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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.Journal of Medical Genetics|June 1, 1992
Limb-girdle type muscular dystrophy in a large family with distal myopathy: homozygous manifestation of a dominant gene?B UddNeurology|March 10, 2012
Eight new mutations and the expanding phenotype variability in muscular dystrophy caused by ANO5S Penttilä, J Palmio, T Suominen, et al.Neuromuscular Disorders : NMD|January 1, 1991
Imaging methods reveal unexpected patchy lesions in late onset distal myopathyB Udd, A Lamminen, H SomerMuscle & Nerve|November 1, 1991
Muscular dystrophy with separate clinical phenotypes in a large familyB Udd, H Kääriänen, H SomerHuman Heredity|January 1, 1992
The first case of familial amyloidotic polyneuropathy (FAP Met30) in the Finnish populationU Drugge, G Holmgren, B UddRevue Neurologique|June 15, 1999
[Tibial muscular dystrophy. A rare form of distal myopathy]J de Seze, B Udd, P VermerschHuman Heredity|March 1, 1996
Linkage analyses in tibial muscular dystrophyP Nokelainen, B Udd, H Somer, et al.Pageof 7