Cardiac anomalies in Williams-Beuren syndrome (Q35604951)

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scientific article published on July 1, 1988

Language	Label	Description	Also known as
English	Cardiac anomalies in Williams-Beuren syndrome	scientific article published on July 1, 1988

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

Cardiac anomalies in Williams-Beuren syndrome (English)

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

author name string

K. A. Hallidie-Smith

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A3415298

8 January 2023

S. Karas

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A3415298

8 January 2023

language of work or name

0 references

publication date

1 July 1988

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

full work available at URL

https://europepmc.org/articles/PMC1779091

online access status

content deliverer

Europe PubMed Central

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A3415298

8 January 2023

https://europepmc.org/articles/PMC1779091?pdf=render

online access status

content deliverer

Europe PubMed Central

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A3415298

8 January 2023

https://syndication.highwire.org/content/doi/10.1136/adc.63.7.809

1 reference

10.1136/ADC.63.7.809

https://api.crossref.org/works/10.1136/ADC.63.7.809

8 January 2023

Archives of Disease in Childhood

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

63

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

7

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

809-813

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

Idiopathic infantile hypercalcaemia--a continuing enigma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1779091

27 July 2018

Collagen composition of normal and myxomatous human mitral heart valves

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1779091

27 July 2018

The relationship between vitamin D and the craniofacial and dental anomalies of the supravalvular aortic stenosis syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1779091

27 July 2018

Autism associated with Williams syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1779091

27 July 2018

Mitral valve prolapse, aortic compliance, and skin collagen in joint hypermobility syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1779091

27 July 2018

Collagen genes and inherited connective tissue disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1779091

27 July 2018

A terminal deletion of the long arm of chromosome 4 [46,XX,del(4)(q33)] in an infant with phenotypic features of Williams syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1779091

27 July 2018

DNA prediction in cystic fibrosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1779091

27 July 2018

Familial occurrence of the Williams syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1779091

27 July 2018

Cross-sectional echocardiographic characterization of aortic obstruction. 1. Supravalvular aortic stenosis and aortic hypoplasia

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1779091

27 July 2018

Effect of Vitamin D on Pregnant Rabbits and Their Offspring

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1779091

27 July 2018

THE SYNDROME OF SUPRAVALVULAR AORTIC STENOSIS, PERIPHERAL PULMONARY STENOSIS, MENTAL RETARDATION AND SIMILAR FACIAL APPEARANCE.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1779091

25 September 2018

Supravalvular aortic stenosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1779091

25 September 2018

Infantile hypercalcemia syndrome in twins.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1779091

25 September 2018

Echocardiographic Detection of Supravalvular Aortic Stenosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1779091

25 September 2018

Supravalvular aortic stenosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/3415298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Vitamin D and the supravalvar aortic stenosis syndrome. The transplacental effects of vitamin D on the aorta of the rabbit

1 reference

https://pubmed.ncbi.nlm.nih.gov/3415298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Supravalvar aortic stenosis. Roentgen analysis of twenty-seven cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/3415298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial supravalvular aortic stenosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/3415298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial supravalvular aortic stenosis. Report of a large family and review of the literature

1 reference

https://pubmed.ncbi.nlm.nih.gov/3415298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Report of the task force on blood pressure control in children

1 reference

https://pubmed.ncbi.nlm.nih.gov/3415298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[The spectrum of supravalvular aortic stenosis: clinical findings of 150 patients with Williams-Beuren syndrome and the isolated lesion (author's transl)]

1 reference

https://pubmed.ncbi.nlm.nih.gov/3415298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mitral valve prolapse: a consistent manifestation of type IV Ehlers-Danlos syndrome. The pathogenetic role of the abnormal production of type III collagen

1 reference

https://pubmed.ncbi.nlm.nih.gov/3415298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Qualitative and quantitative evaluation of supravalvar aortic stenosis by cross-sectional echocardiography. A report of 80 patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/3415298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Localization of the polymorphic human calcitonin gene on chromosome 11

1 reference

https://pubmed.ncbi.nlm.nih.gov/3415298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Systemic hypertension secondary to peripheral vascular anomalies in patients with Williams syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/3415298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Supravalvular aortic stenosis. Clinical and pathologic observations in six patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/3415298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Chronic hyperglycemia, combined with osteosclerosis, hyperazotemia, nanism and congenital malformations]

1 reference

https://pubmed.ncbi.nlm.nih.gov/3415298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital supravalvular aortic stenosis. A morphological study with attempt at classification

1 reference

https://pubmed.ncbi.nlm.nih.gov/3415298

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/ADC.63.7.809

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

9 August 2017

ResearchGate publication ID

0 references

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