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A B Moser

Showing results (31-40 of 86) with videos related to

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American Journal of Medical Genetics|January 1, 1980
Plasma exchange removes glycosphingolipid in Fabry diseaseR E Pyeritz, M D Ullman, A B Moser, et al.
Biochemical Medicine and Metabolic Biology|August 1, 1993
Fatty alcohol accumulation in the autosomal recessive form of rhizomelic chondrodysplasia punctataW B Rizzo, D A Craft, L L Judd, et al.
Biology of the Cell|July 6, 2000
Peroxisomal ghosts are intracellular structures distinct from lysosomal compartments in Zellweger syndrome: a confocal laser scanning microscopy studyM J Santos, S C Henderson, A B Moser, et al.
Journal of Neuropathology and Experimental Neurology|July 1, 1994
Solvent vapor abuse leukoencephalopathy. Comparison to adrenoleukodystrophyM Kornfeld, A B Moser, H W Moser, et al.
Journal of Neuropathology and Experimental Neurology|May 1, 1989
Structural and chemical alterations in the cerebral maldevelopment of fetal cerebro-hepato-renal (Zellweger) syndromeJ M Powers, R C Tummons, V S Caviness, et al.
Journal of the Neurological Sciences|December 1, 1995
Neurodegenerative course in ceramidase deficiency (Farber disease) correlates with the residual lysosomal ceramide turnover in cultured living patient cellsT Levade, H W Moser, A H Fensom, et al.
Human Mutation|March 29, 2000
Determination of 30 X-linked adrenoleukodystrophy mutations, including 15 not previously describedM B Lachtermacher, H N Seuánez, A B Moser, et al.
Journal of Cell Science|May 1, 1995
Identification of three distinct peroxisomal protein import defects in patients with peroxisome biogenesis disordersM L Slawecki, G Dodt, S Steinberg, et al.
Annals of Neurology|June 1, 1980
Adrenoleukodystrophy: elevated C26 fatty acid in cultured skin fibroblastsH W Moser, A B Moser, N Kawamura, et al.
Annals of Neurology|February 1, 1996
Neuronal migration abnormality in peroxisomal bifunctional enzyme defectW E Kaufmann, C Theda, S Naidu, et al.
Pageof 9

Showing results (31-40 of 86) with videos related to

Sort By:
Pageof 9
American Journal of Medical Genetics|January 1, 1980
Plasma exchange removes glycosphingolipid in Fabry diseaseR E Pyeritz, M D Ullman, A B Moser, et al.
Biochemical Medicine and Metabolic Biology|August 1, 1993
Fatty alcohol accumulation in the autosomal recessive form of rhizomelic chondrodysplasia punctataW B Rizzo, D A Craft, L L Judd, et al.
Biology of the Cell|July 6, 2000
Peroxisomal ghosts are intracellular structures distinct from lysosomal compartments in Zellweger syndrome: a confocal laser scanning microscopy studyM J Santos, S C Henderson, A B Moser, et al.
Journal of Neuropathology and Experimental Neurology|July 1, 1994
Solvent vapor abuse leukoencephalopathy. Comparison to adrenoleukodystrophyM Kornfeld, A B Moser, H W Moser, et al.
Journal of Neuropathology and Experimental Neurology|May 1, 1989
Structural and chemical alterations in the cerebral maldevelopment of fetal cerebro-hepato-renal (Zellweger) syndromeJ M Powers, R C Tummons, V S Caviness, et al.
Journal of the Neurological Sciences|December 1, 1995
Neurodegenerative course in ceramidase deficiency (Farber disease) correlates with the residual lysosomal ceramide turnover in cultured living patient cellsT Levade, H W Moser, A H Fensom, et al.
Human Mutation|March 29, 2000
Determination of 30 X-linked adrenoleukodystrophy mutations, including 15 not previously describedM B Lachtermacher, H N Seuánez, A B Moser, et al.
Journal of Cell Science|May 1, 1995
Identification of three distinct peroxisomal protein import defects in patients with peroxisome biogenesis disordersM L Slawecki, G Dodt, S Steinberg, et al.
Annals of Neurology|June 1, 1980
Adrenoleukodystrophy: elevated C26 fatty acid in cultured skin fibroblastsH W Moser, A B Moser, N Kawamura, et al.
Annals of Neurology|February 1, 1996
Neuronal migration abnormality in peroxisomal bifunctional enzyme defectW E Kaufmann, C Theda, S Naidu, et al.
Pageof 9