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

G Meola

Showing results (121-130 of 142) with videos related to

Pageof 15
Sort By:
Rivista Di Neurologia|July 1, 1991
[Expression of a defect in the respiratory chain in cultured human cells]G Meola, G Rotondo, M Velicogna, et al.
Neuromuscular Disorders : NMD|May 11, 2006
140th ENMC International Workshop: Myotonic Dystrophy DM2/PROMM and other myotonic dystrophies with guidelines on managementB Udd, G Meola, R Krahe, et al.
Journal of Neurology|March 1, 1994
Muscle phosphoglycerate mutase (PGAM) deficiency in the first Caucasian patient: biochemistry, muscle culture and 31P-MR spectroscopyG Vita, A Toscano, N Bresolin, et al.
International Journal of Cardiology|December 26, 2012
The frequency and severity of cardiac involvement in myotonic dystrophy type 2 (DM2): long-term outcomesV A Sansone, E Brigonzi, B Schoser, et al.
Journal of Neurology|November 1, 1990
A case of mitochondrial myopathy, lactic acidosis and complex I deficiencyL Bet, N Bresolin, M Moggio, et al.
Electromyography and Clinical Neurophysiology|August 22, 2006
Central nervous system involvement in HCV-related mixed cryoglobulinemiaA Cappellari, L Origgi, M F Spina, et al.
European Journal of Neurology|January 30, 2014
Amyotrophic lateral sclerosis in pregnancy is associated with a vascular endothelial growth factor promoter genotypeC Lunetta, V A Sansone, S Penco, et al.
Neuropsychobiology|January 1, 1988
Low doses of ketazolam in anxiety: a double-blind, placebo-controlled studyE Scarpini, P G Baron, L Bet, et al.
Journal of Neurology|May 1, 1993
Clinical and biochemical evidence of skeletal muscle involvement in galactose-1-phosphate uridyl transferase deficiencyN Bresolin, G P Comi, F Fortunato, et al.
Journal of the Neurological Sciences|September 23, 2008
Colocalization of ribonuclear inclusions with muscle blind like-proteins in a family with myotonic dystrophy type 2 associated with a short CCTG expansionS Lucchiari, S Pagliarani, S Corti, et al.
Pageof 15

Showing results (121-130 of 142) with videos related to

Sort By:
Pageof 15
Rivista Di Neurologia|July 1, 1991
[Expression of a defect in the respiratory chain in cultured human cells]G Meola, G Rotondo, M Velicogna, et al.
Neuromuscular Disorders : NMD|May 11, 2006
140th ENMC International Workshop: Myotonic Dystrophy DM2/PROMM and other myotonic dystrophies with guidelines on managementB Udd, G Meola, R Krahe, et al.
Journal of Neurology|March 1, 1994
Muscle phosphoglycerate mutase (PGAM) deficiency in the first Caucasian patient: biochemistry, muscle culture and 31P-MR spectroscopyG Vita, A Toscano, N Bresolin, et al.
International Journal of Cardiology|December 26, 2012
The frequency and severity of cardiac involvement in myotonic dystrophy type 2 (DM2): long-term outcomesV A Sansone, E Brigonzi, B Schoser, et al.
Journal of Neurology|November 1, 1990
A case of mitochondrial myopathy, lactic acidosis and complex I deficiencyL Bet, N Bresolin, M Moggio, et al.
Electromyography and Clinical Neurophysiology|August 22, 2006
Central nervous system involvement in HCV-related mixed cryoglobulinemiaA Cappellari, L Origgi, M F Spina, et al.
European Journal of Neurology|January 30, 2014
Amyotrophic lateral sclerosis in pregnancy is associated with a vascular endothelial growth factor promoter genotypeC Lunetta, V A Sansone, S Penco, et al.
Neuropsychobiology|January 1, 1988
Low doses of ketazolam in anxiety: a double-blind, placebo-controlled studyE Scarpini, P G Baron, L Bet, et al.
Journal of Neurology|May 1, 1993
Clinical and biochemical evidence of skeletal muscle involvement in galactose-1-phosphate uridyl transferase deficiencyN Bresolin, G P Comi, F Fortunato, et al.
Journal of the Neurological Sciences|September 23, 2008
Colocalization of ribonuclear inclusions with muscle blind like-proteins in a family with myotonic dystrophy type 2 associated with a short CCTG expansionS Lucchiari, S Pagliarani, S Corti, et al.
Pageof 15