(Q45937493)

English

PTPN11 gene mutation and severe neonatal hypertrophic cardiomyopathy: what is the link?

scientific article published on 7 July 2009

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19582499

PTPN11 gene mutation and severe neonatal hypertrophic cardiomyopathy: what is the link? (English)

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19582499

hypertrophic cardiomyopathy

1 reference

based on heuristic

inferred from title

Maria F. Faienza

object named as

Maria Felicia Faienza

1

0 references

Luciano Cavallo

object named as

Luciano Cavallo

5

0 references

author name string

Lucia Giordani

2

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19582499

Marina Ferraris

3

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19582499

Gianni Bona

4

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19582499

publication date

7 July 2009

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19582499

Pediatric Cardiology

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19582499

30

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19582499

7

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19582499

1012-1015

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19582499

https://scigraph.springernature.com/pub.10.1007/s00246-009-9473-7

0 references

Hyperthrophic cardiomyopathy and thePTPN11 gene

1 reference

https://api.crossref.org/works/10.1007%2FS00246-009-9473-7

21 January 2018

Germline KRAS mutations cause Noonan syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/19582499

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19582499

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Grouping of multiple-lentigines/LEOPARD and Noonan syndromes on the PTPN11 gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/19582499

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19582499

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/19582499

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19582499

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

PTPN11 gene mutations: linking the Gln510Glu mutation to the “LEOPARD syndrome phenotype”

1 reference

https://pubmed.ncbi.nlm.nih.gov/19582499

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19582499

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic heterogeneity in LEOPARD syndrome: two families with no mutations in PTPN11.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19582499

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence and clinical significance of cardiovascular abnormalities in patients with the LEOPARD syndrome.

1 reference

https://pubmed.ncbi.nlm.nih.gov/19582499

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel mutation in the PTPN11 gene in a patient with Noonan syndrome and rapidly progressive hypertrophic cardiomyopathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/19582499

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19582499

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00246-009-9473-7

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19582499

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/19582499

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