A. Maillo-rekin lankidetzan egindako argitalpenak (15)

2012

  1. Delineation of commonly deleted chromosomal regions in meningiomas by high-density single nucleotide polymorphism genotyping arrays

    Genes Chromosomes and Cancer, Vol. 51, Núm. 6, pp. 606-617

  2. Immunophenotypic identification and characterization of tumor cells and infiltrating cell populations in meningiomas

    American Journal of Pathology, Vol. 181, Núm. 5, pp. 1749-1761

2009

  1. Gene expression profiles of meningiomas are associated with tumor cytogenetics and patient outcome

    Brain Pathology, Vol. 19, Núm. 3, pp. 409-420

2008

  1. Array-based comparative genomic hybridization of mapped BAC DNA clones to screen for chromosome 14 copy number abnormalities in meningiomas

    European Journal of Human Genetics, Vol. 16, Núm. 12, pp. 1450-1458

2007

  1. Early recurrences in histologically benign/grade i meningiomas are associated with large tumors and coexistence of monosomy 14 and del(1p36) in the ancestral tumor cell clone

    Neuro-Oncology, Vol. 9, Núm. 4, pp. 438-446

  2. Patient gender is associated with distinct patterns of chromosomal abnormalities and sex chromosome-linked gene-expression profiles in meningiomas

    Oncologist, Vol. 12, Núm. 10, pp. 1225-1236

2006

  1. Microarray-based analysis of spinal versus intracranial meningiomas: Different clinical, biological, and genetic characteristics associated with distinct patterns of gene expression

    Journal of Neuropathology and Experimental Neurology, Vol. 65, Núm. 5, pp. 445-454

  2. The cytogenetic relationship between primary and recurrent meningiomas points to the need for new treatment strategies in cases at high risk of relapse

    Clinical Cancer Research, Vol. 12, Núm. 3 I, pp. 772-780

2005

  1. Characterization of chromosome 14 abnormalities by interphase in situ hybridization and comparative genomic hybridization in 124 meningiomas: Correlation with clinical, histopathologic, and prognostic features

    American Journal of Clinical Pathology, Vol. 123, Núm. 5, pp. 744-751

2004

  1. Intratumoral patterns of clonal evolution in meningiomas as defined by multicolor interphase fluorescence in situ hybridization (FISH): Is there a relationship between histopathologically benign and atypical/anaplastic lesions?

    Journal of Molecular Diagnostics, Vol. 6, Núm. 4, pp. 316-325

2003

  1. New classification scheme for the prognostic stratification of meningioma on the basis of chromosome 14 abnormalities, patient age, and tumor histopathology

    Journal of Clinical Oncology, Vol. 21, Núm. 17, pp. 3285-3295

2002

  1. Incidence of Numerical Chromosome Aberrations in Meningioma Tumors as Revealed by Fluorescence in Situ Hybridization Using 10 Chromosome-Specific Probes

    Clinical Cytometry, Vol. 50, Núm. 3, pp. 153-159

2001

  1. Gains of chromosome 22 by fluorescence in situ hybridization in the context of an hyperdiploid karyotype are associated with aggressive clinical features in meningioma patients

    Cancer, Vol. 92, Núm. 2, pp. 377-385

1999

  1. Proportion of S-phase tumor cells measured by flow cytometry is an independent prognostic factor in meningioma tumors

    Communications in Clinical Cytometry, Vol. 38, Núm. 3, pp. 118-123

1994

  1. Meningiomas intracraneales y edema cerebral. Estudio correlativo de diversos factores etiopatogénicos

    Neurocirugia, Vol. 5, Núm. 3, pp. 204-210