Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Carme Cañete Ramírez"'
Autor:
Maria Josep Cabañas Poy, Carme Cañete Ramírez, Sabina X González di Lauro, Virginia Rodríguez Garrido, Gloria Roig Carbajosa, Aurora Fernández-Polo, Susana Clemente Bautista
Publikováno v:
Farmacia Hospitalaria, Vol 40, Iss 5, Pp 427-435 (2016)
The oral administration of drugs to the pediatric population involves the extemporaneous preparation of liquid formulations. These formulations have studies on their physicochemical stability, but they often lack microbiological studies. The objectiv
Externí odkaz:
https://doaj.org/article/dcdba04859064c4d9aa40be4780745e7
Autor:
Cristina Villanueva-Bueno, Elena Montecatine-Alonso, Francisco Jiménez-Parrilla, María González-López, Silvia Manrique-Rodríguez, Francisco Moreno-Ramos, Carme Cañete-Ramírez, Elisenda Dolz, Ana García-Robles, José Manuel Caro-Teller, María Teresa Moral-Pumarega, Elena Bergon-Sendin, María Teresa Gómez-Trevecedo Calvo, Carmen Gallego-Fernández, Concepción Álvarez del Vayo-Benito, Marta Mejías-Trueba, María Victoria Gil-Navarro, Paediatric Antimicrobial Defined Daily Dose Study Group (KiDDDs)
Publikováno v:
Antibiotics, Vol 12, Iss 3, p 602 (2023)
Background: Currently, there is no validated method for estimating antimicrobial consumption in the neonatal population, as it exists for adults using Defined Daily Doses (DDD). In neonatology, although there are different methods, each one with adva
Externí odkaz:
https://doaj.org/article/e803fd3c09ec48b3978a97aff198694e
Autor:
Eugènia Serramontmany, Marina Muñoz, Aurora Fernández-Polo, María Morillo, Laura Gómez-Ganda, Carme Cañete-Ramírez, Gema Ariceta
Publikováno v:
Frontiers in Pediatrics, Vol 8 (2021)
Background: Congenital nephrotic syndrome of the Finnish type (CNF) is a rare, severe glomerular disease caused by mutations in the NPHS1 gene, which codes for nephrin. It is characterised by massive proteinuria and severe edoema. Progression to end-
Externí odkaz:
https://doaj.org/article/960619c2faa445cabc051123dfd9ba6c
Autor:
(KiDDDs), Cristina Villanueva-Bueno, Elena Montecatine-Alonso, Francisco Jiménez-Parrilla, María González-López, Silvia Manrique-Rodríguez, Francisco Moreno-Ramos, Carme Cañete-Ramírez, Elisenda Dolz, Ana García-Robles, José Manuel Caro-Teller, María Teresa Moral-Pumarega, Elena Bergon-Sendin, María Teresa Gómez-Trevecedo Calvo, Carmen Gallego-Fernández, Concepción Álvarez del Vayo-Benito, Marta Mejías-Trueba, María Victoria Gil-Navarro, Paediatric Antimicrobial Defined Daily Dose Study Group (KiDDDs) Paediatric Antimicrobial Defined Daily Dose Study Group
Publikováno v:
Antibiotics; Volume 12; Issue 3; Pages: 602
Background: Currently, there is no validated method for estimating antimicrobial consumption in the neonatal population, as it exists for adults using Defined Daily Doses (DDD). In neonatology, although there are different methods, each one with adva
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=multidiscipl::79d242f23323bd9e3e3a3beceef8dbdd
Autor:
José María Alonso-Herreros, Silvia Berisa-Prado, Carme Cañete-Ramírez, María del Pilar Flox-Benítez, Margarita Ladrón de Guevara-García, Carmen López-Cabezas, Ana María Martín de Rosales-Cabrera, Beatriz Ramos-Martínez
Publikováno v:
Farmacia Hospitalaria, Vol 44, Iss Supl 1, Pp 49-52 (2020)
As in other areas of the health system, COVID-19 has had a dramatic impact on hospital compounding. This area has faced numerous challenges, including the shortage of frequent-use products (hydroalcoholic solutions, lopinavir/ritonavir suspension), t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doajarticles::9e3a4e507620dfdc6b7af6fefc1d63cd
http://www.aulamedica.es/fh/pdf/11492.pdf
http://www.aulamedica.es/fh/pdf/11492.pdf
Autor:
Carme Cañete-Ramírez, Maria Morillo, Marina Muñoz, Gema Ariceta, Laura Gómez-Ganda, Eugènia Serramontmany, Aurora Fernández-Polo
Publikováno v:
Frontiers in Pediatrics
Scientia
Frontiers in Pediatrics, Vol 8 (2021)
Scientia
Frontiers in Pediatrics, Vol 8 (2021)
Background:Congenital nephrotic syndrome of the Finnish type (CNF) is a rare, severe glomerular disease caused by mutations in the NPHS1 gene, which codes for nephrin. It is characterised by massive proteinuria and severe edoema. Progression to end-s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ecdb41245a1e4cb08381d95ab04f1ab4
https://pubmed.ncbi.nlm.nih.gov/33520897
https://pubmed.ncbi.nlm.nih.gov/33520897
Autor:
Maria Josep Cabañas Poy, Maria Roch Santed, Aurora Fernández Polo, Carme Cañete Ramírez, Susana Clemente Bautista, Mireia Del Toro Riera
Publikováno v:
European Journal of Hospital Pharmacy. 24:185-188
Case A child with Niemann-Pick disease type C was started on miglustat therapy at the age of 2 years. Intrathecal administration of hydroxypropyl-β-cyclodextrin was added 5 months later. The initial dose of 175 mg was gradually increased over the fi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::364b6be39d5cbee3af42ac3f0fa3c0d5
https://doi.org/10.1136/ejhpharm-2016-001067
https://doi.org/10.1136/ejhpharm-2016-001067