Navegar por "Pediatría"

13-Valent pneumococcal conjugate vaccine (PCV13) in preterm versus term infants

2015- Concheiro Guisan, Ana; Martinón Torres, Federico

13-valent pneumococcal conjugate vaccine given with meningococcal C-tetanus toxoid conjugate and other routine pediatric vaccinations: Immunogenicity and safety

2012- Martinón Torres, Federico

16p11.2 microdeletion associated to early onset benign childhood seizures

2013- Barros Angueira, Francisco; Castro Gago, Manuel; Gómez Lado, María del Carmen; Perez Gay, Laura; Dacruz Álvarez, David [et al.]

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

2015- Couce Pico, María Luz

A 6q14.1-q15 microdeletion in a male patient with severe autistic disorder, lack of oral language, and dysmorphic features with concomitant presence of a maternally inherited Xp22.31 copy number gain

2015- Quintela, Inés; Fernández Prieto, Montserrat; Gómez Guerrero, Lorena María; Resches, Mariela; Eiris Puñal, Jesús; [et al.]

A community intervention study on patients' resuscitation and defibrillation quality after embedded training in a cardiac rehabilitation program

2019- González Salvado, Violeta; Abelairas-Gomez, C.; Peña Gil, Carlos; Neiro Rey, María Carmen; Barcala-Furelos, R.; [et al.]

A comparison of the McGrath-MAC and Macintosh laryngoscopes for child tracheal intubation during resuscitation by paramedics. A randomized, crossover, manikin study

2015- Rodríguez Núñez, Antonio

A continuous metabolic syndrome score is associated with specific biomarkers of inflammation and CVD risk in prepubertal children

2015- Leis Trabazo, María Rosaura; Tojo Sierra, Rafael

A cross-sectional study of cryptorchidism in children: testicular volume and hormonal function at 18 years of age

2015- Tojo Sierra, Rafael; Pombo Arias, Manuel; Bautista Casasnovas, Adolfo; Méndez Gallart, Roberto; Estévez Martínez, Elina; [et al.]

A gene variant of 11beta-hydroxysteroid dehydrogenase type 1 is associated with obesity in children

2012- Leis Trabazo, María Rosaura; Tojo Sierra, Rafael

A genome-wide study of modern-day Tuscans: revisiting Herodotus's theory on the origin of the Etruscans

2014- Pardo Seco, Jacobo José; Gómez Carballa, Alberto; Amigo Lechuga, Jorge; Martinón Torres, Federico; Salas Ellacuriaga, Antonio [et al.]

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 maternally inherited 16p13.11-p12.3 duplication concomitant with a de novo SOX5 deletion in a male patient with global developmental delay, disruptive and obsessive behaviors and minor dysmorphic features

2015- Carracedo Álvarez, Ángel; Barros Angueira, Francisco; Castro Gago, Manuel; Eiris Puñal, Jesús; Lago Lestón, Ramón Manuel [et al.]

A multinational study of thromboprophylaxis practice in critically ill children

2014- Rodríguez Núñez, Antonio

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

2014- Couce Pico, María Luz

A new technique for collection of cerebrospinal fluid in rat pups

2015- Durán Fernández-Feijoo, Crisitina

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 popular song improves CPR compression rate and skill retention by schoolchildren: A manikin trial

2011- Rodríguez Núñez, Antonio; Busto Cuiñas, María de las Mercedes; García Sanchez, Natalia; Rodríguez Blanco, Silvia

Repositorio digital RUNA

Navegar por "Pediatría"

13-Valent pneumococcal conjugate vaccine (PCV13) in preterm versus term infants ﻿

13-valent pneumococcal conjugate vaccine given with meningococcal C-tetanus toxoid conjugate and other routine pediatric vaccinations: Immunogenicity and safety ﻿

16p11.2 microdeletion associated to early onset benign childhood seizures ﻿

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

A 6q14.1-q15 microdeletion in a male patient with severe autistic disorder, lack of oral language, and dysmorphic features with concomitant presence of a maternally inherited Xp22.31 copy number gain ﻿

A community intervention study on patients' resuscitation and defibrillation quality after embedded training in a cardiac rehabilitation program ﻿

A comparison of the McGrath-MAC and Macintosh laryngoscopes for child tracheal intubation during resuscitation by paramedics. A randomized, crossover, manikin study ﻿

A continuous metabolic syndrome score is associated with specific biomarkers of inflammation and CVD risk in prepubertal children ﻿

A cross-sectional study of cryptorchidism in children: testicular volume and hormonal function at 18 years of age ﻿

A gene variant of 11beta-hydroxysteroid dehydrogenase type 1 is associated with obesity in children ﻿

A genome-wide study of modern-day Tuscans: revisiting Herodotus's theory on the origin of the Etruscans ﻿

A glimpse into past, present, and future DNA sequencing ﻿

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

A maternally inherited 16p13.11-p12.3 duplication concomitant with a de novo SOX5 deletion in a male patient with global developmental delay, disruptive and obsessive behaviors and minor dysmorphic features ﻿

A multinational study of thromboprophylaxis practice in critically ill children ﻿

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

A new technique for collection of cerebrospinal fluid in rat pups ﻿

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 popular song improves CPR compression rate and skill retention by schoolchildren: A manikin trial ﻿

13-Valent pneumococcal conjugate vaccine (PCV13) in preterm versus term infants

13-valent pneumococcal conjugate vaccine given with meningococcal C-tetanus toxoid conjugate and other routine pediatric vaccinations: Immunogenicity and safety

16p11.2 microdeletion associated to early onset benign childhood seizures

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

A 6q14.1-q15 microdeletion in a male patient with severe autistic disorder, lack of oral language, and dysmorphic features with concomitant presence of a maternally inherited Xp22.31 copy number gain

A community intervention study on patients' resuscitation and defibrillation quality after embedded training in a cardiac rehabilitation program

A comparison of the McGrath-MAC and Macintosh laryngoscopes for child tracheal intubation during resuscitation by paramedics. A randomized, crossover, manikin study

A continuous metabolic syndrome score is associated with specific biomarkers of inflammation and CVD risk in prepubertal children

A cross-sectional study of cryptorchidism in children: testicular volume and hormonal function at 18 years of age

A gene variant of 11beta-hydroxysteroid dehydrogenase type 1 is associated with obesity in children

A genome-wide study of modern-day Tuscans: revisiting Herodotus's theory on the origin of the Etruscans

A glimpse into past, present, and future DNA sequencing

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

A maternally inherited 16p13.11-p12.3 duplication concomitant with a de novo SOX5 deletion in a male patient with global developmental delay, disruptive and obsessive behaviors and minor dysmorphic features

A multinational study of thromboprophylaxis practice in critically ill children

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

A new technique for collection of cerebrospinal fluid in rat pups

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 popular song improves CPR compression rate and skill retention by schoolchildren: A manikin trial