Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Belén Ferrer-Lorente"'
Autor:
Javier Arístegui, Santiago Alfayate-Miguelez, Begoña Carazo-Gallego, Elisa Garrote, Laura Díaz-Munilla, Mikel Mendizabal, María Méndez-Hernández, Elia Doménech, Belén Ferrer-Lorente, María Unsaín-Mancisidor, José Tomás Ramos-Amador, Marta Illán-Ramos, Borja Croche-Santander, Fernando Centeno Malfaz, Julián Rodríguez-Suárez, Manuel Cotarelo Suárez, María San-Martín, Jesús Ruiz-Contreras
Publikováno v:
Human Vaccines & Immunotherapeutics, Vol 18, Iss 5 (2022)
Rotavirus (RV) is the most common cause of severe gastroenteritis (GE) in infants and young children worldwide and is associated with a significant clinical and economic burden. The objective of this study was to analyze the characteristics, healthca
Externí odkaz:
https://doaj.org/article/d24272bc6762455dac1e378b33fe333f
Publikováno v:
Anales de Pediatría, Vol 92, Iss 3, Pp 181-182 (2020)
Externí odkaz:
https://doaj.org/article/d0ec3fa8b5454e5cbf5ed1ed12da7e66
Autor:
Purificación Marín-Reina, Antonio Pérez-Aytés, M. Belén Ferrer-Lorente, Francisco Martínez, Carmen Orellana, Mónica Rosello, Ana Herrero-García, Gloria Cabezuelo-Huerta
Publikováno v:
Journal of Pediatric Genetics
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
J Pediatr Genet
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe
instname
J Pediatr Genet
Langer–Giedion's syndrome (LGS) or trichorhinophalangeal syndrome type II (TRPS II; MIM:150230) is a contiguous gene deletion syndrome caused by the haploinsufficiency of the TRPS1 and EXT1 genes. Cornelia de Lange's syndrome (CdLS) is a geneticall
Autor:
Marià Alemany, Sara León Cariñena, Belén Ferrer Lorente, Francisca Moreno Macián, Luis Mifsud Grau
Publikováno v:
Channels
Congenital hyperinsulinemic hypoglycemia is the most frequent cause of persistent and recurrent hypoglycemia in the first years of life and in many patients rare genetic variants can be identified. Recently a case of congenital hyperinsulinemic hypog
Publikováno v:
Anales de Pediatría, Vol 92, Iss 3, Pp 181-182 (2020)
Autor:
Manuel, Oltra-Benavent, Belén, Ferrer-Lorente, Martín, Ródenas Moreno, Laura, Torrejón Rodríguez
Publikováno v:
Anales de pediatria. 92(3)
Autor:
Belén Ferrer-Lorente, Montserrat Évole-Buselli, Antonio Sahuquillo-Torralba, Anaid Calle-Andrino
Publikováno v:
Medicina clinica. 149(9)
Autor:
Belén Ferrer-Lorente, Montserrat Évole-Buselli, Anaid Calle-Andrino, Antonio Sahuquillo-Torralba
Publikováno v:
Medicina Clínica. 149:e49