(Q59215649)

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Noonan syndrome

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scholarly article

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3 references

22 March 2019

22 April 2019

17 June 2019

Noonan syndrome (English)

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Noonan syndrome

3 references

22 March 2019

22 April 2019

17 June 2019

author name string

Ineke van der Burgt

1

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language of work or name

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publication date

14 January 2007

3 references

22 March 2019

22 April 2019

17 June 2019

Orphanet Journal of Rare Diseases

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22 March 2019

22 April 2019

17 June 2019

2

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4

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1

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copyright license

Creative Commons Attribution 2.0 Generic

3 references

Europe PubMed Central

22 March 2019

Europe PubMed Central

22 April 2019

Europe PubMed Central

17 June 2019

copyright status

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on focus list of Wikimedia project

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https://scigraph.springernature.com/pub.10.1186/1750-1172-2-4

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Ocular manifestations of Noonan syndrome in the pediatric patient

1 reference

https://pubmed.ncbi.nlm.nih.gov/17222357

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic heterogeneity in Noonan syndrome: evidence for an autosomal recessive form

1 reference

https://pubmed.ncbi.nlm.nih.gov/17222357

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Keratosis pilaris atrophicans faciei (Ulerythema ophryogenes): a cutaneous marker in the Noonan syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17222357

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Growth and pubertal development in five boys with Noonan's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17222357

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Growth hormone treatment in children with Noonan's syndrome: four year results of a partly controlled trial

1 reference

https://pubmed.ncbi.nlm.nih.gov/17222357

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17222357

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The Noonan syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17222357

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Differential diagnosis of the Williams and the Noonan syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/17222357

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Noonan syndrome: the changing phenotype.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17222357

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Noonan syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17222357

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Cardiovascular dysplasia in Noonan's syndrome. Apropos of 64 cases]

1 reference

https://pubmed.ncbi.nlm.nih.gov/17222357

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Noonan syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17222357

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Noonan syndrome: growth and clinical manifestations in 144 cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/17222357

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bleeding diathesis in Noonan syndrome: a common association.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17222357

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A clinical study of Noonan syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17222357

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hearing loss in Noonan syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17222357

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ocular manifestations of Noonan syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17222357

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genital tract function in men with Noonan syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17222357

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Noonan syndrome. An update and review for the primary pediatrician

1 reference

https://pubmed.ncbi.nlm.nih.gov/17222357

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17222357

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Behavioural aspects and psychiatric findings in Noonan's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17222357

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Noonan syndrome: coagulation and clinical aspects.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17222357

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Multiple temporal bone anomalies associated with Noonan syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17222357

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Audiologic manifestations of Noonan syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17222357

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Noonan's syndrome with sensorineural hearing loss and vestibular abnormalities.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17222357

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal features of Noonan syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17222357

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Chylothorax after surgery for thoracic deformity in Noonan syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17222357

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Psychological profile of children with Noonan syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17222357

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phenotypic and genotypic characterisation of Noonan-like/multiple giant cell lesion syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17222357

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/17222357

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The use of recombinant factor VIIa in a patient with Noonan syndrome and life-threatening bleeding

1 reference

https://pubmed.ncbi.nlm.nih.gov/17222357

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal DNA diagnosis of Noonan syndrome in a fetus with massive hygroma colli, pleural effusion and ascites

1 reference

https://pubmed.ncbi.nlm.nih.gov/17222357

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Noonan syndrome and related disorders: genetics and pathogenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/17222357

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Improved final height with long-term growth hormone treatment in Noonan syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/17222357

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Noonan syndrome: relationships between genotype, growth, and growth factors

1 reference

https://pubmed.ncbi.nlm.nih.gov/17222357

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Germline KRAS mutations cause Noonan syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17222357

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Stops along the RAS pathway in human genetic disease

1 reference

https://pubmed.ncbi.nlm.nih.gov/17222357

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Noonan syndrome and related disorders: dysregulated RAS-mitogen activated protein kinase signal transduction

1 reference

https://pubmed.ncbi.nlm.nih.gov/17222357

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The 'Shp'ing news: SH2 domain-containing tyrosine phosphatases in cell signaling

1 reference

https://pubmed.ncbi.nlm.nih.gov/17222357

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital heart diseases in children with Noonan syndrome: An expanded cardiac spectrum with high prevalence of atrioventricular canal

1 reference

https://pubmed.ncbi.nlm.nih.gov/17222357

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Patterns of cognitive functioning in school-aged children with Noonan syndrome associated with variability in phenotypic expression

1 reference

https://pubmed.ncbi.nlm.nih.gov/17222357

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Paternal germline origin and sex-ratio distortion in transmission of PTPN11 mutations in Noonan syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/17222357

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/1750-1172-2-4

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