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Alessandra Torraco

Showing results (21-30 of 48) with videos related to

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The FEBS Journal|June 14, 2014
Enhancement of mitochondrial ATP production by the Escherichia coli cytotoxic necrotizing factor 1Sara Travaglione, Stefano Loizzo, Teresa Rizza, et al.
Biochimie|March 25, 2014
Effects of levosimendan on mitochondrial function in patients with septic shock: a randomized trialAlessandra Torraco, Rosalba Carrozzo, Fiorella Piemonte, et al.
Molecular Genetics and Metabolism|February 4, 2014
Persistent pulmonary arterial hypertension in the newborn (PPHN): a frequent manifestation of TMEM70 defective patientsMichela Catteruccia, Daniela Verrigni, Diego Martinelli, et al.
Neurogenetics|September 19, 2012
TMEM70: a mutational hot spot in nuclear ATP synthase deficiency with a pivotal role in complex V biogenesisAlessandra Torraco, Daniela Verrigni, Teresa Rizza, et al.
Psychiatry Research|September 6, 2006
Prefrontal dysfunction in schizophrenia controlling for COMT Val158Met genotype and working memory performanceAlessandro Bertolino, Grazia Caforio, Vittoria Petruzzella, et al.
European Journal of Human Genetics : EJHG|January 14, 2010
A new locus on 3p23-p25 for an autosomal-dominant limb-girdle muscular dystrophy, LGMD1HLuigi Bisceglia, Stefano Zoccolella, Alessandra Torraco, et al.
Biochemical and Biophysical Research Communications|October 27, 2011
Novel large-range mitochondrial DNA deletions and fatal multisystemic disorder with prominent hepatopathyMarzia Bianchi, Teresa Rizza, Daniela Verrigni, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|January 31, 2017
Novel mutation in mitochondrial Elongation Factor EF-Tu associated to dysplastic leukoencephalopathy and defective mitochondrial DNA translationMichela Di Nottia, Arianna Montanari, Daniela Verrigni, et al.
Neurogenetics|March 28, 2013
Novel TTC19 mutation in a family with severe psychiatric manifestations and complex III deficiencyCélia Nogueira, José Barros, Maria José Sá, et al.
Neurogenetics|November 12, 2015
Clinical and molecular study in a long-surviving patient with MLASA syndrome due to novel PUS1 mutationsMichelangelo Cao, Marta Donà, M Lucia Valentino, et al.
Pageof 5

Showing results (21-30 of 48) with videos related to

Sort By:
Pageof 5
The FEBS Journal|June 14, 2014
Enhancement of mitochondrial ATP production by the Escherichia coli cytotoxic necrotizing factor 1Sara Travaglione, Stefano Loizzo, Teresa Rizza, et al.
Biochimie|March 25, 2014
Effects of levosimendan on mitochondrial function in patients with septic shock: a randomized trialAlessandra Torraco, Rosalba Carrozzo, Fiorella Piemonte, et al.
Molecular Genetics and Metabolism|February 4, 2014
Persistent pulmonary arterial hypertension in the newborn (PPHN): a frequent manifestation of TMEM70 defective patientsMichela Catteruccia, Daniela Verrigni, Diego Martinelli, et al.
Neurogenetics|September 19, 2012
TMEM70: a mutational hot spot in nuclear ATP synthase deficiency with a pivotal role in complex V biogenesisAlessandra Torraco, Daniela Verrigni, Teresa Rizza, et al.
Psychiatry Research|September 6, 2006
Prefrontal dysfunction in schizophrenia controlling for COMT Val158Met genotype and working memory performanceAlessandro Bertolino, Grazia Caforio, Vittoria Petruzzella, et al.
European Journal of Human Genetics : EJHG|January 14, 2010
A new locus on 3p23-p25 for an autosomal-dominant limb-girdle muscular dystrophy, LGMD1HLuigi Bisceglia, Stefano Zoccolella, Alessandra Torraco, et al.
Biochemical and Biophysical Research Communications|October 27, 2011
Novel large-range mitochondrial DNA deletions and fatal multisystemic disorder with prominent hepatopathyMarzia Bianchi, Teresa Rizza, Daniela Verrigni, et al.
Biochimica Et Biophysica Acta. Molecular Basis of Disease|January 31, 2017
Novel mutation in mitochondrial Elongation Factor EF-Tu associated to dysplastic leukoencephalopathy and defective mitochondrial DNA translationMichela Di Nottia, Arianna Montanari, Daniela Verrigni, et al.
Neurogenetics|March 28, 2013
Novel TTC19 mutation in a family with severe psychiatric manifestations and complex III deficiencyCélia Nogueira, José Barros, Maria José Sá, et al.
Neurogenetics|November 12, 2015
Clinical and molecular study in a long-surviving patient with MLASA syndrome due to novel PUS1 mutationsMichelangelo Cao, Marta Donà, M Lucia Valentino, et al.
Pageof 5