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G Sabetta

Showing results (31-40 of 40) with videos related to

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AJNR. American Journal of Neuroradiology|February 1, 1996
Cranial ultrasonography in maple syrup urine diseaseG Fariello, C Dionisi-Vici, C Orazi, et al.
The Journal of Pediatrics|May 1, 1991
Progressive neuropathy and recurrent myoglobinuria in a child with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiencyC Dionisi Vici, A B Burlina, E Bertini, et al.
European Journal of Pediatrics|February 1, 1992
Peripheral sensory-motor polyneuropathy, pigmentary retinopathy, and fatal cardiomyopathy in long-chain 3-hydroxy-acyl-CoA dehydrogenase deficiencyE Bertini, C Dionisi-Vici, B Garavaglia, et al.
Journal of Inherited Metabolic Disease|May 19, 1998
Intravenous immune globulin in lysinuric protein intoleranceC Dionisi-Vici, L De Felice, M el Hachem, et al.
American Journal of Medical Genetics|January 1, 1988
Agenesis of the corpus callosum, combined immunodeficiency, bilateral cataract, and hypopigmentation in two brothersC Dionisi Vici, G Sabetta, M Gambarara, et al.
Annals of Neurology|October 24, 1997
New familial mitochondrial encephalopathy with macrocephaly, cardiomyopathy, and complex I deficiencyC Dionisi-Vici, W Ruitenbeek, G Fariello, et al.
Journal of Medical Genetics|April 1, 1991
Aldolase B mutations in Italian families affected by hereditary fructose intoleranceG Sebastio, R de Franchis, P Strisciuglio, et al.
Lancet (London, England)|December 14, 1991
New clinical phenotype of branched-chain acyl-CoA oxidation defectA Burlina, F Zacchello, C Dionisi-Vici, et al.
The Journal of Pediatrics|December 1, 1992
Fatal infantile liver failure associated with mitochondrial DNA depletionM R Mazziotta, E Ricci, E Bertini, et al.
The Journal of Pediatrics|January 1, 1994
A new syndrome with ethylmalonic aciduria and normal fatty acid oxidation in fibroblastsA B Burlina, C Dionisi-Vici, M J Bennett, et al.
Pageof 4

Showing results (31-40 of 40) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 40 results.
AJNR. American Journal of Neuroradiology|February 1, 1996
Cranial ultrasonography in maple syrup urine diseaseG Fariello, C Dionisi-Vici, C Orazi, et al.
The Journal of Pediatrics|May 1, 1991
Progressive neuropathy and recurrent myoglobinuria in a child with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiencyC Dionisi Vici, A B Burlina, E Bertini, et al.
European Journal of Pediatrics|February 1, 1992
Peripheral sensory-motor polyneuropathy, pigmentary retinopathy, and fatal cardiomyopathy in long-chain 3-hydroxy-acyl-CoA dehydrogenase deficiencyE Bertini, C Dionisi-Vici, B Garavaglia, et al.
Journal of Inherited Metabolic Disease|May 19, 1998
Intravenous immune globulin in lysinuric protein intoleranceC Dionisi-Vici, L De Felice, M el Hachem, et al.
American Journal of Medical Genetics|January 1, 1988
Agenesis of the corpus callosum, combined immunodeficiency, bilateral cataract, and hypopigmentation in two brothersC Dionisi Vici, G Sabetta, M Gambarara, et al.
Annals of Neurology|October 24, 1997
New familial mitochondrial encephalopathy with macrocephaly, cardiomyopathy, and complex I deficiencyC Dionisi-Vici, W Ruitenbeek, G Fariello, et al.
Journal of Medical Genetics|April 1, 1991
Aldolase B mutations in Italian families affected by hereditary fructose intoleranceG Sebastio, R de Franchis, P Strisciuglio, et al.
Lancet (London, England)|December 14, 1991
New clinical phenotype of branched-chain acyl-CoA oxidation defectA Burlina, F Zacchello, C Dionisi-Vici, et al.
The Journal of Pediatrics|December 1, 1992
Fatal infantile liver failure associated with mitochondrial DNA depletionM R Mazziotta, E Ricci, E Bertini, et al.
The Journal of Pediatrics|January 1, 1994
A new syndrome with ethylmalonic aciduria and normal fatty acid oxidation in fibroblastsA B Burlina, C Dionisi-Vici, M J Bennett, et al.
Pageof 4