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W Moser

Showing results (251-260 of 466) with videos related to

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Neuropediatrics|February 1, 1988
Galactosylceramide-beta-galactosidase deficiency in association with cherry red spotS Naidu, K J Hofmann, H W Moser, et al.
Pediatric Research|February 1, 1991
The 22-kD peroxisomal integral membrane protein in Zellweger syndrome--presence, abundance, and association with a peroxisomal thiolase precursor proteinJ Gärtner, W W Chen, R I Kelley, et al.
Journal of Inherited Metabolic Disease|January 1, 1987
Cherry red spot in association with galactosylceramide-beta-galactosidase deficiencyK J Hofman, S Naidu, H W Moser, et al.
JBJS Case Connector|February 3, 2023
Subacromial-Subdeltoid Bursitis With Rice Bodies After Rotator Cuff Repair With a Collagen Scaffold Implant: A Case ReportKevin T Root, Jonathan O Wright, Nicholas Mandato, et al.
Journal of Cellular Physiology|April 1, 1992
Peroxisome assembly mutations in humans: structural heterogeneity in Zellweger syndromeM J Santos, S Hoefler, A B Moser, et al.
Annals of Neurology|October 1, 1996
Cognitive and brain magnetic resonance imaging findings in adrenomyeloneuropathyD Edwin, L J Speedie, W Kohler, et al.
Clinical Chemistry|January 1, 1981
Direct quantitation of glycosaminoglycans in 2 mL of urine from patients with mucopolysaccharidosesR W Burlingame, G H Thomas, R L Stevens, et al.
Biochemical and Biophysical Research Communications|September 16, 1980
Adrenoleukodystrophy: evidence that abnormal very long chain fatty acids of brain cholesterol esters are of exogenous originY Kishimoto, H W Moser, N Kawamura, et al.
Journal of Molecular Neuroscience : MN|September 29, 2007
"Lorenzo's oil" therapy for X-linked adrenoleukodystrophy: rationale and current assessment of efficacyHugo W Moser, Ann B Moser, Kim Hollandsworth, et al.
Molecular Genetics and Metabolism|March 9, 1999
Accurate DNA-based diagnostic and carrier testing for X-linked adrenoleukodystrophyC D Boehm, G R Cutting, M B Lachtermacher, et al.
Pageof 47

Showing results (251-260 of 466) with videos related to

Sort By:
Pageof 47
Neuropediatrics|February 1, 1988
Galactosylceramide-beta-galactosidase deficiency in association with cherry red spotS Naidu, K J Hofmann, H W Moser, et al.
Pediatric Research|February 1, 1991
The 22-kD peroxisomal integral membrane protein in Zellweger syndrome--presence, abundance, and association with a peroxisomal thiolase precursor proteinJ Gärtner, W W Chen, R I Kelley, et al.
Journal of Inherited Metabolic Disease|January 1, 1987
Cherry red spot in association with galactosylceramide-beta-galactosidase deficiencyK J Hofman, S Naidu, H W Moser, et al.
JBJS Case Connector|February 3, 2023
Subacromial-Subdeltoid Bursitis With Rice Bodies After Rotator Cuff Repair With a Collagen Scaffold Implant: A Case ReportKevin T Root, Jonathan O Wright, Nicholas Mandato, et al.
Journal of Cellular Physiology|April 1, 1992
Peroxisome assembly mutations in humans: structural heterogeneity in Zellweger syndromeM J Santos, S Hoefler, A B Moser, et al.
Annals of Neurology|October 1, 1996
Cognitive and brain magnetic resonance imaging findings in adrenomyeloneuropathyD Edwin, L J Speedie, W Kohler, et al.
Clinical Chemistry|January 1, 1981
Direct quantitation of glycosaminoglycans in 2 mL of urine from patients with mucopolysaccharidosesR W Burlingame, G H Thomas, R L Stevens, et al.
Biochemical and Biophysical Research Communications|September 16, 1980
Adrenoleukodystrophy: evidence that abnormal very long chain fatty acids of brain cholesterol esters are of exogenous originY Kishimoto, H W Moser, N Kawamura, et al.
Journal of Molecular Neuroscience : MN|September 29, 2007
"Lorenzo's oil" therapy for X-linked adrenoleukodystrophy: rationale and current assessment of efficacyHugo W Moser, Ann B Moser, Kim Hollandsworth, et al.
Molecular Genetics and Metabolism|March 9, 1999
Accurate DNA-based diagnostic and carrier testing for X-linked adrenoleukodystrophyC D Boehm, G R Cutting, M B Lachtermacher, et al.
Pageof 47