Navegar Publicación científica por "Dirección Xeral de Asistencia Sanitaria"

A novel ABCA12 pathologic variant identified in an Ecuadorian harlequin ichthyosis patient: A step forward in genotype-phenotype correlations

2019- Montalván-Suárez, M.; Esperón Moldes, Uxía Saraiva; Rodríguez Pazos, Laura; Ordoñez Ugalde, Andrés; Moscoso, F.; [et al.]

A novel ABCA12 pathologic variant identified in an Ecuadorian harlequin ichthyosis patient: A step forward in genotype‐phenotype correlations

2019- Montalván‐Suárez, Martha; Saraiva Esperón, Uxía; Rodríguez Pazos, Laura; Ordóñez‐Ugalde, Andrés; Moscoso, Fernanda; [et al.]

A qPCR expression assay of IFI44L gene differentiates viral from bacterial infections in febrile children

2019- Gómez Carballa, Alberto; Cebey López, Miriam; Pardo Seco, Jacobo José; Barral Arca, Ruth; RIVERO CALLE, IRENE; [et al.]

Acute basophilic leukaemia secondary to MDS with isolated del(5q)

2019- Loyola Holgado, Inés; Fernández González, Raquel; Trastoy, A.

Analysis of social awareness of organ donation in the secondary school population in Galicia

2013- Fernández García, Antón; Sánchez Ibáñez, Jacinto; Bouzas Caamaño, Encarnación; Álvarez Vázquez, Marta

Association analyses identify 31 new risk loci for colorectal cancer susceptibility

2019- Law, P. J.; Timofeeva, M.; Fernández Rozadilla, Ceres; Broderick, P.; Studd, J.; [et al.]

Association study of nonsynonymous single nucleotide polymorphisms in schizophrenia

2012- Carracedo Álvarez, Ángel; Arrojo Romero, Manuel; Ramos Rios, Ramón; Paz Silva, Eduardo; Suárez Rama, Jose Javier; [et al.]

BDNF genetic variants and methylation: effects on cognition in major depressive disorder

2019- Ferrer, A.; Labad, J.; Salvat-Pujol, N.; Barrachina, M.; Costas Costas, Javier; [et al.]

Benchmarking in the process of donation after brain death: a methodology to identify best performer hospitals.

2012- Fernández García, Antón; Sánchez Ibáñez, Jacinto; Bouzas Caamaño, Encarnación

Biogeographical origin and timing of the founder ichthyosis TGM1 c.1187G > A mutation in an isolated Ecuadorian population

2019- Esperón Moldes, Uxía Saraiva; Pardo Seco, Jacobo José; Montalván-Suárez, M.; Fachal Vilar, Laura; Ginarte Val, Manuel Javier; [et al.]

Blood Biomarkers of Uveal Melanoma: Current Perspectives

2020- Bande Rodriguez, Manuel Francisco; Fernández Marta, Beatriz; Lago Baameiro, Nerea; Santiago Varela, Maria; Silva Rodríguez, Paula; [et al.]

Borracheras, conduccion de vehiculos y relaciones sexuales en jovenes consumidores de cocaina y extasis

2011- Fraga Ares, Jaime; Osorio López, Jesús; Arrojo Romero, Manuel; López Crecente, Fernanda; Domínguez González, Nieves [et al.]

Caracteristicas clinicas y pronostico de pacientes con enfermedad cerebrovascular cronica (estudio ICBAR).

2011- González Juanatey, José Ramón; Otero Raviña, Fernando; Vidal Pérez, Rafael Carlos; De Blas Abad, Paula; Castillo Sánchez, José; [et al.]

Cardiopatía isquémica en la mujer. Datos del estudio CIBAR

2012- González Juanatey, José Ramón; Otero Raviña, Fernando; Vidal Pérez, Rafael Carlos; Gómez Vázquez, José Luis; Santos Rodríguez, José Antonio; [et al.]

Cardiovascular risk factors and cardiovascular events in a stroke cohort from a primary care setting. ST-BAR study

2011- González Juanatey, José Ramón; Otero Raviña, Fernando; Vidal Pérez, Rafael Carlos; López Pérez, José Manuel; Domínguez López, Jerónimo Ramón; [et al.]

Common variant at 16p11.2 conferring risk of psychosis

2014- Carracedo Álvarez, Ángel; Arrojo Romero, Manuel; Costas Costas, Javier

Common variants at VRK2 and TCF4 conferring risk of schizophrenia

2011- Carracedo Álvarez, Ángel; Arrojo Romero, Manuel; Costas Costas, Javier; Mattheisen ?, Manuel

A Comparison of Forensic Age Prediction Models Using Data From Four DNA Methylation Technologies

2020- Freire-Aradas, A; Pospiech, E; Aliferi, A; Giron-Santamaria, L; Mosquera-Miguel, A; [et al.]

A compilation of tri-allelic SNPs from 1000 Genomes and use of the most polymorphic loci for a large-scale human identification panel

2020- Phillips, C.; de la Puente, M.; Ruiz-Ramirez, J.; Lareu, M.V.; Amigo Lechuga, Jorge; [et al.]

A compilation of tri-allelic SNPs from 1000 Genomes and use of the most polymorphic loci for a large-scale human identification panel

2020- Phillips, C; Amigo Lechuga, Jorge; Tillmar, AO; Peck, MA; de la Puente, M; [et al.]

Repositorio digital RUNA

Navegar Publicación científica por "Dirección Xeral de Asistencia Sanitaria"

A novel ABCA12 pathologic variant identified in an Ecuadorian harlequin ichthyosis patient: A step forward in genotype-phenotype correlations ﻿

A novel ABCA12 pathologic variant identified in an Ecuadorian harlequin ichthyosis patient: A step forward in genotype‐phenotype correlations ﻿

A qPCR expression assay of IFI44L gene differentiates viral from bacterial infections in febrile children ﻿

Acute basophilic leukaemia secondary to MDS with isolated del(5q) ﻿

Analysis of social awareness of organ donation in the secondary school population in Galicia ﻿

Association analyses identify 31 new risk loci for colorectal cancer susceptibility ﻿

Association study of nonsynonymous single nucleotide polymorphisms in schizophrenia ﻿

BDNF genetic variants and methylation: effects on cognition in major depressive disorder ﻿

Benchmarking in the process of donation after brain death: a methodology to identify best performer hospitals. ﻿

Biogeographical origin and timing of the founder ichthyosis TGM1 c.1187G > A mutation in an isolated Ecuadorian population ﻿

Blood Biomarkers of Uveal Melanoma: Current Perspectives ﻿

Borracheras, conduccion de vehiculos y relaciones sexuales en jovenes consumidores de cocaina y extasis ﻿

Caracteristicas clinicas y pronostico de pacientes con enfermedad cerebrovascular cronica (estudio ICBAR). ﻿

Cardiopatía isquémica en la mujer. Datos del estudio CIBAR ﻿

Cardiovascular risk factors and cardiovascular events in a stroke cohort from a primary care setting. ST-BAR study ﻿

Common variant at 16p11.2 conferring risk of psychosis ﻿

Common variants at VRK2 and TCF4 conferring risk of schizophrenia ﻿

A Comparison of Forensic Age Prediction Models Using Data From Four DNA Methylation Technologies ﻿

A compilation of tri-allelic SNPs from 1000 Genomes and use of the most polymorphic loci for a large-scale human identification panel ﻿

A compilation of tri-allelic SNPs from 1000 Genomes and use of the most polymorphic loci for a large-scale human identification panel ﻿

A novel ABCA12 pathologic variant identified in an Ecuadorian harlequin ichthyosis patient: A step forward in genotype-phenotype correlations

A novel ABCA12 pathologic variant identified in an Ecuadorian harlequin ichthyosis patient: A step forward in genotype‐phenotype correlations

A qPCR expression assay of IFI44L gene differentiates viral from bacterial infections in febrile children

Acute basophilic leukaemia secondary to MDS with isolated del(5q)

Analysis of social awareness of organ donation in the secondary school population in Galicia

Association analyses identify 31 new risk loci for colorectal cancer susceptibility

Association study of nonsynonymous single nucleotide polymorphisms in schizophrenia

BDNF genetic variants and methylation: effects on cognition in major depressive disorder

Benchmarking in the process of donation after brain death: a methodology to identify best performer hospitals.

Biogeographical origin and timing of the founder ichthyosis TGM1 c.1187G > A mutation in an isolated Ecuadorian population

Blood Biomarkers of Uveal Melanoma: Current Perspectives

Borracheras, conduccion de vehiculos y relaciones sexuales en jovenes consumidores de cocaina y extasis

Caracteristicas clinicas y pronostico de pacientes con enfermedad cerebrovascular cronica (estudio ICBAR).

Cardiopatía isquémica en la mujer. Datos del estudio CIBAR

Cardiovascular risk factors and cardiovascular events in a stroke cohort from a primary care setting. ST-BAR study

Common variant at 16p11.2 conferring risk of psychosis

Common variants at VRK2 and TCF4 conferring risk of schizophrenia

A Comparison of Forensic Age Prediction Models Using Data From Four DNA Methylation Technologies

A compilation of tri-allelic SNPs from 1000 Genomes and use of the most polymorphic loci for a large-scale human identification panel

A compilation of tri-allelic SNPs from 1000 Genomes and use of the most polymorphic loci for a large-scale human identification panel