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Rare Tumors in Children: Progress Through Collaboration

Rare Tumors in Children: Progress Through Collaboration

http://www.wikidata.org/entity/Q26797511

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Hepatoblastoma: A Need for Cell Lines and Tissue Banks to Develop Targeted Drug Therapies Approaches to modernize the combination drug development paradigm Integrated genetic and pharmacologic interrogation of rare cancers Importance of an International Registry for and Collaborative Research on Esophageal Atresia.Malignant pleural mesothelioma in a 17-year old boy: A case report and literature review.The burden of rare cancers in the United States.An Update From the Pediatric Proton Consortium Registry.

P2860

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P2860

Rare Tumors in Children: Progress Through Collaboration

http://www.wikidata.org/entity/Q26797511

description

2015 nî lūn-bûn

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2015 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած

@hyw

2015 թվականի սեպտեմբերին հրատարակված գիտական հոդված

@hy

2015年の論文

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2015年論文

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2015年論文

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2015年論文

@zh-hk

2015年論文

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2015年論文

@zh-tw

2015年论文

@wuu

name

Rare Tumors in Children: Progress Through Collaboration

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Rare Tumors in Children: Progress Through Collaboration

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Rare Tumors in Children: Progress Through Collaboration

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type

label

Rare Tumors in Children: Progress Through Collaboration

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Rare Tumors in Children: Progress Through Collaboration

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Rare Tumors in Children: Progress Through Collaboration

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prefLabel

Rare Tumors in Children: Progress Through Collaboration

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Rare Tumors in Children: Progress Through Collaboration

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Rare Tumors in Children: Progress Through Collaboration

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JCO.2014.59.3632

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Journal of Clinical Oncology

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Rare Tumors in Children: Progress Through Collaboration

@en

P2093

Alberto S Pappo

http://www.w3.org/2001/XMLSchema#string

Kris A Schultz

http://www.w3.org/2001/XMLSchema#string

Lee Helman

http://www.w3.org/2001/XMLSchema#string

Mark D Krailo

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Wayne L Furman

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P2860

Towards an international pediatric liver tumor consensus classification: proceedings of the Los Angeles COG liver tumors symposium

Cancer statistics, 2014

Type I pleuropulmonary blastoma: pathology and biology study of 51 cases from the international pleuropulmonary blastoma registry

DICER1 mutations in childhood cystic nephroma and its relationship to DICER1-renal sarcoma

Dose-dense cisplatin-based chemotherapy and surgery for children with high-risk hepatoblastoma (SIOPEL-4): a prospective, single-arm, feasibility study.

Succinate dehydrogenase deficient gastrointestinal stromal tumors (GISTs) - a review.

Succinate dehydrogenase mutation underlies global epigenomic divergence in gastrointestinal stromal tumor

Judicious DICER1 testing and surveillance imaging facilitates early diagnosis and cure of pleuropulmonary blastoma

DICER1 syndrome: clarifying the diagnosis, clinical features and management implications of a pleiotropic tumour predisposition syndrome.

Defects in succinate dehydrogenase in gastrointestinal stromal tumors lacking KIT and PDGFRA mutations.

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3047-54

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577371

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10.1200/JCO.2014.59.3632

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4979197

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