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Acta Neurologica Scandinavica|September 11, 2007
Increased plasma levels of cytokines after seizures in localization-related epilepsyK A Lehtimäki, T Keränen, J Palmio, et al.Epilepsy Research|August 30, 2000
Interleukin-6 and interleukin-1 receptor antagonist in cerebrospinal fluid from patients with recent tonic-clonic seizuresJ Peltola, J Palmio, L Korhonen, et al.American Journal of Human Genetics|April 29, 1998
Assignment of the tibial muscular dystrophy locus to chromosome 2q31H Haravuori, P Mäkelä-Bengs, B Udd, et al.Neurology|July 1, 2011
Late-onset lower motor neuronopathy: a new autosomal dominant disorderM Jokela, S Penttilä, S Huovinen, et al.Acta Neurologica Belgica|April 9, 2014
Laing early-onset distal myopathy in a Belgian familyP Y K Van den Bergh, J J Martin, F Lecouvet, et al.Acta Neurologica Scandinavica|September 2, 1998
High prevalence of Kennedy's disease in Western Finland -- is the syndrome underdiagnosed?B Udd, V Juvonen, L Hakamies, et al.Journal of Neuroimmunology|June 30, 2004
Regulation of IL-6 system in cerebrospinal fluid and serum compartments by seizures: the effect of seizure type and durationK A Lehtimäki, T Keränen, H Huhtala, et al.Clinical Genetics|September 27, 2007
Do carriers of POLG mutation W748S have disease manifestations?M Rantamäki, P Luoma, J J Virta, et al.Neurology|July 9, 2003
A distinct phenotype of distal myopathy in a large Finnish familyI Mahjneh, H Haravuori, A Paetau, et al.Journal of Neurology, Neurosurgery, and Psychiatry|June 24, 2010
Myopathies caused by homozygous titin mutations: limb-girdle muscular dystrophy 2J and variations of phenotypeI Pénisson-Besnier, P Hackman, T Suominen, et al.Pageof 7