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A B Moser

Showing results (1-10 of 86) with videos related to

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Lipids|March 1, 1996
Very long-chain fatty acids in diagnosis, pathogenesis, and therapy of peroxisomal disordersH W Moser, A B Moser
Annals of the New York Academy of Sciences|December 27, 1996
Peroxisomal disorders: overviewH W Moser, A B Moser
Prenatal Diagnosis|March 12, 1999
The prenatal diagnosis of X-linked adrenoleukodystrophyA B Moser, H W Moser
Journal of Inherited Metabolic Disease|May 10, 2002
Lipid status and long-chain polyunsaturated fatty acid concentrations in adults and adolescents with phenylketonuria on phenylalanine-restricted dietK Moseley, R Koch, A B Moser
Archives of Biochemistry and Biophysics|May 1, 1981
Role of lysosomal acid ceramidase in the metabolism of ceramide in human skin fibroblastsW W Chen, A B Moser, H W Moser
The Journal of Cell Biology|May 1, 1985
Ultrastructural and cytochemical demonstration of peroxisomes in cultured fibroblasts from patients with peroxisomal deficiency disordersJ A Arias, A B Moser, S L Goldfischer
Biochemical and Biophysical Research Communications|October 30, 1981
Adrenoleukodystrophy: impaired oxidation of long chain fatty acids in cultured skin fibroblasts an adrenal cortexI Singh, H W Moser, A B Moser, et al.
Journal of Inherited Metabolic Disease|January 1, 1986
Peroxisomes in infantile phytanic acid storage disease: a cytochemical study of skin fibroblastsM E Beard, A B Moser, V Sapirstein, et al.
Developmental Neuroscience|January 1, 1991
Clinical aspects of adrenoleukodystrophy and adrenomyeloneuropathyH W Moser, A B Moser, S Naidu, et al.
Journal of Neuropathology and Experimental Neurology|November 1, 1992
The inflammatory myelinopathy of adreno-leukodystrophy: cells, effector molecules, and pathogenetic implicationsJ M Powers, Y Liu, A B Moser, et al.
Pageof 9

Showing results (1-10 of 86) with videos related to

Sort By:
Pageof 9
Lipids|March 1, 1996
Very long-chain fatty acids in diagnosis, pathogenesis, and therapy of peroxisomal disordersH W Moser, A B Moser
Annals of the New York Academy of Sciences|December 27, 1996
Peroxisomal disorders: overviewH W Moser, A B Moser
Prenatal Diagnosis|March 12, 1999
The prenatal diagnosis of X-linked adrenoleukodystrophyA B Moser, H W Moser
Journal of Inherited Metabolic Disease|May 10, 2002
Lipid status and long-chain polyunsaturated fatty acid concentrations in adults and adolescents with phenylketonuria on phenylalanine-restricted dietK Moseley, R Koch, A B Moser
Archives of Biochemistry and Biophysics|May 1, 1981
Role of lysosomal acid ceramidase in the metabolism of ceramide in human skin fibroblastsW W Chen, A B Moser, H W Moser
The Journal of Cell Biology|May 1, 1985
Ultrastructural and cytochemical demonstration of peroxisomes in cultured fibroblasts from patients with peroxisomal deficiency disordersJ A Arias, A B Moser, S L Goldfischer
Biochemical and Biophysical Research Communications|October 30, 1981
Adrenoleukodystrophy: impaired oxidation of long chain fatty acids in cultured skin fibroblasts an adrenal cortexI Singh, H W Moser, A B Moser, et al.
Journal of Inherited Metabolic Disease|January 1, 1986
Peroxisomes in infantile phytanic acid storage disease: a cytochemical study of skin fibroblastsM E Beard, A B Moser, V Sapirstein, et al.
Developmental Neuroscience|January 1, 1991
Clinical aspects of adrenoleukodystrophy and adrenomyeloneuropathyH W Moser, A B Moser, S Naidu, et al.
Journal of Neuropathology and Experimental Neurology|November 1, 1992
The inflammatory myelinopathy of adreno-leukodystrophy: cells, effector molecules, and pathogenetic implicationsJ M Powers, Y Liu, A B Moser, et al.
Pageof 9