(Q55467569)

12 July 2018

title

Tumor development in three patients with Noonan syndrome. (English)

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12 July 2018

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Helen Fryssira

1

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12 July 2018

George Leventopoulos

2

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12 July 2018

Stavroula Psoni

3

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12 July 2018

Sophia Kitsiou-Tzeli

4

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12 July 2018

Nikolaos Stavrianeas

5

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12 July 2018

Emmanuel Kanavakis

6

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12 July 2018

publication date

5 December 2007

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12 July 2018

European Journal of Pediatrics

published in

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12 July 2018

volume

167

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12 July 2018

issue

9

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12 July 2018

page(s)

1025-1031

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12 July 2018

https://scigraph.springernature.com/pub.10.1007/s00431-007-0636-3

exact match

0 references

cites work

[Immunohistochemistry in oligodendrogliomas].

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00431-007-0636-3

Hypertelorism With Turner Phenotype

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS00431-007-0636-3

The Ullrich-Noonan syndrome (Turner phenotype).

21 January 2018

1 reference

12 December 2020

Clinical and molecular studies in a large Dutch family with Noonan syndrome

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12 December 2020

Pitfalls in the diagnosis of brain tumours

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12 December 2020

Germline KRAS mutations cause Noonan syndrome

1 reference

12 December 2020

Correlation between PTPN11 gene mutations and congenital heart defects in Noonan and LEOPARD syndromes.

1 reference

12 December 2020

Genetic evidence for lineage-related and differentiation stage-related contribution of somatic PTPN11 mutations to leukemogenesis in childhood acute leukemia

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12 December 2020

Clinical behavior and a contemporary management algorithm for prepubertal testis tumors: a summary of the Prepubertal Testis Tumor Registry

1 reference

12 December 2020

Rhabdomyosarcoma in a patient with Noonan syndrome phenotype and review of the literature

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12 December 2020

The role of glial fibrillary acidic protein in the diagnosis of central nervous system tumors

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12 December 2020

Noonan Syndrome and Neuroblastoma

1 reference

12 December 2020

Activating mutations of the noonan syndrome-associated SHP2/PTPN11 gene in human solid tumors and adult acute myelogenous leukemia

1 reference

12 December 2020

Mapping a gene for Noonan syndrome to the long arm of chromosome 12

1 reference

12 December 2020

Association of multiple Abrikossof tumors disseminated on the body and the limbs of an 8 year-old girl with oculocardiac abnormalities

1 reference

12 December 2020

SOS1 is the second most common Noonan gene but plays no major role in cardio-facio-cutaneous syndrome

1 reference

12 December 2020

Noonan's syndrome and seminoma of undescended testicle.

1 reference

12 December 2020

PTPN11 mutations in Noonan syndrome: molecular spectrum, genotype-phenotype correlation, and phenotypic heterogeneity

1 reference

12 December 2020

Granular cell myoblastoma--a misnomer. Electron microscopic and histochemical evidence concerning its Schwann cell derivation and nature (granular cell schwannoma)

1 reference

12 December 2020

Genotype-phenotype correlations in Noonan syndrome

1 reference

12 December 2020

Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome

1 reference

12 December 2020

Multiple subcutaneous granular-cell tumours in a patient with Noonan syndrome

1 reference

12 December 2020

Germline gain-of-function mutations in SOS1 cause Noonan syndrome

1 reference

12 December 2020

Germ-line and somatic PTPN11 mutations in human disease

1 reference

12 December 2020

PTPN11 mutation in a large family with Noonan syndrome and dizygous twinning

1 reference

12 December 2020

Activating PTPN11 mutations play a minor role in pediatric and adult solid tumors

1 reference

12 December 2020

The neurofibromatosis-Noonan syndrome

1 reference

12 December 2020

Genotypic and phenotypic characterization of Noonan syndrome: New data and review of the literature

1 reference

12 December 2020

Cardiac findings in 31 patients with Noonan's syndrome

1 reference

12 December 2020

The clinical value of Ki-67/MIB-1 labeling index in human astrocytomas

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12 December 2020

Mutations of the PTPN11 and RAS genes in rhabdomyosarcoma and pediatric hematological malignancies

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12 December 2020

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12 December 2020

Gain-of-function RAF1 mutations cause Noonan and LEOPARD syndromes with hypertrophic cardiomyopathy

1 reference

12 December 2020

Epidemiology of testicular cancer: an overview

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12 December 2020

Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome.

1 reference

12 December 2020

The new WHO classification of brain tumors

1 reference

12 December 2020

Noonan syndrome and cavernous hemangioma of the brain

1 reference

12 December 2020

Spectrum of mutations in PTPN11 and genotype-phenotype correlation in 96 patients with Noonan syndrome and five patients with cardio-facio-cutaneous syndrome

1 reference

12 December 2020

The spectrum of cardiac anomalies in Noonan syndrome as a result of mutations in the PTPN11 gene

1 reference

12 December 2020

Hypertelorism with Turner phenotype. A new syndrome with associated congenital heart disease

1 reference

12 December 2020

Germline gain-of-function mutations in RAF1 cause Noonan syndrome

1 reference

12 December 2020

10.1007/S00431-007-0636-3

Identifiers

DOI

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12 July 2018

Dimensions Publication ID

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12 July 2018