Zobrazeno 1 - 6
of 6
pro vyhledávání: '"José María Serratosa Fernández"'
Autor:
Irene, García Morales, Cesáreo, Fernández Alonso, Navid, Behzadi Koochani, José María, Serratosa Fernández, Antonio, Gil-Nagel Rein, Manuel, Toledo, Francisco Javier, González, Estevo, Santamarina Pérez
Publikováno v:
Emergencias : revista de la Sociedad Espanola de Medicina de Emergencias. 32(5)
This consensus statement was developed to optimize the emergency management of epileptic seizures in prehospital and hospital settings. A list of clinical questions was drafted and the literature on the emergency treatment of epileptic seizures was r
Autor:
José María Serratosa Fernández, José Tuñón Fernández, Loreto Bravo Calero, Pepa Sánchez Borque, Rafael Sáez Pinel, Ángel Miracle Blanco, Ivana Zamarbide Capdepón, Inmaculada Navas Vinagre, M Araceli García Torres, José Manuel Rubio Campal
Publikováno v:
The American journal of cardiology. 125(3)
Atrial fibrillation (AF) causes a substantial proportion of embolic strokes of undeterminded source (ESUS). Effective detection of subclinical AF (SCAF) has important therapeutic implications. We conducted a prospective study to determine the prevale
Autor:
Daniela Dicapua Sacoto, José María Serratosa Fernández, Paloma Balugo Bengoechea, M.E. García, Irene García Morales, Beatriz G. Giráldez
Publikováno v:
Epileptic Disorders. 15:175-180
Episodes of loss of consciousness are common, even in young, healthy people, and can sometimes represent a diagnostic challenge. The main diagnoses to consider are syncope and epileptic seizures, both of which may have similar symptomatology such as
Publikováno v:
The Neurologist. 13:S38-S46
Background: Despite the currently available armamentarium of antiepileptic drugs, seizures are not adequately controlled in about one-third of epileptic patients. The mechanisms of antiepileptic drug resistance are multiple and not fully clarified. M
Publikováno v:
The neurologist. 13(6 Suppl 1)
Background: The contribution of genetic factors to the origin of different epilepsies is a fact established by epidemiological, clinical, and molecular studies. These studies have made it possible to identify numerous mutations in different genes tha
Publikováno v:
Revista de Neurología. 30:378