Head and Neck Rhabdomyosarcoma: Clinical and Pathologic Characterization of Seven Cases.

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Clinicopathological analysis of head and neck rhabdomyosarcoma: A series of 10 cases and literature review.

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P2860

Head and Neck Rhabdomyosarcoma: Clinical and Pathologic Characterization of Seven Cases.

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2016 nî lūn-bûn

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2016年の論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年論文

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2016年论文

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2016年论文

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2016年论文

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name

Head and Neck Rhabdomyosarcoma: Clinical and Pathologic Characterization of Seven Cases.

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Head and Neck Rhabdomyosarcoma: Clinical and Pathologic Characterization of Seven Cases.

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Head and Neck Rhabdomyosarcoma: Clinical and Pathologic Characterization of Seven Cases.

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Head and Neck Rhabdomyosarcoma: Clinical and Pathologic Characterization of Seven Cases.

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Head and Neck Rhabdomyosarcoma: Clinical and Pathologic Characterization of Seven Cases.

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Head and Neck Rhabdomyosarcoma: Clinical and Pathologic Characterization of Seven Cases.

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P1476

Head and Neck Rhabdomyosarcoma: Clinical and Pathologic Characterization of Seven Cases

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Dolphine Oda

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Neal Futran

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Robert Ricciotti

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P2860

Head and neck rhabdomyosarcoma: follow-up results of four cases and review of the literature

Rhabdomyosarcoma: review of the Children's Oncology Group (COG) Soft-Tissue Sarcoma Committee experience and rationale for current COG studies

Recurrent MYOD1 mutations in pediatric and adult sclerosing and spindle cell rhabdomyosarcomas: evidence for a common pathogenesis.

Sclerosing rhabdomyosarcoma in adults: report of four cases of a hyalinizing, matrix-rich variant of rhabdomyosarcoma that may be confused with osteosarcoma, chondrosarcoma, or angiosarcoma.

Rearrangement of the PAX3 paired box gene in the paediatric solid tumour alveolar rhabdomyosarcoma.

Pleomorphic rhabdomyosarcoma in children: four cases in the pediatric age group.

Fusion of PAX7 to FKHR by the variant t(1;13)(p36;q14) translocation in alveolar rhabdomyosarcoma.

A recurrent neomorphic mutation in MYOD1 defines a clinically aggressive subset of embryonal rhabdomyosarcoma associated with PI3K-AKT pathway mutations.

Comprehensive genomic analysis of rhabdomyosarcoma reveals a landscape of alterations affecting a common genetic axis in fusion-positive and fusion-negative tumors.

Strong immunostaining for myogenin in rhabdomyosarcoma is significantly associated with tumors of the alveolar subclass.

P2888

s12105-016-0771-0

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scholarly article

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10.1007/S12105-016-0771-0

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Eleanor Chen

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2016-11-28T00:00:00Z

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Head and Neck Rhabdomyosarcoma: Clinical and Pathologic Characterization of Seven Cases.

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P2860

P2860

Head and Neck Rhabdomyosarcoma: Clinical and Pathologic Characterization of Seven Cases.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P698

P932

P356

P1433

P1476

P2093

P2860

P2888

P304

P31

P356

P433

P478

P50

P577

P698

P932