Int J Cardiol. 2007 Sep 14;121(1):115-6. doi: 10.1016/j.ijcard.2006.08.049. Epub 2006 Nov 13. Int J Cardiol. 2007. PMID: 17101185

3

Screening of the endothelin1 gene (EDN1) in a cohort of patients with essential left ventricular hypertrophy.

Castro MG, Rodríguez-Pascual F, Magán-Marchal N, Reguero JR, Alonso-Montes C, Morís C, Alvarez V, Lamas S, Coto E. Castro MG, et al. Ann Hum Genet. 2007 Sep;71(Pt 5):601-10. doi: 10.1111/j.1469-1809.2007.00351.x. Epub 2007 Mar 2. Ann Hum Genet. 2007. PMID: 17335511

4

Mitochondrial transcription factor A (TFAM) gene variation in Parkinson's disease.

Alvarez V, Corao AI, Sánchez-Ferrero E, De Mena L, Alonso-Montes C, Huerta C, Blázquez M, Ribacoba R, Guisasola LM, Salvador C, García-Castro M, Coto E. Alvarez V, et al. Neurosci Lett. 2008 Feb 13;432(1):79-82. doi: 10.1016/j.neulet.2007.12.010. Epub 2007 Dec 15. Neurosci Lett. 2008. PMID: 18248889

5

Mitochondrial transcription factor A (TFAM) gene variation and risk of late-onset Alzheimer's disease.

Alvarez V, Corao AI, Alonso-Montes C, Sánchez-Ferrero E, De Mena L, Morales B, García-Castro M, Coto E. Alvarez V, et al. J Alzheimers Dis. 2008 Apr;13(3):275-80. doi: 10.3233/jad-2008-13305. J Alzheimers Dis. 2008. PMID: 18430995

6

Mitochondrial transcription factors TFA, TFB1 and TFB2: a search for DNA variants/haplotypes and the risk of cardiac hypertrophy.

Alonso-Montes C, Castro MG, Reguero JR, Perrot A, Ozcelik C, Geier C, Posch MG, Morís C, Alvarez V, Ruiz-Ortega M, Coto E. Alonso-Montes C, et al. Dis Markers. 2008;25(3):131-9. doi: 10.1155/2008/575323. Dis Markers. 2008. PMID: 19096125 Free PMC article.

7

Mutation analysis of the myocyte enhancer factor 2A gene (MEF2A) in patients with left ventricular hypertrophy/hypertrophic cardiomyopathy.

Coto E, Castro MG, Corao AI, Alonso-Montes C, Reguero JR, Morís C, Alvarez V. Coto E, et al. Am J Med Genet A. 2009 Feb;149A(2):286-9. doi: 10.1002/ajmg.a.32621. Am J Med Genet A. 2009. PMID: 19161138 No abstract available.

8

Bicuspid aortic valve syndrome: a heterogeneous and still unknown condition.

Martín M, Alonso-Montes C, Flórez JP, Pichel IA, Rozado J, Andía JB, Morís C, Rodríguez I. Martín M, et al. Int J Cardiol. 2014 Dec 20;177(3):1105. doi: 10.1016/j.ijcard.2014.09.132. Epub 2014 Oct 2. Int J Cardiol. 2014. PMID: 25449525 No abstract available.

9

Lamin A is involved in the development of vascular calcification induced by chronic kidney failure and phosphorus load.

Quirós-González I, Román-García P, Alonso-Montes C, Barrio-Vázquez S, Carrillo-López N, Naves-Díaz M, Mora MI, Corrales FJ, López-Hernández FJ, Ruiz-Torres MP, Cannata-Andía JB, Fernández-Martín JL. Quirós-González I, et al. Bone. 2016 Mar;84:160-168. doi: 10.1016/j.bone.2016.01.005. Epub 2016 Jan 6. Bone. 2016. PMID: 26769003

10

Direct inhibition of osteoblastic Wnt pathway by fibroblast growth factor 23 contributes to bone loss in chronic kidney disease.

Carrillo-López N, Panizo S, Alonso-Montes C, Román-García P, Rodríguez I, Martínez-Salgado C, Dusso AS, Naves M, Cannata-Andía JB. Carrillo-López N, et al. Kidney Int. 2016 Jul;90(1):77-89. doi: 10.1016/j.kint.2016.01.024. Epub 2016 Mar 24. Kidney Int. 2016. PMID: 27165819 Free article.

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