Listar por autor "Rodríguez Reguero, José Julián"

Aldosterone levels and cardiac hypertrophy in professional cyclists

Iglesias Cubero, Gustavo

; Rodríguez Reguero, José Julián

; Terrados Cepeda, Nicolás

; González, V.; Barriales Villa, Roberto

; Cortina Llosa, Arturo Agustín

(Georg Thieme Verlag, 1995)

Association of the genetic variation in the long non‐coding RNA FENDRR with the risk of developing hypertrophic cardiomyopathy

Cuesta Llavona, Elías; Lorca, R.; Rolle, V.; Alonso, B.; Iglesias, S.; Rodríguez Reguero, José Julián

; Duarte Herrera, I. D.; Pérez Oliveira, S.; Junco Vicente, Alejandro; García Lago, Claudia; Coto García, Eliecer

; Gómez de Oña, Juan

(2022)

Causas, substrato anatómico y evolución clínica de la enfermedad coronaria precoz

Batalla Celorio, Luis Alberto (1999)

Characterization of left ventricular non-compaction cardiomyopathy

Lorca Gutiérrez, Rebeca

; Martín Fernández, María

; Pascual Calleja, Isaac

; Astudillo González, María Aurora

; Díaz Molina, Beatriz

; Cigarrán, Helena; Cuesta Llavona, Elías; Avanzas Fernández, Pablo

; Rodríguez Reguero, José Julián

; Coto García, Eliecer

; Morís de la Tassa, César

; Gómez de Oña, Juan

(2020)

Compound heterozygosity for PTPN11 variants in a subject with Noonan syndrome provides insights into the mechanism of SHP2-related disorders

Lorca Gutiérrez, Rebeca

; Pannone, L.; Cuesta Llavona, Elías; Bocchinfuso, G.; Rodríguez Reguero, José Julián

; Carpentieri, G.; Hernando, Inés; Flex, E.; Tartaglia, M.; Coto García, Eliecer

; Gómez, Juan; Martinelli, S. (2021)

Correlación fenotipo/genotipo en la miocardiopatía hipertrófica y miocardiopatía no compactada

Lorca Gutiérrez, Rebeca

(2018-01-12)

Different phenotypes in monozygotic twins, carriers of the same pathogenic variant for hypertrophic cardiomyopathy

Rodríguez Junquera, Manuel; Salgado, María; González Urbistondo, Francisco; Alen, Alberto; Rodríguez Reguero, José Julián

; Silva, Iria; Coto García, Eliecer

; Avanzas Fernández, Pablo

; Morís de la Tassa, César

; Gómez de Oña, Juan

; Lorca Gutiérrez, Rebeca

(2022)

Differential methylation of lncRNA KCNQ1OT1 promoter polymorphism was associated with symptomatic cardiac long QT

Coto García, Eliecer

; Calvo Temprano, David

; Rodríguez Reguero, José Julián

; Morís de la Tassa, César

; Rubín López, José Manuel

; Díaz Corte, María del Carmen

; Gil Peña, Helena

; Alonso González, Belén

; Iglesias, Sara; Gómez de Oña, Juan

(2017)

Distal renal tubular acidosis. Clinical manifestations in patients with different underlying gene mutations

Alonso Varela, Marta; Gil Peña, Helena

; Coto García, Eliecer

; Gómez de Oña, Juan

; Rodríguez Reguero, José Julián

; Rodríguez-Rubio, Enrique; Santos Rodríguez, Fernando

(2018)

ECG as a part of the preparticipation screening programme: an old and still present international dilemma

Carro Hevia, Amelia

; Fernández, M. M.; Palacio, J. M. A.; Martin, E. H.; Castro, M. G.; Rodríguez Reguero, José Julián

(2011)

Efectos del consumo crónico de tabaco y alcohol sobre lípidos plasmáticos, parámetros cardiovasculares y alpha 1-antitripsina, en una población minera joven

Rodríguez Reguero, José Julián

(1988)

Entendimiento de la miocardiopatía hipertrófica mediante el estudio de una variante patogénica fundadora

Lorca Gutiérrez, Rebeca

; Gómez de Oña, Juan

; Martín, María; Cabanillas Farpón, Rubén

; Calvo Blanco, Juan

; León, Víctor; Pascual Calleja, Isaac

; Morís de la Tassa, César

; Coto García, Eliecer

; Rodríguez Reguero, José Julián

(2019)

Evolución clínica de la enfermedad coronaria precoz. Prevención secundaria y bases genéticas

Martín Fernández, María

(2005-09-09)

Functional polymorphisms in genes of the Angiotensin and Serotonin systems and risk of hypertrophic cardiomyopathy: AT1R as a potential modifier

Coto García, Eliecer

; Palacín Fernández, María

; Martín Fernández, María

; García Castro, Mónica

; Rodríguez Reguero, José Julián

; García Fernández, Cristina; Berrazueta Fernández, José Ramón de; Morís de la Tassa, César

; Morales Cañabete, Blanca

; Ortega Suárez, Francisco José

; Corao Trueba, Ana Isabel

; Díaz González, Marta Elvira

; Tavira Iglesias, Beatriz

; Álvarez Martínez, María Victoria

(2010)

The G263X MYBPC3 mutation is a common and low-penetrant mutation for hypertrophic cardiomyopathy in the region of Asturias (Northern Spain)

Rodríguez Reguero, José Julián

; Gómez de Oña, Juan

; Martín Fernández, María

; Flórez Muñoz, Juan Pablo; Morís de la Tassa, César

; Iglesias, Sara; Alonso González, Belén

; Álvarez Martínez, María Victoria

; Coto García, Eliecer

(2013)

Gene variants in the NF-KB pathway (NFKB1, NFKBIA, NFKBIZ) and risk for early-onset coronary artery disease

Coto García, Eliecer

; Rodríguez Reguero, José Julián

; Avanzas Fernández, Pablo

; Pascual Calleja, Isaac

; Martín, M.; Hevia Nava, Sergio

; Morís de la Tassa, César

; Díaz Molina, Beatriz

; Rodríguez Lambert, José Luis

; Alonso González, Belén

; Cuesta Llavona, Elías; Díaz Corte, María del Carmen

; Gómez, Juan (2019)

Gene variants in the NF-KB pathway (NFKB1, NFKBIA, NFKBIZ) and their association with type 2 diabetes and impaired renal function

Coto García, Eliecer

; Díaz Corte, María del Carmen

; Tranche Iparraguirre, Salvador

; Gómez de Oña, Juan

; Alonso González, Belén

; Iglesias, Sara; Rodríguez Reguero, José Julián

; López Larrea, Carlos

; Coto Segura, Pablo

(2018)

Genetic variation at the long noncoding RNA H19 gene is associated with the risk of hypertrophic cardiomyopathy

Gómez de Oña, Juan

; Lorca Gutiérrez, Rebeca

; Rodríguez Reguero, José Julián

; Martín Fernández, María

; Morís de la Tassa, César

; Alonso González, Belén

; Iglesias, Sara; Díaz Molina, Beatriz

; Avanzas Fernández, Pablo

; Coto García, Eliecer

(2018)

Genetic Variation in the H19-IGF2 Cluster Might Confer Risk of Developing Impaired Renal Function

Coto García, Eliecer

; Díaz Corte, María del Carmen

; Tranche Iparraguirre, Salvador

; Gómez de Oña, Juan

; Rodríguez Reguero, José Julián

; Alonso González, Belén

; Iglesias, Sara; Gil Peña, Helena

; Yin, Xueqian; Coto Segura, Pablo

(2018-10-08)

Genetic variation in the renin-angiotensin system and athletic performance

Álvarez Díaz, Ruth; Terrados Cepeda, Nicolás

; Ortolano Ríos, Raquel; Iglesias Cubero, Gustavo

; Rodríguez Reguero, José Julián

; Batalla, Alberto; Cortina Llosa, Arturo Agustín

; Fernández García, Benjamín

; Casañas Rodríguez, Carmen; Braga, Socorro; Asensi Álvarez, Víctor

; Coto García, Eliecer

(2000)

Listar por autor "Rodríguez Reguero, José Julián"

Aldosterone levels and cardiac hypertrophy in professional cyclists ﻿

Association of the genetic variation in the long non‐coding RNA FENDRR with the risk of developing hypertrophic cardiomyopathy ﻿

Causas, substrato anatómico y evolución clínica de la enfermedad coronaria precoz ﻿

Characterization of left ventricular non-compaction cardiomyopathy ﻿

Compound heterozygosity for PTPN11 variants in a subject with Noonan syndrome provides insights into the mechanism of SHP2-related disorders ﻿

Correlación fenotipo/genotipo en la miocardiopatía hipertrófica y miocardiopatía no compactada ﻿

Different phenotypes in monozygotic twins, carriers of the same pathogenic variant for hypertrophic cardiomyopathy ﻿

Differential methylation of lncRNA KCNQ1OT1 promoter polymorphism was associated with symptomatic cardiac long QT ﻿

Distal renal tubular acidosis. Clinical manifestations in patients with different underlying gene mutations ﻿

ECG as a part of the preparticipation screening programme: an old and still present international dilemma ﻿

Efectos del consumo crónico de tabaco y alcohol sobre lípidos plasmáticos, parámetros cardiovasculares y alpha 1-antitripsina, en una población minera joven ﻿

Entendimiento de la miocardiopatía hipertrófica mediante el estudio de una variante patogénica fundadora ﻿

Evolución clínica de la enfermedad coronaria precoz. Prevención secundaria y bases genéticas ﻿

Functional polymorphisms in genes of the Angiotensin and Serotonin systems and risk of hypertrophic cardiomyopathy: AT1R as a potential modifier ﻿

The G263X MYBPC3 mutation is a common and low-penetrant mutation for hypertrophic cardiomyopathy in the region of Asturias (Northern Spain) ﻿

Gene variants in the NF-KB pathway (NFKB1, NFKBIA, NFKBIZ) and risk for early-onset coronary artery disease ﻿

Gene variants in the NF-KB pathway (NFKB1, NFKBIA, NFKBIZ) and their association with type 2 diabetes and impaired renal function ﻿

Genetic variation at the long noncoding RNA H19 gene is associated with the risk of hypertrophic cardiomyopathy ﻿

Genetic Variation in the H19-IGF2 Cluster Might Confer Risk of Developing Impaired Renal Function ﻿

Genetic variation in the renin-angiotensin system and athletic performance ﻿

Aldosterone levels and cardiac hypertrophy in professional cyclists

Association of the genetic variation in the long non‐coding RNA FENDRR with the risk of developing hypertrophic cardiomyopathy

Causas, substrato anatómico y evolución clínica de la enfermedad coronaria precoz

Characterization of left ventricular non-compaction cardiomyopathy

Compound heterozygosity for PTPN11 variants in a subject with Noonan syndrome provides insights into the mechanism of SHP2-related disorders

Correlación fenotipo/genotipo en la miocardiopatía hipertrófica y miocardiopatía no compactada

Different phenotypes in monozygotic twins, carriers of the same pathogenic variant for hypertrophic cardiomyopathy

Differential methylation of lncRNA KCNQ1OT1 promoter polymorphism was associated with symptomatic cardiac long QT

Distal renal tubular acidosis. Clinical manifestations in patients with different underlying gene mutations

ECG as a part of the preparticipation screening programme: an old and still present international dilemma

Efectos del consumo crónico de tabaco y alcohol sobre lípidos plasmáticos, parámetros cardiovasculares y alpha 1-antitripsina, en una población minera joven

Entendimiento de la miocardiopatía hipertrófica mediante el estudio de una variante patogénica fundadora

Evolución clínica de la enfermedad coronaria precoz. Prevención secundaria y bases genéticas

Functional polymorphisms in genes of the Angiotensin and Serotonin systems and risk of hypertrophic cardiomyopathy: AT1R as a potential modifier

The G263X MYBPC3 mutation is a common and low-penetrant mutation for hypertrophic cardiomyopathy in the region of Asturias (Northern Spain)

Gene variants in the NF-KB pathway (NFKB1, NFKBIA, NFKBIZ) and risk for early-onset coronary artery disease

Gene variants in the NF-KB pathway (NFKB1, NFKBIA, NFKBIZ) and their association with type 2 diabetes and impaired renal function

Genetic variation at the long noncoding RNA H19 gene is associated with the risk of hypertrophic cardiomyopathy

Genetic Variation in the H19-IGF2 Cluster Might Confer Risk of Developing Impaired Renal Function

Genetic variation in the renin-angiotensin system and athletic performance