(Q48256123)

27 June 2018

title

Cantú syndrome with coexisting familial pituitary adenoma. (English)

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27 June 2018

1 reference

8

Márta Korbonits

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author name string

Pedro Marques

1

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27 June 2018

Rupert Spencer

2

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27 June 2018

Patrick J Morrison

3

1 reference

27 June 2018

Ian M Carr

4

1 reference

27 June 2018

Mary N Dang

5

1 reference

27 June 2018

David T Bonthron

6

1 reference

27 June 2018

Steven Hunter

7

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27 June 2018

publication date

11 January 2018

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27 June 2018

full work available at URL

http://eprints.whiterose.ac.uk/127493/

content deliverer

White Rose Research Online

object has role

published version

copyright license

Creative Commons Attribution 4.0 International

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published in

Endocrine

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27 June 2018

volume

59

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27 June 2018

page(s)

677-684

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27 June 2018

issue

3

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27 June 2018

Creative Commons Attribution 4.0 International

copyright license

start time

11 January 2018

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

exact match

https://scigraph.springernature.com/pub.10.1007/s12020-017-1497-9

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cites work

Genetic Aspects of Pituitary Adenomas

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5847123

Neurologic and neuroimaging manifestations of Cantú syndrome: A case series

30 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5847123

Differential mechanisms of Cantú syndrome-associated gain of function mutations in the ABCC9 (SUR2) subunit of the KATP channel

30 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5847123

Cantú syndrome resulting from activating mutation in the KCNJ8 gene

30 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5847123

Epidemiology and etiopathogenesis of pituitary adenomas

30 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5847123

KATP channels and cardiovascular disease: suddenly a syndrome

30 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5847123

Dominant missense mutations in ABCC9 cause Cantú syndrome.

30 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5847123

Cantú syndrome is caused by mutations in ABCC9.

30 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5847123

An autosomal dominant syndrome of acromegaloid facial appearance and generalised hypertrichosis terminalis

30 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5847123

An autosomal dominant syndrome with 'acromegaloid' features and thickened oral mucosa.

30 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5847123

Sulfation of minoxidil in keratinocytes and hair follicles and the stimulatory effect of minoxidil on the biosynthesis of glycosaminoglycans

30 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5847123

Minoxidil-Associated Pleuropericardial Effusion

30 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5847123

De Novo Mutation in ABCC9 Causes Hypertrichosis Acromegaloid Facial Features Disorder.

14 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5847123

Aortic aneurysm and craniosynostosis in a family with Cantu syndrome

14 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5847123

Wide clinical variability in conditions with coarse facial features and hypertrichosis caused by mutations inABCC9

14 August 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS12020-017-1497-9

Cantú syndrome: Report of nine new cases and expansion of the clinical phenotype

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1007%2FS12020-017-1497-9

10.1007/S12020-017-1497-9

21 January 2018

Identifiers

DOI

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27 June 2018

Dimensions Publication ID

0 references

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27 June 2018

PubMed ID

29327300

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27 June 2018