Browse by Author "Couce Pico, María Luz"

Carglumic acid (NCG) as treatment of hyperammonemia episodes in organic acidemias/acidurias (OAS): A retrospective observational study in patients from Europe and Turkey

2011- Couce Pico, María Luz

Characterization of New Proteomic Biomarker Candidates in Mucopolysaccharidosis Type IVA

2020- Álvarez, V. J.; Bravo López, Susana Belén; Chantada Vázquez, María Pilar; Colón Mejeras, Cristobal; De Castro López, María José; [et al.]

Cierre parcial del ductus arterioso intrautero asociado a consumo materno de flavonoides

2014- Couce Pico, María Luz; Pérez Muñuzuri, Alejandro; López Suárez, Olalla Elena; Fariña Nogueira, Sabela

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.]

Clinical manifestations in female carriers of mucopolysaccharidosis type II: A spanish cross-sectional study

2013- Couce Pico, María Luz

Clinical Utility of LCT Genotyping in Children with Suspected Functional Gastrointestinal Disorder

2020- Couce Pico, María Luz; Sánchez Pintos, Paula; González Vioque, Emiliano; Leis Trabazo, María Rosaura

Clinical, genetic, and therapeutic diversity in 2 patients with severe mevalonate kinase deficiency

2012- Couce Pico, María Luz; Baña Souto, Ana Maria

Congenital hypothyroidism with neurological and respiratory alterations: A case detected using a variable diagnostic threshold for Tsh

2011- Couce Pico, María Luz; Gómez Lado, María del Carmen; Pombo Arias, Manuel; Cabanas Rodríguez, Paloma; Castro Feijoo, Lidia; [et al.]

Corrigendum to

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

Corticoides antenatales y prevención del distrés respiratorio del recién nacido prematuro: utilidad de la terapia de rescate

2014- Couce Pico, María Luz; Baña Souto, Ana Maria; Pérez Muñuzuri, Alejandro; López Suárez, Olalla Elena; García Magán, Carlos; [et al.]

Cost-effectiveness analysis of a national newborn screening program for biotinidase deficiency

2015- Couce Pico, María Luz

Cross-sectional study of 168 patients with hepatorenal tyrosinaemia and implications for clinical practice

2014- Couce Pico, María Luz; Cocho de Juan, José Ángel

Cuidados al paciente neonato con hipotermia inducida

2015- Couce Pico, María Luz; Pérez Muñuzuri, Alejandro; Fernández Tuñas, María del Carmen; Prego Boente, Raquel

Cuidados enfermeros en la extrofia vesical neonatal

2014- Couce Pico, María Luz; Pérez Muñuzuri, Alejandro; Fernández Tuñas, María del Carmen; Turnes Paredes, Margarita; Ces Tarrio, María del Carmen [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.]

Dimethylarginines as biomarkers for the kidney transplant management in methylmalonic aciduria

2015- Couce Pico, María Luz

Discovery of Biomarker Panels for Neural Dysfunction in Inborn Errors of Amino Acid Metabolism

2019- Castells, A. A.; Gueraldi, D.; Balada, R.; Tristán-Noguero, A.; Cortès-Saladelafont, E.; [et al.]

Diversity of approaches to classic galactosemia around the world: A comparison of diagnosis, intervention, and outcomes

2012- Couce Pico, María Luz

Effect of allopurinol in addition to hypothermia treatment in neonates for hypoxic-ischemic brain injury on neurocognitive outcome (ALBINO): study protocol of a blinded randomized placebo-controlled parallel group multicenter trial for superiority (phase III)

2019- Maiwald, C. A.; Annink, K. V.; Rudiger, M.; Benders, Mjnl; van Bel, F.; [et al.]

RUNA digital repository

Browse by Author "Couce Pico, María Luz"

Carglumic acid (NCG) as treatment of hyperammonemia episodes in organic acidemias/acidurias (OAS): A retrospective observational study in patients from Europe and Turkey ﻿

Characterization of New Proteomic Biomarker Candidates in Mucopolysaccharidosis Type IVA ﻿

Cierre parcial del ductus arterioso intrautero asociado a consumo materno de flavonoides ﻿

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) ﻿

Clinical manifestations in female carriers of mucopolysaccharidosis type II: A spanish cross-sectional study ﻿

Clinical Utility of LCT Genotyping in Children with Suspected Functional Gastrointestinal Disorder ﻿

Clinical, genetic, and therapeutic diversity in 2 patients with severe mevalonate kinase deficiency ﻿

Congenital hypothyroidism with neurological and respiratory alterations: A case detected using a variable diagnostic threshold for Tsh ﻿

Corrigendum to ﻿

Corticoides antenatales y prevención del distrés respiratorio del recién nacido prematuro: utilidad de la terapia de rescate ﻿

Cost-effectiveness analysis of a national newborn screening program for biotinidase deficiency ﻿

Cross-sectional study of 168 patients with hepatorenal tyrosinaemia and implications for clinical practice ﻿

Cuidados al paciente neonato con hipotermia inducida ﻿

Cuidados enfermeros en la extrofia vesical neonatal ﻿

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

Dimethylarginines as biomarkers for the kidney transplant management in methylmalonic aciduria ﻿

Discovery of Biomarker Panels for Neural Dysfunction in Inborn Errors of Amino Acid Metabolism ﻿

Diversity of approaches to classic galactosemia around the world: A comparison of diagnosis, intervention, and outcomes ﻿

Effect of allopurinol in addition to hypothermia treatment in neonates for hypoxic-ischemic brain injury on neurocognitive outcome (ALBINO): study protocol of a blinded randomized placebo-controlled parallel group multicenter trial for superiority (phase III) ﻿

Carglumic acid (NCG) as treatment of hyperammonemia episodes in organic acidemias/acidurias (OAS): A retrospective observational study in patients from Europe and Turkey

Characterization of New Proteomic Biomarker Candidates in Mucopolysaccharidosis Type IVA

Cierre parcial del ductus arterioso intrautero asociado a consumo materno de flavonoides

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)

Clinical manifestations in female carriers of mucopolysaccharidosis type II: A spanish cross-sectional study

Clinical Utility of LCT Genotyping in Children with Suspected Functional Gastrointestinal Disorder

Clinical, genetic, and therapeutic diversity in 2 patients with severe mevalonate kinase deficiency

Congenital hypothyroidism with neurological and respiratory alterations: A case detected using a variable diagnostic threshold for Tsh

Corrigendum to

Corticoides antenatales y prevención del distrés respiratorio del recién nacido prematuro: utilidad de la terapia de rescate

Cost-effectiveness analysis of a national newborn screening program for biotinidase deficiency

Cross-sectional study of 168 patients with hepatorenal tyrosinaemia and implications for clinical practice

Cuidados al paciente neonato con hipotermia inducida

Cuidados enfermeros en la extrofia vesical neonatal

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

Dimethylarginines as biomarkers for the kidney transplant management in methylmalonic aciduria

Discovery of Biomarker Panels for Neural Dysfunction in Inborn Errors of Amino Acid Metabolism

Diversity of approaches to classic galactosemia around the world: A comparison of diagnosis, intervention, and outcomes

Effect of allopurinol in addition to hypothermia treatment in neonates for hypoxic-ischemic brain injury on neurocognitive outcome (ALBINO): study protocol of a blinded randomized placebo-controlled parallel group multicenter trial for superiority (phase III)