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European Journal of Neurology|May 9, 2025
Novel SCN4A Variants Associated With Myalgic Myotonic Disorder or ParamyotoniaVesa Periviita, Roope Männikkö, Manu Jokela, et al.Journal of Communication Disorders|April 26, 2016
Oral motor functions, speech and communication before a definitive diagnosis of amyotrophic lateral sclerosisTanja Makkonen, Anna-Maija Korpijaakko-Huuhka, Hanna Ruottinen, et al.Psychiatry Research|April 10, 2010
Electroconvulsive therapy and biomarkers of neuronal injury and plasticity: Serum levels of neuron-specific enolase and S-100b proteinJohanna Palmio, Martti Huuhka, Seppo Laine, et al.Acta Neuropathologica Communications|February 6, 2016
Diagnostically important muscle pathology in DNAJB6 mutated LGMD1DSatu Sandell, Sanna Huovinen, Johanna Palmio, et al.Epilepsy Research|July 4, 2008
Elevated serum neuron-specific enolase in patients with temporal lobe epilepsy: a video-EEG studyJohanna Palmio, Tapani Keränen, Tiina Alapirtti, et al.Neurology. Genetics|June 14, 2019
Novel mutation in TNPO3 causes congenital limb-girdle myopathy with slow progressionAnna Vihola, Johanna Palmio, Olof Danielsson, et al.Psychiatry Research|November 22, 2005
Changes in plasma amino acids after electroconvulsive therapy of depressed patientsJohanna Palmio, Martti Huuhka, Pirjo Saransaari, et al.Neurology. Genetics|June 12, 2018
Absence of NEFL in patient-specific neurons in early-onset Charcot-Marie-Tooth neuropathyMarkus T Sainio, Emil Ylikallio, Laura Mäenpää, et al.Journal of the Neurological Sciences|June 11, 2015
Spontaneous activity in electromyography may differentiate certain benign lower motor neuron disease forms from amyotrophic lateral sclerosisManu E Jokela, Satu K Jääskeläinen, Satu Sandell, et al.Neuromuscular Disorders : NMD|June 21, 2011
Distinct distal myopathy phenotype caused by VCP gene mutation in a Finnish familyJohanna Palmio, Satu Sandell, Tiina Suominen, et al.Pageof 7