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Journal of Lipid Research
|
January 1, 1979
Analysis and quantitation of free ceramide containing nonhydroxy and 2-hydroxy fatty acids, and phytosphingosine by high-performance liquid chromatography
M Iwamori, C Costello, H W Moser
Journal of Lipid Research
|
July 1, 1975
Specific tritium labeling of cerebrosides at the 3-positions of erythro-sphingosine and threo-sphingosine
M Iwamori, H W Moser, Y Kishimoto
Current Opinion in Neurology
|
May 24, 2001
Leukodystrophies: recent developments in genetics, molecular biology, pathogenesis and treatment
J Berger, H W Moser, S Forss-Petter
Journal of Inherited Metabolic Disease
|
January 1, 1987
Adrenoleukodystrophy: biochemical procedures in diagnosis, prevention and treatment
P A Watkins, S Naidu, H W Moser
Archives of Neurology
|
April 6, 1999
Mutational analysis and the pathogenesis of variant X-linked adrenoleukodystrophy phenotypes
H W Moser, S Kemp, K D Smith
Biotechnology and Bioengineering
|
March 1, 1970
Proteases of the genus Bacillus. II. Alkaline proteases
L Keay, P W Moser, B S Wildi
Rheumatic Diseases Clinics of North America
|
May 31, 2013
Ultrasound and treatment algorithms of RA and JIA
Sam R Dalvi, David W Moser, Jonathan Samuels
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
JAMA
|
December 29, 2005
Adrenoleukodystrophy: new approaches to a neurodegenerative disease
Hugo W Moser, Gerald V Raymond, Prachi Dubey
Page
of 47
Search research articles
Search
Showing results (121-130 of 466) with videos related to
Sort By:
Page
of 47
Journal of Lipid Research
|
January 1, 1979
Analysis and quantitation of free ceramide containing nonhydroxy and 2-hydroxy fatty acids, and phytosphingosine by high-performance liquid chromatography
M Iwamori, C Costello, H W Moser
Journal of Lipid Research
|
July 1, 1975
Specific tritium labeling of cerebrosides at the 3-positions of erythro-sphingosine and threo-sphingosine
M Iwamori, H W Moser, Y Kishimoto
Current Opinion in Neurology
|
May 24, 2001
Leukodystrophies: recent developments in genetics, molecular biology, pathogenesis and treatment
J Berger, H W Moser, S Forss-Petter
Journal of Inherited Metabolic Disease
|
January 1, 1987
Adrenoleukodystrophy: biochemical procedures in diagnosis, prevention and treatment
P A Watkins, S Naidu, H W Moser
Archives of Neurology
|
April 6, 1999
Mutational analysis and the pathogenesis of variant X-linked adrenoleukodystrophy phenotypes
H W Moser, S Kemp, K D Smith
Biotechnology and Bioengineering
|
March 1, 1970
Proteases of the genus Bacillus. II. Alkaline proteases
L Keay, P W Moser, B S Wildi
Rheumatic Diseases Clinics of North America
|
May 31, 2013
Ultrasound and treatment algorithms of RA and JIA
Sam R Dalvi, David W Moser, Jonathan Samuels
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
JAMA
|
December 29, 2005
Adrenoleukodystrophy: new approaches to a neurodegenerative disease
Hugo W Moser, Gerald V Raymond, Prachi Dubey
Page
of 47