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Pediatric Research
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September 1, 1979
gamma-Glutamyl transferase: studies of normal and cystinotic human leukocytes, rabbit neutrophiles, and rat liver
A D Patrick, R D Berlin, J D Schulman
Archives of Disease in Childhood
|
June 1, 1972
Galactocerebrosidase deficiency in globoid cell leucodystrophy of late onset
E Young, J Wilson, A D Patrick, et al.
Developmental Neuroscience
|
January 1, 1991
Recent biochemical and genetic advances in our understanding of Batten's disease (ceroid-lipofuscinosis)
N A Hall, B D Lake, A D Patrick
Journal of Medical Genetics
|
February 1, 1976
Prenatal diagnosis of Wolman's disease
A D Patrick, P Willcox, R Stephens, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1980
Glutathionuria: gamma-glutamyl transpeptidase deficiency
E C Wright, J Stern, R Ersser, et al.
Journal of Medical Genetics
|
September 1, 1975
Variability of acid hydrolase activities in cultured skin fibroblasts and amniotic fluid cells
E Young, P Willcox, A E Whitfield, et al.
Prenatal Diagnosis
|
May 1, 1988
Multiple sulphatase deficiency: prenatal diagnosis using chorionic villi
A D Patrick, E Young, C Ellis, et al.
Lancet (London, England)
|
July 16, 1977
Prenatal diagnosis of Niemann-Pick disease type A using chromogenic substrate
A D Patrick, E Young, W J Kleijer, et al.
The Biochemical Journal
|
April 1, 1991
Lysosomal storage of subunit c of mitochondrial ATP synthase in Batten's disease (ceroid-lipofuscinosis)
N A Hall, B D Lake, N N Dewji, et al.
The Proceedings of the Nutrition Society
|
December 1, 1979
Fructose I,6 diphosphatase deficiency
M J Tarlow, A D Patrick, D R Carlton, et al.
Page
of 6
Search research articles
Search
Showing results (21-30 of 53) with videos related to
Sort By:
Page
of 6
Pediatric Research
|
September 1, 1979
gamma-Glutamyl transferase: studies of normal and cystinotic human leukocytes, rabbit neutrophiles, and rat liver
A D Patrick, R D Berlin, J D Schulman
Archives of Disease in Childhood
|
June 1, 1972
Galactocerebrosidase deficiency in globoid cell leucodystrophy of late onset
E Young, J Wilson, A D Patrick, et al.
Developmental Neuroscience
|
January 1, 1991
Recent biochemical and genetic advances in our understanding of Batten's disease (ceroid-lipofuscinosis)
N A Hall, B D Lake, A D Patrick
Journal of Medical Genetics
|
February 1, 1976
Prenatal diagnosis of Wolman's disease
A D Patrick, P Willcox, R Stephens, et al.
Journal of Inherited Metabolic Disease
|
January 1, 1980
Glutathionuria: gamma-glutamyl transpeptidase deficiency
E C Wright, J Stern, R Ersser, et al.
Journal of Medical Genetics
|
September 1, 1975
Variability of acid hydrolase activities in cultured skin fibroblasts and amniotic fluid cells
E Young, P Willcox, A E Whitfield, et al.
Prenatal Diagnosis
|
May 1, 1988
Multiple sulphatase deficiency: prenatal diagnosis using chorionic villi
A D Patrick, E Young, C Ellis, et al.
Lancet (London, England)
|
July 16, 1977
Prenatal diagnosis of Niemann-Pick disease type A using chromogenic substrate
A D Patrick, E Young, W J Kleijer, et al.
The Biochemical Journal
|
April 1, 1991
Lysosomal storage of subunit c of mitochondrial ATP synthase in Batten's disease (ceroid-lipofuscinosis)
N A Hall, B D Lake, N N Dewji, et al.
The Proceedings of the Nutrition Society
|
December 1, 1979
Fructose I,6 diphosphatase deficiency
M J Tarlow, A D Patrick, D R Carlton, et al.
Page
of 6