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Molecular Genetics and Metabolism
|
October 11, 2001
Nonketotic hyperglycinemia (glycine encephalopathy): laboratory diagnosis
D A Applegarth, J R Toone
Journal of Inherited Metabolic Disease
|
January 1, 1980
Uptake of lysosomal enzymes by human fibroblasts: lack of uptake of fungal or plant glycosidases in comparison with a mammalian enzyme
K C Dooley, D A Applegarth
Clinical Genetics
|
June 1, 1988
Carrier detection in Sanfilippo A syndrome
J R Toone, D A Applegarth
Clinical Biochemistry
|
April 1, 1979
Hyperprolinemia type II: evidence of the excretion of 3-hydroxy delta 1-pyrroline 5-carboxylic acid
K C Dooley, D A Applegarth
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
November 9, 1991
Micromethod for the assay of glutamate: glyoxylate aminotransferase and modifications of a micromethod for the assay of alanine: glyoxylate aminotransferase. Implications for the prenatal diagnosis of type I hyperoxaluria by fetal liver biopsy
J R Toone, D A Applegarth
Perspectives in Pediatric Pathology
|
January 1, 1993
Pathology of peroxisomal disorders
J E Dimmick, D A Applegarth
Journal of Inherited Metabolic Disease
|
July 27, 2004
Glycine encephalopathy (nonketotic hyperglycinaemia) : review and update
D A Applegarth, J R Toone
Annals of the New York Academy of Sciences
|
January 1, 1983
Characterization of alpha 2-macroglobulin in cystic fibrosis
M A Bridges, D A Applegarth
Carbohydrate Research
|
July 1, 1986
Diagnosis of mucopolysaccharidoses using 1H-n.m.r. spectroscopy of glycosaminoglycans
A V Savage, D A Applegarth
Medical Hypotheses
|
June 1, 1983
Is cystic fibrosis a disease confined to epithelial cells?
D A Applegarth, M A Bridges
Page
of 13
Search research articles
Search
Showing results (11-20 of 125) with videos related to
Sort By:
Page
of 13
Molecular Genetics and Metabolism
|
October 11, 2001
Nonketotic hyperglycinemia (glycine encephalopathy): laboratory diagnosis
D A Applegarth, J R Toone
Journal of Inherited Metabolic Disease
|
January 1, 1980
Uptake of lysosomal enzymes by human fibroblasts: lack of uptake of fungal or plant glycosidases in comparison with a mammalian enzyme
K C Dooley, D A Applegarth
Clinical Genetics
|
June 1, 1988
Carrier detection in Sanfilippo A syndrome
J R Toone, D A Applegarth
Clinical Biochemistry
|
April 1, 1979
Hyperprolinemia type II: evidence of the excretion of 3-hydroxy delta 1-pyrroline 5-carboxylic acid
K C Dooley, D A Applegarth
Clinica Chimica Acta; International Journal of Clinical Chemistry
|
November 9, 1991
Micromethod for the assay of glutamate: glyoxylate aminotransferase and modifications of a micromethod for the assay of alanine: glyoxylate aminotransferase. Implications for the prenatal diagnosis of type I hyperoxaluria by fetal liver biopsy
J R Toone, D A Applegarth
Perspectives in Pediatric Pathology
|
January 1, 1993
Pathology of peroxisomal disorders
J E Dimmick, D A Applegarth
Journal of Inherited Metabolic Disease
|
July 27, 2004
Glycine encephalopathy (nonketotic hyperglycinaemia) : review and update
D A Applegarth, J R Toone
Annals of the New York Academy of Sciences
|
January 1, 1983
Characterization of alpha 2-macroglobulin in cystic fibrosis
M A Bridges, D A Applegarth
Carbohydrate Research
|
July 1, 1986
Diagnosis of mucopolysaccharidoses using 1H-n.m.r. spectroscopy of glycosaminoglycans
A V Savage, D A Applegarth
Medical Hypotheses
|
June 1, 1983
Is cystic fibrosis a disease confined to epithelial cells?
D A Applegarth, M A Bridges
Page
of 13