about
Methotrexate for high-grade osteosarcoma in children and young adultsMolecular profiling of isolated histological components of wilms tumor implicates a common role for the Wnt signaling pathway in kidney and tumor developmentLow prevalence of HPV in Brazilian children with retinoblastoma.Recurrent somatic mutation in DROSHA induces microRNA profile changes in Wilms tumourSocioeconomic status and the incidence of non-central nervous system childhood embryonic tumours in BrazilRFC-1 80G>A polymorphism in case-mother/control-mother dyads is associated with risk of nephroblastoma and neuroblastomaHepatocellular Carcinoma in Children: Does Modified Platinum- and Doxorubicin-Based Chemotherapy Increase Tumor Resectability and Change Outcome? Lessons Learned From the SIOPEL 2 and 3 Studies.Maternal and Birth Characteristics and Childhood Embryonal Solid Tumors: A Population-Based Report from Brazil.Translation and cultural adaptation of Health Utilities Index (HUI) Mark 2 (HUI2) and Mark 3 (HUI3) with application to survivors of childhood cancer in Brazil.Childhood cancer mortality trends in Brazil, 1979-2008.Cultural adaptation, translation and validation of a functional outcome questionnaire (TESS) to Portuguese with application to patients with lower extremity osteosarcoma.Treatment of relapsed Wilms tumors: lessons learned.Trends in childhood leukemia mortality in Brazil and correlation with social inequalities.Incidence Trends of Cervical Cancer in Adolescents and Young Adults: Brazilian Population Based Data.Trends in Cancer Mortality Among Adolescents and Young Adults in Brazil.Large germline copy number variations as predisposing factor in childhood neoplasms.Clear cell sarcomas of the kidney registered on International Society of Pediatric Oncology (SIOP) 93-01 and SIOP 2001 protocols: a report of the SIOP Renal Tumour Study Group.P-glycoprotein expression, tumor weight, age, and relapse in patients with stage I and II favorable-histology Wilms' tumor.Cancer incidence among children and adolescents in Brazil: first report of 14 population-based cancer registries.Early childhood leukemia incidence trends in Brazil.Omission of doxorubicin from the treatment of stage II-III, intermediate-risk Wilms' tumour (SIOP WT 2001): an open-label, non-inferiority, randomised controlled trial.Cancer Incidence Among Adolescents and Young Adults (15 to 29 Years) in Brazil.Aberrant DNA methylation of ESR1 and p14ARF genes could be useful as prognostic indicators in osteosarcoma.A simple cost-effective lactate dehydrogenase level measurement can stratify patients with Ewing's tumor into low and high risk.Extraocular retinoblastoma: a 13-year experience.Epithelial salivary glands neoplasms in children and adolescents: a forty-four-year experience.Cisplatin and etoposide in childhood germ cell tumor: brazilian pediatric oncology society protocol GCT-91.Isolated CNS involvement in Ewing sarcoma.Position paper: Rationale for the treatment of children with CCSK in the UMBRELLA SIOP-RTSG 2016 protocol.The contribution of chest CT-scan at diagnosis in children with unilateral Wilms' tumour. Results of the SIOP 2001 study.Childhood leukemia incidence in Brazil according to different geographical regions.Prognostic impact of adenomatous polyposis coli gene expression in osteosarcoma of the extremities.Outcome of localised blastemal-type Wilms tumour patients treated according to intensified treatment in the SIOP WT 2001 protocol, a report of the SIOP Renal Tumour Study Group (SIOP-RTSG).The clinical phenotype of YWHAE-NUTM2B/E positive pediatric clear cell sarcoma of the kidney.Gene expression analysis of blastemal component reveals genes associated with relapse mechanism in Wilms tumour.DNA damage in lymphocytes and buccal mucosa cells of children with malignant tumours undergoing chemotherapy.PON1 Q192R polymorphism (rs662) is associated with childhood embryonal tumors.Malignant rhabdoid tumours of the kidney (MRTKs), registered on recent SIOP protocols from 1993 to 2005: A report of the SIOP renal tumour study groupAbdominal Recurrence of Osteogenic SarcomaIntrathecal Vincristine
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P50
description
onderzoeker
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researcher ORCID ID = 0000-0002-5794-1042
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name
Beatriz de Camargo
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Beatriz de Camargo
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Beatriz de Camargo
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Beatriz de Camargo
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type
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Beatriz de Camargo
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Beatriz de Camargo
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Beatriz de Camargo
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Beatriz de Camargo
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prefLabel
Beatriz de Camargo
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Beatriz de Camargo
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Beatriz de Camargo
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Beatriz de Camargo
@nl
P106
P21
P31
P496
0000-0002-5794-1042