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B Udd

Showing results (1-10 of 54) with videos related to

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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 Udd
Revue Neurologique|September 18, 2016
Myofibrillar and distal myopathiesJ Palmio, B Udd
Current Opinion in Neurology|September 20, 2001
Distal myopathiesB Udd, R Griggs
Neuromuscular Disorders : NMD|January 1, 1991
Imaging methods reveal unexpected patchy lesions in late onset distal myopathyB Udd, A Lamminen, H Somer
Muscle & Nerve|November 1, 1991
Muscular dystrophy with separate clinical phenotypes in a large familyB Udd, H Kääriänen, H Somer
Human Heredity|January 1, 1992
The first case of familial amyloidotic polyneuropathy (FAP Met30) in the Finnish populationU Drugge, G Holmgren, B Udd
Revue Neurologique|June 15, 1999
[Tibial muscular dystrophy. A rare form of distal myopathy]J de Seze, B Udd, P Vermersch
Human Heredity|March 1, 1996
Linkage analyses in tibial muscular dystrophyP Nokelainen, B Udd, H Somer, et al.
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.
Pageof 6

Showing results (1-10 of 54) with videos related to

Sort By:
Pageof 6
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 Udd
Revue Neurologique|September 18, 2016
Myofibrillar and distal myopathiesJ Palmio, B Udd
Current Opinion in Neurology|September 20, 2001
Distal myopathiesB Udd, R Griggs
Neuromuscular Disorders : NMD|January 1, 1991
Imaging methods reveal unexpected patchy lesions in late onset distal myopathyB Udd, A Lamminen, H Somer
Muscle & Nerve|November 1, 1991
Muscular dystrophy with separate clinical phenotypes in a large familyB Udd, H Kääriänen, H Somer
Human Heredity|January 1, 1992
The first case of familial amyloidotic polyneuropathy (FAP Met30) in the Finnish populationU Drugge, G Holmgren, B Udd
Revue Neurologique|June 15, 1999
[Tibial muscular dystrophy. A rare form of distal myopathy]J de Seze, B Udd, P Vermersch
Human Heredity|March 1, 1996
Linkage analyses in tibial muscular dystrophyP Nokelainen, B Udd, H Somer, et al.
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.
Pageof 6