(Q54165480)

25 May 2018

title

Rhabdomyosarcomas in children with neurofibromatosis type I: A national historical cohort. (English)

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25 May 2018

main subject

neurofibromatosis type I

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1 reference

12

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25 May 2018

Wilfrid Richer

Wilfrid Richer

2

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Franck Bourdeaut

15

Franck Bourdeaut

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25 May 2018

3

Laurence Brugières

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25 May 2018

Daniel Orbach

14

Daniel Orbach

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25 May 2018

Dominique Ranchere-Vince

13

Dominique Ranchere-Vince

1 reference

25 May 2018

Stephan Roche

6

Jean-Louis Stephan

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25 May 2018

Aude Marie-Cardine

5

Aude Marie-Cardine

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25 May 2018

Martine Munzer

9

Martine Munzer

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25 May 2018

Brigitte Lacour

10

Brigitte Lacour

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25 May 2018

author name string

Anne Crucis

1

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25 May 2018

Christophe Bergeron

4

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25 May 2018

Pauline Girard

7

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25 May 2018

Nadege Corradini

8

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25 May 2018

Veronique Minard-Colin

11

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25 May 2018

publication date

20 April 2015

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25 May 2018

published in

Pediatric Blood Cancer

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25 May 2018

volume

62

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25 May 2018

issue

10

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25 May 2018

page(s)

1733-1738

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25 May 2018

Prevalence of germline TP53 mutations and history of Li-Fraumeni syndrome in families with childhood adrenocortical tumors, choroid plexus tumors, and rhabdomyosarcoma: a population-based survey.

cites work

1 reference

Second cranio-facial malignancies in hereditary retinoblastoma survivors previously treated with radiation therapy: clinic and radiologic characteristics and survival outcomes

21 January 2018

1 reference

DICER1 mutations in embryonal rhabdomyosarcomas from children with and without familial PPB-tumor predisposition syndrome.

21 January 2018

1 reference

DICER1 mutations in an adolescent with cervical embryonal rhabdomyosarcoma (cERMS).

21 January 2018

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Constitutional aneuploidy and cancer predisposition caused by biallelic mutations in BUB1B.

21 January 2018

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Rhabdomyosarcoma in patients with constitutional mismatch-repair-deficiency syndrome

21 January 2018

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Association of alveolar rhabdomyosarcoma with the Beckwith-Wiedemann syndrome.

21 January 2018

1 reference

Beckwith-Wiedemann syndrome: growth pattern and tumor risk according to molecular mechanism, and guidelines for tumor surveillance

21 January 2018

1 reference

Rhabdomyosarcoma, Wilms tumor, and deletion of the patched gene in Gorlin syndrome

21 January 2018

1 reference

Five additional Costello syndrome patients with rhabdomyosarcoma: proposal for a tumor screening protocol

21 January 2018

1 reference

Cancer in Noonan, Costello, cardiofaciocutaneous and LEOPARD syndromes.

21 January 2018

1 reference

Noonan syndrome, the SOS1 gene and embryonal rhabdomyosarcoma

21 January 2018

1 reference

Mechanisms in the pathogenesis of malignant tumours in neurofibromatosis type 1.

21 January 2018

1 reference

The diagnostic evaluation and multidisciplinary management of neurofibromatosis 1 and neurofibromatosis 2.

21 January 2018

1 reference

The Intergroup Rhabdomyosarcoma Study-I. A final report

21 January 2018

1 reference

Randomized comparison of intensified six-drug versus standard three-drug chemotherapy for high-risk nonmetastatic rhabdomyosarcoma and other chemotherapy-sensitive childhood soft tissue sarcomas: long-term results from the International Society of P

21 January 2018

1 reference

Treatment of nonmetastatic rhabdomyosarcoma in childhood and adolescence: third study of the International Society of Paediatric Oncology--SIOP Malignant Mesenchymal Tumor 89.

21 January 2018

1 reference

A faster circular binary segmentation algorithm for the analysis of array CGH data

21 January 2018

1 reference

Neurofibromatosis in children with Rhabdomyosarcoma: a report from the Intergroup Rhabdomyosarcoma study IV.

21 January 2018

1 reference

Neurofibromatosis type 1 and childhood cancer

21 January 2018

1 reference

Mortality in neurofibromatosis 1: in North West England: an assessment of actuarial survival in a region of the UK since 1989.

21 January 2018

1 reference

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

21 January 2018

1 reference

High-resolution array CGH identifies common mechanisms that drive embryonal rhabdomyosarcoma pathogenesis.

21 January 2018

1 reference

RAS signaling dysregulation in human embryonal Rhabdomyosarcoma

21 January 2018

1 reference

Oncogene mutation profiling of pediatric solid tumors reveals significant subsets of embryonal rhabdomyosarcoma and neuroblastoma with mutated genes in growth signaling pathways

21 January 2018

1 reference

Radiation-induced cerebral vasculopathy in children with neurofibromatosis and optic pathway glioma.

21 January 2018

1 reference

Fusion gene-negative alveolar rhabdomyosarcoma is clinically and molecularly indistinguishable from embryonal rhabdomyosarcoma.

21 January 2018

1 reference

Characterization of genetic lesions in rhabdomyosarcoma using a high-density single nucleotide polymorphism array

21 January 2018

1 reference

The mutational landscape of adenoid cystic carcinoma

21 January 2018

1 reference

Dissecting the genomic complexity underlying medulloblastoma

21 January 2018

1 reference

Familial neurofibromatosis microdeletion syndrome complicated by rhabdomyosarcoma

21 January 2018

1 reference

Optic pathway glioma associated with orbital rhabdomyosarcoma and bilateral optic nerve sheath dural ectasia in a child with neurofibromatosis-1.

21 January 2018

1 reference

Orbital embryonal rhabdomyosarcoma in association with neurofibromatosis type 1.

21 January 2018

1 reference

Soft tissue sarcomas and central nervous system tumors in children with neurofibromatosis type 1.

21 January 2018

1 reference

Genotype-phenotype associations in neurofibromatosis type 1 (NF1): an increased risk of tumor complications in patients with NF1 splice-site mutations?

21 January 2018

1 reference

Association of childhood rhabdomyosarcoma with neurofibromatosis type I and birth defects

21 January 2018

1 reference

Two neurofibromatosis type 1 cases associated with rhabdomyosarcoma of bladder, one with a large deletion in the NF1 gene

21 January 2018

1 reference

TP53 germline mutation testing in 180 families suspected of Li-Fraumeni syndrome: mutation detection rate and relative frequency of cancers in different familial phenotypes

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1002/PBC.25556

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25 May 2018

PubMed ID

25893277

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25 May 2018