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F Piemonte

Showing results (21-30 of 34) with videos related to

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Gut|January 26, 2008
Waist circumference correlates with liver fibrosis in children with non-alcoholic steatohepatitisM Manco, G Bedogni, M Marcellini, et al.
Neuromuscular Disorders : NMD|July 19, 2000
A novel SURF1 mutation results in Leigh syndrome with peripheral neuropathy caused by cytochrome c oxidase deficiencyL Santoro, R Carrozzo, A Malandrini, et al.
European Journal of Clinical Investigation|December 12, 2001
Glutathione in blood of patients with Friedreich's ataxiaF Piemonte, A Pastore, G Tozzi, et al.
American Journal of Medical Genetics|April 5, 2000
Novel 7-DHCR mutation in a child with Smith-Lemli-Opitz syndromeC Patrono, C Rizzo, A Tessa, et al.
Neuromuscular Disorders : NMD|December 4, 2001
Hypertrophic cardiomyopathy and mtDNA depletion. Successful treatment with heart transplantationF M Santorelli, M G Gagliardi, C Dionisi-Vici, et al.
Experientia|December 1, 1986
Enhancement of peritoneal macrophage activity by bovine gamma globulin in miceP Di Nardo, G De Sanctis, P De Sole, et al.
Neurology|July 27, 2001
Fatal infantile leukodystrophy: a severe variant of CACH/VWM syndrome, allelic to chromosome 3q27P Francalanci, E Eymard-Pierre, C Dionisi-Vici, et al.
Neurology|October 15, 2003
Atypical Leigh syndrome associated with the D393N mutation in the mitochondrial ND5 subunitV Petruzzella, G Di Giacinto, S Scacco, et al.
Archives of Disease in Childhood|April 24, 2002
Antioxidant enzymes in blood of patients with Friedreich's ataxiaG Tozzi, M Nuccetelli, M Lo Bello, et al.
Clinical Genetics|November 29, 2016
Novel mutations in KARS cause hypertrophic cardiomyopathy and combined mitochondrial respiratory chain defectD Verrigni, D Diodato, M Di Nottia, et al.
Pageof 4

Showing results (21-30 of 34) with videos related to

Sort By:
Pageof 4
Gut|January 26, 2008
Waist circumference correlates with liver fibrosis in children with non-alcoholic steatohepatitisM Manco, G Bedogni, M Marcellini, et al.
Neuromuscular Disorders : NMD|July 19, 2000
A novel SURF1 mutation results in Leigh syndrome with peripheral neuropathy caused by cytochrome c oxidase deficiencyL Santoro, R Carrozzo, A Malandrini, et al.
European Journal of Clinical Investigation|December 12, 2001
Glutathione in blood of patients with Friedreich's ataxiaF Piemonte, A Pastore, G Tozzi, et al.
American Journal of Medical Genetics|April 5, 2000
Novel 7-DHCR mutation in a child with Smith-Lemli-Opitz syndromeC Patrono, C Rizzo, A Tessa, et al.
Neuromuscular Disorders : NMD|December 4, 2001
Hypertrophic cardiomyopathy and mtDNA depletion. Successful treatment with heart transplantationF M Santorelli, M G Gagliardi, C Dionisi-Vici, et al.
Experientia|December 1, 1986
Enhancement of peritoneal macrophage activity by bovine gamma globulin in miceP Di Nardo, G De Sanctis, P De Sole, et al.
Neurology|July 27, 2001
Fatal infantile leukodystrophy: a severe variant of CACH/VWM syndrome, allelic to chromosome 3q27P Francalanci, E Eymard-Pierre, C Dionisi-Vici, et al.
Neurology|October 15, 2003
Atypical Leigh syndrome associated with the D393N mutation in the mitochondrial ND5 subunitV Petruzzella, G Di Giacinto, S Scacco, et al.
Archives of Disease in Childhood|April 24, 2002
Antioxidant enzymes in blood of patients with Friedreich's ataxiaG Tozzi, M Nuccetelli, M Lo Bello, et al.
Clinical Genetics|November 29, 2016
Novel mutations in KARS cause hypertrophic cardiomyopathy and combined mitochondrial respiratory chain defectD Verrigni, D Diodato, M Di Nottia, et al.
Pageof 4