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American Journal of Nephrology
|
September 1, 1983
Silicon nephropathy mimicking Fabry's disease
D E Banks, J Milutinovic, R J Desnick, et al.
The Journal of Biological Chemistry
|
June 25, 1986
Human acid beta-glucosidase. Use of conduritol B epoxide derivatives to investigate the catalytically active normal and Gaucher disease enzymes
G A Grabowski, K Osiecki-Newman, T Dinur, et al.
Journal of Lipid Research
|
April 6, 2001
Lysosomal acid lipase-deficient mice: depletion of white and brown fat, severe hepatosplenomegaly, and shortened life span
H Du, M Heur, M Duanmu, et al.
Progress in Clinical and Biological Research
|
January 1, 1982
Gaucher disease in the dog
B R Farrow, W J Hartley, A C Pollard, et al.
Enzyme
|
January 1, 1988
Human acid beta-glucosidase: inhibition studies using glucose analogues and pH variation to characterize the normal and Gaucher disease glycon binding sites
K Osiecki-Newman, G Legler, M Grace, et al.
Pediatric Research
|
May 1, 1992
Enzyme augmentation in moderate to life-threatening Gaucher disease
S Fallet, M E Grace, A Sibille, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
June 30, 1995
Hyaluronic acid and dermatan sulfate in non-lesional pseudoxanthoma elasticum skin
M Lebwohl, M O Longas, J Konstadt, et al.
Clinical Genetics
|
August 1, 1984
Reduced plasma concentrations of total, low density lipoprotein and high density lipoprotein cholesterol in patients with Gaucher type I disease
H Ginsberg, G A Grabowski, J C Gibson, et al.
Journal of Pediatric Surgery
|
June 1, 1989
Gaucher disease: fate of the splenic remnant after partial splenectomy--a case of rapid enlargement
P R Fleshner, D J Astion, M D Ludman, et al.
Muscle & Nerve
|
March 1, 1988
Hexosaminidase A activity and amyotrophic lateral sclerosis
M Gudesblatt, M D Ludman, J A Cohen, et al.
Page
of 13
Search research articles
Search
Showing results (101-110 of 126) with videos related to
Sort By:
Page
of 13
American Journal of Nephrology
|
September 1, 1983
Silicon nephropathy mimicking Fabry's disease
D E Banks, J Milutinovic, R J Desnick, et al.
The Journal of Biological Chemistry
|
June 25, 1986
Human acid beta-glucosidase. Use of conduritol B epoxide derivatives to investigate the catalytically active normal and Gaucher disease enzymes
G A Grabowski, K Osiecki-Newman, T Dinur, et al.
Journal of Lipid Research
|
April 6, 2001
Lysosomal acid lipase-deficient mice: depletion of white and brown fat, severe hepatosplenomegaly, and shortened life span
H Du, M Heur, M Duanmu, et al.
Progress in Clinical and Biological Research
|
January 1, 1982
Gaucher disease in the dog
B R Farrow, W J Hartley, A C Pollard, et al.
Enzyme
|
January 1, 1988
Human acid beta-glucosidase: inhibition studies using glucose analogues and pH variation to characterize the normal and Gaucher disease glycon binding sites
K Osiecki-Newman, G Legler, M Grace, et al.
Pediatric Research
|
May 1, 1992
Enzyme augmentation in moderate to life-threatening Gaucher disease
S Fallet, M E Grace, A Sibille, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
June 30, 1995
Hyaluronic acid and dermatan sulfate in non-lesional pseudoxanthoma elasticum skin
M Lebwohl, M O Longas, J Konstadt, et al.
Clinical Genetics
|
August 1, 1984
Reduced plasma concentrations of total, low density lipoprotein and high density lipoprotein cholesterol in patients with Gaucher type I disease
H Ginsberg, G A Grabowski, J C Gibson, et al.
Journal of Pediatric Surgery
|
June 1, 1989
Gaucher disease: fate of the splenic remnant after partial splenectomy--a case of rapid enlargement
P R Fleshner, D J Astion, M D Ludman, et al.
Muscle & Nerve
|
March 1, 1988
Hexosaminidase A activity and amyotrophic lateral sclerosis
M Gudesblatt, M D Ludman, J A Cohen, et al.
Page
of 13