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Neuromuscular Disorders : NMD|July 23, 1998
Tibial muscular dystrophy--from clinical description to linkage on chromosome 2q31B Udd, H Haravuori, H Kalimo, et al.Neuropathology and Applied Neurobiology|July 5, 2012
Altered expression and splicing of Ca(2+) metabolism genes in myotonic dystrophies DM1 and DM2A Vihola, M Sirito, L L Bachinski, et al.Journal of Neurology|September 23, 2008
High frequency of co-segregating CLCN1 mutations among myotonic dystrophy type 2 patients from Finland and GermanyT Suominen, B Schoser, O Raheem, et al.Neurology|November 23, 2005
Similar brain tau pathology in DM2/PROMM and DM1/Steinert diseaseC A Maurage, B Udd, M M Ruchoux, et al.Neurology|July 13, 2000
Autoantibodies to glutamic acid decarboxylase in patients with therapy-resistant epilepsyJ Peltola, P Kulmala, J Isojärvi, et al.Acta Neurologica Scandinavica|July 10, 2004
Muscle magnetic resonance imaging shows distinct diagnostic patterns in Welander and tibial muscular dystrophyI Mahjneh, A E Lamminen, B Udd, et al.Archives of Neurology|June 1, 1993
Tibial muscular dystrophy. Late adult-onset distal myopathy in 66 Finnish patientsB Udd, J Partanen, P Halonen, et al.Neurology|November 21, 2008
Premutation allele pool in myotonic dystrophy type 2L L Bachinski, T Czernuszewicz, L S Ramagli, et al.The American Journal of Medicine|January 4, 2001
Antiphospholipid and antinuclear antibodies in patients with epilepsy or new-onset seizure disordersJ T Peltola, A Haapala, J I Isojärvi, et al.Neuromuscular Disorders : NMD|July 16, 2002
Congenital myasthenic syndrome associated with episodic apnea and sudden infant deathR F Byring, H Pihko, A Tsujino, et al.Pageof 7