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B Udd

Showing results (21-30 of 54) with videos related to

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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.
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.
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.
European Journal of Neurology|February 25, 2017
Association study reveals novel risk loci for sporadic inclusion body myositisM Johari, M Arumilli, J Palmio, et al.
Pageof 6

Showing results (21-30 of 54) with videos related to

Sort By:
Pageof 6
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.
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.
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.
European Journal of Neurology|February 25, 2017
Association study reveals novel risk loci for sporadic inclusion body myositisM Johari, M Arumilli, J Palmio, et al.
Pageof 6