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H W Moser

Showing results (61-70 of 283) with videos related to

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Science (New York, N.Y.)|December 8, 1972
Ceramidase deficiency in Farber's disease (lipogranulomatosis)M Sugita, J T Dulaney, H W Moser
Journal of Neurology, Neurosurgery, and Psychiatry|August 1, 1996
Nerve conduction studies in adrenomyeloneuropathyV Chaudhry, H W Moser, D R Cornblath
Pediatric Neurology|January 1, 1988
Phenotypic and genotypic variability of generalized peroxisomal disordersS Naidu, A E Moser, H W Moser
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 1, 1976
Detection of the carrier state of Hurler's syndrome by assay of alpha-L-iduronidase in leukocytesJ T Dulaney, A Milunsky, H W Moser
Journal of Lipid Research|May 1, 1974
Structure and composition of sulfatides isolated from livers of patients with metachromatic leukodystrophy: galactosyl sulfatide and lactosyl sulfatideM Sugita, J T Dulaney, H W Moser
The American Journal of Pathology|July 1, 1982
Neonatal adrenoleukodystrophy: clinical, pathologic, and biochemical delineation of a syndrome affecting both males and femalesR Jaffe, P Crumrine, Y Hashida, et al.
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
Archives of Neurology|May 1, 1987
Adrenoleukodystrophy carrier state presenting as a chronic nonprogressive spinal cord disorderM J Noetzel, W M Landau, H W Moser
Advances in Experimental Medicine and Biology|January 1, 1976
The biochemical defect in Farber's diseaseJ Dulaney, H W Moser, J Sidbury, et al.
Brain Pathology (Zurich, Switzerland)|July 1, 1995
Adrenoleukodystrophy: molecular genetics, pathology, and Lorenzo's oilH W Moser, J M Powers, K D Smith
Pageof 29

Showing results (61-70 of 283) with videos related to

Sort By:
Pageof 29
Science (New York, N.Y.)|December 8, 1972
Ceramidase deficiency in Farber's disease (lipogranulomatosis)M Sugita, J T Dulaney, H W Moser
Journal of Neurology, Neurosurgery, and Psychiatry|August 1, 1996
Nerve conduction studies in adrenomyeloneuropathyV Chaudhry, H W Moser, D R Cornblath
Pediatric Neurology|January 1, 1988
Phenotypic and genotypic variability of generalized peroxisomal disordersS Naidu, A E Moser, H W Moser
Clinica Chimica Acta; International Journal of Clinical Chemistry|June 1, 1976
Detection of the carrier state of Hurler's syndrome by assay of alpha-L-iduronidase in leukocytesJ T Dulaney, A Milunsky, H W Moser
Journal of Lipid Research|May 1, 1974
Structure and composition of sulfatides isolated from livers of patients with metachromatic leukodystrophy: galactosyl sulfatide and lactosyl sulfatideM Sugita, J T Dulaney, H W Moser
The American Journal of Pathology|July 1, 1982
Neonatal adrenoleukodystrophy: clinical, pathologic, and biochemical delineation of a syndrome affecting both males and femalesR Jaffe, P Crumrine, Y Hashida, et al.
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
Archives of Neurology|May 1, 1987
Adrenoleukodystrophy carrier state presenting as a chronic nonprogressive spinal cord disorderM J Noetzel, W M Landau, H W Moser
Advances in Experimental Medicine and Biology|January 1, 1976
The biochemical defect in Farber's diseaseJ Dulaney, H W Moser, J Sidbury, et al.
Brain Pathology (Zurich, Switzerland)|July 1, 1995
Adrenoleukodystrophy: molecular genetics, pathology, and Lorenzo's oilH W Moser, J M Powers, K D Smith
Pageof 29