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DiMauro

Showing results (411-420 of 942) with videos related to

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Journal of the Neurological Sciences|February 11, 1976
Luft's disease. Further biochemical and ultrastructural studies of skeletal muscle in the second caseS DiMauro, E Bonilla, C P Lee, et al.
Muscle & Nerve|February 1, 1991
Polyglucosan body diseaseM S Cafferty, R E Lovelace, A P Hays, et al.
Biochemical and Biophysical Research Communications|September 10, 1998
A splice junction mutation in the alpha(M) gene of phosphorylase kinase in a patient with myopathyC Bruno, G Manfredi, A L Andreu, et al.
Physical Review Letters|April 11, 2026
Nonadiabatic Strong-Field Photoionization RevisitedSpencer Walker, Abdulaziz Alqasem, Abraham Camacho Garibay, et al.
Multiple Sclerosis and Related Disorders|October 10, 2021
Patients' experiences of self-identification, seeking support, and anticipation of potential relapse in multiple sclerosisCharlotte R Wicks, Rob Sloan, Sophie DiMauro, et al.
Animal Genetics|January 26, 2013
Use of the canonical discriminant analysis to select SNP markers for bovine breed assignment and traceability purposesC Dimauro, M Cellesi, R Steri, et al.
Optics Letters|November 16, 2019
High relative-phase precision beam duplicator for mid-infrared femtosecond pulsesAntoine Camper, Hyunwook Park, Stephen J Hageman, et al.
Epidemiologia E Prevenzione|June 22, 2001
[Mortality in a cohort of alcoholics from Arezzo in 1979-1997]F Cipriani, M L Cucinelli, P E Dimauro, et al.
Annals of Neurology|July 12, 2002
Deficiency of tetralinoleoyl-cardiolipin in Barth syndromeMichael Schlame, Jeffrey A Towbin, Paul M Heerdt, et al.
Neurology|April 1, 1995
High levels of mitochondrial DNA with an unstable 260-bp duplication in a patient with a mitochondrial myopathyG Manfredi, S Servidei, E Bonilla, et al.
Pageof 95

Showing results (411-420 of 942) with videos related to

Sort By:
Pageof 95
Journal of the Neurological Sciences|February 11, 1976
Luft's disease. Further biochemical and ultrastructural studies of skeletal muscle in the second caseS DiMauro, E Bonilla, C P Lee, et al.
Muscle & Nerve|February 1, 1991
Polyglucosan body diseaseM S Cafferty, R E Lovelace, A P Hays, et al.
Biochemical and Biophysical Research Communications|September 10, 1998
A splice junction mutation in the alpha(M) gene of phosphorylase kinase in a patient with myopathyC Bruno, G Manfredi, A L Andreu, et al.
Physical Review Letters|April 11, 2026
Nonadiabatic Strong-Field Photoionization RevisitedSpencer Walker, Abdulaziz Alqasem, Abraham Camacho Garibay, et al.
Multiple Sclerosis and Related Disorders|October 10, 2021
Patients' experiences of self-identification, seeking support, and anticipation of potential relapse in multiple sclerosisCharlotte R Wicks, Rob Sloan, Sophie DiMauro, et al.
Animal Genetics|January 26, 2013
Use of the canonical discriminant analysis to select SNP markers for bovine breed assignment and traceability purposesC Dimauro, M Cellesi, R Steri, et al.
Optics Letters|November 16, 2019
High relative-phase precision beam duplicator for mid-infrared femtosecond pulsesAntoine Camper, Hyunwook Park, Stephen J Hageman, et al.
Epidemiologia E Prevenzione|June 22, 2001
[Mortality in a cohort of alcoholics from Arezzo in 1979-1997]F Cipriani, M L Cucinelli, P E Dimauro, et al.
Annals of Neurology|July 12, 2002
Deficiency of tetralinoleoyl-cardiolipin in Barth syndromeMichael Schlame, Jeffrey A Towbin, Paul M Heerdt, et al.
Neurology|April 1, 1995
High levels of mitochondrial DNA with an unstable 260-bp duplication in a patient with a mitochondrial myopathyG Manfredi, S Servidei, E Bonilla, et al.
Pageof 95