Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Aurea Cervera"'
Autor:
Griselda Vallés, Pablo Velasco, José Antonio Salinas, Eduardo J. Bardón Cancho, David Beneitez, Thais Murciano, Cristina Beléndez, Elena Cela, Aurea Cervera, Anna Ruiz-Llobet, Ainhoa Gondra, Mar Bermúdez, Cruz Vecilla, Rubén Berrueco, Bienvenida Argilés, Marina García-Morín
Publikováno v:
Medicina Clínica (English Edition). 155:95-103
Background and objective Patients with thalassaemia major (TM) and sickle cell disease (SCD) in Spain have been counted since the creation of the Spanish registry of haemoglobinopathies (REHem). The objective of this paper is to update the published
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f8f910cc36f75096485d7b598c57c081
https://doi.org/10.1016/j.medcle.2019.10.007
https://doi.org/10.1016/j.medcle.2019.10.007
Autor:
Eduardo J. Bardón Cancho, Pablo Velasco, Aurea Cervera, Marina García-Morín, Rubén Berrueco, Mar Bermúdez, Ainhoa Gondra, José Antonio Salinas, Griselda Vallés, Thais Murciano, Cristina Beléndez, David Beneitez, Anna Ruiz-Llobet, Elena Cela, Bienvenida Argilés, Cruz Vecilla
Publikováno v:
Medicina Clínica. 155:95-103
Resumen Antecedentes y objetivo Los pacientes con talasemia mayor (TM) y enfermedad de celulas falciformes (ECF) en Espana se han empezado a contabilizar desde la creacion del registro espanol de hemoglobinopatias (REHem). El objetivo del trabajo es
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2a24e493bc3551a717e3b43ac78c4d44
https://doi.org/10.1016/j.medcli.2019.10.011
https://doi.org/10.1016/j.medcli.2019.10.011
Autor:
Grupo Español de Eritropatología, Silvia de la Iglesia, David Beneitez, Marta Morado Arias, Aurea Cervera, Beatriz Arrizabalaga, Ana Villegas, Isabel Gutiérrez Jomarrón, Montserrat López Rubio, Ascensión Herrera, María Isabel Sáez, Valle Recasens
Publikováno v:
Medicina Clínica (English Edition). 154:331-337
Introduction Autoimmune haemolytic anaemia (AIHA) is an infrequent and heterogeneous disease in its pathophysiology and clinical behaviour, therefore it is generally managed empirically. Patients and methods We conducted an observational, retrospecti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::65a32f19e918f48d8384586c622cf78e
https://doi.org/10.1016/j.medcle.2019.06.025
https://doi.org/10.1016/j.medcle.2019.06.025
Autor:
Grupo Español de Eritropatología, Ascensión Herrera, Valle Recasens, Silvia de la Iglesia, Marta Morado Arias, David Beneitez, María Isabel Sáez, Ana Villegas, Montserrat López Rubio, Aurea Cervera, Beatriz Arrizabalaga, Isabel Gutiérrez Jomarrón
Publikováno v:
Medicina Clínica. 154:331-337
Resumen Introduccion Las anemias hemoliticas autoinmunes (AHAI) son enfermedades poco frecuentes y heterogeneas en su fisiopatologia y comportamiento clinico, siendo el manejo de las mismas fundamentalmente empirico. Pacientes y metodos Realizamos un
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d9bab5ed489c05f3118a22f1d9ecf0f3
https://doi.org/10.1016/j.medcli.2019.06.024
https://doi.org/10.1016/j.medcli.2019.06.024
Autor:
Aurea Cervera, Emilio Monteagudo, José Luis Dapena, Itziar Astigarraga, Rubén Berrueco, María Angeles Dasí, Ana Sastre
Publikováno v:
Anales de Pediatría, Vol 91, Iss 2, Pp 127.e1-127.e10 (2019)
Resumen: La trombocitopenia inmune primaria, anteriormente conocida como púrpura trombocitopénica inmune, es una enfermedad cuyo manejo diagnóstico y terapéutico ha sido siempre controvertido. La Sociedad Española de Hematología y Oncología Pe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9feaddd7b0bd9a124e0e08672738d0c4
http://www.sciencedirect.com/science/article/pii/S1695403319301821
http://www.sciencedirect.com/science/article/pii/S1695403319301821
Autor:
Isabel, Gutiérrez Jomarrón, Montserrat, López Rubio, Marta, Morado Arias, Beatriz, Arrizabalaga, Silvia, de la Iglesia, David, Beneitez, María Isabel, Sáez, Aurea, Cervera, Valle, Recasens, Ascensión, Herrera, Ana María, Villegas
Publikováno v:
Medicina clinica. 154(9)
Autoimmune haemolytic anaemia (AIHA) is an infrequent and heterogeneous disease in its pathophysiology and clinical behaviour, therefore it is generally managed empirically.We conducted an observational, retrospective and multicentre study of 93 pati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::223ffbf060b16929ffc670c1634a61de
https://pubmed.ncbi.nlm.nih.gov/31488259
https://pubmed.ncbi.nlm.nih.gov/31488259
Autor:
Aurea Cervera, Ana Sastre, José Luis Dapena, Emilio Monteagudo, Rubén Berrueco, María Angeles Dasí, Itziar Astigarraga
Publikováno v:
Anales de Pediatría (English Edition), Vol 91, Iss 2, Pp 127.e1-127.e10 (2019)
Primary immune thrombocytopenia, formerly known as immune thrombocytopenic purpura, is a disease for which the clinical and therapeutic management has always been controversial. The ITP working group of the Spanish Society of Paediatric Haematology a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e7008e1531b633be0b168ccebd8d95a
https://doi.org/10.1016/j.anpede.2019.04.008
https://doi.org/10.1016/j.anpede.2019.04.008
Autor:
Aurea Cervera, Félix de la Fuente-Gonzalo, Jorge Martínez-Nieto, Lara Vinuesa, Ana Villegas, Paloma Ropero, Elena Cela, Joaquín Díaz-Mediavilla, Cristina Beléndez, Fernando A. González
Publikováno v:
Hemoglobin. 37:112-118
In the 5' untranslated region (5'UTR), which is transcribed but not translated and is involved in posttranscriptional regulation of the gene promoting and stabilizing the mRNA translation, several mutations associated with mild β-thalassemia (β-tha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::95496a9162e5e784db978e566d1d36ef
https://doi.org/10.3109/03630269.2013.766620
https://doi.org/10.3109/03630269.2013.766620
Autor:
Elena, Cela, José M, Bellón, María, de la Cruz, Cristina, Beléndez, Rubén, Berrueco, Anna, Ruiz, Izaskun, Elorza, Cristina, Díaz de Heredia, Aurea, Cervera, Griselda, Vallés, J Antonio, Salinas, M Teresa, Coll, Mar, Bermúdez, Marta, Prudencio, Bienvenida, Argilés, Cruz, Vecilla
Publikováno v:
Pediatric bloodcancer. 64(7)
Although highly prevalent throughout the world, the accurate prevalence of hemoglobinopathies in Spain is unknown.This study presents data on the national registry of hemoglobinopathies of patients with thalassemia major (TM), thalassemia intermedia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::3fd67ff9fdea38b1c80f64a87de97540
https://pubmed.ncbi.nlm.nih.gov/28371007
https://pubmed.ncbi.nlm.nih.gov/28371007
Autor:
Leticia Albert, Rosario Cogollos, Rebeca Villares, Miguel A. Roa, Abdulkareem Alarabe, Rogelio López-Vélez, Juan Arnaez, Aurea Cervera, José M. Rubio
Publikováno v:
Journal of Travel Medicine. 17:221-227
Background. In Europe, imported malarial cases occur in returning travelers and immigrants mostly from African countries. There have been an increasing number of cases in the past years in Spain. Methods. An analysis of all cases of malaria who atten
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39f6be6de62c58e50985962e39b71361
https://doi.org/10.1111/j.1708-8305.2010.00416.x
https://doi.org/10.1111/j.1708-8305.2010.00416.x