Eric H. Legius

Leuven, VLG, Belgium

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 142 publications

Cherry Angiomas in Individuals With Neurofibromatosis Type 1.

Cherry Angiomas in Individuals With Neurofibromatosis Type 1.

Journal: JAMA dermatology

Published: August 19, 2026

From clinical suspicion to molecular detection of low-level mosaicism in NF2-related schwannomatosis via ultra-sensitive duplex sequencing.

From clinical suspicion to molecular detection of low-level mosaicism in NF2-related schwannomatosis via ultra-sensitive duplex sequencing.

Journal: Molecular medicine (Cambridge, Mass.)

Published: May 29, 2026

Pigmentary mosaicism: a literature review

Pigmentary mosaicism: a literature review

Journal: Revue medicale suisse

Published: March 26, 2026

Novel Identical Likely Pathogenic ACTB Variant in Congenital Smooth Muscle Hamartoma: A Report of Two Pediatric Cases.

Novel Identical Likely Pathogenic ACTB Variant in Congenital Smooth Muscle Hamartoma: A Report of Two Pediatric Cases.

Journal: Pediatric dermatology

Published: August 05, 2025

Emerging insights into mosaic errors of immunity.

Emerging insights into mosaic errors of immunity.

Journal: Trends in immunology

Published: July 07, 2025

Reply to Taal et al. Comment on "Iasella et al. Close Follow-Up of Patients with Neurofibromatosis Type 1 Reduces the Incidence of Malignant Peripheral Nerve Sheath Tumour. Cancers 2025, 17, 1306".

Reply to Taal et al. Comment on "Iasella et al. Close Follow-Up of Patients with Neurofibromatosis Type 1 Reduces the Incidence of Malignant Peripheral Nerve Sheath Tumour. Cancers 2025, 17, 1306".

Journal: Cancers

Published: June 25, 2025

Close Follow-Up of Patients with Neurofibromatosis Type 1 Reduces the Incidence of Malignant Peripheral Nerve Sheath Tumour.

Close Follow-Up of Patients with Neurofibromatosis Type 1 Reduces the Incidence of Malignant Peripheral Nerve Sheath Tumour.

Journal: Cancers

Published: March 06, 2025

Neonatal Epidermolytic Ichthyosis Caused by a KRT10 Mutation (c.467G>A, p.Arg156His): A Case Report.

Neonatal Epidermolytic Ichthyosis Caused by a KRT10 Mutation (c.467G>A, p.Arg156His): A Case Report.

Journal: Clinical case reports

Published: September 09, 2024

Platform trial design for neurofibromatosis type 1, NF2-related schwannomatosis and non-NF2-related schwannomatosis: A potential model for rare diseases.

Platform trial design for neurofibromatosis type 1, NF2-related schwannomatosis and non-NF2-related schwannomatosis: A potential model for rare diseases.

Journal: Neuro-oncology practice

Published: July 15, 2024

Legius syndrome mutations in the Ras-regulator SPRED1 abolish its membrane localization and potentially cause neurodegeneration.

Legius syndrome mutations in the Ras-regulator SPRED1 abolish its membrane localization and potentially cause neurodegeneration.

Journal: The Journal of biological chemistry

Published: July 13, 2024

The phenotypic and genotypic spectrum of individuals with mono- or biallelic ANK3 variants.

The phenotypic and genotypic spectrum of individuals with mono- or biallelic ANK3 variants.

Journal: Clinical genetics

Published: May 03, 2024

Pigment epithelium derived factor drives melanocyte proliferation and migration in neurofibromatosis café au lait macules.

Pigment epithelium derived factor drives melanocyte proliferation and migration in neurofibromatosis café au lait macules.

Journal: Skin health and disease

Published: December 06, 2023

Showing 1-12 of 142

Last Updated: 09/26/2026