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H Somer

Showing results (91-100 of 123) with videos related to

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Brain & Development|January 1, 1995
Ocular findings in muscle-eye-brain (MEB) disease: a follow-up studyH Pihko, M Lappi, C Raitta, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1993
[McArdle's disease]M Löfberg, M Junes, H Seppänen, et al.
European Journal of Nuclear Medicine|October 1, 1994
Antimyosin scintigraphy in patients with acquired and hereditary muscular disordersM Löfberg, K Liewendahl, S Savolainen, et al.
Biochemical and Biophysical Research Communications|March 30, 1990
Amyloid protein in familial amyloidosis (Finnish type) is homologous to gelsolin, an actin-binding proteinM Haltia, F Prelli, J Ghiso, et al.
The Journal of Clinical Investigation|July 1, 1992
Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthalmoplegiaA Suomalainen, A Majander, M Haltia, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1985
[Diagnosis of Duchenne's muscular dystrophy using recombinant DNA technics]M Lindlöf, P Ammälä, H Somer, et al.
American Journal of Human Genetics|April 29, 1998
Assignment of the tibial muscular dystrophy locus to chromosome 2q31H Haravuori, P Mäkelä-Bengs, B Udd, et al.
Muscle & Nerve|January 1, 1993
Progressive unilateral hypertrophic myopathy: a case studyH Pihko, I Lehtinen, H Tikkanen, 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.
Archives of Disease in Childhood|August 1, 1992
Reversible mitochondrial myopathy with cytochrome c oxidase deficiencyM K Salo, J Rapola, H Somer, et al.
Pageof 13

Showing results (91-100 of 123) with videos related to

Sort By:
Pageof 13
Brain & Development|January 1, 1995
Ocular findings in muscle-eye-brain (MEB) disease: a follow-up studyH Pihko, M Lappi, C Raitta, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1993
[McArdle's disease]M Löfberg, M Junes, H Seppänen, et al.
European Journal of Nuclear Medicine|October 1, 1994
Antimyosin scintigraphy in patients with acquired and hereditary muscular disordersM Löfberg, K Liewendahl, S Savolainen, et al.
Biochemical and Biophysical Research Communications|March 30, 1990
Amyloid protein in familial amyloidosis (Finnish type) is homologous to gelsolin, an actin-binding proteinM Haltia, F Prelli, J Ghiso, et al.
The Journal of Clinical Investigation|July 1, 1992
Multiple deletions of mitochondrial DNA in several tissues of a patient with severe retarded depression and familial progressive external ophthalmoplegiaA Suomalainen, A Majander, M Haltia, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1985
[Diagnosis of Duchenne's muscular dystrophy using recombinant DNA technics]M Lindlöf, P Ammälä, H Somer, et al.
American Journal of Human Genetics|April 29, 1998
Assignment of the tibial muscular dystrophy locus to chromosome 2q31H Haravuori, P Mäkelä-Bengs, B Udd, et al.
Muscle & Nerve|January 1, 1993
Progressive unilateral hypertrophic myopathy: a case studyH Pihko, I Lehtinen, H Tikkanen, 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.
Archives of Disease in Childhood|August 1, 1992
Reversible mitochondrial myopathy with cytochrome c oxidase deficiencyM K Salo, J Rapola, H Somer, et al.
Pageof 13