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F Rocchiccioli

Showing results (51-60 of 56) with videos related to

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The New England Journal of Medicine|September 9, 1993
A two-year trial of oleic and erucic acids ("Lorenzo's oil") as treatment for adrenomyeloneuropathyP Aubourg, C Adamsbaum, M C Lavallard-Rousseau, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 28, 1995
Retroviral-mediated gene transfer corrects very-long-chain fatty acid metabolism in adrenoleukodystrophy fibroblastsN Cartier, J Lopez, P Moullier, et al.
The New England Journal of Medicine|June 28, 1990
Reversal of early neurologic and neuroradiologic manifestations of X-linked adrenoleukodystrophy by bone marrow transplantationP Aubourg, S Blanche, I Jambaqué, et al.
Acta Paediatrica Scandinavica|January 1, 1982
Congenital lactic acidosis, alpha-ketoglutaric aciduria and variant form of maple syrup urine disease due to a single enzyme defect: dihydrolipoyl dehydrogenase deficiencyA Munnich, J M Saudubray, J Taylor, et al.
Journal of Inherited Metabolic Disease|January 1, 1985
The prenatal diagnosis of glutaric aciduria type II, using quantitative GC-MSR A Chalmers, B M Tracey, G S King, et al.
Lancet (London, England)|April 14, 1984
Prenatal diagnosis of dysmorphic neonatal-lethal type II glutaricaciduriaJ Boué, R A Chalmers, B M Tracey, et al.
Pageof 6

Showing results (51-60 of 56) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 56 results.
The New England Journal of Medicine|September 9, 1993
A two-year trial of oleic and erucic acids ("Lorenzo's oil") as treatment for adrenomyeloneuropathyP Aubourg, C Adamsbaum, M C Lavallard-Rousseau, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 28, 1995
Retroviral-mediated gene transfer corrects very-long-chain fatty acid metabolism in adrenoleukodystrophy fibroblastsN Cartier, J Lopez, P Moullier, et al.
The New England Journal of Medicine|June 28, 1990
Reversal of early neurologic and neuroradiologic manifestations of X-linked adrenoleukodystrophy by bone marrow transplantationP Aubourg, S Blanche, I Jambaqué, et al.
Acta Paediatrica Scandinavica|January 1, 1982
Congenital lactic acidosis, alpha-ketoglutaric aciduria and variant form of maple syrup urine disease due to a single enzyme defect: dihydrolipoyl dehydrogenase deficiencyA Munnich, J M Saudubray, J Taylor, et al.
Journal of Inherited Metabolic Disease|January 1, 1985
The prenatal diagnosis of glutaric aciduria type II, using quantitative GC-MSR A Chalmers, B M Tracey, G S King, et al.
Lancet (London, England)|April 14, 1984
Prenatal diagnosis of dysmorphic neonatal-lethal type II glutaricaciduriaJ Boué, R A Chalmers, B M Tracey, et al.
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