Sudden death in Williams syndrome: report of ten cases (Q41273020)

29 September 2017

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title

Sudden death in Williams syndrome: report of ten cases (English)

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29 September 2017

8

Morris C

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author name string

Bird LM

1

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29 September 2017

Billman GF

2

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29 September 2017

Lacro RV

3

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29 September 2017

Spicer RL

4

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29 September 2017

Jariwala LK

5

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29 September 2017

Hoyme HE

6

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29 September 2017

Zamora-Salinas R

7

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29 September 2017

Viskochil D

9

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29 September 2017

Frikke MJ

10

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29 September 2017

Jones MC

11

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29 September 2017

language of work or name

English

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publication date

1 December 1996

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The Journal of Pediatrics

29 September 2017

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29 September 2017

129

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29 September 2017

6

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29 September 2017

926-931

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The Williams elfin facies syndrome. A new perspective

29 September 2017

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https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970042-2

Williams-Beuren syndrome: a 30-year follow-up of natural and postoperative course

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970042-2

Cardiac findings in idiopathic hypercalcemia of infancy

7 January 2021

1 reference

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ASSOCIATION BETWEEN AORTIC STENOSIS AND FACIES OF SEVERE INFANTILE HYPERCALCAEMIA

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970042-2

Myocardial infarction associated with supravalvular aortic stenosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970042-2

Myocardial infarction leading to sudden death in the Williams syndrome: report of three cases

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970042-2

Sudden death in supravalvular aortic stenosis: fusion of a coronary leaflet to the sinus ridge, dysplasia and stenosis of aortic and pulmonic valves

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970042-2

Supravalvular aortic stenosis: clinical, hemodynamic and pathologic observations

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970042-2

Generalized arterial fibromuscular dysplasia and myocardial infarction in familial supravalvular aortic stenosis syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970042-2

A Developmental Complex Including Supravalvular Stenosis of the Aorta and Pulmonary Trunk

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970042-2

Obstruction to left coronary artery blood flow secondary to obliteration of the coronary ostium in supravalvular aortic stenosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970042-2

Supravalvular aortic stenosis in adults

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970042-2

Supra-aortic stenosis; congenital, supraaortic valvular, stenosing membrane on the aortic cusps

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970042-2

Supravalvular aortic stenosis

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970042-2

Familial supravalvular aortic stenosis

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970042-2

Systemic and pulmonary artery dysplasia associated with unexpected death in infancy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970042-2

The elastin gene is disrupted by a translocation associated with supravalvular aortic stenosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970042-2

A human vascular disorder, supravalvular aortic stenosis, maps to chromosome 7.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970042-2

Autosomal dominant supravalvular aortic stenosis: localization to chromosome 7

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970042-2

Confirmation of linkage of supravalvular aortic stenosis to the elastin gene on chromosome 7q

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970042-2

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970042-2

Supravalvular aortic stenosis associated with a deletion disrupting the elastin gene

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970042-2

Supravalvar aortic stenosis: a 29-year review of surgical experience

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970042-2

Supravalvar aortic stenosis

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970042-2

Spectrum of renal anomalies in patients with Williams syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970042-2

Cerebral artery stenoses in Williams syndrome cause strokes in childhood

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970042-2

Ischemic stroke and intracranial multifocal cerebral arteriopathy in Williams syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970042-2

Natural history of supravalvular aortic stenosis and pulmonary artery stenosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970042-2

Three decades of follow-up of aortic and pulmonary vascular lesions in the Williams-Beuren syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970042-2

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2896%2970042-2

inferred from DOI database lookup

7 January 2021

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Identifiers

DOI

10.1016/S0022-3476(96)70042-2

1 reference

29 September 2017

1 reference