Aude Beyens

Clinical and Molecular Delineation of Cutis Laxa Syndromes: Paradigms for Homeostasis.

B. Callewaert, P. Sips, Aude Beyens, 2021, Advances in experimental medicine and biology.

Cutis laxa: A comprehensive overview of clinical characteristics and pathophysiology

A. Boel, B. Callewaert, S. Symoens, 2020, Clinical genetics.

Severe congenital cutis laxa: Identification of novel homozygous LOX gene variants in two families

F. McKenzie, G. Baynam, K. Mina, 2021, Clinical genetics.

ATP6V0A2‐related cutis laxa in 10 novel patients: Focus on clinical variability and expansion of the phenotype

C. Bodemer, Elif Yilmaz Gulec, A. Gezdirici, 2018, Experimental dermatology.

Identification of Codon 146 KRAS Variants in Isolated Epidermal Nevus and Multiple Lesions in Oculoectodermal Syndrome: Confirmation of the Phenotypic Continuum of Mosaic RASopathies

P. de Paepe, S. de Schepper, H. Brems, 2022, International journal of molecular sciences.

Arterial Tortuosity Syndrome: an ascorbate compartmentalization disorder?

Csilla E. Németh, É. Margittai, A. Boel, 2019, Antioxidants & redox signaling.