Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Rosa Goterris Viciedo"'
Recommendations for the diagnosis and treatment of patients with thrombotic thrombocytopenic purpura
Autor:
María Eva Mingot Castellano, Cristina Pascual Izquierdo, Ataulfo González, Aurora Viejo Llorente, David Valcarcel Ferreiras, Elena Sebastián, Faustino García Candel, Héctor Sarmiento Palao, Inés Gómez Seguí, Javier de la Rubia, Joan Cid, Jorge Martínez Nieto, Luis Hernández Mateo, Rosa Goterris Viciedo, Teresa Fidalgo, Ramon Salinas, Julio del Rio-Garma
Publikováno v:
Medicina Clínica (English Edition). 158:630.e1-630.e14
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fa43b5c82cc114cea28bf59b0d2c09cf
https://doi.org/10.1016/j.medcle.2021.03.038
https://doi.org/10.1016/j.medcle.2021.03.038
Autor:
Joan Cid, Inés Gómez Seguí, Rosa Goterris Viciedo, Julio del Río-Garma, Jorge M. Nieto, Luis M. Hernández Mateo, Elena Sebastián, A. González, Javier de la Rubia, Ramón Salinas, Teresa Fidalgo, Grupo Español de Aféresis, María Eva Mingot Castellano, David Valcarcel Ferreiras, Faustino García Candel, Cristina Pascual Izquierdo, Aurora Viejo Llorente, Hector Sarmiento Palao
Publikováno v:
Medicina Clínica. 158:630.e1-630.e14
Thrombotic thrombocytopenic purpura (TTP) is a thrombotic microangiopathy (TMA) characterized by the development of microangiopathic haemolytic anaemia, thrombocytopenia, and ischaemic organ dysfunction associated with ADAMTS13 levels lower than 10%
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c5183f687f8a22133740423bf6a22232
https://doi.org/10.1016/j.medcli.2021.03.040
https://doi.org/10.1016/j.medcli.2021.03.040
Autor:
Rosa Goterris-Viciedo, Víctor Alegre de Miquel, Maria Macarena Giacaman-von der Weth, Amparo Pérez-Ferriols, Felipe Partarrieu-Mejías
Publikováno v:
Dermatologic Therapy
r-INCLIVA. Repositorio Institucional de Producción Científica de INCLIVA
instname
r-INCLIVA. Repositorio Institucional de Producción Científica de INCLIVA
instname
Eosinophilic fasciitis (EF) is an uncommon fibrosing disease of the fascia with characteristic cutaneous and hematologic manifestations. Although EF is most commonly treated with corticosteroids at the beginning, a considerable number of patients sho
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6cddeccf419ae5dafe464146b86468e4
https://pubmed.ncbi.nlm.nih.gov/31025428
https://pubmed.ncbi.nlm.nih.gov/31025428
Autor:
Partarrieu‐Mejías, Felipe1 fpartarrieu@gmail.com, Giacaman‐Von der Weth, María Macarena1, Pérez‐Ferriols, Amparo1, Goterris‐Viciedo, Rosa2, Alegre‐de Miquel, Victor1
Publikováno v:
Dermatologic Therapy. Jul2019, Vol. 32 Issue 4, pN.PAG-N.PAG. 1p.
Publikováno v:
Blood Transfusion (17232007); 2011 Supplement, ps113-s188, 76p