Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Sara Alvarez, de Andrés"'
Autor:
Isabel Benavente, Ana Rodríguez-Valle, Elvira Orduna-Hospital, Francisco Javier Fernández-Tirado, Sara Alvarez-de Andrés, José Gazulla, Pedro Osorio-Caicedo, José Berciano, Elena García-González, Jesús Fraile-Rodrigo
Publikováno v:
Journal of neurology. 267(8)
To report clinical and ancillary findings in a kindred with spinocerebellar ataxia 38 (SCA38). Five family members spanning two generations developed gait ataxia and intermittent diplopia. On examination, a cerebellar syndrome accompanied by downbeat
Autor:
Laura Valle, Angel Martinez-Ramirez, Javier Benitez, Juan C. Cigudosa, Miguel Urioste, María José Calasanz, David Blesa, Klaas Kok, Lorenzo Melchor, Sara Alvarez de Andrés
Publikováno v:
Genes, Chromosomes and Cancer. 42:287-298
Molecular cytogenetic techniques enabled us to clarify numerical and structural alterations previously detected by conventional cytogenetic techniques in 37 patients who had myelodysplastic syndromes with complex karyotypes. Using high-resolution com
Autor:
Angel Martinez-Ramirez, Javier Benitez, Sandra Rodriguez-Perales, Laura Valle, Juan C. Cigudosa, Sara Alvarez de Andrés, Miguel Urioste
Publikováno v:
Cancer Genetics and Cytogenetics. 148:35-43
Alveolar rhabdomyosarcomas (ARMS) are soft-tissue tumors that are genetically characterized by the presence of reciprocal translocations that generate the fusion gene PAX3-FOXO1A or PAX7-FOXO1A. For the study of the biologic consequences of such rear
Autor:
Angel, Martínez-Ramírez, Miguel, Urioste, Lorenzo, Melchor, David, Blesa, Laura, Valle, Sara Alvarez, de Andrés, Klaas, Kok, Maria José, Calasanz, Juan Cruz, Cigudosa, Javier, Benítez
Publikováno v:
Genes, chromosomescancer. 42(3)
Molecular cytogenetic techniques enabled us to clarify numerical and structural alterations previously detected by conventional cytogenetic techniques in 37 patients who had myelodysplastic syndromes with complex karyotypes. Using high-resolution com