Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Cristina Martínez Faci"'
Autor:
Beatriz Palenzuela Afonso, Ana B. Caparrós Nieto, Macarena González Cruz, Cristina Martínez Faci
Publikováno v:
Anales de Pediatría (English Edition), Vol 98, Iss 2, Pp 141-142 (2023)
Externí odkaz:
https://doaj.org/article/492dd8b4d8384e80be60d95ee72f862f
Autor:
Beatriz Palenzuela Afonso, Ana B. Caparrós Nieto, Macarena González Cruz, Cristina Martínez Faci
Publikováno v:
Anales de Pediatría, Vol 98, Iss 2, Pp 141-142 (2023)
Externí odkaz:
https://doaj.org/article/64500627ff214123be52328d1ecaef9d
Autor:
Carmen Rodríguez-Vigil Iturrate, Maria Pilar Sanz de Miguel, Cristina Martínez Faci, Laura Murillo Sanjuan, Carlota Calvo Escribano, Juan Pablo García Íñiguez, Maria Pilar Samper Villagrasa
Publikováno v:
Anales de Pediatría, Vol 93, Iss 1, Pp 16-23 (2020)
Resumen: Introducción: La trombocitopenia inmune primaria (PTI) es poco frecuente en la infancia, pero es la causa más habitual de trombocitopenia. Se han intentado establecer factores de riesgo para predecir su evolución, con el objetivo de poder
Externí odkaz:
https://doaj.org/article/14e0d6b5b6854d87a9ddd2e6f63cdc93
Autor:
Carmen Rodríguez-Vigil Iturrate, Maria Pilar Sanz de Miguel, Cristina Martínez Faci, Laura Murillo Sanjuan, Carlota Calvo Escribano, Juan Pablo García Íñiguez, Maria Pilar Samper Villagrasa
Publikováno v:
Anales de Pediatría (English Edition), Vol 93, Iss 1, Pp 16-23 (2020)
Introduction: Although primary immune thrombocytopenia (ITP) is rare in childhood, it is the most frequent cause of thrombocytopenia. There have been attempts to establish risk factors to predict the progression of the disease in order to optimise it
Externí odkaz:
https://doaj.org/article/b2d4a96f67c643e38625e50e5f35e04d
Autor:
Juan Pablo García Íñiguez, María Pilar Samper Villagrasa, Carlota Calvo Escribano, Laura Murillo Sanjuan, Carmen Rodríguez-Vigil Iturrate, Maria Pilar Sanz de Miguel, Cristina Martínez Faci
Publikováno v:
Anales de Pediatría (English Edition), Vol 93, Iss 1, Pp 16-23 (2020)
Zaguán. Repositorio Digital de la Universidad de Zaragoza
instname
Zaguán: Repositorio Digital de la Universidad de Zaragoza
Universidad de Zaragoza
Zaguán. Repositorio Digital de la Universidad de Zaragoza
instname
Zaguán: Repositorio Digital de la Universidad de Zaragoza
Universidad de Zaragoza
Introduction: Although primary immune thrombocytopenia (ITP) is rare in childhood, it is the most frequent cause of thrombocytopenia. There have been attempts to establish risk factors to predict the progression of the disease in order to optimise it
Publikováno v:
Archivos Argentinos de Pediatria. 119
Unlike adults, ovarian tumors are infrequent in the pediatric population, predominating the germ line at this age, with high survival rates. The objective is to present the epidemiological, clinical, diagnosis and therapeutic characteristics of 0 to
Autor:
Carmen Rodríguez-Vigil Iturrate, Laura Murillo Sanjuan, Cristina Martínez Faci, Alicia Montaner Ramón, Carmelo Guerrero Laleona
Publikováno v:
Archivos Argentinos de Pediatria. 115
Chronic granulomatous disease (CGD) is a primary immunodeficiency with an incidence of 1/200,000-250,000 live births. CGD affects mainly male patients, most of the mutations being X-linked, and autosomal recessive forms occur more frequently in commu
Autor:
Ascensión Muñoz Mellado, Cristina Martínez Faci, Laura Murillo Sanjuan, Carmen Rodríguez-Vigil Iturrate, José Miguel Martínez de Zabarte Fernández, Inmaculada García Jiménez
Publikováno v:
Archivos Argentinos de Pediatria. 115
Anemia is very common in infants. Although its causes are usually not severe and treatable, proper etiologic diagnosis should be established. When anemia is non-regenerative, it can be caused by aplastic anemia, myelodysplastic syndrome, bone marrow
Autor:
Maria Ángeles Carlota Calvo Escribano, Carmen Rodríguez-Vigil Iturrate, Laura Murillo Sanjuan, Ana Carboné Bañeres, Ines Martinez Redondo, Cristina Martínez Faci, Maria C. Vera Sáez-Benito
Publikováno v:
Journal of pediatric hematology/oncology. 39(1)
Autor:
Alicia, Montaner Ramón, Laura, Murillo Sanjuán, Cristina, Martínez Faci, Carmelo, Guerrero Laleona, Carmen, Rodríguez-Vigil Iturrate
Publikováno v:
Archivos argentinos de pediatria. 115(2)
Chronic granulomatous disease (CGD) is a primary immunodeficiency with an incidence of 1/200,000-250,000 live births. CGD affects mainly male patients, most of the mutations being X-linked, and autosomal recessive forms occur more frequently in commu