(Q87548740)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25113270%20AND%20SRC:MED&resulttype=core&format=json

12 March 2020

title

Total serum transforming growth factor-β1 is elevated in the entire spectrum of genetic aortic syndromes (English)

1 reference

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12 March 2020

13

Stefan Blankenberg

1 reference

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12 March 2020

12

Tanja Zeller

1 reference

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12 March 2020

11

Thomas S Mir

1 reference

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12 March 2020

15

Britta Goldmann

1 reference

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12 March 2020

1

Mathias Hillebrand

1 reference

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12 March 2020

author name string

Nathalie Millot

2

1 reference

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12 March 2020

Sara Sheikhzadeh

3

1 reference

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12 March 2020

Meike Rybczynski

4

1 reference

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12 March 2020

Sabine Gerth

5

1 reference

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12 March 2020

Tilo Kölbel

6

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12 March 2020

Britta Keyser

7

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12 March 2020

Kerstin Kutsche

8

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12 March 2020

Peter N Robinson

9

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12 March 2020

Jürgen Berger

10

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12 March 2020

Yskert von Kodolitsch

14

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12 March 2020

publication date

11 August 2014

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12 March 2020

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12 March 2020

volume

37

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12 March 2020

issue

11

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12 March 2020

page(s)

672-679

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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

12 March 2020

cites work

1 reference

7 January 2021

The revised Ghent nosology for the Marfan syndrome

1 reference

7 January 2021

Matrix-dependent perturbation of TGFβ signaling and disease

1 reference

7 January 2021

Losartan, an AT1 antagonist, prevents aortic aneurysm in a mouse model of Marfan syndrome

1 reference

7 January 2021

Effect of perindopril on large artery stiffness and aortic root diameter in patients with Marfan syndrome: a randomized controlled trial

1 reference

7 January 2021

Circulating transforming growth factor-beta in Marfan syndrome

1 reference

7 January 2021

Positive correlation between the dysregulation of transforming growth factor-β1 and aneurysmal pathological changes in patients with Marfan syndrome

1 reference

7 January 2021

Circulating transforming growth factor β-1 level in Japanese patients with Marfan syndrome

1 reference

7 January 2021

Circulating transforming growth factor-β as a prognostic biomarker in Marfan syndrome.

1 reference

7 January 2021

Biomarkers in TAA-the Holy Grail

1 reference

7 January 2021

A 1-bp duplication in TGFB2 in three family members with a syndromic form of thoracic aortic aneurysm

1 reference

7 January 2021

Heritable thoracic aortic disorders

1 reference

7 January 2021

Genetics of thoracic aortic aneurysm: at the crossroad of transforming growth factor-β signaling and vascular smooth muscle cell contractility

1 reference

7 January 2021

Revised diagnostic criteria for the Marfan syndrome

1 reference

7 January 2021

A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2

1 reference

7 January 2021

Aneurysm syndromes caused by mutations in the TGF-beta receptor

1 reference

7 January 2021

Evaluation of the adolescent or adult with some features of Marfan syndrome

1 reference

7 January 2021

Normal limits in relation to age, body size and gender of two-dimensional echocardiographic aortic root dimensions in persons ≥15 years of age.

1 reference

7 January 2021

Recommendations for chamber quantification

1 reference

7 January 2021

Augmentation index relates to progression of aortic disease in adults with Marfan syndrome.

1 reference

7 January 2021

Notch signaling in descending thoracic aortic aneurysm and dissection

1 reference

7 January 2021

Syndromic and non-syndromic aneurysms of the human ascending aorta share activation of the Smad2 pathway.

1 reference

7 January 2021

Novel MYH11 and ACTA2 mutations reveal a role for enhanced TGFβ signaling in FTAAD.

1 reference

7 January 2021

Angiotensin II blockade in Marfan's syndrome

1 reference

7 January 2021

Mutations in the TGFβ binding-protein-like domain 5 of FBN1 are responsible for acromicric and geleophysic dysplasias

1 reference

7 January 2021

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

1 reference

7 January 2021

Comprehensive analysis of dural ectasia in 150 patients with a causative FBN1 mutation

1 reference

12 December 2020

Dural ectasia in Loeys-Dietz syndrome: comprehensive study of 30 patients with a TGFBR1 or TGFBR2 mutation.

1 reference

12 December 2020

Loeys-Dietz syndrome: a primer for diagnosis and management

1 reference

12 December 2020

A formula to estimate the approximate surface area if height and weight be known. 1916.

1 reference

12 December 2020

Revised diagnostic criteria for the Marfan syndrome

1 reference

12 December 2020

Identifiers

DOI

10.1002/CLC.22320

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25113270%20AND%20SRC:MED&resulttype=core&format=json

12 March 2020

1 reference

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12 March 2020

PubMed publication ID

25113270

1 reference