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J Kovanen

Showing results (21-30 of 28) with videos related to

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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.
Journal of the Neurological Sciences|August 1, 1979
Familial Creutzfeldt-Jakob diseaseM Haltia, J Kovanen, H Van Crevel, et al.
European Journal of Epidemiology|September 1, 1991
Familial Creutzfeldt-Jakob disease in Finland: epidemiological, clinical, pathological and molecular genetic studiesM Haltia, J Kovanen, L G Goldfarb, et al.
Journal of Computer Assisted Tomography|January 1, 1985
Cerebral MR and CT imaging in Creutzfeldt-Jakob diseaseJ Kovanen, T Erkinjuntti, M Iivanainen, et al.
Annals of Neurology|March 11, 1992
Phenotypic characteristics of familial Creutzfeldt-Jakob disease associated with the codon 178Asn PRNP mutationP Brown, L G Goldfarb, J Kovanen, et al.
Lancet (London, England)|February 16, 1991
New mutation in scrapie amyloid precursor gene (at codon 178) in Finnish Creutzfeldt-Jakob kindredL G Goldfarb, M Haltia, P Brown, et al.
Annals of Neurology|March 1, 1992
Creutzfeldt-Jakob disease cosegregates with the codon 178Asn PRNP mutation in families of European originL G Goldfarb, P Brown, M Haltia, et al.
Parkinsonism & Related Disorders|February 8, 2003
Economic burden and quality of life impairment increase with severity of PDT Keränen, S Kaakkola, K Sotaniemi, et al.
Pageof 3

Showing results (21-30 of 28) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 28 results.
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.
Journal of the Neurological Sciences|August 1, 1979
Familial Creutzfeldt-Jakob diseaseM Haltia, J Kovanen, H Van Crevel, et al.
European Journal of Epidemiology|September 1, 1991
Familial Creutzfeldt-Jakob disease in Finland: epidemiological, clinical, pathological and molecular genetic studiesM Haltia, J Kovanen, L G Goldfarb, et al.
Journal of Computer Assisted Tomography|January 1, 1985
Cerebral MR and CT imaging in Creutzfeldt-Jakob diseaseJ Kovanen, T Erkinjuntti, M Iivanainen, et al.
Annals of Neurology|March 11, 1992
Phenotypic characteristics of familial Creutzfeldt-Jakob disease associated with the codon 178Asn PRNP mutationP Brown, L G Goldfarb, J Kovanen, et al.
Lancet (London, England)|February 16, 1991
New mutation in scrapie amyloid precursor gene (at codon 178) in Finnish Creutzfeldt-Jakob kindredL G Goldfarb, M Haltia, P Brown, et al.
Annals of Neurology|March 1, 1992
Creutzfeldt-Jakob disease cosegregates with the codon 178Asn PRNP mutation in families of European originL G Goldfarb, P Brown, M Haltia, et al.
Parkinsonism & Related Disorders|February 8, 2003
Economic burden and quality of life impairment increase with severity of PDT Keränen, S Kaakkola, K Sotaniemi, et al.
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