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

N Bresolin

Showing results (121-130 of 206) with videos related to

Pageof 21
Sort By:
American Journal of Human Genetics|December 1, 1990
Nucleus-driven multiple large-scale deletions of the human mitochondrial genome: a new autosomal dominant diseaseM Zeviani, N Bresolin, C Gellera, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|January 1, 1989
Cytochrome c oxidase during human fetal developmentM Moggio, N Bresolin, E Scarpini, et al.
Journal of the Neurological Sciences|May 12, 2009
Transthyretin Asn90 variant: amyloidogenic or non-amyloidogenic roleA Bersano, R Del Bo, E Ballabio, et al.
Journal of Cellular and Molecular Medicine|December 18, 2009
Growth factors in ischemic strokeS Lanfranconi, F Locatelli, S Corti, et al.
Human Genetics|September 3, 2010
Long-term balancing selection maintains trans-specific polymorphisms in the human TRIM5 geneR Cagliani, M Fumagalli, M Biasin, et al.
Annals of Neurology|June 1, 1987
Progressive cytochrome c oxidase deficiency in a case of Kearns-Sayre syndrome: morphological, immunological, and biochemical studies in muscle biopsies and autopsy tissuesN Bresolin, M Moggio, L Bet, et al.
Neuromuscular Disorders : NMD|July 1, 1994
Cognitive impairment in Duchenne muscular dystrophyN Bresolin, E Castelli, G P Comi, et al.
Clinical Therapeutics|January 1, 1988
Treatment of anxiety with ketazolam in elderly patientsN Bresolin, G Monza, E Scarpini, et al.
Clinical Genetics|September 20, 2007
Amino acid changes in the amino terminus of the Na,K-adenosine triphosphatase alpha-2 subunit associated to familial and sporadic hemiplegic migraineA Tonelli, A Gallanti, A Bersano, et al.
Journal of Neurology|July 1, 1994
Multiple sclerosis and mitochondrial myopathy: an unusual combination of diseasesL Bet, M Moggio, G P Comi, et al.
Pageof 21

Showing results (121-130 of 206) with videos related to

Sort By:
Pageof 21
American Journal of Human Genetics|December 1, 1990
Nucleus-driven multiple large-scale deletions of the human mitochondrial genome: a new autosomal dominant diseaseM Zeviani, N Bresolin, C Gellera, et al.
International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience|January 1, 1989
Cytochrome c oxidase during human fetal developmentM Moggio, N Bresolin, E Scarpini, et al.
Journal of the Neurological Sciences|May 12, 2009
Transthyretin Asn90 variant: amyloidogenic or non-amyloidogenic roleA Bersano, R Del Bo, E Ballabio, et al.
Journal of Cellular and Molecular Medicine|December 18, 2009
Growth factors in ischemic strokeS Lanfranconi, F Locatelli, S Corti, et al.
Human Genetics|September 3, 2010
Long-term balancing selection maintains trans-specific polymorphisms in the human TRIM5 geneR Cagliani, M Fumagalli, M Biasin, et al.
Annals of Neurology|June 1, 1987
Progressive cytochrome c oxidase deficiency in a case of Kearns-Sayre syndrome: morphological, immunological, and biochemical studies in muscle biopsies and autopsy tissuesN Bresolin, M Moggio, L Bet, et al.
Neuromuscular Disorders : NMD|July 1, 1994
Cognitive impairment in Duchenne muscular dystrophyN Bresolin, E Castelli, G P Comi, et al.
Clinical Therapeutics|January 1, 1988
Treatment of anxiety with ketazolam in elderly patientsN Bresolin, G Monza, E Scarpini, et al.
Clinical Genetics|September 20, 2007
Amino acid changes in the amino terminus of the Na,K-adenosine triphosphatase alpha-2 subunit associated to familial and sporadic hemiplegic migraineA Tonelli, A Gallanti, A Bersano, et al.
Journal of Neurology|July 1, 1994
Multiple sclerosis and mitochondrial myopathy: an unusual combination of diseasesL Bet, M Moggio, G P Comi, et al.
Pageof 21