Silke De Feyter (S De Feyter)

Publication Activity (10 Years)

Years Active: 2021-2023
Publications (10 Years): 6

Top Topics

Systematic Review

Magnetic Resonance

Top Venues

Journal of inherited metabolic disease

This page only lists publications with an associated author ORCID identifier.

Publications

Silke De Feyter, Aude Beyens, Bert Callewaert
ATP7A-related copper transport disorders: A systematic review and definition of the clinical subtypes. Journal of inherited metabolic disease (2023)
Silke De Feyter, Aude Beyens, Bert Callewaert
ATP7A-related copper transport disorders: A systematic review and definition of the clinical subtypes. Journal of inherited metabolic disease 46 (2) (2023)
Silke De Feyter, Aude Beyens, Bert Callewaert
ATP7A-related copper transport disorders: A systematic review and definition of the clinical subtypes. Journal of inherited metabolic disease (2023)
Silke De Feyter, Aude Beyens, Bert Callewaert
ATP7A-related copper transport disorders: A systematic review and definition of the clinical subtypes. Journal of inherited metabolic disease 46 (2) (2023)
Silke De Feyter, Aude Beyens, Bert Callewaert
ATP7A-related copper transport disorders: a systematic review and definition of the clinical subtypes. Journal of inherited metabolic disease (2023)
Maxim Verlee, Aude Beyens, Alper Gezdirici, Elif Yilmaz Gulec, Lore Pottie, Silke De Feyter, Michiel Vanhooydonck, Piyanoot Tapaneeyaphan, Sofie Symoens, Bert Callewaert
Loss-of-Function Variants in EFEMP1 Cause a Recognizable Connective Tissue Disorder Characterized by Cutis Laxa and Multiple Herniations. Genes 12 (4) (2021)