Browsing by author "Alonso Montes, Cristina"

Bicuspid aortic valve syndrome: A heterogeneous and still unknown condition

Martín Fernández, María

; Alonso Montes, Cristina

; Flórez Muñoz, Juan Pablo; Álvarez Pichel, Irene; Rozado Castaño, José; Cannata Andía, Jorge Benito

; Morís de la Tassa, César

; Rodríguez Fernández, Isabel

(Elsevier Ireland Ltd, 2014)

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

Carrillo López, Natalia

; Panizo García, Sara; Alonso Montes, Cristina

; Román García, Pablo

; Rodríguez Fernández, Isabel

; Martínez Salgado, Carlos; Dusso, Adriana S.; Naves Díaz, Manuel Luis; Cannata Andía, Jorge Benito

(2016)

Factores de transcripción mitocondriales y cardiacos en la miocardiopatía hipertrófica

Alonso Montes, Cristina

(Universidad de Oviedo, 2012-12-21)

High-serum phosphate and parathyroid hormone distinctly regulate bone loss and vascular calcification in experimental chronic kidney disease

Carrillo López, Natalia

; Panizo García, Sara; Alonso Montes, Cristina

; Martínez Arias, Laura; Avello Llano, Noelia

; Sosa, Patricia; Dusso, Adriana S.; Cannata Andía, Jorge Benito

; Naves Díaz, Luis Manuel (2019)

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

Quirós González, Isabel

; Román García, Pablo

; Alonso Montes, Cristina

; Barrio Vázquez, Sara

; Carrillo López, Natalia

; Naves Díaz, Manuel Luis; Mora, M. I.; Corrales, F. J.; López Hernández, Francisco José; Ruiz Torres, María Piedad; Cannata Andía, Jorge Benito

; Fernández Martín, José Luis (Elsevier, 2016)

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

Álvarez Martínez, María Victoria

; Corao Trueba, Ana Isabel

; Alonso Montes, Cristina

; Sánchez Ferrero, Elena

; Mena Álvarez, Lorena de

; Morales Cañabete, Blanca

; García Castro, Mónica

; Coto García, Eliecer

(2008)

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

Álvarez Martínez, María Victoria

; Corao Trueba, Ana Isabel

; Sánchez Ferrero, Elena

; Mena Álvarez, Lorena de

; Alonso Montes, Cristina

; Huerta Arias, Cecilia

; Blázquez Estrada, Marta

; Ribacoba Montero, Renée

; Menéndez Guisasola, Luis María

; Salvador Aguiar, Carlos

; García Castro, Mónica

; Coto García, Eliecer

(2008)

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

Alonso Montes, Cristina

; García Castro, Mónica

; Rodríguez Reguero, José Julián

; Perrot, A.; Özcelik, C.; Geier, C.; Posch, M. G.; Morís de la Tassa, César

; Álvarez Antuña, Víctor Manuel

; Ruiz Ortega, Marta; Coto García, Eliecer

(IOS Press, 2008)

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

Coto García, Eliecer

; García Castro, Mónica

; Corao Trueba, Ana Isabel

; Alonso Montes, Cristina

; Rodríguez Reguero, José Julián

; Morís de la Tassa, César

; Álvarez Martínez, María Victoria

(2009)

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

Alonso Montes, Cristina

; Naves Díaz, Manuel Luis; Fernández Martín, José Luis; Rodríguez Reguero, José Julián

; Morís de la Tassa, César

; Coto García, Eliecer

; Cannata Andía, Jorge Benito

; Rodríguez Fernández, Isabel

(2012)

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

García Castro, Mónica

; Rodríguez Reguero, José Julián

; Morís de la Tassa, César

; Alonso Montes, Cristina

; Berrazueta Fernández, José Ramón de; Sainz, Rocío; Álvarez Martínez, María Victoria

; Coto García, Eliecer

(Elsevier, 2007)

Rare genetic variants in GATA transcription factors in patients with hypertrophic cardiomyopathy

Alonso Montes, Cristina

; Rodríguez Reguero, José Julián

; Martín Luengo, M. A.; Gómez de Oña, Juan

; Coto García, Eliecer

; Naves Díaz, Manuel Luis; Morís de la Tassa, César

; Cannata Andía, Jorge Benito

; Rodríguez Fernández, Isabel

(2017)

Regeneration of mandibular defects using adipose tissue mesenchymal stromal cells in combination with human serum-derived scaffolds

Peña González, Ignacio

; Álvarez Viejo, María

; Alonso Montes, Cristina

; Menéndez Menéndez, Yolanda; Gutiérrez Álvarez, Fernando; de Vicente, Juan C.

; Otero Hernández, Jesús; Meana Infiesta, Álvaro Enrique

(Churchill Livingstone, 2016)

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

Castro, M. G.; Rodríguez-Pascual, F.; Magán-Marchal, N.; Rodríguez Reguero, José Julián

; Alonso Montes, Cristina

; Morís de la Tassa, César

; Álvarez Martínez, María Victoria

; Lamas, S.; Coto García, Eliecer

(2007)

Variants in cardiac GATA genes associated with bicuspid aortic valve

Alonso Montes, Cristina

; Martín Luengo, M. A.; Martínez Arias, Laura; Coto García, Eliecer

; Naves Díaz, Manuel Luis; Morís de la Tassa, César

; Cannata Andía, Jorge Benito

; Rodríguez Fernández, Isabel

(2018)

Browsing by author "Alonso Montes, Cristina"

Bicuspid aortic valve syndrome: A heterogeneous and still unknown condition ﻿

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

Factores de transcripción mitocondriales y cardiacos en la miocardiopatía hipertrófica ﻿

High-serum phosphate and parathyroid hormone distinctly regulate bone loss and vascular calcification in experimental chronic kidney disease ﻿

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

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

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

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

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

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

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

Rare genetic variants in GATA transcription factors in patients with hypertrophic cardiomyopathy ﻿

Regeneration of mandibular defects using adipose tissue mesenchymal stromal cells in combination with human serum-derived scaffolds ﻿

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

Variants in cardiac GATA genes associated with bicuspid aortic valve ﻿

Bicuspid aortic valve syndrome: A heterogeneous and still unknown condition

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

Factores de transcripción mitocondriales y cardiacos en la miocardiopatía hipertrófica

High-serum phosphate and parathyroid hormone distinctly regulate bone loss and vascular calcification in experimental chronic kidney disease

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

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

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

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

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

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

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

Rare genetic variants in GATA transcription factors in patients with hypertrophic cardiomyopathy

Regeneration of mandibular defects using adipose tissue mesenchymal stromal cells in combination with human serum-derived scaffolds

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

Variants in cardiac GATA genes associated with bicuspid aortic valve