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 (81-90 of 123) with videos related to

Pageof 13
Sort By:
Archives of Neurology|July 1, 1989
Neurological outcome after out-of-hospital cardiac arrest. Prediction by cerebrospinal fluid enzyme analysisR O Roine, H Somer, M Kaste, et al.
American Journal of Medical Genetics|July 1, 1992
Terminal deletion of chromosome 4p (4p16.3) shows a breakpoint between loci linked to Huntington diseaseE Ikonen, A Salo, M Somer, et al.
Neurology|March 1, 1991
Celiac disease, brain atrophy, and dementiaP Collin, T Pirttilä, T Nurmikko, et al.
Journal of the Neurological Sciences|September 1, 1988
Microangiopathy with encephalopathy, hearing loss and retinal arteriolar occlusions: two new casesH Heiskala, H Somer, J Kovanen, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 1, 1978
A new cause of increased serum aspartate aminotransferase activityA Konttinen, J Murros, K Ojala, et al.
Journal of the Neurological Sciences|September 1, 1989
Lymphocytic beta-adrenergic receptors in X-linked muscular dystrophyT Mäki, H Somer, H Pihko, et al.
Neuroradiology|August 1, 1994
MRI of the brain in muscle-eye-brain (MEB) diseaseL Valanne, H Pihko, K Katevuo, et al.
Journal of Neurology|July 12, 2002
Axial myopathy--an unrecognised entityIbrahim Mahjneh, G Marconi, A Paetau, et al.
Neuromuscular Disorders : NMD|February 13, 2001
Dysferlinopathy (LGMD2B): a 23-year follow-up study of 10 patients homozygous for the same frameshifting dysferlin mutationsI Mahjneh, G Marconi, K Bushby, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1986
[Huntington's disease]J Palo, H Somer, L Palotie, et al.
Pageof 13

Showing results (81-90 of 123) with videos related to

Sort By:
Pageof 13
Archives of Neurology|July 1, 1989
Neurological outcome after out-of-hospital cardiac arrest. Prediction by cerebrospinal fluid enzyme analysisR O Roine, H Somer, M Kaste, et al.
American Journal of Medical Genetics|July 1, 1992
Terminal deletion of chromosome 4p (4p16.3) shows a breakpoint between loci linked to Huntington diseaseE Ikonen, A Salo, M Somer, et al.
Neurology|March 1, 1991
Celiac disease, brain atrophy, and dementiaP Collin, T Pirttilä, T Nurmikko, et al.
Journal of the Neurological Sciences|September 1, 1988
Microangiopathy with encephalopathy, hearing loss and retinal arteriolar occlusions: two new casesH Heiskala, H Somer, J Kovanen, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|March 1, 1978
A new cause of increased serum aspartate aminotransferase activityA Konttinen, J Murros, K Ojala, et al.
Journal of the Neurological Sciences|September 1, 1989
Lymphocytic beta-adrenergic receptors in X-linked muscular dystrophyT Mäki, H Somer, H Pihko, et al.
Neuroradiology|August 1, 1994
MRI of the brain in muscle-eye-brain (MEB) diseaseL Valanne, H Pihko, K Katevuo, et al.
Journal of Neurology|July 12, 2002
Axial myopathy--an unrecognised entityIbrahim Mahjneh, G Marconi, A Paetau, et al.
Neuromuscular Disorders : NMD|February 13, 2001
Dysferlinopathy (LGMD2B): a 23-year follow-up study of 10 patients homozygous for the same frameshifting dysferlin mutationsI Mahjneh, G Marconi, K Bushby, et al.
Duodecim; Laaketieteellinen Aikakauskirja|January 1, 1986
[Huntington's disease]J Palo, H Somer, L Palotie, et al.
Pageof 13