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Neurology|February 25, 2005
Titinopathies and extension of the M-line mutation phenotype beyond distal myopathy and LGMD2JB Udd, A Vihola, J Sarparanta, et al.Journal of the Neurological Sciences|December 1, 1992
Nonvacuolar myopathy in a large family with both late adult onset distal myopathy and severe proximal muscular dystrophyB Udd, J Rapola, P Nokelainen, et al.Neuromuscular Disorders : NMD|June 1, 1997
Proximal myotonic dystrophy--a family with autosomal dominant muscular dystrophy, cataracts, hearing loss and hypogonadism: heterogeneity of proximal myotonic syndromes?B Udd, R Krahe, C Wallgren-Pettersson, et al.Journal of the Neurological Sciences|February 13, 2001
Normal CSF neuron-specific enolase and S-100 protein levels in patients with recent non-complicated tonic-clonic seizuresJ Palmio, J Peltola, P Vuorinen, et al.European Journal of Neurology|April 24, 2010
Mutations in CHMP2B are not a cause of frontotemporal lobar degeneration in Finnish patientsA-L Kaivorinne, J Krüger, B Udd, et al.Neurology|September 26, 2001
Adult-onset autosomal recessive ataxia with thalamic lesions in a Finnish familyM Rantamäki, R Krahe, A Paetau, et al.European Journal of Neurology|December 4, 2008
Low prevalence of progranulin mutations in Finnish patients with frontotemporal lobar degenerationJ Krüger, A-L Kaivorinne, B Udd, et al.Journal of Neuromuscular Diseases|November 18, 2016
GNE-Myopathy in a Greek Romani Family with Unusual Calf Phenotype and Protein Aggregation PathologyG K Papadimas, A Evilä, C Papadopoulos, et al.European Journal of Neurology|July 20, 2013
'Pathognomonic' muscle imaging findings in DNAJB6 mutated LGMD1DS M Sandell, I Mahjneh, J Palmio, et al.European Journal of Neurology|February 14, 2018
Novel mutations in DNAJB6 cause LGMD1D and distal myopathy in French familiesP H Jonson, J Palmio, M Johari, et al.Pageof 7