Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Macarena Piñero-Saavedra"'
Publikováno v:
Journal of Rare Diseases Research & Treatment. 2:14-19
Autor:
Blanca Sáenz de San Pedro, Belén Hinojosa, Macarena Piñero-Saavedra, Pedro Bobadilla-González, Cristina Alcaraz, Raúl García-Lozano, T González-Quevedo, Lourdes Fernández-Vieira
Publikováno v:
Annals of Allergy, Asthma & Immunology. 117:520-526
Background Information on F12 mutation hereditary angioedema (HAE) is still limited, but Spain is now recognized as having one of the highest concentrations of cases in Western Europe. Objective To describe unique features of HAE in Spanish carriers
Autor:
Teresa Gonzalez-Quevedo, Anna Sala Cunill, Mar Guilarte, Macarena Piñero-Saavedra, Alicia Prieto-García, Ignacio Jauregui, Maria Pedrosa, Marta Ferrer, Teresa Caballero, Stefan Cimbollek
Publikováno v:
Annals of Medicine. 46:607-618
Angioedema refers to a localized, transient swelling of the deep skin layers or the upper respiratory or gastrointestinal mucosa. It develops as a result of mainly two different vasoactive peptides, histamine or bradykinin. Pathophysiology, as well a
Autor:
Isabel Gonzalez-Martin, Belen Hinojosa-Jara, Macarena Piñero-Saavedra, Marta Rodriguez-Lantaron, Marina Lluncor
Publikováno v:
Journal of Allergy and Clinical Immunology. 143:AB277
Autor:
Macarena, Piñero-Saavedra, Teresa, González-Quevedo, Blanca, Saenz de San Pedro, Cristina, Alcaraz, Pedro, Bobadilla-González, Lourdes, Fernández-Vieira, Belén, Hinojosa, Raúl, García-Lozano
Publikováno v:
Annals of allergy, asthmaimmunology : official publication of the American College of Allergy, Asthma,Immunology. 117(5)
Information on F12 mutation hereditary angioedema (HAE) is still limited, but Spain is now recognized as having one of the highest concentrations of cases in Western Europe.To describe unique features of HAE in Spanish carriers of the F12 mutation an
Autor:
Manuel Prados Castaño, Santiago Leguisamo Milla, Maria Ortega Camarero, Macarena Piñero-Saavedra
Publikováno v:
Blood Coagulation & Fibrinolysis. 24:576-578
Drug reaction with eosinophlia and systemic symptoms (DRESS) syndrome describes a severe medication-induced adverse reaction, which shows skin, blood and solid-organ features. Up to 50 drugs have been described to cause DRESS. The main responsible dr
Autor:
Macarena Piñero-Saavedra, Prados Castaño M, Sánchez B, Jm, Lucena Soto, Avila Castellanos R, Ortega-Camarero M
Publikováno v:
Europe PubMed Central