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Acta Neuropathologica
|
January 1, 1987
Neuronal lipidosis and neuroaxonal dystrophy in cerebro-hepato-renal (Zellweger) syndrome
J M Powers, R C Tummons, A B Moser, et al.
Pediatric Neurology
|
November 1, 1993
Neonatal adrenoleukodystrophy presenting as infantile progressive spinal muscular atrophy
D 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 disease
T Levade, M C Tempesta, H W Moser, et al.
Archives of Pathology & Laboratory Medicine
|
February 1, 1987
Pathologic findings in adrenoleukodystrophy heterozygotes
J M Powers, H W Moser, A B Moser, et al.
Journal of Cell Science
|
April 23, 1999
Metabolic control of peroxisome abundance
C C Chang, S South, D Warren, et al.
Brain : a Journal of Neurology
|
December 1, 1989
Polyneuropathy in feline Niemann-Pick disease
P 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 acids
F 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. 1981
H 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 leukodystrophy
F R Brown, H Shimizu, J M McDonald, et al.
Neurology
|
October 1, 1981
Adrenoleukodystrophy: increased plasma content of saturated very long chain fatty acids
H W Moser, A B Moser, K K Frayer, et al.
Page
of 9
Search research articles
Search
Showing results (51-60 of 86) with videos related to
Sort By:
Page
of 9
Acta Neuropathologica
|
January 1, 1987
Neuronal lipidosis and neuroaxonal dystrophy in cerebro-hepato-renal (Zellweger) syndrome
J M Powers, R C Tummons, A B Moser, et al.
Pediatric Neurology
|
November 1, 1993
Neonatal adrenoleukodystrophy presenting as infantile progressive spinal muscular atrophy
D 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 disease
T Levade, M C Tempesta, H W Moser, et al.
Archives of Pathology & Laboratory Medicine
|
February 1, 1987
Pathologic findings in adrenoleukodystrophy heterozygotes
J M Powers, H W Moser, A B Moser, et al.
Journal of Cell Science
|
April 23, 1999
Metabolic control of peroxisome abundance
C C Chang, S South, D Warren, et al.
Brain : a Journal of Neurology
|
December 1, 1989
Polyneuropathy in feline Niemann-Pick disease
P 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 acids
F 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. 1981
H 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 leukodystrophy
F R Brown, H Shimizu, J M McDonald, et al.
Neurology
|
October 1, 1981
Adrenoleukodystrophy: increased plasma content of saturated very long chain fatty acids
H W Moser, A B Moser, K K Frayer, et al.
Page
of 9