Kristien Peeters

Publication Activity (10 Years)

Years Active: 2021-2021
Publications (10 Years): 2

Top Topics

Magnetic Resonance Imaging

Chemotherapy Induced

Top Venues

Molecular genetics & genomic medicine

Orphanet journal of rare diseases

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

Publications

Bianca de Aguiar Coelho Silva Madeiro, Kristien Peeters, Elker Lene Santos de Lima, Silvia Amor-Barris, Els De Vriendt, Albena Jordanova, Maria Tereza Cartaxo Muniz, Carolina da Cunha Correia
HINT1 founder mutation causing axonal neuropathy with neuromyotonia in South America: A case report. Molecular genetics & genomic medicine 9 (10) (2021)
Silvia Amor-Barris, Helle Høyer, Lin V Brauteset, Els De Vriendt, Linda Strand, Albena Jordanova, Geir J Braathen, Kristien Peeters
HINT1 neuropathy in Norway: clinical, genetic and functional profiling. Orphanet journal of rare diseases 16 (1) (2021)