Zobrazeno 1 - 8
of 8
pro vyhledávání: '"María Angeles Dasí"'
Autor:
Emilio Monteagudo, Itziar Astigarraga, Áurea Cervera, María Angeles Dasí, Ana Sastre, Rubén Berrueco, José Luis Dapena
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://doaj.org/article/f46c7b3158284b6395ecbf461a0189a0
Autor:
Emilio Monteagudo, Itziar Astigarraga, Áurea Cervera, María Angeles Dasí, Ana Sastre, Rubén Berrueco, José Luis Dapena
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://doaj.org/article/2d7e1390fdd34e4fb991946fe1708244
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:
Emilio, Monteagudo, Itziar, Astigarraga, Áurea, Cervera, María Angeles, Dasí, Ana, Sastre, Rubén, Berrueco, José Luis, Dapena
Publikováno v:
Anales de pediatria. 91(2)
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=pmid________::0e9e67034a23a16d3601c2307bece4ee
https://pubmed.ncbi.nlm.nih.gov/31178291
https://pubmed.ncbi.nlm.nih.gov/31178291
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, Itziar Astigarraga, Emilio Monteagudo, Ana Sastre, T Toll, A. Llort, J. Molina, María Angeles Dasí, Rafael Fernández-Delgado
Publikováno v:
Anales de Pediatría, Vol 74, Iss 6, Pp 414.e1-414.e8 (2011)
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___::705e6e8a99eff6fa7d587db884e1dd60
https://doi.org/10.1016/j.anpedi.2010.11.004
https://doi.org/10.1016/j.anpedi.2010.11.004
Autor:
Judith Reina-Castillón, Roser Pujol, Marcos López-Sánchez, Benjamín Rodríguez-Santiago, Miriam Aza-Carmona, Juan Ramón González, José Antonio Casado, Juan Antonio Bueren, Julián Sevilla, Isabel Badel, Albert Català, Cristina Beléndez, María Ángeles Dasí, Cristina Díaz de Heredia, Jean Soulier, Detlev Schindler, Luis Alberto Pérez-Jurado, Jordi Surrallés
Publikováno v:
Blood Advances, Vol 1, Iss 5, Pp 319-329 (2017)
Abstract: Detectable clonal mosaicism for large chromosomal events has been associated with aging and an increased risk of hematological and some solid cancers. We hypothesized that genetic cancer predisposition disorders, such as Fanconi anemia (FA)
Externí odkaz:
https://doaj.org/article/2a05af7ecf714c17916551b30f0cd80f
Autor:
Pilar Casaña, Noelia Cabrera, Ana Rosa Cid, Saturnino Haya, Magdalena Beneyto, Carmen Espinós, Vicente Cortina, Maria Angeles Dasí, Josè Antonio Aznar
Publikováno v:
Haematologica, Vol 93, Iss 7 (2008)
Hemophilia A is an X-linked recessive disorder caused by a lack or decrease of factor VIII activity. Its socio-economic impact is high given its high bleeding expression and treatment cost. Our aim was to establish the mutation of each patient to imp
Externí odkaz:
https://doaj.org/article/3ed4722f199947ed995035b721d7a152