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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 adrenomyeloneuropathy
P 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 fibroblasts
N 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 transplantation
P 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 deficiency
A 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-MS
R A Chalmers, B M Tracey, G S King, et al.
Lancet (London, England)
|
April 14, 1984
Prenatal diagnosis of dysmorphic neonatal-lethal type II glutaricaciduria
J Boué, R A Chalmers, B M Tracey, et al.
Page
of 6
Search research articles
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Showing results (51-60 of 56) with videos related to
Sort By:
Page
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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 adrenomyeloneuropathy
P 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 fibroblasts
N 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 transplantation
P 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 deficiency
A 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-MS
R A Chalmers, B M Tracey, G S King, et al.
Lancet (London, England)
|
April 14, 1984
Prenatal diagnosis of dysmorphic neonatal-lethal type II glutaricaciduria
J Boué, R A Chalmers, B M Tracey, et al.
Page
of 6