Navegar por autor "Couce Pico, María Luz"

6R-tetrahydrobiopterin treated PKU patients below 4years of age: Physical outcomes, nutrition and genotype

2015- Couce Pico, María Luz

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 new case of maternal phenylketonuria treated with sapropterin dihydrochloride (6R-BH4)

2014- Couce Pico, María Luz

A novel form of CAP myopathy in absence of heart disease associated with recessive TTN gene mutations

2015- Couce Pico, María Luz; Fernández Marmiesse, Ana

A novel stop mutation in the vascular endothelial growth factor-C gene (VEGFC) results in Milroy-like disease

2014- Carracedo Álvarez, Ángel; Barros Angueira, Francisco; Couce Pico, María Luz; Balboa Beltran, Emilia; Pérez Muñuzuri, Alejandro; [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

Acylcarnitine profile in neonatal hypoxic-ischemic encephalopathy: The value of butyrylcarnitine as a prognostic marker

2019- López Suárez, Olalla Elena; CONCHEIRO GUISAN, ANA; Sánchez Pintos, Paula; Cocho, J. A.; FERNANDEZ LORENZO, JOSE RAMON; [et al.]

Albinismo oculocutáneo 1B asociado a una nueva mutación en el gen TYR

2013- Cortés Pereira, Estefania; Couce Pico, María Luz; Porras Hurtado, Liliana; Fernández Seara, María José; Vidal-Rios Vázquez, Pablo [et al.]

Anthropometric characteristics and nutrition in a cohort of PAH-deficient patients

2014- Couce Pico, María Luz

Anthropometric characteristics and nutrition in a cohort of PAH-deficient patients

2013- Couce Pico, María Luz

Are we giving our phenylketonuric patients the adequate amount of micronutrients?

2015- Iglesias Vázquez, José Antonio; Couce Pico, María Luz; De Castro López, María José; Sánchez Pintos, Paula; Crujeiras Martínez, Vanesa [et al.]

Arginine-guanidinoacetate-creatine pathway in preterm newborns: Creatine biosynthesis in newborns

2013- Couce Pico, María Luz

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.]

Azul de metileno: utilidad en el tratamiento de la hipotension arterial refractaria en prematuros.

2011- López Suárez, Olalla; Pérez Muñuzuri, Alejandro; Baña Souto, Ana Maria; Crespo Suárez, Pilar Adelaida; Couce Pico, María Luz; [et al.]

Repositorio digital RUNA

Navegar por autor "Couce Pico, María Luz"

6R-tetrahydrobiopterin treated PKU patients below 4years of age: Physical outcomes, nutrition and genotype ﻿

A glimpse into past, present, and future DNA sequencing ﻿

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

A new case of maternal phenylketonuria treated with sapropterin dihydrochloride (6R-BH4) ﻿

A novel form of CAP myopathy in absence of heart disease associated with recessive TTN gene mutations ﻿

A novel stop mutation in the vascular endothelial growth factor-C gene (VEGFC) results in Milroy-like disease ﻿

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

Acylcarnitine profile in neonatal hypoxic-ischemic encephalopathy: The value of butyrylcarnitine as a prognostic marker ﻿

Albinismo oculocutáneo 1B asociado a una nueva mutación en el gen TYR ﻿

Anthropometric characteristics and nutrition in a cohort of PAH-deficient patients ﻿

Anthropometric characteristics and nutrition in a cohort of PAH-deficient patients ﻿

Are we giving our phenylketonuric patients the adequate amount of micronutrients? ﻿

Arginine-guanidinoacetate-creatine pathway in preterm newborns: Creatine biosynthesis in newborns ﻿

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 ﻿

Azul de metileno: utilidad en el tratamiento de la hipotension arterial refractaria en prematuros. ﻿

Betaine anhydrous in homocystinuria: results from the RoCH registry ﻿

Bone Mineralization and Calcium Phosphorus Metabolism ﻿

Bone Status in Patients with Phenylketonuria: A Systematic Review ﻿

6R-tetrahydrobiopterin treated PKU patients below 4years of age: Physical outcomes, nutrition and genotype

A glimpse into past, present, and future DNA sequencing

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

A new case of maternal phenylketonuria treated with sapropterin dihydrochloride (6R-BH4)

A novel form of CAP myopathy in absence of heart disease associated with recessive TTN gene mutations

A novel stop mutation in the vascular endothelial growth factor-C gene (VEGFC) results in Milroy-like disease

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

Acylcarnitine profile in neonatal hypoxic-ischemic encephalopathy: The value of butyrylcarnitine as a prognostic marker

Albinismo oculocutáneo 1B asociado a una nueva mutación en el gen TYR

Anthropometric characteristics and nutrition in a cohort of PAH-deficient patients

Anthropometric characteristics and nutrition in a cohort of PAH-deficient patients

Are we giving our phenylketonuric patients the adequate amount of micronutrients?

Arginine-guanidinoacetate-creatine pathway in preterm newborns: Creatine biosynthesis in newborns

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

Azul de metileno: utilidad en el tratamiento de la hipotension arterial refractaria en prematuros.

Betaine anhydrous in homocystinuria: results from the RoCH registry

Bone Mineralization and Calcium Phosphorus Metabolism

Bone Status in Patients with Phenylketonuria: A Systematic Review