(Q75195993)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14687249%20AND%20SRC:MED&resulttype=core&format=json

16 November 2019

title

Severe hypoplasia of the abdominal aorta and its branches in a patient and his daughter (English)

1 reference

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16 November 2019

7

1 reference

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16 November 2019

author name string

A Dejardin

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14687249%20AND%20SRC:MED&resulttype=core&format=json

16 November 2019

P Goffette

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14687249%20AND%20SRC:MED&resulttype=core&format=json

16 November 2019

P Moulin

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14687249%20AND%20SRC:MED&resulttype=core&format=json

16 November 2019

R Verhelst

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14687249%20AND%20SRC:MED&resulttype=core&format=json

16 November 2019

G Cornu

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14687249%20AND%20SRC:MED&resulttype=core&format=json

16 November 2019

J F De Plaen

6

1 reference

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16 November 2019

publication date

1 January 2004

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14687249%20AND%20SRC:MED&resulttype=core&format=json

Journal of Internal Medicine

16 November 2019

published in

1 reference

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16 November 2019

volume

255

1 reference

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16 November 2019

issue

1

1 reference

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16 November 2019

page(s)

130-136

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Anomalies of the abdominal aorta in Williams-Beuren syndrome--another cause of arterial hypertension

16 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1046%2FJ.0954-6820.2003.01240.X

[Hypoplasia of abdominal aorta, rare cause of hypertension in childhood]

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0954-6820.2003.01240.X

Analysis of cardiovascular phenotype and genotype-phenotype correlation in individuals with a JAG1 mutation and/or Alagille syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0954-6820.2003.01240.X

Butterfly vertebra: a case report

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0954-6820.2003.01240.X

Jagged1 gene mutation for abdominal coarctation of the aorta in Alagille syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0954-6820.2003.01240.X

Familial syndrome of progressive arterial occlusive disease consistent with fibromuscular dysplasia, hypertension, congenital cardiac defects, bone fragility, brachysyndactyly, and learning disabilities.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0954-6820.2003.01240.X

Possible familial origin of multifocal renal artery fibromuscular dysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0954-6820.2003.01240.X

Phenotypes of patients with "simple" Mendelian disorders are complex traits: thresholds, modifiers, and systems dynamics

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0954-6820.2003.01240.X

Insights into the pathogenesis of neurofibromatosis 1 vasculopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0954-6820.2003.01240.X

Coexistence of fibromuscular dysplasia and cystic medial necrosis in a patient with Marfan's syndrome and bilateral carotid artery dissections

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0954-6820.2003.01240.X

Hemizygosity at the elastin locus in a developmental disorder, Williams syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0954-6820.2003.01240.X

A 1.5 million-base pair inversion polymorphism in families with Williams-Beuren syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0954-6820.2003.01240.X

Polymorphisms of the renin-angiotensin system in patients with multifocal renal arterial fibromuscular dysplasia

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.0954-6820.2003.01240.X

10.1046/J.0954-6820.2003.01240.X

21 January 2018

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:14687249%20AND%20SRC:MED&resulttype=core&format=json

16 November 2019

1 reference