Josefine de Stricker Borch (Josefine de S Borch, Josefine D S Borch)

Publication Activity (10 Years)

Years Active: 2021-2022
Publications (10 Years): 3

Top Topics

Multiple Sclerosis

Inflammatory Response

Muscular Dystrophy

Top Venues

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

Publications

Josefine de Stricker Borch, Thomas Krag, Sonja D Holm-Yildiz, Hakan Cetin, Tuva A Solheim, Freja Fornander, Volker Straub, Morten Duno, John Vissing
Three novel FHL1 variants cause a mild phenotype of Emery-Dreifuss muscular dystrophy. Human mutation 43 (9) (2022)
Mads G Stemmerik, Josefine de Stricker Borch, Morten Dunø, Thomas O Krag, John Vissing
Myopathy can be a key phenotype of membrin (GOSR2) deficiency. Human mutation 42 (9) (2021)
Josefine de Stricker Borch, Jeppe Lohfert Haslund-Vinding, Frederik Vilhardt, Andrea Daniela Maier, Tiit Illimar Mathiesen
Meningioma-Brain Crosstalk: A Scoping Review. Cancers 13 (17) (2021)