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The Journal of Pediatrics
|
May 1, 1988
Biochemical abnormalities in rhizomelic chondrodysplasia punctata
G 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 Registry
C 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 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.
Molecular Genetics and Metabolism
|
September 4, 2016
Triheptanoin treatment in patients with pediatric cardiomyopathy associated with long chain-fatty acid oxidation disorders
J 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 trial
A Amalfitano, A R Bengur, R P Morse, et al.
Journal of Dental Research
|
June 16, 2012
Dental abnormalities in Schimke immuno-osseous dysplasia
M Morimoto, O Kérourédan, M Gendronneau, et al.
Page
of 5
Search research articles
Search
Showing results (41-50 of 47) with videos related to
Sort By:
Page
of 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 punctata
G 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 Registry
C 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 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.
Molecular Genetics and Metabolism
|
September 4, 2016
Triheptanoin treatment in patients with pediatric cardiomyopathy associated with long chain-fatty acid oxidation disorders
J 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 trial
A Amalfitano, A R Bengur, R P Morse, et al.
Journal of Dental Research
|
June 16, 2012
Dental abnormalities in Schimke immuno-osseous dysplasia
M Morimoto, O Kérourédan, M Gendronneau, et al.
Page
of 5