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A D Patrick

Showing results (21-30 of 53) with videos related to

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Pediatric Research|September 1, 1979
gamma-Glutamyl transferase: studies of normal and cystinotic human leukocytes, rabbit neutrophiles, and rat liverA D Patrick, R D Berlin, J D Schulman
Archives of Disease in Childhood|June 1, 1972
Galactocerebrosidase deficiency in globoid cell leucodystrophy of late onsetE 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 diseaseA D Patrick, P Willcox, R Stephens, et al.
Journal of Inherited Metabolic Disease|January 1, 1980
Glutathionuria: gamma-glutamyl transpeptidase deficiencyE 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 cellsE Young, P Willcox, A E Whitfield, et al.
Prenatal Diagnosis|May 1, 1988
Multiple sulphatase deficiency: prenatal diagnosis using chorionic villiA D Patrick, E Young, C Ellis, et al.
Lancet (London, England)|July 16, 1977
Prenatal diagnosis of Niemann-Pick disease type A using chromogenic substrateA 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 deficiencyM J Tarlow, A D Patrick, D R Carlton, et al.
Pageof 6

Showing results (21-30 of 53) with videos related to

Sort By:
Pageof 6
Pediatric Research|September 1, 1979
gamma-Glutamyl transferase: studies of normal and cystinotic human leukocytes, rabbit neutrophiles, and rat liverA D Patrick, R D Berlin, J D Schulman
Archives of Disease in Childhood|June 1, 1972
Galactocerebrosidase deficiency in globoid cell leucodystrophy of late onsetE 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 diseaseA D Patrick, P Willcox, R Stephens, et al.
Journal of Inherited Metabolic Disease|January 1, 1980
Glutathionuria: gamma-glutamyl transpeptidase deficiencyE 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 cellsE Young, P Willcox, A E Whitfield, et al.
Prenatal Diagnosis|May 1, 1988
Multiple sulphatase deficiency: prenatal diagnosis using chorionic villiA D Patrick, E Young, C Ellis, et al.
Lancet (London, England)|July 16, 1977
Prenatal diagnosis of Niemann-Pick disease type A using chromogenic substrateA 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 deficiencyM J Tarlow, A D Patrick, D R Carlton, et al.
Pageof 6