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N Bresolin

Showing results (21-30 of 206) with videos related to

Pageof 21
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Mitochondrion|October 16, 2012
PINK1 parkinsonism and Parkinson disease: distinguishable brain mitochondrial function and metabolomicsM Rango, A Arighi, G Marotta, et al.
Journal of Neurology|April 15, 2004
Transient response to immune therapies in post-irradiation lumbosacral radiculoplexopathyA Bersano, M Carpo, A Cappellari, et al.
Pediatric Research|October 1, 1984
Histiocytoid cardiomyopathy of infancy: deficiency of reducible cytochrome b in heart mitochondriaA Papadimitriou, H B Neustein, S Dimauro, et al.
Neurology|October 1, 1983
Congenital myopathy due to phosphorylase deficiencyF Cornelio, N Bresolin, S DiMauro, et al.
Lancet (London, England)|March 27, 1999
Absence of brain Dp140 isoform and cognitive impairment in Becker muscular dystrophyA Bardoni, M Sironi, G Felisari, et al.
Muscle & Nerve|September 1, 1984
Phosphoglycerate kinase deficiency myopathy: biochemical and immunological studies of the mutant enzymeN Bresolin, A Miranda, H W Chang, et al.
Neurology|August 1, 1983
Muscle phosphoglycerate mutase (PGAM) deficiency: a second caseN Bresolin, Y I Ro, M Reyes, et al.
Journal of Neurology|December 1, 1987
Recessive carnitine palmityl transferase deficiency: biochemical studies in tissue cultures and plateletsG Meola, N Bresolin, M Rimoldi, et al.
Journal of Neurology|July 1, 1990
McArdle's disease: two clinical expressions in the same pedigreeA Papadimitriou, P Manta, R Divari, et al.
Journal of Neurology|January 1, 1984
Carnitine and acyltransferase in experimental neurogenic atrophies: changes with treatmentN Bresolin, L Freddo, V Tegazzin, et al.
Pageof 21

Showing results (21-30 of 206) with videos related to

Sort By:
Pageof 21
Mitochondrion|October 16, 2012
PINK1 parkinsonism and Parkinson disease: distinguishable brain mitochondrial function and metabolomicsM Rango, A Arighi, G Marotta, et al.
Journal of Neurology|April 15, 2004
Transient response to immune therapies in post-irradiation lumbosacral radiculoplexopathyA Bersano, M Carpo, A Cappellari, et al.
Pediatric Research|October 1, 1984
Histiocytoid cardiomyopathy of infancy: deficiency of reducible cytochrome b in heart mitochondriaA Papadimitriou, H B Neustein, S Dimauro, et al.
Neurology|October 1, 1983
Congenital myopathy due to phosphorylase deficiencyF Cornelio, N Bresolin, S DiMauro, et al.
Lancet (London, England)|March 27, 1999
Absence of brain Dp140 isoform and cognitive impairment in Becker muscular dystrophyA Bardoni, M Sironi, G Felisari, et al.
Muscle & Nerve|September 1, 1984
Phosphoglycerate kinase deficiency myopathy: biochemical and immunological studies of the mutant enzymeN Bresolin, A Miranda, H W Chang, et al.
Neurology|August 1, 1983
Muscle phosphoglycerate mutase (PGAM) deficiency: a second caseN Bresolin, Y I Ro, M Reyes, et al.
Journal of Neurology|December 1, 1987
Recessive carnitine palmityl transferase deficiency: biochemical studies in tissue cultures and plateletsG Meola, N Bresolin, M Rimoldi, et al.
Journal of Neurology|July 1, 1990
McArdle's disease: two clinical expressions in the same pedigreeA Papadimitriou, P Manta, R Divari, et al.
Journal of Neurology|January 1, 1984
Carnitine and acyltransferase in experimental neurogenic atrophies: changes with treatmentN Bresolin, L Freddo, V Tegazzin, et al.
Pageof 21