Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Nuria Padullés, Zamora"'
Autor:
Gabriel Mercadal-Orfila, Piedad López Sánchez, Aranzazu Pou Alonso, Olatz Ibarra-Barrueta, Emilio Monte-Boquet, Joaquin Borrás Blasco, Nuria Padullés Zamora, Patricia Sanmartin-Fenollera, Cristina Capilla Montes, M. Ángeles Bernabéu Martínez, Salvador Herrera-Pérez
Publikováno v:
Frontiers in Medicine, Vol 11 (2024)
Background and purposePsoriasis is a chronic, immune-mediated inflammatory skin disease that significantly impacts patients’ quality of life. The integration of telepharmacy has the potential to enhance patient care by providing flexible and person
Externí odkaz:
https://doaj.org/article/b775a92269e34efaa27d8bf339311880
Autor:
Albert Garcia-Sumalla, Raul Rigo, José Castellote, Inmaculada Grau, Fe Tubau, Alberto Amador, Nuria Padullés Zamora, Ariadna Padullés, Sara Cobo
Publikováno v:
Journal of Hepatology. 70:e628-e629
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1d7426abb4c03a8537fd722c7c012f3a
https://doi.org/10.1016/s0618-8278(19)31252-6
https://doi.org/10.1016/s0618-8278(19)31252-6
Autor:
Francisco Rodriguez Frias, José Bruno Montoro Ronsano, Nuria Padullés Zamora, Ferran Sala Piñol, Rosendo Jardí Margalef, Rafael Vidal Pla
Publikováno v:
Archivos de Bronconeumología. 42:553-556
Objetivo El deficit de alfa-1-antitripsina (AAT) es una enfermedad genetica autosomica codominante, que predispone a enfermedad pulmonar obstructiva cronica y enfisema. El tratamiento especifico consiste en la administracion intravenosa sistematica d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ada6603c45b85700a81239265ad8d83d
https://doi.org/10.1157/13093399
https://doi.org/10.1157/13093399
Autor:
Francisco Rodriguez Frias, Rosendo Jardi Margaleff, Nuria Padullés Zamora, Ferran Sala Piñol, Rafael Vidal Pla, José Bruno Montoro Ronsano
Publikováno v:
Archivos de Bronconeumología ((English Edition)). 42:553-556
Objective α1-antitrypsin (AAT) deficiency is a codominant autosomal genetic disorder that predisposes a patient to chronic obstructive pulmonary disease and emphysema. Specific treatment is systemic, consisting of intravenous infusion of AAT. The pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e847b5286acc2349d766ab86fcf6a6a6
https://doi.org/10.1016/s1579-2129(06)60583-1
https://doi.org/10.1016/s1579-2129(06)60583-1
Autor:
Nuria Padullés, Zamora, Rafael Vidal, Pla, Pilar Gispert, Del Rio, Rosendo Jardi, Margaleff, Francisco Rodriguez, Frias, Jose Bruno Montoro, Ronsano, Jose Bruono Montoro, Ronsano
Publikováno v:
The Annals of pharmacotherapy. 42(5)
Background: Severs forms of α1-antitrypsin (AAT) deficiency require augmentation therapy by intravenous administration of purified preparations of AAT concentrate. Although standard AAT treatment schedules are widely available, pharmacokinetic studi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1e2fee0c342f63a628845801b4bb59c
https://pubmed.ncbi.nlm.nih.gov/18413692
https://pubmed.ncbi.nlm.nih.gov/18413692
Autor:
Lourdes Girona-Brumos, Juan Carlos Juárez-Giménez, Pilar Lalueza-Broto, Nuria Padullés-Zamora
Publikováno v:
Medicina Clínica. 129:558-559
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b25dfa4a0249e01c39b86d00942b068
https://doi.org/10.1157/13111422
https://doi.org/10.1157/13111422