(Q48743544)

English

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

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/18925407

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

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/18925407

1 reference

based on heuristic

inferred from title

Marfan syndrome

1 reference

based on heuristic

inferred from title

author name string

M Klintschar

1

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/18925407

U Bilkenroth

2

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/18925407

M Arslan-Kirchner

3

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/18925407

J Schmidtke

4

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/18925407

D Stiller

5

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/18925407

publication date

17 October 2008

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/18925407

International Journal of Legal Medicine

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/18925407

123

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/18925407

1

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/18925407

55-58

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/18925407

https://scigraph.springernature.com/pub.10.1007/s00414-008-0288-5

0 references

The role of alpharadrenergic and muscarinic receptors in cardiac function

1 reference

https://api.crossref.org/works/10.1007%2FS00414-008-0288-5

21 January 2018

Multi-exon out of frame deletion of the FBN1 gene leading to a severe juvenile onset cardiovascular phenotype in Marfan syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/18925407

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sudden cardiac death in hereditary hemochromatosis: an underestimated cause of death?

1 reference

https://pubmed.ncbi.nlm.nih.gov/18925407

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Marfan syndrome. A contribution to forensic medicine cases]

1 reference

https://pubmed.ncbi.nlm.nih.gov/18925407

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Marfan syndrome and sudden death within a family - aetiologic, molecular and diagnostic issues at autopsy

1 reference

https://pubmed.ncbi.nlm.nih.gov/18925407

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Marfan's syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/18925407

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The molecular pathogenesis of the Marfan syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/18925407

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dissecting aneurysm of the aorta: a review of 505 cases.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18925407

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clustering of mutations associated with mild Marfan-like phenotypes in the 3? region ofFBN1 suggests a potential genotype-phenotype correlation

1 reference

https://pubmed.ncbi.nlm.nih.gov/18925407

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sudden infant death syndrome and long QT syndrome: an epidemiological and genetic study.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18925407

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two cases of unexpected sudden death due to cystic medionecrosis of the aorta associated with bloodless aortic dissection

1 reference

https://pubmed.ncbi.nlm.nih.gov/18925407

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Ehlers-Danlos syndrome type IV

1 reference

https://pubmed.ncbi.nlm.nih.gov/18925407

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/18925407

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Marfan syndrome: an update of genetics, medical and surgical management

1 reference

https://pubmed.ncbi.nlm.nih.gov/18925407

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Life expectancy in the Marfan syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/18925407

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Marfan's disease and Erdheim's cystic medionecrosis. A study of their pathology.

1 reference

https://pubmed.ncbi.nlm.nih.gov/18925407

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Recent data for frequency of autopsy in Germany

1 reference

https://pubmed.ncbi.nlm.nih.gov/18925407

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular genetics of Marfan syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/18925407

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00414-008-0288-5

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/18925407

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

15 February 2018

http://europepmc.org/abstract/MED/18925407

ResearchGate publication ID

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