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H Somer

Showing results (111-120 of 123) with videos related to

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Annals of Neurology|February 1, 1997
Muscle-eye-brain disease: a neuropathological studyM Haltia, I Leivo, H Somer, et al.
Human Genetics|October 1, 1990
Linkage disequilibrium detected between dystrophia myotonica and APOC2 locus in the Finnish populationP Nokelainen, L Alanen-Kurki, R Winqvist, et al.
Clinical Genetics|April 1, 1993
The DM mutation; diagnostic applications in the Finnish populationP Nokelainen, P Shelbourne, D Shaw, et al.
American Journal of Human Genetics|April 1, 1989
Gene deletions in X-linked muscular dystrophyM Lindlöf, A Kiuru, H Kääriäinen, et al.
Neuromuscular Disorders : NMD|March 11, 2000
Muscle membrane-skeleton protein changes and histopathological characterization of muscle-eye-brain diseaseM Auranen, J Rapola, H Pihko, et al.
Scandinavian Journal of Medicine & Science in Sports|February 13, 2001
Serum concentrations of collagen degrading enzymes and their inhibitors after downhill runningS O Koskinen, M Höyhtyä, T Turpeenniemi-Hujanen, et al.
Journal of the Neurological Sciences|March 10, 1997
Absence of calpain 3 in a form of limb-girdle muscular dystrophy (LGMD2A)M J Spencer, J G Tidball, L V Anderson, et al.
Neurology|April 11, 2001
Secondary calpain3 deficiency in 2q-linked muscular dystrophy: titin is the candidate geneH Haravuori, A Vihola, V Straub, et al.
Neurogenetics|October 8, 2003
Novel splice site CACNA1A mutation causing episodic ataxia type 2M A Kaunisto, H Harno, M Kallela, et al.
Neurology|May 1, 1997
Autosomal dominant progressive external ophthalmoplegia with multiple deletions of mtDNA: clinical, biochemical, and molecular genetic features of the 10q-linked diseaseA Suomalainen, A Majander, M Wallin, et al.
Pageof 13

Showing results (111-120 of 123) with videos related to

Sort By:
Pageof 13
Annals of Neurology|February 1, 1997
Muscle-eye-brain disease: a neuropathological studyM Haltia, I Leivo, H Somer, et al.
Human Genetics|October 1, 1990
Linkage disequilibrium detected between dystrophia myotonica and APOC2 locus in the Finnish populationP Nokelainen, L Alanen-Kurki, R Winqvist, et al.
Clinical Genetics|April 1, 1993
The DM mutation; diagnostic applications in the Finnish populationP Nokelainen, P Shelbourne, D Shaw, et al.
American Journal of Human Genetics|April 1, 1989
Gene deletions in X-linked muscular dystrophyM Lindlöf, A Kiuru, H Kääriäinen, et al.
Neuromuscular Disorders : NMD|March 11, 2000
Muscle membrane-skeleton protein changes and histopathological characterization of muscle-eye-brain diseaseM Auranen, J Rapola, H Pihko, et al.
Scandinavian Journal of Medicine & Science in Sports|February 13, 2001
Serum concentrations of collagen degrading enzymes and their inhibitors after downhill runningS O Koskinen, M Höyhtyä, T Turpeenniemi-Hujanen, et al.
Journal of the Neurological Sciences|March 10, 1997
Absence of calpain 3 in a form of limb-girdle muscular dystrophy (LGMD2A)M J Spencer, J G Tidball, L V Anderson, et al.
Neurology|April 11, 2001
Secondary calpain3 deficiency in 2q-linked muscular dystrophy: titin is the candidate geneH Haravuori, A Vihola, V Straub, et al.
Neurogenetics|October 8, 2003
Novel splice site CACNA1A mutation causing episodic ataxia type 2M A Kaunisto, H Harno, M Kallela, et al.
Neurology|May 1, 1997
Autosomal dominant progressive external ophthalmoplegia with multiple deletions of mtDNA: clinical, biochemical, and molecular genetic features of the 10q-linked diseaseA Suomalainen, A Majander, M Wallin, et al.
Pageof 13