Fleur S. Van Dijk

Amsterdam, NH, Netherlands

Last Updated: 09/26/2026

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Found 64 publications

Spontaneous coronary artery dissection and vascular Ehlers-Danlos syndrome: a systematic review and case series.

Spontaneous coronary artery dissection and vascular Ehlers-Danlos syndrome: a systematic review and case series.

Journal: European journal of human genetics : EJHG

Published: July 23, 2025

Editorial.

Editorial.

Journal: Medizinische Genetik : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V

Published: December 04, 2024

Clinical diagnosis of the monogenic Ehlers-Danlos syndromes.

Clinical diagnosis of the monogenic Ehlers-Danlos syndromes.

Journal: Medizinische Genetik : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V

Published: December 04, 2024

Non-genetic diagnostic investigations in monogenic Ehlers-Danlos syndromes.

Non-genetic diagnostic investigations in monogenic Ehlers-Danlos syndromes.

Journal: Medizinische Genetik : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V

Published: December 04, 2024

Genetic diagnosis of the Ehlers-Danlos syndromes.

Genetic diagnosis of the Ehlers-Danlos syndromes.

Journal: Medizinische Genetik : Mitteilungsblatt des Berufsverbandes Medizinische Genetik e.V

Published: December 04, 2024

Novel Insights Aortic Root Dilatation in an Individual with 3p21.31 Deletion.

Novel Insights Aortic Root Dilatation in an Individual with 3p21.31 Deletion.

Journal: Molecular syndromology

Published: November 11, 2024

The Natural History of Dermatosparaxis Ehlers Danlos Syndrome: An Adult Case Series.

The Natural History of Dermatosparaxis Ehlers Danlos Syndrome: An Adult Case Series.

Journal: American journal of medical genetics. Part A

Published: September 12, 2024

Vascular Ehlers-Danlos syndrome in children: evaluating the importance of diagnosis and follow-up during childhood.

Vascular Ehlers-Danlos syndrome in children: evaluating the importance of diagnosis and follow-up during childhood.

Journal: European journal of human genetics : EJHG

Published: June 27, 2024

Tenascin-X Deficiency Causing Classical-Like Ehlers-Danlos Syndrome Type 1 in Humans is a Significant Risk Factor of Gastrointestinal and Tracheal Ruptures.

Tenascin-X Deficiency Causing Classical-Like Ehlers-Danlos Syndrome Type 1 in Humans is a Significant Risk Factor of Gastrointestinal and Tracheal Ruptures.

Journal: Clinical and translational gastroenterology

Published: June 26, 2024

Vascular Ehlers Danlos Syndrome and Chromosome 2q32 Microdeletion Syndrome.

Vascular Ehlers Danlos Syndrome and Chromosome 2q32 Microdeletion Syndrome.

Journal: European journal of human genetics : EJHG

Published: April 19, 2024

Genetic testing in patients with unexplained coronary aneurysms or dilation.

Genetic testing in patients with unexplained coronary aneurysms or dilation.

Journal: European heart journal

Published: April 17, 2024

Pleiotropic effects of a recessive Col1a2 mutation occurring in a mouse model of severe osteogenesis imperfecta.

Pleiotropic effects of a recessive Col1a2 mutation occurring in a mouse model of severe osteogenesis imperfecta.

Journal: PloS one

Published: March 08, 2024

Showing 1-12 of 64

Last Updated: 09/26/2026