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W B Rizzo

Showing results (61-70 of 71) with videos related to

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Nature Genetics|January 1, 1996
Sjögren-Larsson syndrome is caused by mutations in the fatty aldehyde dehydrogenase geneV De Laurenzi, G R Rogers, D J Hamrock, et al.
Pediatric Dermatology|December 12, 2001
Unusual clinical presentation in two cases of multiple sulfatase deficiencyM E Blanco-Aguirre, S H Kofman-Alfaro, M R Rivera-Vega, et al.
The Journal of Pediatrics|August 1, 1989
Sjögren-Larsson syndrome: inherited defect in the fatty alcohol cycleW B Rizzo, A L Dammann, D A Craft, et al.
The Journal of Investigative Dermatology|July 1, 1997
Sjögren-Larsson syndrome is caused by a common mutation in northern European and Swedish patientsV De Laurenzi, G R Rogers, E Tarcsa, et al.
Gastroenterology|March 27, 2001
Nonalcoholic steatohepatitis: association of insulin resistance and mitochondrial abnormalitiesA J Sanyal, C Campbell-Sargent, F Mirshahi, et al.
Neurology|November 1, 1989
Dietary erucic acid therapy for X-linked adrenoleukodystrophyW B Rizzo, R T Leshner, A Odone, et al.
The Journal of Biological Chemistry|April 25, 1992
Mutants in a macrophage-like cell line are defective in plasmalogen biosynthesis, but contain functional peroxisomesR A Zoeller, S Rangaswamy, H Herscovitz, et al.
Prenatal Diagnosis|July 1, 1994
Prenatal diagnosis of Sjögren-Larsson syndrome using enzymatic methodsW B Rizzo, D A Craft, T L Kelson, et al.
The British Journal of Dermatology|March 16, 2006
Sjögren-Larsson syndrome in Brazil is caused by a common c.1108-1G-->C splice-site mutation in the ALDH3A2 geneM P Auada, M B Puzzi, M L Cintra, et al.
The Johns Hopkins Medical Journal|October 1, 1982
Adrenoleukodystrophy: effects of dietary restriction of very long chain fatty acids and of administration of carnitine and clofibrate on clinical status and plasma fatty acidsF R Brown, M A Van Duyn, A B Moser, et al.
Pageof 8

Showing results (61-70 of 71) with videos related to

Sort By:
Pageof 8
Nature Genetics|January 1, 1996
Sjögren-Larsson syndrome is caused by mutations in the fatty aldehyde dehydrogenase geneV De Laurenzi, G R Rogers, D J Hamrock, et al.
Pediatric Dermatology|December 12, 2001
Unusual clinical presentation in two cases of multiple sulfatase deficiencyM E Blanco-Aguirre, S H Kofman-Alfaro, M R Rivera-Vega, et al.
The Journal of Pediatrics|August 1, 1989
Sjögren-Larsson syndrome: inherited defect in the fatty alcohol cycleW B Rizzo, A L Dammann, D A Craft, et al.
The Journal of Investigative Dermatology|July 1, 1997
Sjögren-Larsson syndrome is caused by a common mutation in northern European and Swedish patientsV De Laurenzi, G R Rogers, E Tarcsa, et al.
Gastroenterology|March 27, 2001
Nonalcoholic steatohepatitis: association of insulin resistance and mitochondrial abnormalitiesA J Sanyal, C Campbell-Sargent, F Mirshahi, et al.
Neurology|November 1, 1989
Dietary erucic acid therapy for X-linked adrenoleukodystrophyW B Rizzo, R T Leshner, A Odone, et al.
The Journal of Biological Chemistry|April 25, 1992
Mutants in a macrophage-like cell line are defective in plasmalogen biosynthesis, but contain functional peroxisomesR A Zoeller, S Rangaswamy, H Herscovitz, et al.
Prenatal Diagnosis|July 1, 1994
Prenatal diagnosis of Sjögren-Larsson syndrome using enzymatic methodsW B Rizzo, D A Craft, T L Kelson, et al.
The British Journal of Dermatology|March 16, 2006
Sjögren-Larsson syndrome in Brazil is caused by a common c.1108-1G-->C splice-site mutation in the ALDH3A2 geneM P Auada, M B Puzzi, M L Cintra, et al.
The Johns Hopkins Medical Journal|October 1, 1982
Adrenoleukodystrophy: effects of dietary restriction of very long chain fatty acids and of administration of carnitine and clofibrate on clinical status and plasma fatty acidsF R Brown, M A Van Duyn, A B Moser, et al.
Pageof 8