Zobrazeno 1 - 10
of 58
pro vyhledávání: '"Andrés, Bruno"'
Autor:
Bernardo Frider, Amalia Castillo, Raquel Gordo-Gilart, Andrés Bruno, Marcelo Amante, Luis Alvarez, Verónica Mathet
Publikováno v:
Annals of Hepatology, Vol 14, Iss 5, Pp 745-751 (2015)
Introduction. Progressive familial intrahepatic cholestasis type 3 (PFIC-3) is a severe liver disorder associated with inherited dysfunction of multidrug resistance protein 3 (MDR3/ABCB4), which functions as a phospholipid floppase, translocating pho
Externí odkaz:
https://doaj.org/article/55e78ab0a46f4361ab5210d9411349cf
Publikováno v:
Participatory Educational Research; Jul2023, Vol. 10 Issue 4, p218-236, 19p
Publikováno v:
Acta Gastroenterológica Latinoamericana, Vol 41, Iss 1, Pp 55-59 (2011)
The IgG4-related sclerosing disease is characterized by the presence of plasmatic IgG4 positive cells and Tlymphocytes infiltration in different organs. We herein report a case of cholest asis due to autoimmune cholangitis associated to IgG4 disease.
Externí odkaz:
https://doaj.org/article/ee9752d0b9764d3fa4a96691e92ebb9e
Autor:
Enrique M Baldessari, Mariana Cecilia Herrero, María Pilar Cean, Andrés Mendez Villarroel, Didier Andrés Bruno, Raquel Liliana Vazquez, Graciela Vita
Publikováno v:
Medicina Paliativa.
Introduction: The prevalence of heart failure is on the rise. In its advanced stage (AHF) the condition manifests with incapacitating symptoms. Exacerbations, frequent admissions, and high morbidity and mortality represent conditions amenable to pall
Publikováno v:
Proceedings of the International Conference on Industrial Engineering & Operations Management; 8/16/2021, p408-415, 8p
Akademický článek
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Vía clínica para el tratamiento del neumotórax espontáneo primario en un servicio de cirugía general
Autor:
Soria, Víctor, Flores, Benito, Miguel, Joana, Coll, Antonio, de Andrés, Bruno, Antonio Torralba, José, Campillo, Álvaro, Fe Candel, Mari, Carrasco, Milagros, Luis Aguayo, José
Publikováno v:
In Cirugia Espanola 2005 77(6):343-350
Autor:
Carcedo de Andrés, Bruno P.
Publikováno v:
Espacio, Tiempo y Forma: Serie II, Historia Antigua; 2022, Issue 35, p263-277, 15p
Publikováno v:
Archivos espanoles de urologia. 72(5)
Herlyn-Werner-Wunderlich syndrome (HWW) is a rare congenital anomaly difficult to diagnose due to an alteration in the common embryological development of the reproductive and urinary tract, with renal agenesis, double collecting system, renal duplic