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The Journal of Pediatrics
|
July 1, 1996
Acceleration of retarded growth in children with Gaucher disease after treatment with alglucerase
P Kaplan, A Mazur, O Manor, et al.
Pediatric Research
|
May 19, 1998
Molecular characterization of pyruvate carboxylase deficiency in two consanguineous families
I D Wexler, D S Kerr, Y Du, et al.
Enzyme
|
January 1, 1989
Mevalonate kinase in lysates of cultured human fibroblasts and lymphoblasts: kinetic properties, assay conditions, carrier detection and measurement of residual activity in a patient with mevalonic aciduria
K M Gibson, J L Lohr, R L Broock, et al.
Prenatal Diagnosis
|
February 1, 1996
Prenatal diagnosis of mitochondrial fatty acid oxidation defects
M A Nada, C Vianey-Saban, C R Roe, et al.
Journal of Lipid Research
|
March 1, 1990
3-Hydroxy-3-methylglutaryl coenzyme A reductase activity in cultured fibroblasts from patients with mevalonate kinase deficiency: differential response to lipid supplied by fetal bovine serum in tissue culture medium
K M Gibson, G Hoffmann, A Schwall, et al.
Archives of Internal Medicine
|
October 12, 2000
The Gaucher registry: demographics and disease characteristics of 1698 patients with Gaucher disease
J Charrow, H C Andersson, P Kaplan, et al.
Archives of Internal Medicine
|
September 17, 1998
Gaucher disease: recommendations on diagnosis, evaluation, and monitoring
J Charrow, J A Esplin, T J Gribble, et al.
Page
of 3
Search research articles
Search
Showing results (21-30 of 27) with videos related to
Sort By:
Page
of 3
You have reached the last page of results.
This site can display upto 27 results.
The Journal of Pediatrics
|
July 1, 1996
Acceleration of retarded growth in children with Gaucher disease after treatment with alglucerase
P Kaplan, A Mazur, O Manor, et al.
Pediatric Research
|
May 19, 1998
Molecular characterization of pyruvate carboxylase deficiency in two consanguineous families
I D Wexler, D S Kerr, Y Du, et al.
Enzyme
|
January 1, 1989
Mevalonate kinase in lysates of cultured human fibroblasts and lymphoblasts: kinetic properties, assay conditions, carrier detection and measurement of residual activity in a patient with mevalonic aciduria
K M Gibson, J L Lohr, R L Broock, et al.
Prenatal Diagnosis
|
February 1, 1996
Prenatal diagnosis of mitochondrial fatty acid oxidation defects
M A Nada, C Vianey-Saban, C R Roe, et al.
Journal of Lipid Research
|
March 1, 1990
3-Hydroxy-3-methylglutaryl coenzyme A reductase activity in cultured fibroblasts from patients with mevalonate kinase deficiency: differential response to lipid supplied by fetal bovine serum in tissue culture medium
K M Gibson, G Hoffmann, A Schwall, et al.
Archives of Internal Medicine
|
October 12, 2000
The Gaucher registry: demographics and disease characteristics of 1698 patients with Gaucher disease
J Charrow, H C Andersson, P Kaplan, et al.
Archives of Internal Medicine
|
September 17, 1998
Gaucher disease: recommendations on diagnosis, evaluation, and monitoring
J Charrow, J A Esplin, T J Gribble, et al.
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of 3