A simple clinical model to estimate the probability of Marfan syndrome (Q56988676)

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22 January 2020

title

A simple clinical model to estimate the probability of Marfan syndrome (English)

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22 January 2020

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10

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22 January 2020

author name string

S Sheikhzadeh

1

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22 January 2020

M L Kusch

2

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22 January 2020

M Rybczynski

3

1 reference

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22 January 2020

C Kade

4

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22 January 2020

B Keyser

5

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22 January 2020

A M Bernhardt

6

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22 January 2020

M Hillebrand

7

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22 January 2020

T S Mir

8

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22 January 2020

B Fuisting

9

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22 January 2020

J Berger

11

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22 January 2020

V Lorenzen

12

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22 January 2020

J Schmidtke

13

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22 January 2020

S Blankenberg

14

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22 January 2020

Y von Kodolitsch

15

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22 January 2020

language of work or name

English

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publication date

1 February 2012

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QJM: An International Journal of Medicine

22 January 2020

published in

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22 January 2020

volume

105

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22 January 2020

issue

6

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22 January 2020

page(s)

527-535

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22 January 2020

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https://api.crossref.org/works/10.1093%2FQJMED%2FHCS008

The revised Ghent nosology for the Marfan syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FQJMED%2FHCS008

The spectrum of syndromes and manifestations in individuals screened for suspected Marfan syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FQJMED%2FHCS008

Prevalence data on all Ghent features in a cross-sectional study of 87 adults with proven Marfan syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FQJMED%2FHCS008

Identification of 29 novel and nine recurrent fibrillin-1 (FBN1) mutations and genotype-phenotype correlations in 76 patients with Marfan syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FQJMED%2FHCS008

TGFBR1 and TGFBR2 mutations in patients with features of Marfan syndrome and Loeys-Dietz syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FQJMED%2FHCS008

Dural ectasia in individuals with Marfan-like features but exclusion of mutations in the genes FBN1, TGFBR1 and TGFBR2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FQJMED%2FHCS008

Young patients with chest pain: 1-year outcomes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FQJMED%2FHCS008

2010 ACCF/AHA/AATS/ACR/ASA/SCA/SCAI/SIR/STS/SVM guidelines for the diagnosis and management of patients with Thoracic Aortic Disease: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guideli

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FQJMED%2FHCS008

Clinical prediction of acute aortic dissection.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FQJMED%2FHCS008

The genetic message of a sudden, unexpected death due to thoracic aortic dissection.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FQJMED%2FHCS008

Marfan syndrome: clinical consequences resulting from a medicolegal autopsy of a case of sudden death due to aortic rupture.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FQJMED%2FHCS008

Improving clinical recognition of Marfan syndrome.

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FQJMED%2FHCS008

Effect of mutation type and location on clinical outcome in 1,013 probands with Marfan syndrome or related phenotypes and FBN1 mutations: an international study

21 January 2018

1 reference

https://api.crossref.org/works/10.1093%2FQJMED%2FHCS008

Letter: Nomogram for Bayes theorem

21 January 2018

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https://api.crossref.org/works/10.1093%2FQJMED%2FHCS008

21 January 2018

Identifiers

DOI

10.1093/QJMED/HCS008

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22301820%20AND%20SRC:MED&resulttype=core&format=json

22 January 2020

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