Anna Vihola (A Vihola)

Publication Activity (10 Years)

Years Active: 2017-2021
Publications (10 Years): 3

Top Topics

Dna Methylation

Muscular Dystrophy

Genome Wide Analysis

Top Venues

Neuropathology and applied neurobiology

Neurology. Genetics

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

Publications

Peter Hackman, Salla M Rusanen, Mridul Johari, Anna Vihola, Per Harald Jonson, Jaakko Sarparanta, Kati Donner, Päivi Lahermo, Sampo Koivunen, Helena Luque, Merja Soininen, Ibrahim Mahjneh, Mari Auranen, Meharji Arumilli, Marco Savarese, Bjarne Udd
Dominant Distal Myopathy 3 (MPD3) Caused by a Deletion in the HNRNPA1 Gene. Neurology. Genetics 7 (6) (2021)
Manu Jokela, Giorgio Tasca, Anna Vihola, Eugenio Mercuri, Per Harald Jonson, Sara Lehtinen, Salla M Rusanen, Marika Pane, Maria Donati, Mridul Johari, Marco Savarese, Sanna Huovinen, Pirjo Isohanni, Johanna Palmio, Päivi Hartikainen, Bjarne Udd
An unusual ryanodine receptor 1 (RYR1) phenotype: Mild calf-predominant myopathy. Neurology 92 (14) (2019)
Anna Vihola, H Luque, M Savarese, S Penttilä, M Lindfors, F Leturcq, B Eymard, Giorgio Tasca, B Brais, T Conte, K Charton, I Richard, B Udd
Diagnostic anoctamin-5 protein defect in patients with ANO5-mutated muscular dystrophy. Neuropathology and applied neurobiology 44 (5) (2017)