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H Somer

Showing results (101-110 of 123) with videos related to

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The American Journal of Pathology|June 1, 1990
Amyloid in familial amyloidosis, Finnish type, is antigenically and structurally related to gelsolinM Haltia, J Ghiso, F Prelli, et al.
Neurology|July 9, 2003
A distinct phenotype of distal myopathy in a large Finnish familyI Mahjneh, H Haravuori, A Paetau, et al.
Neuromuscular Disorders : NMD|January 1, 1991
Benign muscular dystrophy with autosomal dominant inheritanceH Somer, V Laulumaa, L Paljärvi, et al.
Brain & Development|January 1, 1989
Muscle-eye-brain disease (MEB)P Santavuori, H Somer, K Sainio, et al.
American Journal of Human Genetics|January 1, 1990
Huntington disease in Finland: linkage disequilibrium of chromosome 4 RFLP haplotypes and exclusion of a tight linkage between the disease and D4S43 locusE Ikonen, J Palo, J Ott, et al.
Neuromuscular Disorders : NMD|May 23, 2001
ATP, phosphocreatine and lactate in exercising muscle in mitochondrial disease and McArdle's diseaseM Löfberg, H Lindholm, H Näveri, et al.
American Journal of Medical Genetics|July 1, 1990
Muscle-eye-brain disease and Walker-Warburg syndromeP Santavuori, H Pihko, K Sainio, et al.
Nature Genetics|February 1, 1995
An autosomal locus predisposing to deletions of mitochondrial DNAA Suomalainen, J Kaukonen, P Amati, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1992
[Peripheral myopathies in Finland--a new kind of muscular dystrophy in the leg]B Udd, J Partanen, P Halonen, et al.
Journal of the Neurological Sciences|August 18, 1999
Molecular characterization of McArdle's disease in two large Finnish familiesC Bruno, M Löfberg, L Tamburino, et al.
Pageof 13

Showing results (101-110 of 123) with videos related to

Sort By:
Pageof 13
The American Journal of Pathology|June 1, 1990
Amyloid in familial amyloidosis, Finnish type, is antigenically and structurally related to gelsolinM Haltia, J Ghiso, F Prelli, et al.
Neurology|July 9, 2003
A distinct phenotype of distal myopathy in a large Finnish familyI Mahjneh, H Haravuori, A Paetau, et al.
Neuromuscular Disorders : NMD|January 1, 1991
Benign muscular dystrophy with autosomal dominant inheritanceH Somer, V Laulumaa, L Paljärvi, et al.
Brain & Development|January 1, 1989
Muscle-eye-brain disease (MEB)P Santavuori, H Somer, K Sainio, et al.
American Journal of Human Genetics|January 1, 1990
Huntington disease in Finland: linkage disequilibrium of chromosome 4 RFLP haplotypes and exclusion of a tight linkage between the disease and D4S43 locusE Ikonen, J Palo, J Ott, et al.
Neuromuscular Disorders : NMD|May 23, 2001
ATP, phosphocreatine and lactate in exercising muscle in mitochondrial disease and McArdle's diseaseM Löfberg, H Lindholm, H Näveri, et al.
American Journal of Medical Genetics|July 1, 1990
Muscle-eye-brain disease and Walker-Warburg syndromeP Santavuori, H Pihko, K Sainio, et al.
Nature Genetics|February 1, 1995
An autosomal locus predisposing to deletions of mitochondrial DNAA Suomalainen, J Kaukonen, P Amati, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1992
[Peripheral myopathies in Finland--a new kind of muscular dystrophy in the leg]B Udd, J Partanen, P Halonen, et al.
Journal of the Neurological Sciences|August 18, 1999
Molecular characterization of McArdle's disease in two large Finnish familiesC Bruno, M Löfberg, L Tamburino, et al.
Pageof 13