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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 adrenomyeloneuropathy
V Chaudhry, H W Moser, D R Cornblath
Pediatric Neurology
|
January 1, 1988
Phenotypic and genotypic variability of generalized peroxisomal disorders
S 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 leukocytes
J 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 sulfatide
M 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 females
R 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 fibroblasts
W W Chen, A B Moser, H W Moser
Archives of Neurology
|
May 1, 1987
Adrenoleukodystrophy carrier state presenting as a chronic nonprogressive spinal cord disorder
M J Noetzel, W M Landau, H W Moser
Advances in Experimental Medicine and Biology
|
January 1, 1976
The biochemical defect in Farber's disease
J Dulaney, H W Moser, J Sidbury, et al.
Brain Pathology (Zurich, Switzerland)
|
July 1, 1995
Adrenoleukodystrophy: molecular genetics, pathology, and Lorenzo's oil
H W Moser, J M Powers, K D Smith
Page
of 29
Search research articles
Search
Showing results (61-70 of 283) with videos related to
Sort By:
Page
of 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 adrenomyeloneuropathy
V Chaudhry, H W Moser, D R Cornblath
Pediatric Neurology
|
January 1, 1988
Phenotypic and genotypic variability of generalized peroxisomal disorders
S 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 leukocytes
J 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 sulfatide
M 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 females
R 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 fibroblasts
W W Chen, A B Moser, H W Moser
Archives of Neurology
|
May 1, 1987
Adrenoleukodystrophy carrier state presenting as a chronic nonprogressive spinal cord disorder
M J Noetzel, W M Landau, H W Moser
Advances in Experimental Medicine and Biology
|
January 1, 1976
The biochemical defect in Farber's disease
J Dulaney, H W Moser, J Sidbury, et al.
Brain Pathology (Zurich, Switzerland)
|
July 1, 1995
Adrenoleukodystrophy: molecular genetics, pathology, and Lorenzo's oil
H W Moser, J M Powers, K D Smith
Page
of 29