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A B Moser

Showing results (51-60 of 86) with videos related to

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Acta Neuropathologica|January 1, 1987
Neuronal lipidosis and neuroaxonal dystrophy in cerebro-hepato-renal (Zellweger) syndromeJ M Powers, R C Tummons, A B Moser, et al.
Pediatric Neurology|November 1, 1993
Neonatal adrenoleukodystrophy presenting as infantile progressive spinal muscular atrophyD A Paul, L S Goldsmith, D K Miles, et al.
Biochemical and Molecular Medicine|April 1, 1995
Sulfatide and sphingomyelin loading of living cells as tools for the study of ceramide turnover by lysosomal ceramidase--implications for the diagnosis of Farber diseaseT Levade, M C Tempesta, H W Moser, et al.
Archives of Pathology & Laboratory Medicine|February 1, 1987
Pathologic findings in adrenoleukodystrophy heterozygotesJ M Powers, H W Moser, A B Moser, et al.
Journal of Cell Science|April 23, 1999
Metabolic control of peroxisome abundanceC C Chang, S South, D Warren, et al.
Brain : a Journal of Neurology|December 1, 1989
Polyneuropathy in feline Niemann-Pick diseaseP A Cuddon, R J Higgins, I D Duncan, et al.
The Johns Hopkins Medical Journal|December 1, 1982
Cerebro-hepato-renal (Zellweger) syndrome and neonatal adrenoleukodystrophy: similarities in phenotype and accumulation of very long chain fatty acidsF R Brown, A J McAdams, J W Cummins, et al.
Neurology|August 26, 1998
Adrenoleukodystrophy: increased plasma content of saturated very long chain fatty acids. 1981H W Moser, A B Moser, K K Frayer, et al.
Neurology|August 1, 1981
Auditory evoked brainstem response and high-performance liquid chromatography sulfatide assay as early indices of metachromatic leukodystrophyF R Brown, H Shimizu, J M McDonald, et al.
Neurology|October 1, 1981
Adrenoleukodystrophy: increased plasma content of saturated very long chain fatty acidsH W Moser, A B Moser, K K Frayer, et al.
Pageof 9

Showing results (51-60 of 86) with videos related to

Sort By:
Pageof 9
Acta Neuropathologica|January 1, 1987
Neuronal lipidosis and neuroaxonal dystrophy in cerebro-hepato-renal (Zellweger) syndromeJ M Powers, R C Tummons, A B Moser, et al.
Pediatric Neurology|November 1, 1993
Neonatal adrenoleukodystrophy presenting as infantile progressive spinal muscular atrophyD A Paul, L S Goldsmith, D K Miles, et al.
Biochemical and Molecular Medicine|April 1, 1995
Sulfatide and sphingomyelin loading of living cells as tools for the study of ceramide turnover by lysosomal ceramidase--implications for the diagnosis of Farber diseaseT Levade, M C Tempesta, H W Moser, et al.
Archives of Pathology & Laboratory Medicine|February 1, 1987
Pathologic findings in adrenoleukodystrophy heterozygotesJ M Powers, H W Moser, A B Moser, et al.
Journal of Cell Science|April 23, 1999
Metabolic control of peroxisome abundanceC C Chang, S South, D Warren, et al.
Brain : a Journal of Neurology|December 1, 1989
Polyneuropathy in feline Niemann-Pick diseaseP A Cuddon, R J Higgins, I D Duncan, et al.
The Johns Hopkins Medical Journal|December 1, 1982
Cerebro-hepato-renal (Zellweger) syndrome and neonatal adrenoleukodystrophy: similarities in phenotype and accumulation of very long chain fatty acidsF R Brown, A J McAdams, J W Cummins, et al.
Neurology|August 26, 1998
Adrenoleukodystrophy: increased plasma content of saturated very long chain fatty acids. 1981H W Moser, A B Moser, K K Frayer, et al.
Neurology|August 1, 1981
Auditory evoked brainstem response and high-performance liquid chromatography sulfatide assay as early indices of metachromatic leukodystrophyF R Brown, H Shimizu, J M McDonald, et al.
Neurology|October 1, 1981
Adrenoleukodystrophy: increased plasma content of saturated very long chain fatty acidsH W Moser, A B Moser, K K Frayer, et al.
Pageof 9