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Neuropediatrics
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February 1, 1988
Galactosylceramide-beta-galactosidase deficiency in association with cherry red spot
S 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 protein
J 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 deficiency
K 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 Report
Kevin 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 syndrome
M J Santos, S Hoefler, A B Moser, et al.
Annals of Neurology
|
October 1, 1996
Cognitive and brain magnetic resonance imaging findings in adrenomyeloneuropathy
D 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 mucopolysaccharidoses
R 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 origin
Y 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 efficacy
Hugo 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 adrenoleukodystrophy
C D Boehm, G R Cutting, M B Lachtermacher, et al.
Page
of 47
Search research articles
Search
Showing results (251-260 of 466) with videos related to
Sort By:
Page
of 47
Neuropediatrics
|
February 1, 1988
Galactosylceramide-beta-galactosidase deficiency in association with cherry red spot
S 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 protein
J 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 deficiency
K 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 Report
Kevin 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 syndrome
M J Santos, S Hoefler, A B Moser, et al.
Annals of Neurology
|
October 1, 1996
Cognitive and brain magnetic resonance imaging findings in adrenomyeloneuropathy
D 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 mucopolysaccharidoses
R 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 origin
Y 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 efficacy
Hugo 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 adrenoleukodystrophy
C D Boehm, G R Cutting, M B Lachtermacher, et al.
Page
of 47