Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

H Somer

Showing results (71-80 of 123) with videos related to

Pageof 13
Sort By:
Lancet (London, England)|October 3, 1987
Low prevalence of Huntington's disease in FinlandJ Palo, H Somer, E Ikonen, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1983
[Carnitine palmitoyltransferase deficiency: fatty acid utilization defect causing myopathy]A Lehtonen, L Paljärvi, B Falck, et al.
Journal of the Neurological Sciences|June 10, 1998
Serum gelsolin and rhabdomyolysisM Löfberg, T Paunio, R Tähtelä, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1992
[Mitochondrial diseases]H Pihko, A Suomalainen, H Somer, et al.
Neurology|June 1, 1979
Myasthenia gravis and monoclonal IgG gammopathyH Somer, R Pirskanen, A K Lefvert, et al.
Neurology|February 1, 1980
Duchenne carriers: lactate dehydrogenase isoenzyme 5 in serum and muscleH Somer, J Willner, R P DeCresce, et al.
Journal of the Neurological Sciences|March 1, 1986
Cerebrospinal fluid lysozyme and beta 2-microglobulin in neurosarcoidosisV Oksanen, C Grönhagen-Riska, S Tikanoja, et al.
Annals of Clinical Research|January 1, 1986
Three different pathogenic mechanisms for paraparesis in association with bacterial infectionsJ Syrjänen, M Iivanainen, M Kallio, et al.
Lancet (London, England)|November 28, 1992
Inherited idiopathic dilated cardiomyopathy with multiple deletions of mitochondrial DNAA Suomalainen, A Paetau, H Leinonen, et al.
Clinical Genetics|August 1, 1985
Duchenne-like muscular dystrophy in two sisters with normal karyotypes: evidence for autosomal recessive inheritanceH Somer, A Voutilainen, S Knuutila, et al.
Pageof 13

Showing results (71-80 of 123) with videos related to

Sort By:
Pageof 13
Lancet (London, England)|October 3, 1987
Low prevalence of Huntington's disease in FinlandJ Palo, H Somer, E Ikonen, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1983
[Carnitine palmitoyltransferase deficiency: fatty acid utilization defect causing myopathy]A Lehtonen, L Paljärvi, B Falck, et al.
Journal of the Neurological Sciences|June 10, 1998
Serum gelsolin and rhabdomyolysisM Löfberg, T Paunio, R Tähtelä, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1992
[Mitochondrial diseases]H Pihko, A Suomalainen, H Somer, et al.
Neurology|June 1, 1979
Myasthenia gravis and monoclonal IgG gammopathyH Somer, R Pirskanen, A K Lefvert, et al.
Neurology|February 1, 1980
Duchenne carriers: lactate dehydrogenase isoenzyme 5 in serum and muscleH Somer, J Willner, R P DeCresce, et al.
Journal of the Neurological Sciences|March 1, 1986
Cerebrospinal fluid lysozyme and beta 2-microglobulin in neurosarcoidosisV Oksanen, C Grönhagen-Riska, S Tikanoja, et al.
Annals of Clinical Research|January 1, 1986
Three different pathogenic mechanisms for paraparesis in association with bacterial infectionsJ Syrjänen, M Iivanainen, M Kallio, et al.
Lancet (London, England)|November 28, 1992
Inherited idiopathic dilated cardiomyopathy with multiple deletions of mitochondrial DNAA Suomalainen, A Paetau, H Leinonen, et al.
Clinical Genetics|August 1, 1985
Duchenne-like muscular dystrophy in two sisters with normal karyotypes: evidence for autosomal recessive inheritanceH Somer, A Voutilainen, S Knuutila, et al.
Pageof 13