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Journal of the American Society of Nephrology : JASN
|
April 6, 2007
Weekly enzyme replacement therapy may slow decline of renal function in patients with Fabry disease who are on long-term biweekly dosing
Raphael Schiffmann, Hasan Askari, Margaret Timmons, et al.
Biochemical Medicine
|
February 1, 1985
Lectin-specific targeting of beta-glucocerebrosidase to different liver cells via glycosylated liposomes
P K Das, G J Murray, G C Zirzow, et al.
Addiction Biology
|
January 7, 2016
Butyrylcholinesterase: an enzyme antidote for cocaine intoxication
C E Mattes, G W Belendiuk, T J Lynch, et al.
Annals of Neurology
|
December 1, 1985
Monoclonal IgM in a patient with paraproteinemic polyneuropathy binds to gangliosides containing disialosyl groups
A A Ilyas, R H Quarles, M C Dalakas, et al.
Human Mutation
|
January 29, 2000
Five novel mutations in fourteen patients with Fabry Disease
K M Rosenberg, R Schiffmann, C Kaneski, et al.
Journal of Neurochemistry
|
December 1, 1975
Characterization and protein analysis of myelin subfractions in rat brain: developmental and regional comparisons
A W Zimmerman, R H Quarles, H de Webster, et al.
Biochemical and Biophysical Research Communications
|
December 16, 1980
A new group of glucocerebrosidase isozymes found in human white blood cells
E I Ginns, R O Brady, D W Stowens, et al.
Science (New York, N.Y.)
|
April 15, 1977
Niemann-Pick disease experimental model: sphingomyelinase reduction induced by AY-9944
N Sakuragawa, M Sakuragaw, T Kuwabara, et al.
Plos One
|
July 30, 2011
The saccadic and neurological deficits in type 3 Gaucher disease
William Benko, Markus Ries, Edythe A Wiggs, et al.
Pediatric Research
|
September 1, 1972
Prenatal Niemann-Pick disease: biochemical and histologic examination of a 19-gestational week fetus
E L Schneider, W G Ellis, R O Brady, et al.
Page
of 54
Search research articles
Search
Showing results (301-310 of 536) with videos related to
Sort By:
Page
of 54
Journal of the American Society of Nephrology : JASN
|
April 6, 2007
Weekly enzyme replacement therapy may slow decline of renal function in patients with Fabry disease who are on long-term biweekly dosing
Raphael Schiffmann, Hasan Askari, Margaret Timmons, et al.
Biochemical Medicine
|
February 1, 1985
Lectin-specific targeting of beta-glucocerebrosidase to different liver cells via glycosylated liposomes
P K Das, G J Murray, G C Zirzow, et al.
Addiction Biology
|
January 7, 2016
Butyrylcholinesterase: an enzyme antidote for cocaine intoxication
C E Mattes, G W Belendiuk, T J Lynch, et al.
Annals of Neurology
|
December 1, 1985
Monoclonal IgM in a patient with paraproteinemic polyneuropathy binds to gangliosides containing disialosyl groups
A A Ilyas, R H Quarles, M C Dalakas, et al.
Human Mutation
|
January 29, 2000
Five novel mutations in fourteen patients with Fabry Disease
K M Rosenberg, R Schiffmann, C Kaneski, et al.
Journal of Neurochemistry
|
December 1, 1975
Characterization and protein analysis of myelin subfractions in rat brain: developmental and regional comparisons
A W Zimmerman, R H Quarles, H de Webster, et al.
Biochemical and Biophysical Research Communications
|
December 16, 1980
A new group of glucocerebrosidase isozymes found in human white blood cells
E I Ginns, R O Brady, D W Stowens, et al.
Science (New York, N.Y.)
|
April 15, 1977
Niemann-Pick disease experimental model: sphingomyelinase reduction induced by AY-9944
N Sakuragawa, M Sakuragaw, T Kuwabara, et al.
Plos One
|
July 30, 2011
The saccadic and neurological deficits in type 3 Gaucher disease
William Benko, Markus Ries, Edythe A Wiggs, et al.
Pediatric Research
|
September 1, 1972
Prenatal Niemann-Pick disease: biochemical and histologic examination of a 19-gestational week fetus
E L Schneider, W G Ellis, R O Brady, et al.
Page
of 54