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2007, Biblioteca di studi linguistici filologici, ISBN 8876360832, Volume 8, viii, 339
Book
Journal of Neuropathology & Experimental Neurology, ISSN 0022-3069, 04/2019, Volume 78, Issue 4, pp. 297 - 304
Abstract We investigated 113 adult Brazilian patients with glioblastoma (GBM) for comparison with patients from distinct geographical areas and evaluation of... 
NTRK1 | PDGFRA | KIT | Fluorescence in situ hybridization | Glioblastoma | KDR | ROS1 | SURVIVAL | RECEPTOR-TYROSINE-KINASES | PROGNOSTIC-FACTORS | IDH1 | GENOMIC ANALYSIS | PATHOLOGY | CANCER | NEUROSCIENCES | EGFR | CLINICAL NEUROLOGY | PDGFRA AMPLIFICATION | GENE FUSION | STRATIFICATION
Journal Article
Journal of Neuro-Oncology, ISSN 0167-594X, 12/2017, Volume 135, Issue 3, pp. 465 - 472
Glioblastoma stands out as the most frequent central nervous system neoplasia, presenting a poor prognosis. The aim of this study was to verify the frequency... 
Neurology | Medicine & Public Health | Glioblastoma | FISH | PTEN | Oncology | 1p19q codeletion | TP53 | Survival | EGFR | GROWTH-FACTOR-RECEPTOR | MALIGNANT ASTROCYTOMA | IN-SITU HYBRIDIZATION | MUTANT TP53 | MULTIFORME | CLINICAL NEUROLOGY | BRAIN-TUMORS | MOLECULAR MARKERS | ONCOLOGY | CENTRAL-NERVOUS-SYSTEM | PROGNOSTIC-SIGNIFICANCE | Receptor, Epidermal Growth Factor - genetics | Humans | Middle Aged | Brain Neoplasms - pathology | Aneuploidy | Male | Brain Neoplasms - surgery | Tumor Suppressor Protein p53 - genetics | Chromosomes, Human, Pair 1 | Glioblastoma - genetics | Aged, 80 and over | Brazil | Adult | Female | PTEN Phosphohydrolase - genetics | Kaplan-Meier Estimate | Brain Neoplasms - genetics | Chromosomes, Human, Pair 7 | Glioblastoma - epidemiology | Glioblastoma - surgery | Glioblastoma - pathology | Aged | Mutation | Chromosomes, Human, Pair 10 | Brain Neoplasms - epidemiology | Genes | Medical genetics | Genetic research | Cytogenetics | Tumor proteins | Health aspects | Glioblastoma multiforme | Chromosome 19 | Prognosis | Epidermal growth factor receptors | p53 Protein | Central nervous system | Chromosome 7 | Chromosome deletion | Neurosurgery | Gene deletion | Chromosome 1 | Clonal deletion | Medical prognosis | Fluorescence in situ hybridization | Chromosome 10 | Chromosomes | PTEN protein | Age | Monosomy | Cancer
Journal Article
Journal Article
Pediatric Neurology, ISSN 0887-8994, 2014, Volume 50, Issue 6, pp. 612 - 615
Journal Article
Journal Article
Sao Paulo Medical Journal, ISSN 1516-3180, 07/2015, Volume 133, Issue 4, pp. 377 - 380
CONTEXT: The autosomal recessive form of microcephaly-chorioretinopathy syndrome is a rare genetic condition that is considered to be an important differential... 
Retina | Consanguinity | Intellectual disability | Microcephaly | Toxoplasmosis | MEDICINE, GENERAL & INTERNAL | DYSPLASIA | Microcephaly - genetics | Pedigree | Humans | Retinal Pigment Epithelium - abnormalities | Male | Child | Cerebral Palsy - genetics | Syndrome | Intellectual Disability - genetics
Journal Article
SAO PAULO MEDICAL JOURNAL, ISSN 1516-3180, 2011, Volume 129, Issue 6, pp. 428 - 432
CONTEXT: Mosaic trisomy 9 is considered to be a rare chromosomal abnormality with limited survival. Our objective was to report on two patients with mosaic... 
Survivorship (Public health) | MEDICINE, GENERAL & INTERNAL | Goldenhar syndrome | Mosaicism | MATERNAL UNIPARENTAL DISOMY | CHILD | Chromosome aberrations | Chromosomes, human, pair 9 | CHROMOSOME-9 | Chromosomes, Human, Pair 9 - genetics | Phenotype | Trisomy - genetics | Humans | Survivors | Child, Preschool | Female | Male | Child | Abnormalities, Multiple - genetics
Journal Article
Revista Paulista de Pediatria, ISSN 0103-0582, 01/2013, Volume 31, Issue 1, pp. 111 - 120
Journal Article
Revista paulista de pediatria : orgao oficial da Sociedade de Pediatria de Sao Paulo, ISSN 0103-0582, 09/2013, Volume 31, Issue 3, pp. 293 - 298
Journal Article
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