Survival and toxicity outcomes of hematopoietic stem cell transplantation for pediatric patients with Fanconi anemia: a unified multicentric national study from the Spanish Working Group for Bone Marrow Transplantation in Children

Autor: A Sastre Urgelles, M. L. Uria Oficialdegui, A Rodríguez Villa, I. Badell Serra, B. Argiles Aparicio, Marta González-Vicent, C Beléndez-Bieler, L. Murillo-Sanjuán, Cristina Diaz-de-Heredia, M López-Duarte, J Sevilla Navarro

Publikováno v: BONE MARROW TRANSPLANTATION
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
r-IIS La Fe. Repositorio Institucional de Producción Científica del Instituto de Investigación Sanitaria La Fe

Hematopoietic stem cell transplantation (HSCT) is currently the only curative option for hematological manifestations in patients with Fanconi anemia (FA). We report the outcome of 34 patients with FA inside a collaborative multicenter national study

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35d8aeeeb6b84e39d8579895417b9622
https://pubmed.ncbi.nlm.nih.gov/33303901

Evaluation of bone mineral density in children with sickle cell disease

Autor: E. Cela de Julián, C. Beléndez Bieler, M. Pérez Díaz, C. Garrido Colino

Publikováno v: Anales de Pediatría (English Edition), Vol 82, Iss 4, Pp 216-221 (2015)

Objective: To evaluate bone mineral density (BMD) in children with sickle cell disease (SCD) in the Community of Madrid. Materials and methods: The BMD was estimated in 40 children with SCD, and with an age range between 3 and 16 years, using densito

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c420de1fe3f7f8dd7de222b8d6f1ca9a
https://doi.org/10.1016/j.anpede.2015.03.006

The treatment for primary immune thrombocytopenia with romiplostim in adult and paediatric patients: use experience at a Spanish university hospital

Autor: Vicente Escudero-Vilaplana, S Pernía, I Marquínez-Alonso, C Beléndez Bieler, María Sanjurjo-Sáez, Cecilia M. Fernández-Llamazares

Publikováno v: Journal of Clinical Pharmacy and Therapeutics. 39:376-382

SummaryWhat is known and objective Primary immune thrombocytopenia (ITP) is characterized by accelerated platelet destruction, as well as suboptimal platelet production. Thrombopoietin (TPO) receptor agonists bind to and activate human TPO receptor,

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::473eee0613441e841b1dc3977b22cc1b
https://doi.org/10.1111/jcpt.12156

Evaluación en el tercer año de implantación del cribado neonatal universal de anemia falciforme en la Comunidad de Madrid

Autor: E. Dulín Íñiguez, M. García Arias, M. Arranz Leirado, E. Cela de Julián, M. Guerrero Soler, P. Galarón García, A. Cantalejo López, J.M. Bellón Cano, C. Beléndez Bieler

Publikováno v: Anales de Pediatría, Vol 66, Iss 4, Pp 382-386 (2007)

Antecedentes: La anemia falciforme es una enfermedad hereditaria que como resultado de las migraciones, constituye una de las alteraciones genéticas más frecuentes en el noroeste de Europa. Las complicaciones secundarias a la enfermedad son frecuen

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8ecb5f22f3c5803f3a468608dc41842
http://www.sciencedirect.com/science/article/pii/S1695403307704319

Anemia hemolítica autoinmunitaria por crioaglutininas secundaria a neumonía neumocócica

Autor: J. Saavedra Lozano, P. Galarón García, C. Beléndez Bieler, F. González Martínez, A. Rodríguez Ogando, M.J. Rodríguez Castaño

Publikováno v: Anales de Pediatría, Vol 72, Iss 6, Pp 440-442 (2010)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5bdcf1782e462c7661b9d7448dd75e97
https://doi.org/10.1016/j.anpedi.2010.02.006