Complete surgical resection is curative for children with hepatoblastoma with pure fetal histology: a report from the Children's Oncology Group. - Wikidata - awgldk - TriplyDB

Complete surgical resection is curative for children with hepatoblastoma with pure fetal histology: a report from the Children's Oncology Group.

Complete surgical resection is curative for children with hepatoblastoma with pure fetal histology: a report from the Children's Oncology Group.

http://www.wikidata.org/entity/Q35172214

about

Rare Tumors in Children: Progress Through Collaboration Towards an international pediatric liver tumor consensus classification: proceedings of the Los Angeles COG liver tumors symposium Hepatoblastoma clinical research: lessons learned and future challenges Surgical treatment of hepatoblastoma The Children's Hepatic tumors International Collaboration (CHIC): Novel global rare tumor database yields new prognostic factors in hepatoblastoma and becomes a research model A Challenging Case of Hepatoblastoma Concomitant with Autosomal Recessive Polycystic Kidney Disease and Caroli Syndrome-Review of the Literature.Small cell undifferentiated variant of hepatoblastoma: adverse clinical and molecular features similar to rhabdoid tumors.The treatment of hepatoblastoma: Its evolution and the current status as per the SIOPEL trials.New concepts and outcomes for children with hepatoblastoma based on the experience of a tertiary center over the last 21 years.CITED1 expression in liver development and hepatoblastoma.Hepatoblastoma Associated with Trisomy 18 Predictors of survival and incidence of hepatoblastoma in the paediatric population Surgical complications in pediatric surgical oncology.Chemotherapeutic approaches for newly diagnosed hepatoblastoma: past, present, and future strategies.Children's Oncology Group's 2013 blueprint for research: rare tumors.Current chemotherapeutic approaches for hepatoblastoma.Current therapeutic strategies for childhood hepatic tumors: surgical and interventional treatments for hepatoblastoma.International pediatric liver cancer pathological classification: current trend.Utility of PAS and β-catenin staining in histological categorisation and prediction of prognosis of hepatoblastomas.Pediatric hepatoblastoma: diagnosis and treatment.Novel Advances in Understanding of Molecular Pathogenesis of Hepatoblastoma: A Wnt/β-Catenin Perspective.Risk-stratified staging in paediatric hepatoblastoma: a unified analysis from the Children's Hepatic tumors International Collaboration.A single-center retrospective study of pediatric hepatoblastoma.Management of Hepatoblastoma: ICMR Consensus Document.Low expression of N-myc downstream-regulated gene 2 (NDRG2) correlates with poor prognosis in hepatoblastoma.Opioid growth factor (OGF) for hepatoblastoma: a novel non-toxic treatment.Genomic analysis of hepatoblastoma identifies distinct molecular and prognostic subgroups.Pure fetal histology subtype was associated with better prognosis of children with hepatoblastoma: A Chinese population-based study.Glypican 3 as a Serum Marker for Hepatoblastoma.Quantification of glypican 3, β-catenin and claudin-1 protein expression in hepatoblastoma and paediatric hepatocellular carcinoma by colour deconvolution.Cure of Hepatoblastoma Through Transcatheter Arterial Chemoembolization.Identification of differentially expressed genes, lncRNAs and miRNAs which are associated with tumor malignant phenotypes in hepatoblastoma patients.Hepatoblastoma: current understanding, recent advances, and controversies.Current therapeutic strategies for childhood hepatic malignant tumors.FNAC Aided Diagnosis and Categorization of Hepatoblastoma:: A Report of Three Cases.Histological and immunohistochemical study of hepatoblastoma: correlation with tumour behaviour and survival.

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P2860

Complete surgical resection is curative for children with hepatoblastoma with pure fetal histology: a report from the Children's Oncology Group.

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2011 թվականի հուլիսին հրատարակված գիտական հոդված

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2011年の論文

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Howard M Katzenstein

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Joel Haas

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Jon M Rowland

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P2860

Hepatoblastoma with a low serum alpha-fetoprotein level at diagnosis: the SIOPEL group experience

Small cell undifferentiated variant of hepatoblastoma: adverse clinical and molecular features similar to rhabdoid tumors.

Predictive value of the pretreatment extent of disease system in hepatoblastoma: results from the International Society of Pediatric Oncology Liver Tumor Study Group SIOPEL-1 study.

Intensified platinum therapy is an ineffective strategy for improving outcome in pediatric patients with advanced hepatoblastoma.

Predictive power of pretreatment prognostic factors in children with hepatoblastoma: a report from the Children's Oncology Group.

Primary hepatic tumors of childhood.

Improved outcome for children with hepatoblastoma.

Histopathology and prognosis in childhood hepatoblastoma and hepatocarcinoma.

Effective treatment of unresectable or metastatic hepatoblastoma with cisplatin and continuous infusion doxorubicin chemotherapy: a report from the Childrens Cancer Study Group.

Risk-adapted treatment for childhood hepatoblastoma. final report of the second study of the International Society of Paediatric Oncology--SIOPEL 2.

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