(Q36805804)

16 August 2017

Cardiovascular malformations in Turner's and Noonan's syndrome (English)

1 reference

16 August 2017

1 reference

L. G. Van der Hauwaert

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A656215

18 July 2022

J. P. Fryns

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A656215

18 July 2022

M. Dumoulin

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A656215

18 July 2022

N. Logghe

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A656215

18 July 2022

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=656215

18 July 2022

publication date

1 May 1978

1 reference

PMC publication ID

483435

full work available at URL

16 August 2017

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/656215/?tool=EBI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A656215

https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/656215/pdf/?tool=EBI

18 July 2022

file format

Portable Document Format

online access status

open access

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A656215

https://europepmc.org/articles/PMC483435

18 July 2022

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A656215

https://europepmc.org/articles/PMC483435?pdf=render

18 July 2022

file format

Portable Document Format

online access status

open access

content deliverer

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A656215

18 July 2022

published in

British Heart Journal

1 reference

16 August 2017

40

1 reference

16 August 2017

5

1 reference

16 August 2017

500-509

1 reference

ULLRICH-TURNER SYNDROME ASSOCIATED WITH CYSTIC MEDIAL NECROSIS OF THE AORTA AND GREAT VESSELS: CASE REPORT AND REVIEW OF THE LITERATURE.

16 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=483435

Congenital anomalies associated with gonadal aplasia; review of 55 cases.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=483435

A sex-chromosome anomaly in a case of gonadal dysgenesis (Turner's syndrome).

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=483435

The Ullrich-Noonan syndrome (Turner phenotype).

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=483435

Pulmonary valvular dysplasia. A cardiofacial syndrome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=483435

Congenital heart disease in male and female subjects with somatic features of Turner's syndrome and normal sex chromosomes (Ullrich's and related syndromes).

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=483435

Hypertelorism with Turner phenotype. A new syndrome with associated congenital heart disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=483435

Cardiomyopathy in Noonan's syndrome. Report of 3 cases

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=483435

'Isolated' pulmonary valve stenosis as part of more widespread cardiovascular disease

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=483435

Echocardiographic Studies of Left Ventricular Disease in Ullrich-Noonan Syndrome

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=483435

Rapidly progressive obstructive cardiomyopathy in infants with Noonan's syndrome. Report of two cases

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=483435

Pulmonary stenosis in patients with the Turner phenotype in the male.

29 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=483435

Chromosomal abnormalities and congenital heart disease.

27 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=483435

CARDIOVASCULAR MALFORMATION IN TURNER'S SYNDROME

27 June 2018

1 reference

12 December 2020

Colour-blindness in ovarian agenesis (gonadal dysplasia)

1 reference

12 December 2020

Congenital pulmonary stenosis resulting from dysplasia of valve

1 reference

12 December 2020

Eccentric Ventricular Hypertrophy in Familial and Sporadic Instances of 46 XX, XY Turner Phenotype

1 reference

12 December 2020

The heart in Turner-Ullrich syndrome. (Study of 26 personal cases and review of cases comprising a chromosomal study)

1 reference

12 December 2020

Systolic prolapse of the mitral valve in Noonan's syndrome

1 reference

12 December 2020

Characteristic cardiovascular anomalies of XO Turner syndrome, XX and XY phenotype and XO/XX Turner mosaic

1 reference

12 December 2020

[The syndrome called "male Turner" (6 cases)]

1 reference

12 December 2020

Noonan's Syndrome and Ebstein's Malformation of the Tricuspid Valve

1 reference

12 December 2020

THE XO SYNDROME. A STUDY OF THE DIFFERENTIATED PHENOTYPE IN 25 PATIENTS

1 reference

12 December 2020

Identifiers

DOI

10.1136/HRT.40.5.500

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=656215

18 July 2022

1 reference

PMC publication ID

483435

16 August 2017

1 reference

PMC publication ID

483435