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J Charrow

Showing results (41-50 of 47) with videos related to

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The Journal of Pediatrics|May 1, 1988
Biochemical abnormalities in rhizomelic chondrodysplasia punctataG Hoefler, S Hoefler, P A Watkins, et al.
Journal of Inherited Metabolic Disease|March 10, 2007
Fabry disease: baseline medical characteristics of a cohort of 1765 males and females in the Fabry RegistryC M Eng, J Fletcher, W R Wilcox, 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.
Molecular Genetics and Metabolism|September 4, 2016
Triheptanoin treatment in patients with pediatric cardiomyopathy associated with long chain-fatty acid oxidation disordersJ Vockley, J Charrow, J Ganesh, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 5, 2001
Recombinant human acid alpha-glucosidase enzyme therapy for infantile glycogen storage disease type II: results of a phase I/II clinical trialA Amalfitano, A R Bengur, R P Morse, et al.
Journal of Dental Research|June 16, 2012
Dental abnormalities in Schimke immuno-osseous dysplasiaM Morimoto, O Kérourédan, M Gendronneau, et al.
Pageof 5

Showing results (41-50 of 47) with videos related to

Sort By:
Pageof 5
You have reached the last page of results.This site can display upto 47 results.
The Journal of Pediatrics|May 1, 1988
Biochemical abnormalities in rhizomelic chondrodysplasia punctataG Hoefler, S Hoefler, P A Watkins, et al.
Journal of Inherited Metabolic Disease|March 10, 2007
Fabry disease: baseline medical characteristics of a cohort of 1765 males and females in the Fabry RegistryC M Eng, J Fletcher, W R Wilcox, 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.
Molecular Genetics and Metabolism|September 4, 2016
Triheptanoin treatment in patients with pediatric cardiomyopathy associated with long chain-fatty acid oxidation disordersJ Vockley, J Charrow, J Ganesh, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 5, 2001
Recombinant human acid alpha-glucosidase enzyme therapy for infantile glycogen storage disease type II: results of a phase I/II clinical trialA Amalfitano, A R Bengur, R P Morse, et al.
Journal of Dental Research|June 16, 2012
Dental abnormalities in Schimke immuno-osseous dysplasiaM Morimoto, O Kérourédan, M Gendronneau, et al.
Pageof 5