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Neuromuscular Disorders : NMD|July 23, 2014
Screening for late-onset Pompe disease in FinlandJohanna Palmio, Mari Auranen, Sari Kiuru-Enari, et al.Neurology|March 24, 2017
Predominantly myalgic phenotype caused by the c.3466G>A p.A1156T mutation in SCN4A geneJohanna Palmio, Satu Sandell, Michael G Hanna, et al.BMC Neurology|August 31, 2012
Ubiquitin carboxy-terminal hydrolase L1 (UCH-L1) is increased in cerebrospinal fluid and plasma of patients after epileptic seizureStefania Mondello, Johanna Palmio, Jackson Streeter, et al.Neurochemical Research|March 3, 2004
Plasma and cerebrospinal fluid amino acids in epileptic patientsSirpa Rainesalo, Tapani Keränen, Johanna Palmio, et al.Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|October 26, 2012
TARDBP mutations are not a frequent cause of ALS in Finnish patientsHanna-Kaisa Mentula, Laura Tuovinen, Sini Penttilä, et al.Plos One|March 22, 2016
Distinct Muscle Biopsy Findings in Genetically Defined Adult-Onset Motor Neuron DisordersManu Jokela, Sanna Huovinen, Olayinka Raheem, et al.Neurology|September 7, 2023
CACNA1S Variant Associated With a Myalgic Myopathy PhenotypeVesa Periviita, Johanna Palmio, Manu Jokela, et al.The Journal of ECT|April 2, 2008
Increase in plasma proinflammatory cytokines after electroconvulsive therapy in patients with depressive disorderKai Lehtimäki, Tapani Keränen, Martti Huuhka, et al.European Journal of Neurology|February 17, 2026
Over-Representation of TTN Truncating Variants in a Finnish Cohort of Patients With Axial MyopathyMaria Francesca Di Feo, Giuliana Capece, Marco Savarese, et al.Journal of Neurology|April 10, 2019
A novel COL6A2 mutation causing late-onset limb-girdle muscular dystrophyManu Jokela, Sara Lehtinen, Johanna Palmio, et al.Pageof 7