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DiMauro

Showing results (761-770 of 942) with videos related to

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Journal of the Neurological Sciences|December 21, 2004
Congenital or late-onset myopathy in patients with the T14709C mtDNA mutationMichelangelo Mancuso, Silvio Ferraris, Yutaka Nishigaki, et al.
Experimental Neurology|March 5, 2008
Mitochondrial fusion and function in Charcot-Marie-Tooth type 2A patient fibroblasts with mitofusin 2 mutationsElizabeth A Amiott, Paul Lott, Jamie Soto, et al.
Neurology|January 26, 2006
Coenzyme Q10 deficiency and isolated myopathyR Horvath, P Schneiderat, B G H Schoser, et al.
Neurology|June 27, 2001
Surprises of genetic engineering: a possible model of polyglucosan body diseaseN Raben, M Danon, N Lu, et al.
Neurology|February 27, 2001
Autosomal dominant limb-girdle muscular dystrophy: a large kindred with evidence for anticipationJ Gamez, C Navarro, A L Andreu, et al.
Annals of Neurology|May 1, 1979
Debrancher deficiency: neuromuscular disorder in 5 adultsS DiMauro, G B Hartwig, A Hays, et al.
Bioorganic & Medicinal Chemistry Letters|March 26, 2016
Creation of a S1P Lyase bacterial surrogate for structure-based drug designMaria A Argiriadi, David Banach, Elzbieta Radziejewska, et al.
Physical Review Letters|February 2, 2013
Laser-induced electron diffraction for probing rare gas atomsJunliang Xu, Cosmin I Blaga, Anthony D DiChiara, et al.
Journal of the Neurological Sciences|April 10, 2012
Decreased hippocampal expression of calbindin D28K and cognitive impairment in MELASValentina Emmanuele, Angels Garcia-Cazorla, Hua-Bin Huang, et al.
Pediatric Research|May 1, 1996
Clinical heterogeneity associated with the mitochondrial DNA T8993C point mutationF M Santorelli, S C Mak, M E Vazquez-Memije, et al.
Pageof 95

Showing results (761-770 of 942) with videos related to

Sort By:
Pageof 95
Journal of the Neurological Sciences|December 21, 2004
Congenital or late-onset myopathy in patients with the T14709C mtDNA mutationMichelangelo Mancuso, Silvio Ferraris, Yutaka Nishigaki, et al.
Experimental Neurology|March 5, 2008
Mitochondrial fusion and function in Charcot-Marie-Tooth type 2A patient fibroblasts with mitofusin 2 mutationsElizabeth A Amiott, Paul Lott, Jamie Soto, et al.
Neurology|January 26, 2006
Coenzyme Q10 deficiency and isolated myopathyR Horvath, P Schneiderat, B G H Schoser, et al.
Neurology|June 27, 2001
Surprises of genetic engineering: a possible model of polyglucosan body diseaseN Raben, M Danon, N Lu, et al.
Neurology|February 27, 2001
Autosomal dominant limb-girdle muscular dystrophy: a large kindred with evidence for anticipationJ Gamez, C Navarro, A L Andreu, et al.
Annals of Neurology|May 1, 1979
Debrancher deficiency: neuromuscular disorder in 5 adultsS DiMauro, G B Hartwig, A Hays, et al.
Bioorganic & Medicinal Chemistry Letters|March 26, 2016
Creation of a S1P Lyase bacterial surrogate for structure-based drug designMaria A Argiriadi, David Banach, Elzbieta Radziejewska, et al.
Physical Review Letters|February 2, 2013
Laser-induced electron diffraction for probing rare gas atomsJunliang Xu, Cosmin I Blaga, Anthony D DiChiara, et al.
Journal of the Neurological Sciences|April 10, 2012
Decreased hippocampal expression of calbindin D28K and cognitive impairment in MELASValentina Emmanuele, Angels Garcia-Cazorla, Hua-Bin Huang, et al.
Pediatric Research|May 1, 1996
Clinical heterogeneity associated with the mitochondrial DNA T8993C point mutationF M Santorelli, S C Mak, M E Vazquez-Memije, et al.
Pageof 95