(Q51990523)

English

Segmental overgrowth, lipomatosis, arteriovenous malformation and epidermal nevus (SOLAMEN) syndrome is related to mosaic PTEN nullizygosity.

scientific article published on 28 March 2007

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17392703

Segmental overgrowth, lipomatosis, arteriovenous malformation and epidermal nevus (SOLAMEN) syndrome is related to mosaic PTEN nullizygosity. (English)

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17392703

arteriovenous malformation

1 reference

based on heuristic

inferred from title

epidermal nevus

1 reference

based on heuristic

inferred from title

6

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17392703

author name string

Frédéric Caux

1

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17392703

Henri Plauchu

2

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17392703

Frédéric Chibon

3

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17392703

Laurence Faivre

4

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17392703

Olivier Fain

5

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17392703

Françoise Bonnet

7

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17392703

Zied Ben Selma

8

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17392703

Liliane Laroche

9

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17392703

Marion Gérard

10

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17392703

Michel Longy

11

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17392703

publication date

28 March 2007

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17392703

European Journal of Human Genetics

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17392703

15

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17392703

7

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17392703

767-773

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17392703

https://scigraph.springernature.com/pub.10.1038/sj.ejhg.5201823

0 references

Association of germline mutation in the PTEN tumour suppressor gene and Proteus and Proteus-like syndromes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201823

7 January 2021

based on heuristic

inferred from DOI database lookup

The multifaceted challenges of Proteus syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201823

7 January 2021

based on heuristic

inferred from DOI database lookup

Proteus syndrome: Misdiagnosis with PTEN mutations

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201823

7 January 2021

based on heuristic

inferred from DOI database lookup

Will the real Cowden syndrome please stand up: revised diagnostic criteria

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201823

7 January 2021

based on heuristic

inferred from DOI database lookup

No evidence for germline PTEN mutations in families with breast and brain tumours

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201823

7 January 2021

based on heuristic

inferred from DOI database lookup

Allelic imbalance study of 16q in human primary breast carcinomas using microsatellite markers

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201823

7 January 2021

based on heuristic

inferred from DOI database lookup

PTEN mutation spectrum and genotype-phenotype correlations in Bannayan-Riley-Ruvalcaba syndrome suggest a single entity with Cowden syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201823

7 January 2021

based on heuristic

inferred from DOI database lookup

PTEN: one gene, many syndromes

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201823

7 January 2021

based on heuristic

inferred from DOI database lookup

Proteus syndrome: diagnostic criteria, differential diagnosis, and patient evaluation

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201823

7 January 2021

based on heuristic

inferred from DOI database lookup

PTEN mutations and proteus syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201823

7 January 2021

based on heuristic

inferred from DOI database lookup

Reassessment of the Proteus syndrome literature: application of diagnostic criteria to published cases.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201823

7 January 2021

based on heuristic

inferred from DOI database lookup

Germline and germline mosaic PTEN mutations associated with a Proteus-like syndrome of hemihypertrophy, lower limb asymmetry, arteriovenous malformations and lipomatosis

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201823

7 January 2021

based on heuristic

inferred from DOI database lookup

Epidermal naevus in Proteus syndrome showing loss of heterozygosity for an inherited PTEN mutation

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201823

7 January 2021

based on heuristic

inferred from DOI database lookup

Knudson's hypothesis and the TP53 revolution

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201823

7 January 2021

based on heuristic

inferred from DOI database lookup

Segmental forms of autosomal dominant skin disorders: different types of severity reflect different states of zygosity

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201823

7 January 2021

based on heuristic

inferred from DOI database lookup

Allelic loss underlies type 2 segmental Hailey-Hailey disease, providing molecular confirmation of a novel genetic concept

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201823

7 January 2021

based on heuristic

inferred from DOI database lookup

The multiple roles of PTEN in tumor suppression

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201823

7 January 2021

based on heuristic

inferred from DOI database lookup

PTEN: from pathology to biology

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201823

7 January 2021

based on heuristic

inferred from DOI database lookup

Germline mutation of the tumour suppressor PTEN in Proteus syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201823

7 January 2021

based on heuristic

inferred from DOI database lookup

PTEN mutations are uncommon in Proteus syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201823

7 January 2021

based on heuristic

inferred from DOI database lookup

Mutation analysis of the tumor suppressor PTEN and the glypican 3 (GPC3) gene in patients diagnosed with Proteus syndrome.

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201823

7 January 2021

based on heuristic

inferred from DOI database lookup

PTEN mutations and proteus syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201823

7 January 2021

based on heuristic

inferred from DOI database lookup

Will the real Cowden syndrome please stand up (again)? Expanding mutational and clinical spectra of the PTEN hamartoma tumour syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201823

7 January 2021

based on heuristic

inferred from DOI database lookup

Evolution of skin lesions in Proteus syndrome

1 reference

https://api.crossref.org/works/10.1038%2FSJ.EJHG.5201823

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1038/SJ.EJHG.5201823

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17392703

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

19 April 2018

http://europepmc.org/abstract/MED/17392703

ResearchGate publication ID

0 references

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