Navegar por autor "Fraga Bermúdez, José María"

A glimpse into past, present, and future DNA sequencing

2013- Couce Pico, María Luz; Castiñeiras Ramos, Daisy E; Cocho de Juan, José Ángel; Fraga Bermúdez, José María; Morey Villar, Marcos; [et al.]

A glimpse into past, present, and future DNA sequencing (vol 110, pg 3, 2013)

2015- Couce Pico, María Luz; Castiñeiras Ramos, Daisy E; Cocho de Juan, José Ángel; Fraga Bermúdez, José María; Morey Villar, Marcos; [et al.]

A Rare Cause of Neonatal Obstructive Jaundice Answer to the Clinical Challenges and Images in GI Question: Image 6: Mirizzi Syndrome

2015- Couce Pico, María Luz; Fraga Bermúdez, José María; De Castro López, María José

Assasement of omega-6/omega-3 ratio supplementation and psychomotor development in very preterm infants; a randomized controlled trial

2015- Couce Pico, María Luz; Baña Souto, Ana Maria; Fraga Bermúdez, José María; Pérez Muñuzuri, Alejandro; Fernández Seara, María José; [et al.]

Assessment of a targeted resequencing assay as a support tool in the diagnosis of lysosomal storage disorders

2014- Couce Pico, María Luz; Castiñeiras Ramos, Daisy E; Cocho de Juan, José Ángel; Fraga Bermúdez, José María; Castro Gago, Manuel; [et al.]

Assessment of the prevalence of major anomalies as a cause of neonatal death. Study in a cohort of 55.140 newborn infants

2014- Couce Pico, María Luz; Fraga Bermúdez, José María; Pérez Muñuzuri, Alejandro; Iglesias Deus, Alicia; Rodríguez Cervilla, José; [et al.]

Clinical and metabolic findings in patients with methionine adenosyltransferase I/III deficiency detected by newborn screening

2013- Couce Pico, María Luz; Castiñeiras Ramos, Daisy E; Bóveda Fontán, María Dolores; Fraga Bermúdez, José María; Fernández Marmiesse, Ana [et al.]

Clinical and metabolic findings in patients with methionine adenosyltransferase I/III deficiency detected by newborn screening (vol 110, pg 218, 2013)

2015- Couce Pico, María Luz; Castiñeiras Ramos, Daisy E; Bóveda Fontán, María Dolores; Fraga Bermúdez, José María; Fernández Marmiesse, Ana [et al.]

Corrigendum to

2015- Leis Trabazo, María Rosaura; Couce Pico, María Luz; Bóveda Fontán, María Dolores; Fraga Bermúdez, José María

Determinación de ácido etilendiaminotetraacético por espectrometría de masas en tándem en muestras de sangre impregnadas en papel. Utilidad en la medida de tirotropina para cribado neonatal de hipotiroidismo congénito

2012- Castiñeiras Ramos, Daisy E; Bóveda Fontán, María Dolores; Cocho de Juan, José Ángel; Fraga Bermúdez, José María; Pérez Suarez, Luis Fernando; [et al.]

Development of electrospray ionization tandem mass spectrometry methods for the study of a high number of urine markers of inborn errors of metabolism

2012- Couce Pico, María Luz; Rebollido Fernández, María; Castiñeiras Ramos, Daisy E; Bóveda Fontán, María Dolores; Cocho de Juan, José Ángel; [et al.]

Early extrauterine life adaptation. Assessment between two cohort groups of livebirths in the last ten years

2014- Baña Souto, Ana Maria; Fraga Bermúdez, José María; Pérez Muñuzuri, Alejandro; López Suárez, Olalla Elena; Rodríguez Cervilla, José; [et al.]

Effects of different arachidonic acid supplementation on psychomotor development in very preterm infants; A randomized controlled trial

2015- Couce Pico, María Luz; Baña Souto, Ana Maria; Fraga Bermúdez, José María; Pérez Muñuzuri, Alejandro; De Castro López, María José; [et al.]

Effects of different omega-6/omega-3 ratio supplementation on growth and evoked potentials in very preterm infants; a randomized controlled trial

2015- Couce Pico, María Luz; Baña Souto, Ana Maria; Fraga Bermúdez, José María; Pérez Muñuzuri, Alejandro; Fernández Seara, María José; [et al.]

Evaluation and long-term follow-up of infants with inborn errors of metabolism identified in an expanded screening programme

2011- Couce Pico, María Luz; Baña Souto, Ana Maria; Castiñeiras Ramos, Daisy E; Bóveda Fontán, María Dolores; Cocho de Juan, José Ángel; [et al.]

Evolution of patients with methionine adenosyltransferase (MAT) I/III deficiency detected by neonatal screening in Spain

2013- Couce Pico, María Luz; Castiñeiras Ramos, Daisy E; Bóveda Fontán, María Dolores; Fraga Bermúdez, José María; Iglesias Rodríguez, Agustín Javier [et al.]

Fetal growth restriction: Comparative assessment between naturally conceived pregnancies and by assisted reproductive techniques

2014- Couce Pico, María Luz; Baña Souto, Ana Maria; Fraga Bermúdez, José María; Pérez Muñuzuri, Alejandro; Rodríguez Cervilla, José; [et al.]

Glutaric aciduria type I: outcome of patients with early- versus late-diagnosis

2013- Couce Pico, María Luz; Castiñeiras Ramos, Daisy E; Bóveda Fontán, María Dolores; Cocho de Juan, José Ángel; Fraga Bermúdez, José María; [et al.]

Hallazgos clinicos y geneticos en pacientes con deficiencia de biotinidasa detectados en el cribado neonatal o selectivo de sordera o de enfermedades metabolicas hereditarias.

2011- Couce Pico, María Luz; Castiñeiras Ramos, Daisy E; Fraga Bermúdez, José María

Immunohistochemical evaluation of EGFR expression in lip squamous cell carcinoma. Correlation with clinicopathological characteristics

2014- Gude Sampedro, Francisco; Ginarte Val, Manuel Javier; García-Caballero Parada, Tomas; Antúnez López, José Ramón; Fraga Bermúdez, José María [et al.]

Repositorio digital RUNA

Navegar por autor "Fraga Bermúdez, José María"

A glimpse into past, present, and future DNA sequencing ﻿

A glimpse into past, present, and future DNA sequencing (vol 110, pg 3, 2013) ﻿

A Rare Cause of Neonatal Obstructive Jaundice Answer to the Clinical Challenges and Images in GI Question: Image 6: Mirizzi Syndrome ﻿

Assasement of omega-6/omega-3 ratio supplementation and psychomotor development in very preterm infants; a randomized controlled trial ﻿

Assessment of a targeted resequencing assay as a support tool in the diagnosis of lysosomal storage disorders ﻿

Assessment of the prevalence of major anomalies as a cause of neonatal death. Study in a cohort of 55.140 newborn infants ﻿

Clinical and metabolic findings in patients with methionine adenosyltransferase I/III deficiency detected by newborn screening ﻿

Clinical and metabolic findings in patients with methionine adenosyltransferase I/III deficiency detected by newborn screening (vol 110, pg 218, 2013) ﻿

Corrigendum to ﻿

Determinación de ácido etilendiaminotetraacético por espectrometría de masas en tándem en muestras de sangre impregnadas en papel. Utilidad en la medida de tirotropina para cribado neonatal de hipotiroidismo congénito ﻿

Development of electrospray ionization tandem mass spectrometry methods for the study of a high number of urine markers of inborn errors of metabolism ﻿

Early extrauterine life adaptation. Assessment between two cohort groups of livebirths in the last ten years ﻿

Effects of different arachidonic acid supplementation on psychomotor development in very preterm infants; A randomized controlled trial ﻿

Effects of different omega-6/omega-3 ratio supplementation on growth and evoked potentials in very preterm infants; a randomized controlled trial ﻿

Evaluation and long-term follow-up of infants with inborn errors of metabolism identified in an expanded screening programme ﻿

Evolution of patients with methionine adenosyltransferase (MAT) I/III deficiency detected by neonatal screening in Spain ﻿

Fetal growth restriction: Comparative assessment between naturally conceived pregnancies and by assisted reproductive techniques ﻿

Glutaric aciduria type I: outcome of patients with early- versus late-diagnosis ﻿

Hallazgos clinicos y geneticos en pacientes con deficiencia de biotinidasa detectados en el cribado neonatal o selectivo de sordera o de enfermedades metabolicas hereditarias. ﻿

Immunohistochemical evaluation of EGFR expression in lip squamous cell carcinoma. Correlation with clinicopathological characteristics ﻿

A glimpse into past, present, and future DNA sequencing

A glimpse into past, present, and future DNA sequencing (vol 110, pg 3, 2013)

A Rare Cause of Neonatal Obstructive Jaundice Answer to the Clinical Challenges and Images in GI Question: Image 6: Mirizzi Syndrome

Assasement of omega-6/omega-3 ratio supplementation and psychomotor development in very preterm infants; a randomized controlled trial

Assessment of a targeted resequencing assay as a support tool in the diagnosis of lysosomal storage disorders

Assessment of the prevalence of major anomalies as a cause of neonatal death. Study in a cohort of 55.140 newborn infants

Clinical and metabolic findings in patients with methionine adenosyltransferase I/III deficiency detected by newborn screening

Clinical and metabolic findings in patients with methionine adenosyltransferase I/III deficiency detected by newborn screening (vol 110, pg 218, 2013)

Corrigendum to

Determinación de ácido etilendiaminotetraacético por espectrometría de masas en tándem en muestras de sangre impregnadas en papel. Utilidad en la medida de tirotropina para cribado neonatal de hipotiroidismo congénito

Development of electrospray ionization tandem mass spectrometry methods for the study of a high number of urine markers of inborn errors of metabolism

Early extrauterine life adaptation. Assessment between two cohort groups of livebirths in the last ten years

Effects of different arachidonic acid supplementation on psychomotor development in very preterm infants; A randomized controlled trial

Effects of different omega-6/omega-3 ratio supplementation on growth and evoked potentials in very preterm infants; a randomized controlled trial

Evaluation and long-term follow-up of infants with inborn errors of metabolism identified in an expanded screening programme

Evolution of patients with methionine adenosyltransferase (MAT) I/III deficiency detected by neonatal screening in Spain

Fetal growth restriction: Comparative assessment between naturally conceived pregnancies and by assisted reproductive techniques

Glutaric aciduria type I: outcome of patients with early- versus late-diagnosis

Hallazgos clinicos y geneticos en pacientes con deficiencia de biotinidasa detectados en el cribado neonatal o selectivo de sordera o de enfermedades metabolicas hereditarias.

Immunohistochemical evaluation of EGFR expression in lip squamous cell carcinoma. Correlation with clinicopathological characteristics