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R S Wappner

Showing results (21-30 of 27) with videos related to

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The Journal of Pediatrics|July 1, 1996
Acceleration of retarded growth in children with Gaucher disease after treatment with algluceraseP Kaplan, A Mazur, O Manor, et al.
Pediatric Research|May 19, 1998
Molecular characterization of pyruvate carboxylase deficiency in two consanguineous familiesI 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 aciduriaK M Gibson, J L Lohr, R L Broock, et al.
Prenatal Diagnosis|February 1, 1996
Prenatal diagnosis of mitochondrial fatty acid oxidation defectsM 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 mediumK 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 diseaseJ Charrow, H C Andersson, P Kaplan, et al.
Archives of Internal Medicine|September 17, 1998
Gaucher disease: recommendations on diagnosis, evaluation, and monitoringJ Charrow, J A Esplin, T J Gribble, et al.
Pageof 3

Showing results (21-30 of 27) with videos related to

Sort By:
Pageof 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 algluceraseP Kaplan, A Mazur, O Manor, et al.
Pediatric Research|May 19, 1998
Molecular characterization of pyruvate carboxylase deficiency in two consanguineous familiesI 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 aciduriaK M Gibson, J L Lohr, R L Broock, et al.
Prenatal Diagnosis|February 1, 1996
Prenatal diagnosis of mitochondrial fatty acid oxidation defectsM 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 mediumK 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 diseaseJ Charrow, H C Andersson, P Kaplan, et al.
Archives of Internal Medicine|September 17, 1998
Gaucher disease: recommendations on diagnosis, evaluation, and monitoringJ Charrow, J A Esplin, T J Gribble, et al.
Pageof 3