Paucar M

Acute Vestibular Syndrome Unmasking an RFC1-Spectrum Disorder.

Verrecchia L, Alm V, Thonberg H, ..., Nilsson D, Paucar M

Neurol Genet 11 (1) e200238 [2025-02-00; online 2025-01-16]

Comment to: "SCA4 Unravelled After More than 25 Years Using Advanced Genomic Technologies".

Paucar M, Nilsson D, Engvall M, ..., Wedell A, Svenningsson P

Mov Disord 39 (6) 1077 [2024-06-00; online 2024-06-26]

V374A KCND3 Pathogenic Variant Associated With Paroxysmal Ataxia Exacerbations.

Paucar M, Ågren R, Li T, ..., Nilsson J, Svenningsson P

Neurol Genet 7 (1) e546 [2021-02-00; online 2021-01-06]

Phenotypic variability in chorea-acanthocytosis associated with novel VPS13A mutations.

Niemelä V, Salih A, Solea D, ..., Dahl N, Paucar M

Neurol Genet 6 (3) e426 [2020-06-00; online 2020-04-27]

Rare variants in dynein heavy chain genes in two individuals with situs inversus and developmental dyslexia

Bieder A, Einarsdottir E, Matsson H, ..., Kere J, Tapia-Páez I

- - (-) - [2020-03-31; online 2020-03-31]