Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Manuel Cidrás"'
Autor:
Juan José Agüera Arenas, María del Valle Viedma Guiard, Cristina Martínez García, Olga Micol Martínez, Miguel Alcaraz Saura, María del Rocío Pérez Crespo, Manuel Cidrás Pidre
Background: The use of less invasive surfactant administration (LISA) has been increasingly investigated, since neonatal respiratory distress syndrome (RDS) due to surfactant deficiency is associated with high morbidity and mortality in preterm infan
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a615ece160f95048cd9d1899f2b6deb7
https://doi.org/10.21203/rs.3.rs-38999/v1
https://doi.org/10.21203/rs.3.rs-38999/v1
Autor:
Gerardo Martínez-Munar, Carmen Fuentes-Gutiérrez, Antonio Martínez-Gimeno, Ana García-González, José Luis Leante-Castellanos, Manuel Cidrás-Pidré
Publikováno v:
Pediatric Infectious Disease Journal. 36:e293-e297
BACKGROUND The prognosis for late-onset sepsis depends largely on a timely diagnosis. We assess central-peripheral temperature difference monitoring as a marker for late-onset neonatal sepsis diagnosis. METHODS We performed a prospective, observation
Autor:
Manuel Cidrás
Publikováno v:
OALib. :1-8
Background: Body mass index (BMI) is a squared-height power function. Nevertheless, some studies show a significant exponential weight-height correlation. Objectives: To demonstrate that the weight-height relationship from 2 to 20 years of age is bet
Autor:
Lorenzo Quesada-Dorigne, Ángel Bernardo Brea-Lamas, Manuel Cidrás-Pidré, Juan José Quesada López, Sonia Valero-Portero
Publikováno v:
Archives of Disease in Childhood - Fetal and Neonatal Edition. 102:F224-F225
A preterm newborn (24 weeks gestational age, birth weight 710 g) was admitted to the neonatal intensive care unit. On day 30 of life, he was receiving respiratory support with nasal continuous positive airway pressure (CPAP), full breast milk feeds a
Autor:
Daniel Grinberg, Raül Santamaria, Lluïsa Vilageliu, Manuel Cidrás, Magdalena Montfort, Anna Diaz-Font, Amparo Chabás, Laura Gort
Publikováno v:
Blood Cells, Molecules, and Diseases. 35:253-258
Gaucher disease, the most common lysosomal storage disorder, encompasses a wide spectrum of clinical symptoms. The perinatal lethal form is very rare and is considered a distinct form of classic type 2 Gaucher disease. Prominent features of the sever