Zobrazeno 1 - 10
of 66
pro vyhledávání: '"V. Castel Sánchez"'
Autor:
S. Navarro Fos, M. Piqueras Franco, R. Noguera Salvá, A. Ruiz Saurí, V. Castel Sánchez, Antonio Llombart-Bosch
Publikováno v:
Anales de Pediatría, Vol 64, Iss 5, Pp 449-456 (2006)
El neuroblastoma presenta alteraciones genéticas que predicen su evolución clínica. Ganancias cromosómicas completas están asociadas a estadios clínicos no avanzados y evolución favorable, mientras que pérdidas de 1p, ganancia de 17q y amplif
Autor:
V. Castel Sánchez, J.M. Fernández Navarro, V. Verdeguer Miralles, L. López Ferrer, B. Pozuelo Muñoz, P. Ortí Martínez, A. Cañete Nieto
Publikováno v:
Anales de Pediatría, Vol 52, Iss 1, Pp 41-46 (2000)
La hospitalización a domicilio para niños con cáncerempezó a funcionar en la Unidad de Oncología Pediátrica(UOP) del Hospital Infantil La Fe en abril de 1997. Recogemos en este trabajo la asistencia realizada en los primeros 17 meses de experie
Autor:
G, Sanchís Blanco, M, Andrés Moreno, A F, Gregoraci, J, Cortés Sáez, A, Marco Macián, J M, Rubio Rubio, E, Novella Maestre, V, Castel Sánchez, C, García-Sala Viguer
Publikováno v:
Cirugia pediatrica : organo oficial de la Sociedad Espanola de Cirugia Pediatrica. 24(4)
Ovarian cortex cryopreservation (OCC) for future autotransplant represents a treatment alternative for those paediatric cancer survivors affected of ovarian failure and fertility disorders.Patients with high gonadotoxic risk are included in the Oncol
Autor:
Jose A. Martinez-Climent, J. Ferris i Tortajada, A Verdeguer Miralles, C. Esquembre Menor, V. Castel Sánchez
Publikováno v:
Journal of Neuro-Oncology. 22:67-76
Evaluation of quality of life of survivors of brain tumors is an important aspect of outcome that must be included in clinical studies.We have developed a new scale for assessing quality of life (QL) of pediatric long-term survivors of posterior foss
Publikováno v:
Clinicaltranslational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico. 9(7)
Synovial sarcoma (SS) is a rare disease in the paediatric population, predominating in adolescents. Surgery remains the best treatment strategy for resectable cases. Adjuvant chemotherapy or radiotherapy can be used but have not proven efficacy. Meta
Autor:
R, Noguera Salvá, M, Piqueras Franco, A, Ruiz Saurí, A, Llombart-Bosch, V, Castel Sánchez, S, Navarro Fos
Publikováno v:
Anales de pediatria (Barcelona, Spain : 2003). 64(5)
Different subtypes of neuroblastoma (NB) carry associated genetic aberrations that predict their clinical course. Whole chromosome gains are usually associated with early clinical stages and good prognosis, while 1p deletion, 17q gain and MYCN amplif
Autor:
J, Balaguer Guill, J Maria, Fernández Navarro, A, Cañete Nieto, Maria D, Muro Velilla, M, Hernández Martí, V, Castel Sánchez
Publikováno v:
Anales de pediatria (Barcelona, Spain : 2003). 64(5)
To determine the frequency and distribution of primary renal tumors diagnosed in a pediatric oncology unit in children younger than 1 year and identify their clinical and histopathological characteristics, the treatment used, and outcomes.We retrospe
Autor:
J, Bernabeu Verdu, B, López Luengo, C, Fournier del Castillo, A, Cañete Nieto, J, Suárez Rodríguez, V, Castel Sánchez
Publikováno v:
Revista de neurologia. 38(5)
Childhood cancer treatments have made a spectacular advance in recent years, obtaining survival rates of about 70%. These survival rates have permitted many children to reach adulthood, but also involve the appearance of previously unknown neurocogni
Autor:
M, Bermúdez Cortés, A, Verdeguer Miralles, C, Jovaní Casano, A, Cañete Nieto, J M, Fernández, J, Ferris Tortajada, V, Castel Sánchez
Publikováno v:
Anales espanoles de pediatria. 48(6)
Children with Down's Syndrome (DS) have a high risk for leukemia and need special clinical management. For this reason we have reviewed our experience.All children with DS diagnosed a having acute leukemia during a 21-year period were reviewed retros
Autor:
V, Castel Sánchez, C, Melero Moreno, P, García-Miguel García-Rosados, A, Navajas Gutiérrez, J I, Ruiz Jiménez, S, Navarro Fos, J C, Garín Valle, M, Galbe Sada
Publikováno v:
Anales espanoles de pediatria. 47(6)
Our objective was to carry out a prospective multicenter study of neuroblastoma patients diagnosed between 0 and 12 months of age.Diagnostic procedures included histology, catecholamine excretion, bone marrow cytology and MIBG-scan. Staging was evalu