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N Bresolin

Showing results (101-110 of 206) with videos related to

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Journal of the Neurological Sciences|May 1, 1994
Multiple deletions of mitochondrial DNA in sporadic and atypical cases of encephalomyopathyN Checcarelli, A Prelle, M Moggio, et al.
Neurology|October 1, 1987
Biochemical and immunologic studies in a case of congenital myopathy with unusual morphologic featuresD Biral, E Damiani, E Scarpini, et al.
Neurology|October 15, 2003
Remarkable infidelity of polymerase gammaA associated with mutations in POLG1 exonuclease domainR Del Bo, A Bordoni, M Sciacco, et al.
American Journal of Human Genetics|April 25, 2000
Intragenic inversion of mtDNA: a new type of pathogenic mutation in a patient with mitochondrial myopathyO Musumeci, A L Andreu, S Shanske, et al.
American Journal of Medical Genetics|April 27, 2002
Clinical and genetic variability of glycogen storage disease type IIIa: seven novel AGL gene mutations in the Mediterranean areaS Lucchiari, I Fogh, A Prelle, et al.
Human Gene Therapy|December 16, 1998
Insertion of two independent enhancers in the long terminal repeat of a self-inactivating vector results in high-titer retroviral vectors with tissue-specific expressionA Fassati, A Bardoni, M Sironi, et al.
European Neurology|January 1, 1993
Bezafibrate-induced myopathy: no evidence for defects in muscle metabolismG Vita, A Toscano, G Mileto, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 19, 2008
Effect of steroid treatment in cerebellar ataxia associated with anti-glutamic acid decarboxylase antibodiesR Virgilio, S Corti, P Agazzi, et al.
Cellular and Molecular Life Sciences : CMLS|November 8, 2008
Stem cell therapy in strokeF Locatelli, A Bersano, E Ballabio, et al.
Neuromuscular Disorders : NMD|January 1, 1992
Congenital myopathy associated with abnormal accumulation of desmin and dystrophinA Prelle, M Moggio, G P Comi, et al.
Pageof 21

Showing results (101-110 of 206) with videos related to

Sort By:
Pageof 21
Journal of the Neurological Sciences|May 1, 1994
Multiple deletions of mitochondrial DNA in sporadic and atypical cases of encephalomyopathyN Checcarelli, A Prelle, M Moggio, et al.
Neurology|October 1, 1987
Biochemical and immunologic studies in a case of congenital myopathy with unusual morphologic featuresD Biral, E Damiani, E Scarpini, et al.
Neurology|October 15, 2003
Remarkable infidelity of polymerase gammaA associated with mutations in POLG1 exonuclease domainR Del Bo, A Bordoni, M Sciacco, et al.
American Journal of Human Genetics|April 25, 2000
Intragenic inversion of mtDNA: a new type of pathogenic mutation in a patient with mitochondrial myopathyO Musumeci, A L Andreu, S Shanske, et al.
American Journal of Medical Genetics|April 27, 2002
Clinical and genetic variability of glycogen storage disease type IIIa: seven novel AGL gene mutations in the Mediterranean areaS Lucchiari, I Fogh, A Prelle, et al.
Human Gene Therapy|December 16, 1998
Insertion of two independent enhancers in the long terminal repeat of a self-inactivating vector results in high-titer retroviral vectors with tissue-specific expressionA Fassati, A Bardoni, M Sironi, et al.
European Neurology|January 1, 1993
Bezafibrate-induced myopathy: no evidence for defects in muscle metabolismG Vita, A Toscano, G Mileto, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 19, 2008
Effect of steroid treatment in cerebellar ataxia associated with anti-glutamic acid decarboxylase antibodiesR Virgilio, S Corti, P Agazzi, et al.
Cellular and Molecular Life Sciences : CMLS|November 8, 2008
Stem cell therapy in strokeF Locatelli, A Bersano, E Ballabio, et al.
Neuromuscular Disorders : NMD|January 1, 1992
Congenital myopathy associated with abnormal accumulation of desmin and dystrophinA Prelle, M Moggio, G P Comi, et al.
Pageof 21