Zobrazeno 1 - 10
of 12
pro vyhledávání: '"José María Rodríguez-Barbero"'
Autor:
José María Rodríguez-Barbero, Alfonso Muriel, Nicolás Nin, Andrés Esteban, Oscar Peñuelas, Eva Aguilar-Rivilla, Julián Panizo-Alcañiz, Carlos Jaramillo, Fernando Frutos-Vivar, Arnaud W. Thille
Publikováno v:
Journal of Critical Care. 60:6-9
Evaluate diagnostic accuracy of portable chest radiograph in mechanically ventilated patients taking autopsy findings as the gold standard and the interobserver agreement among intensivists and radiologists.Retrospective study of 422 patients over 22
Autor:
Aida Ballen, Rebeca Padilla, Andrés Esteban, Fernando Frutos-Vivar, José María Rodríguez-Barbero, Elena Abril, Eva Tejerina, José A. Lorente
Publikováno v:
Human pathology. 76
We evaluate the evolution over time of discrepancies between clinical diagnoses and postmortem findings in critically ill patients and assess the factors associated with these discrepancies. We conducted a prospective study of all consecutive patient
Autor:
Sagrario Fuerte-Ruiz, José María Rodríguez-Barbero, José María Jover-Navalón, Miguel Ángel Hernández-Bartolomé, Alba Manuel Vázquez
Publikováno v:
Revista de Senología y Patología Mamaria. 29:44-46
Autor:
Manuel Zamora, Esther Martin, José Antonio Aramburu, José María Rodríguez-Barbero, Miguel A. Huertas, Pedro Medina, Isabel Solis, Rosario Granados, Beatriz Calvo, Encarnación Camarmo, Teresa Alcaide, Hilda Tellez-Safina, Teresa Corrales, Paloma Bajo, Francisco Mateos, Laura Anta
Publikováno v:
Diagnostic cytopathology. 45(12)
Background European guidelines recommend primary HPV testing for cervical cancer screening. However, the starting age remains to be defined, with an undecided window between 30 and 35 years. This pilot study compares the effectiveness of primary HPV
Publikováno v:
Diagnostic Cytopathology. 28:76-81
Chondroblastoma is a benign tumor arising in the epiphysis of long bones. The extraskeletal presentation is most unusual. We report the first cytological description of a soft tissue chondroblastoma. It was a subcutaneous mass in the leg of a 62-yr-o
Autor:
María Rodríguez Ortega, Manuel Limones Esteban, Alfonso Monereo Alonso, Enrique Montano Navarro, Alberto Carabias Hernández, José María Rodríguez Barbero
Publikováno v:
Gastroenterología y Hepatología. 30:229-231
We present a case of obstructive jaundice due to duodenal amyloidosis presenting as a bulbar pseudotumor (amyloidoma). The duodenal and biliary obstruction were treated by double bypass, hepatojejunostomy and gastroenterostomy. Our case suggests that
Autor:
Liliam El-Bouayadi, Elisa Aguirre, Joaquin Costa, Isabel Roca-Cerezo, Inmaculada Alía, Fernando Frutos-Vivar, Karen Gómez-Mediavilla, Andrés Esteban, José María Rodríguez-Barbero
Publikováno v:
D56. INTENSIVE CARE UNIT PROCEDURES, ULTRASOUND, AND NEW DEVICES.
Autor:
José Antonio Aramburu, Andrés Esteban, Eva Tejerina, Pilar Fernández-Segoviano, José María Rodríguez-Barbero, Fernando Frutos-Vivar, D. Ballesteros
Publikováno v:
Journal of critical care. 25(1)
Methods We studied patients requiring mechanical ventilation for more than 48 hours who died in the intensive care unit and whose bodies were autopsied. We evaluated 3 clinical definitions of ventilator-associated pneumonia: loose definition, defined
Autor:
María, Rodríguez Ortega, Alberto, Carabias Hernández, Enrique, Montano Navarro, Alfonso, Monereo Alonso, José María, Rodríguez Barbero, Manuel, Limones Esteban
Publikováno v:
Gastroenterologia y hepatologia. 30(4)
We present a case of obstructive jaundice due to duodenal amyloidosis presenting as a bulbar pseudotumor (amyloidoma). The duodenal and biliary obstruction were treated by double bypass, hepatojejunostomy and gastroenterostomy. Our case suggests that
Autor:
María, Rodríguez Ortega, Alberto, Carabias Hernández, José María, Rodríguez Barbero, Paloma, Garaulet González, Manuel, Limones Esteban
Publikováno v:
Cirugia espanola. 80(3)
Linitis plastica is a malignant disease that usually occurs in the stomach, although it can affect any segment of the alimentary tract. Typically, this entity shows slow progression and insidious clinical course. We present the case of a patient with