Lotte F. Van Den Heuvel

Antwerpen, VLG, Belgium

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 9 publications

Variations across Europe in National Guidelines and Clinical Practice Regarding Screening of Cognitive and Emotional Consequences after Aneurysmal Subarachnoid Hemorrhage.

Variations across Europe in National Guidelines and Clinical Practice Regarding Screening of Cognitive and Emotional Consequences after Aneurysmal Subarachnoid Hemorrhage.

Journal: Cerebrovascular diseases (Basel, Switzerland)

Published: February 22, 2026

An exploration of alternative therapeutic targets for aortic disease in Marfan syndrome.

An exploration of alternative therapeutic targets for aortic disease in Marfan syndrome.

Journal: Drug discovery today

Published: February 27, 2024

A generated induced pluripotent stem cell (iPSC) line (CMGANTi005-A) of a Marfan syndrome patient with an FBN1 c.7754T > C (p.Ile2585Thr) variation.

A generated induced pluripotent stem cell (iPSC) line (CMGANTi005-A) of a Marfan syndrome patient with an FBN1 c.7754T > C (p.Ile2585Thr) variation.

Journal: Stem cell research

Published: December 30, 2022

The Frequency of CYP2C19 Loss-of-Function Variants in Patients with Non-Cardioembolic Ischemic Stroke or Transient Ischemic Attack in the Dutch Population.

The Frequency of CYP2C19 Loss-of-Function Variants in Patients with Non-Cardioembolic Ischemic Stroke or Transient Ischemic Attack in the Dutch Population.

Journal: Cerebrovascular diseases (Basel, Switzerland)

Published: December 19, 2022

Molecular characterization and investigation of the role of genetic variation in phenotypic variability and response to treatment in a large pediatric Marfan syndrome cohort.

Molecular characterization and investigation of the role of genetic variation in phenotypic variability and response to treatment in a large pediatric Marfan syndrome cohort.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: September 13, 2021

Novel LOX Variants in Five Families with Aortic/Arterial Aneurysm and Dissection with Variable Connective Tissue Findings.

Novel LOX Variants in Five Families with Aortic/Arterial Aneurysm and Dissection with Variable Connective Tissue Findings.

Journal: International journal of molecular sciences

Published: June 04, 2021

A human importin-β-related disorder: Syndromic thoracic aortic aneurysm caused by bi-allelic loss-of-function variants in IPO8.

A human importin-β-related disorder: Syndromic thoracic aortic aneurysm caused by bi-allelic loss-of-function variants in IPO8.

Journal: American journal of human genetics

Published: January 24, 2021

Enrichment of Rare Variants in Loeys-Dietz Syndrome Genes in Spontaneous Coronary Artery Dissection but Not in Severe Fibromuscular Dysplasia.

Enrichment of Rare Variants in Loeys-Dietz Syndrome Genes in Spontaneous Coronary Artery Dissection but Not in Severe Fibromuscular Dysplasia.

Journal: Circulation

Published: September 08, 2020

Clinically relevant variants in a large cohort of Indian patients with Marfan syndrome and related disorders identified by next-generation sequencing.

Clinically relevant variants in a large cohort of Indian patients with Marfan syndrome and related disorders identified by next-generation sequencing.

Journal: Scientific reports

Published: July 06, 2020

Showing 1-9 of 9

Last Updated: 09/26/2026